Operation Rescue
Essential Solutions For Immunity From The Silent War
Compiled And Written, June 1997,
BY ANANDA
We all shudder when we again remind ourselves of the gas chambers used during world war 2. Since 1954, however, a new form of warfare was implemented on the global populace - a quite war. The testimony of former military personnel, doctors, bankers, and court released documents, define and demonstrate, overwhelmingly the intentional existence of this silent war, which utilises quite weapons, such as economic tools, biological additives, and cancer forming drugs etc. Overpopulation management, is the excuse, at the forefront, for this gradual attack on the human populces health, and mind. It is not in the scope of this small book to cover the detailed documentation, here (see my book Sovereignty: The Emergency For Independence From The Europian Slave Machine, for documentation, 1993).
With the deliberate suppression of the various cancer cures and causes by the medical CORPORATE establishment when we are now in a global cancer crissis, requires the absolute alertness of ALL who care to survive into the next century and into the next years.
With 1 out 1 persons, in the US, in their lifetimes coming down with one form of cancer or another, and this unbelievably is increasing to with an accelleration of more than one cancer per person, appearing in one lifetime. People, due to lack of inquisiteveness, and lack of reduntent energy, due to extra survivel stress in economic maintainence, are willing to line up to the modern gas chambres, known as Chemo Therapy. Here the nuclear waste, which usually costs billions, each year for the energy corporations to dispose off, is "usefully" dispossed of with a profit, from the sick, and which often disposes of the individual (especially, if they have not negotiated radioactive dosing with their doctors).
In this booklet we then compile, the solutions all around, which are not new, but which have been there all the time, and will be a requirement for all. As we are to help our friends and surrounding sincere fellow human beings, of all backgrounds, inthe balance of the rainbow races, that humanity is a remenent off.
Vitamin C, a rainbow of beauty at the crystal microscopic perspective.
EMERGENCY EMERGED FROM THE MEDICAL CORPORATE STATE
The Orthodox Cancer Cure Hoax
"Everyone should know that most cancer research is largely a fraud
and that the major cancer research organisations are derelict in their
duties to the people who support them."
- Linus Pauling PhD (Two-time Nobel Prize winner).
In the United Kingdom alone, the Cancer Research Fund-Raising Syndicate are now
clawing in over £100 million per year. An army of commission-paid agents, old
ladies with their life savings, school children, posers walking in the Alps with
elephants, marathon runners, tin wavers and unpaid volunteers, have all helped to
create by far the most successful fraud in history.
"Economics and politics simply intertwine in shaping conventional medicine's
approach to cancer. Very simply put, treating disease is enormously profitable,
preventing disease is not."
-British Cancer Control Society.
Nearly one in two of the population have, or will develop, cancer. The vast majority
will choose the drug/radiation/surgery package produced by the vivisection
laboratories, and over half will be dead within two years. According to America's
leading cancer statistician, Professor Hardin B Jones, the orthodox onslaught kills the
patient up to four times faster than the disease does.
By all pointers - incidence, severity and death-rate, the disease has long been out of
control. The causes of cancer are too numerous to list fully, suffice to say that certain
sections of society have been allowed a free hand to do as they wish with our food,
drink, medicine and environment. The petrochemical industry and, in particular, its
pharmaceutical wing, the general practitioner, food processor, cigarette
manufacturer, farmer and radiologist, can all stake their claim as cancer producers.
An endless saturation of the environment with synthetic poisons; a million
prescriptions for petro-derivative drugs, per day, from UK doctors; vaccination;
fluoride waste dumping in the water supply; cigarettes; X-radiation used as though it
were sunshine; and poisoned, adulterated food, have all helped to push cancer
beyond epidemic levels, and yet the attitude of the public is to look the other way and
hope the thing disappears.
The five year survival rates for the major cancers are:
Stomach - 5%
Trachea, bronchus and lung - 5%
Breast - 50%
Oesophagus - 5%
Large intestine - 22%
Pancreas - 4%
Liver - 2%
The definition of cure in cancer is the restoration of health to the cancer patient; the
restoration of the immune system, and the elimination of cancer through this
system. Detecting cancer early enough, attacking the tumour with the
slash/burn/poison version of cancer therapy, and then pronouncing "cured" after
the five year survival period has elapsed, has, of course, nothing remotely to do with
the successful treatment of the disease.
Patients who die from the effects of chemo of radio "therapy" after more than five
years have passed are counted as cured. Being dead or dying does not exclude one
from the figures of the cancer industry's creative statisticians. Claims, by the
fund-raisers and their media-lackeys, of "One third of cases can now be cured" and
"80,000 cured each year"' , may have pushed contributions past the golden £100
million a year mark, but these have only year helped to ensure that the cancer
holocaust continues to worsen.
The only "breakthroughs" by the Cancer Business have been financial. Agencies vie
with each other to relieve the public of their cash in order to fund an endless stream
of totally fraudulent research projects, and keep an army of vivisectors, animal
breeders, and administrators, in cigars and brandy and yachts and aeroplanes.
The cancer industry is sustained by a policy of deliberately facing in the wrong
direction, as was accurately summed up by the American newsmen, Robert Houston
and Gary Null:
"A solution to cancer would mean the termination of research
programs, the obsolescence of skills, the end of dreams of personal
glory, triumph over cancer would dry up contributions to
self-perpetuating charities....It would mortally threaten the present
clinical establishments by rendering obsolete the expensive surgical,
radiological and chemotherapeutic treatments in which so much
money, training and equipment is invested....The new therapy must
be disbelieved, denied, discouraged and disallowed at all costs,
regardless of actual testing results, and preferably without any testing
at all."
The multitude of highly paid vivisectors, animal breeders, petrochemical drug
interests, salesmen, prescribers, surgeons, radiation machine makers and operatives,
equipment makers and the rest, aided and abetted by agents in government, health
departments and the mass media, suppress or attempt to discredit all information on
the safe, effective, rational approach to the disease.
Every couple of months the media agents announce a cancer research breakthrough,
with a particularly good fund-raiser being to parade a "cured" child on the television
screen. Ignoring mischievous cancer statisticians: " I wouldn't be surprised if they are
curing a lot of leukaemia that never existed", the lengthening of survival times
("cures") is down to the fact that less children are being killed within weeks or days
through the effects of lethal, class six, super poisonous "chemotherapy". And whilst
any lessening of the petrochemical drug lunacy is, of course, to be welcomed, the
notion that these cases are steps on the way to the "conquest of cancer" is too bizarre
to warrant intelligent discussion.
Cancer is, basically, a nutritional/environmental disease - it has never been
incurable, nor is it anything to do with bad luck. The medical orthodoxy resisted
vitamin C as a cure for scurvy for over 200 years; the British Navy, alone, lost over a
million men before the academic blockheads could be persuaded to give up their
search for mystery "germs" and wonder cures from the chemical industry and turn
towards the "witch-doctor cures of ignorant savages." All over the world countless
people have been restored to health using naturopathic and other therapies, yet they
have been ruthlessly suppressed in order to protect the vested interests of the cancer
industry.
"The use of animals in cancer research has been attacked as
unnecessary cruelty to animals, and defended as absolutely essential
for research progress....From a scientific standpoint, what is pertinent
is that what are called 'animal model systems' in cancer research have
been a total failure....The moral is that animal model systems not only
kill animals, they also kill humans. There is no good factual evidence
to show that the use of animals in cancer research has led to the
prevention or cure of a single human cancer."
-Dr Irwin D Bross PhD
For over two hundred years the inmates of the vivisection laboratories have
tormented to death hundreds of millions of animals. Over 800 ways of inducing
tumours in animals have been found, not one of which is remotely related to a
cancer which has developed spontaneously in a human.
Tumours are implanted under the skin, and then observed as the growth takes over
the body, animals are radiated, limbs become gangrenous and fall off, force feeding
large amounts of toxic substances causes vomiting and fits - until death intervenes.
"The ably exploited fear of this dread disease, caused mainly by the
products issuing from chemical and industrial laboratories, has
become an inexhaustible source of income for the researchers, for the
pharmaceutical industry, and the medical establishment. In the course
of our century, so-called cancer research and cancer therapy have
become a source of solid gold without precedent."
-medical historian, Hans Ruesch (from his book, Naked Empress)
Animal-based "cancer research" fund-raisers include: The Imperial Cancer Research
Fund, The Cancer Research Campaign, The Leukaemia Research Fund, Tenovus
Cancer Research, The Yorkshire Cancer Research Campaign, Cancer and Leukaemia
in Childhood Trust, Institute of Cancer Research, World Cancer Research Fund.
If you support animal-based "cancer research" you are supporting the biggest fraud,
medical or otherwise, in history, and the cruel and senseless torture and killing of
your fellow beings; both human and animal.
You can help to bring vivisection's end one step nearer by joining the BAVA.
Members receive the BAVA journal, the New Abolitionist, four times per year. The
36 page booklet, Cancer Epidemic - A Question of Survival, by naturopath Patrick
Rattigan, is available from the BAVA, price £2.00 inc p&p.
British Anti-Vivisection Association, PO Box 82, Kingswood, Bristol, BS15 1YF
"While the people are being lied to...and drugged and inoculated for the
benefit of the huge chemical combines who own the Press and Radio, it is
obviously necessary to hit back with the truth."
-Lionel Dole, The Blood Poisoners, 1965.
"Everyone has the right to freedom of opinion and expression; this right
includes freedom to hold opinions without interference and to seek,
receive and impart information and ideas through any media and
regardless of frontiers".
-Article 19, Universal Declaration of Human Rights.
The Ultimate Cancer Conspiracy:
Vitamin B17 and Laetrile
by Joe Vialls
During 1950 after many years of research, a dedicated biochemist
by the name of Dr. Ernst T. Krebs, Jr., isolated a new vitamin
that he numbered B17 and called 'Laetrile'. As the years rolled
by, thousands became convinced that Krebs had finally found the
complete control for all cancers, a conviction that even more
people share today. Back in 1950 Ernst Krebs could have had
little idea of the hornet's nest he was about to stir up. The
pharmaceutical multinationals, unable to patent or claim
exclusive rights to the vitamin, launched a propaganda attack of
unprecedented viciousness against B17, despite the fact that hard
proof of its efficiency in controlling all forms of cancer
surrounds us in overwhelming abundance.
In his brilliantly researched 1974 book World Without Cancer,
researcher and author G. Edward Griffin explains the
trophoblastic theory of cancer proposed by Professor John Beard
of Edinburgh University, which states that certain pre-embryonic
cells in pregnancy differ in no discernible way from
highly-malignant cancer cells. Edwards Griffin continues:
"The trophoblast in pregnancy indeed does exhibit all the
classical characteristics of cancer. It spreads and multiplies
rapidly as it eats its way into the uterus wall preparing a place
where the embryo can attach itself for maternal protection and
nourishment."
The trophoblast is formed in a chain reaction by another cell
that Griffin simplifies down to the 'total life' cell, which has
the total capacity to evolve into any organ or tissue, or a
complete embryo. When the total life cell is triggered into
producing trophoblast by contact with the hormone estrogen,
present in both males and females, one of two different things
happens. In the case of pregnancy the result is conventional
development of a placenta and umbilical cord. If the trophoblast
is triggered as part of a healing process however, the result is
cancer or, as Edward Griffin cautions: "To be more accurate, we
should say it is cancer if the healing process is not terminated
upon completion of its task."
Stunning proof of this claim is readily available. All
trophoblast cells produce a unique hormone called the chorionic
gonadotrophic (CGH) which is easily detected in urine. Thus if a
person is either pregnant or has cancer, a simple CGH pregnancy
test should confirm either or both. It does, with an accuracy of
better than 92% in all cases. If the urine sample shows positive
it means either normal pregnancy or abnormal malignant cancer.
Griffin notes: "If the patient is a woman, she either is pregnant
or has cancer. If he is a man, cancer can be the only cause." So
why all of the expensive, dangerous biopsies carried to 'detect'
cancerous growths? One can only assume that medicare pays doctors
a larger fee for biopsies than pregnancy tests.
So how is it that any of us gets cancer in the first place. Is it
exposure to cigarette smoking, intense sunlight or perhaps the
effect of toxic food additives? Dr. Krebs thinks not. All of the
hard biochemical evidence points to the fact that cancer is a
simple deficiency disease of vitamin B17, long ago removed from
our highly refined, western diets. Krebs postulates that the
so-called 'carcinogens' are merely stress triggers that finally
expose the B17 deficiency with devastating effect.
The proof Krebs has presented over the years to support his claim
is impressive. Centuries ago we used to eat millet bread, rich in
B17, but now we chew our way through wheat which has none at all.
For generations our grandmothers used to carefully crush the
seeds of plums, greengages, cherries, apples, apricots and other
members of the botanical family Rosaceae, and diligently mix them
with their home made jams and preserves. Grandma probably didn't
know why she was doing it, but the seeds of all these fruits are
the most potent source of B17 in the world. In the tropics, large
quantities of B17 are found in cassava, also known as tapioca.
When did you last eat some?
Independent research has also proved that a Himalayan tribe known
as the 'Hunza' never contract cancer of any kind so long as they
stick to their native diet which is exceptionally high in both
apricots and millet. However, once exposed to western diets they
become as vulnerable as the rest of us.
The implications of these findings are staggering of course. If
we managed to control Scurvy (vitamin C deficiency) centuries
ago, how is it we cannot do the same for cancer today? The fact
of the matter is that we could if our respective governments
would allow it. Unfortunately most governments have buckled under
the pressure exerted by the pharmaceutical multinationals, the
American Food & Drug Administration, and the American Medical
Association. All three have mounted highly successful 'scare'
campaigns based on the fact that vitamin B17 contains quantities
of 'deadly' cyanide; conveniently forgetting that vitamin B12
also contains significant quantities of cyanide, and has long
been available in health food shops world-wide.
Dr. Kreb's B17 Laetrile was derived from apricot seeds and then
synthesized into crystalline form using his own unique process.
Suddenly, the American FDA bombarded the media with a story about
an unfortunate couple who had poisoned themselves by eating raw
apricot seeds in San Francisco. The story made headline news
across the U.S.A. although several suspicious journalists never
managed to establish the identity of the unfortunate couple,
despite many determined attempts. But the multinational
pharmaceutical/FDA boot had been put in with a vengeance. From
that point onwards eating apricot seeds or B17 Laetrile became
synonymous with committing suicide...
Back in the fifties Dr. Ernst Krebs proved beyond doubt that B17
was completely harmless to humans in the most convincing way
possible. After testing the vitamin on animals, he filled a large
hypodermic with a mega-dose which he then injected into his own
arm! Drastic perhaps, but the adventurous Dr. Krebs is still
alive and well today.
The vitamin is harmless to healthy tissue for a very simple
reason: Each molecule of B17 contains one unit of cyanide, one
unit of benzaldehyde and two of glucose (sugar) tightly locked
together. In order for the cyanide to become dangerous it is
first necessary to 'unlock' the molecule to release it, a trick
that can only be performed by an enzyme called beta-glucosidase.
This enzyme is present all over the body in minute quantities,
but in huge quantities (up to 100 times as high) at cancerous
tumour sites.
Thus the cyanide is released only at the cancer site with drastic
results, which become utterly devastating to the cancer cells
because the benzaldehyde unit also unlocks at the same time.
Benzaldehyde is a deadly poison in its own right, which then acts
synergistically with the cyanide to produce a poison 100 times
more deadly than either in isolation. The combined effect on the
cancer cells is best left to the imagination.
But what about danger to the rest of the body's cells? Another
enzyme, rhodanese, always present in larger quantities than the
unlocking enzyme beta-glucosidase in healthy tissues has the easy
ability to completely break down both cyanide and benzaldehyde
into beneficial body products. Predictably perhaps, malignant
cancer cells contain no rhodanese at all, leaving them completely
at the mercy of the cyanide and benzaldehyde.
Any physician reading this article will probably be shaking with
self-righteous indignation at this stage, muttering to himself:
'Yes, but where is the PROOF???'
Right here! Most people have heard of 'spontaneous remission',
where the cancer simply goes away, hopefully never to reappear.
Spontaneous remissions are exceedingly rare and vary from one
form of cancer to another. One virulent variety known as
testicular chorionepithelioma has never been known to produce a
single spontaneous remission. Perhaps for that precise reason,
Dr. Krebs singled it out for special attention when proving the
effectiveness of B17 Laetrile in providing total control for
cancers. As Edward Griffin recounts:
"In a banquet speech in San Francisco on November 19, 1967, Dr.
Ernst T. Krebs, Jr., briefly reviewed six such cases. Then he
added:
Now there is an advantage in not having had prior radiation,
because if you have not received prior radiation that has failed,
then you cannot enjoy the imagined benefits of the delayed
effects of prior radiation. So this boy falls into the category
of the "spontaneous regression... "
And when we look at this scientifically, we know that spontaneous
regression occurs in fewer than one in 150,000 cases of cancer.
The statistical possibility of spontaneous regression accounting
for the complete resolution of successive cases of testicular
chorionepithelioma is far greater than the statistical
improbability of the sun not rising tomorrow morning."
Wisely perhaps, Griffin notes that because of the adverse
publicity against B17 Laetrile, and because of the difficulties
in obtaining the 'banned' substance, most cancer sufferers turn
to the vitamin as a last resort, long after they have been burned
by radiation therapy, and/or poisoned by chemotherapy. He points
out that once the body organs have been savagely damaged in this
way, there is little if any chance of B17 Laetrile being able to
effect a cure. The body is simply too far gone.
When World Without Cancer was written back in 1974, B17 Laetrile
was freely available in Australia. It is not now. A recent check
with the Australian Cancer Foundation and health authorities
revealed that nowadays Canberra considers each individual case on
its merits, then decides whether the patient should be allowed to
import sufficient of the material for his or her own personal
use. If he or she manages to jump that hurdle, it is then his or
her own responsibility to find a doctor prepared to inject it.
Seemingly the multinational pharmaceutical lobbyists managed to
get to our politicians before Dr. Krebs could get to the
Australian public. Radiation and chemotherapy are highly
profitable, and oncologists have to make a decent living...
Only a few months ago Australian nationwide television carried
the delightful information that two out of every three
Australians can expect to suffer skin cancer at least once during
their lifetimes. On the massive evidence provided by Dr. Ernst
Krebs, Jr. and G. Edward Griffin, that figure could be crushed to
a tiny percentage of the anticipated numbers if Australians were
allowed freedom of choice where B17 Laetrile is concerned. It is
time for Australians to take a stand on this lethal issue.
Now many of the alternative cures for the silent WW3 generated diseases, are being placed under the labels of drugs. Such ancient traditional remedies such as herbs, and in our day vitamins, are already being placed under the drug catagory. Injectable vitamin C, beyond one gram, even in homeopathic form (that is no physical molecule) is illegal and is considered a drug, today in Italy. Hard to believe? Thought you knew you could trust the good old corporations? Perhaps you never had a chance to think. Here is food for thought of prime examples:
Attack On Essential NutrientS By The Health Protection Branch (HPB):
The Who Codex Connection
By Saul Kent, President of The Life Extension Foundation
Kava kava, a rather innocuous anti-stress herbal remedy in use
for several decades in Canada without incident, was recently
prohibited (November, 1996) from sale by the HPB (Health
Protection Branch).
DHEA, a very popular health food store supplement extracted from
wild yam was also the target of the HPB supplement police
(November 13, 1996). Several months previous to this, melatonin
was the HPB victim. All this has gone on despite zero deaths or
even any serious adverse reactions taking place as a result of
Kava kava, DHEA, or melatonin.
Meanwhile, the death toll continues to rise as a direct result of
"safe and effective" prescription and over the counter drugs like
non-steroidal anti-inflammatories (NSAIDS), cough and cold
remedies containing pseudephedrine, and broad spectrum
antibiotics.
Drugs like the NSAIDS which can cause gastrointestinal hemorrhage
and which were previously available on prescription only are now
easily obtainable over the counter. Narcotics like codeine (in
ASA + caffeine + codeine pain tablets) can also be obtained
without any difficulty just by asking the pharmacist.
In the USA, this is not possible and every narcotic requires a
written doctor's prescription. Acid suppressing drugs which can
also cause impotence and candida overgrowth were previously only
available by prescription. The public is now welcome to
experience these side effects via the over the counter route. As
more and more potentially dangerous drugs are accessible to the
public, less and less natural health care products remain
available.
Why is this Happening?
Some of you by now must be wondering if there is any sense that
can be made out of this recent illogical behaviour of the HPB. An
understanding of the Codex connection will suddenly make things
quite clear. Codex is officially known as the United
Nations/World Health Organization (WHO) Codex Alimentarious
(Nutrition Code) Commission. It meets every 2 years, usually in
Rome, and is considered by many legal experts to be the greatest
threat to health freedom in the world today. You will not find
much in the mainstream media on Codex, a secretive group that
would prefer to remain anonymous. Most of what follows is taken
from various web sites on the Internet.
Codex is empowered by governments to set standards of operation
for the health industry. Over 90% of the international
organizations "allowed" to send delegates to the meetings
represent giant multinational pharmaceutical corporations. The
only "consumer" organization is the "International Organization
of Consumer Unions". Neither the natural health care industry nor
the general public have any representation at Codex meetings.
In October, 1996, Codex met in Bonn, Germany, to make radical
changes in the rules governing dietary supplements for member
nations. The proposals of greatest concern were those made by the
German delegation ("Proposed Draft Guidelines for Dietary
Supplements"), which is being sponsored by Hoechst, Bayer, and
BASF.
These are the three drug companies formed when the Nuremberg War
Trials disbanded IG Farben, manufacturer of the poison gas used
in Nazi concentration camps. Although IG Farben may have been
disbanded, none of its directors were ever penalized for their
actions during the war. They simply divided what remained from
the company and split into three separate entities.
The three Nazi-connected German drug companies have stated their
main purpose as being to "...create a set of international
standards to guide the world's growing food industry and to
protect the health of consumers." If you really believe that, I
have some ocean front property for you at half price in
Saskatoon. The drug company backed proposals call for the
following:
1. No vitamin, mineral, herb, etc., can be sold for
prophylactic (preventative) or therapeutic reasons.
2. Natural remedies can be sold as food but they must not
exceed the potency (dosage) levels set by the commission.
This means that consumer access to dietary supplements will
be limited to the RDA dosage as a maximum limit for vitamins
(vitamin C - 60 mg, vitamin E - 15 mg, etc.). Supplements
without an RDA (e.g. coenzyme Q10) would be illegal to sell
because they would all become drugs.
3. Codex regulations for dietary supplements would become
binding, eliminating the escape clause within the General
Agreement of Tariffs and Trade (GATT) that allows a nation
to set its own standards. This applies to all member
countries of the U.N. Any nation that does not accept and
apply these new standards will be heavily fined by the World
Trade Organization (WTO), creating the potential for
crippling entire sectors of the nation's economy.
4. All new supplements would be banned unless they went through
the Codex approval process.
Five steps have already been taken in the Codex process over the
past few years. Remember Canadian Bill C-7 which was passed
eventually in Canada as C-8? The similarity of the process, the
secrecy, and the wording between the Codex proposals and the
Canadian laws is uncanny.
Voting in favour of adopting the German proposal has been
overwhelming (16 for and 2 against in the most recent vote). The
Codex process is now at "Step Five" - formalization and debate
concerning the specific features. In two years, Codex could jump
from step 5 to step 8 to finalize these restrictions. The Codex
proposals already exist as law in Norway and Germany, where the
entire health food industry has literally been taken over by the
drug companies. In these countries, vitamin C above 200 mg is
illegal as is vitamin E above 45 IU, Vitamin B1 over 2.4 mg and
so on. Shering-Plough, the Norway pharmaceutical giant, now
controls an echinacea tincture which is being sold there as an
OTC drug at grossly inflated prices. The same is true of ginkgo
and many other herbs. Only one government controlled pharmacy has
the right to import supplements as medicines which they can sell
to health food stores, convenience stores, or pharmacies.
According to Dr. Matthias Rath, researcher and author who
discovered a correlation between vitamin C deficiency and heart
disease, the three Nazi-linked drug companies pushing so hard for
the German proposal - Hoechst, Bayer and BASF - are also
manufacturers of heart drugs. Obviously, with the vitamin
competition gone, nothing will stop their profits.
The Spies Among Us
"HPB is interested in receiving any information for
purposes of following up on any firms that continue to
sell or distribute DHEA in violation of the Food & Drug
Act and Regulations".
-D.W. Shelly, Chief, Drug & Environmental Health
Inspection Division.
HPB Chief Shelly is asking you to report any of your colleagues
obstinate enough to sell DHEA. This sort of unpaid spy work was a
favorite tactic of totalitarian regimes like the Nazis before WW
II and the Communists before the Berlin wall came down. How
economical!!
About a month ago, I was asked by Alive magazine to write an
article about Codex. At the time, Rhody Lake, editor of Alive was
told by representatives of both the HPB and the CNHPA (Canadian
Natural Health Products Association) that Codex was not a threat
to public access to natural health care products.
The facts do not support this belief. While the CNHPA says that
it works on behalf of the natural products industry, it appears
to support the HPB's removal of products from health food store
shelves.
For example, in an Oct. 9, 1996 press release, the CNHPA said,
"In light of the recent crackdown by Health Canada on the sale of
the hormone, melatonin, in health food stores, the Association
recommends that stores cease the sale of DHEA immediately."
Is the CNHPA in collusion with the HPB? Their actions seem to
indicate that. So do their words: "...the Supplement
Manufacturers' Committee is in almost daily negotiations with
Health Canada in the area of regulatory affairs and working, with
some success, toward special recognition..." What success? The
reality is that these "daily negotiations" have been a dismal
failure, making public access to health products worse than at
any time in the history of Canada. According to John C. Hammell,
legal advocate for the U.S. based Life Extension Foundation, the
Nazi-linked proposals have the backing of Canadian and French
Codex commission representatives.
In June of 1996, the Codex Executive committee created an "expert
panel" on herbs which was expected generate a "negative list" to
prevent public access to certain herbs internationally. The
formation of this "expert panel" was advocated by none other than
the Canadian and Austrailian representatives.
During the October 1996 Bonn, Germany Codex discussions only the
United States and the United Kingdom voted against such a list
and against limiting other supplements to a maximum international
RDA.
Why then are the HPB and the CNHPA denying that the Codex
proposals will have any impact on the availability of nutritional
supplements in Canada? Either spokespersons for these two groups
are ignorant about the proposals or they are lying to the public
in order to protect drug company interests. After all, several
voting member companies of the CNHPA are owned by or are
subsidiaries of major drug manufacturers or pharmaceutical
chains.
Neither group can be trusted to give the public straight answers
about the Codex scam when, in fact, they are a part of the group
trying to outlaw melatonin, DHEA, Kava kava, amino acids, and
several dozen herbs. Some members of the CNHPA are in a clear
conflict of interest since they stand to gain financially when
the supplement prices are boosted through the roof. It should be
noted that the CNHPA was formerly called the Canadian Health Food
Association. Did changing its name have anything to do with drug
company wishes? Further evidence of Canadian involvement with
Codex is the HPB position on what is or is not a food or a drug.
For example, garlic, ginger, licorice, and peppermint are
considered to be foods when sold as spices. If a grocery store
manager makes claims for their therapeutic effects, they then
become drugs via a hocus pocus mechanism which still remains to
be defined. Perhaps one of the drug owned supplement firms that
are members of the CNHPA can explain how this occurs.
If Codex and the HPB have their way, your favourite supplements
will be replaced by expensive, patented, over-the-counter or
prescription drugs. Just look what has already happened to amino
acids like tryptophan. Once available for under $20 for a bottle
of 100 tablets of 500 mg at your local health food store, the
same tablet is now only available by prescription at a cost of
over $120 by prescription.
For more information, documentation, and a plan of action that
you can take to fight the Government(s)/Codex Connection,
contact:
Canada:
Write or phone your federal MPs and make them aware of
the situation and how you feel about it. If you you do
not know who your federal representative is, phone
1-800-282-8060 (in Manitoba), or 1-800-667-3355
(everywhere else in Canada). No postage is required for
letters sent to MPs while parliament is in session.
Also write to the Honourable David Dingwall, Minister
of Health, Health Canada, Brooke Claxton Building, Room
091-6A, Tunney's Pasture, Ottawa, ON K1A 0K9.
Canadian Natural Health Products Association
Suite 205 - 550 Alden Rd, Markham, ON L3R 6A8
Phone: (800) 661-4510, (905) 479-6939
fax: (905) 479-1516
Start a chain letter, creating a cover letter stating
"Make ten copies of this cover page and newsletter,
send it to 10 people locally or around the world.
Continuing this chain letter will bring you more than
just luck, it will help save our God given right to
health freedom and access to natural and safe
supplements World wide."
U.S.A.
John Hammell
Legislative Advocate
The Life Extension Foundation
2411 Monroe St. #2, Hollywood, FL 33020 USA
Phone: (800) 333-2553, (954) 929-2905
fax: (954) 929-0507
e-mail: John@lef.org
Everyone:
Phone, fax, E-mail, write as many natural health
supplement manufacturer/distributors and make them
aware of your views and ask them to also represent you.
Look under health foods or vitamins in your local
yellow pages and/or go to a library to find other phone
books to locate out of town companies or ask your local
health food store to supply you with addresses.
Boycott all Hoechst, Bayer, and BASF products. Write to
them and tell them your views.
Please help protect your right of access to natural
products. The entire planet is counting on it!
Here are less serious versions being implemented of the same above procedures, but now in England:
UK THREAT TO HERBAL MEDICINES
The Department of Health (DoH) is planning
to implement a European Directive
which is likely to lead to the removal
of many herbal products from shops, cut
off supplies to practising herbalists
and put herbal companies out of
business. This change is being rushed
through by the UK government before
the end of 1995.
EUROPEAN DIRECTIVE
Officials from the DoH met with members
of the herb industry on 21 September 1994
to say that their lawyers had just
discovered that Section 12 of the 1968
Medicines Act was out of step with a
European Directive (65/65) due to come
into force at the beginning of 1995. The
DoH would be seeking immediate repeal of
Section 12 which gives herbal practitioners
and companies the right to supply herbal
medicines without a medicines licence. This
legislation was passed after considerable
public and parliamentary debate and reflects
rights of practice going back to the
Herbalists Charter of 1543.
DESTRUCTION OF HERB INDUSTRY
Dried or fresh herbs would still be available
but processed herbs including tinctures, pills,
concentrates, capsules and ointments would
all require a licence. Since a medicines'
licence costs 84,000 alone for administrative
fees and as plants cannot be patented there is
no chance of herbal suppliers recouping their
costs. Food law does not apply as European
law defines a medicine as anything which can
be demonstrated to have a medicinal or
physiological effect. The effect of Directive
65/65 will be the destruction of the herb
industry and hence the rights of people to
have access to traditional and natural
medicines.
CHANGES TO BE RUSHED THROUGH
Other European governments are not
implementing this Directive and the German
government has voted for a 10 year delay
before implementation. The US government
has just recently reversed legislation so
that herbs and vitamins can be sold freely.
In Australia there is a Traditional Medicines
Evaluation Committee with representatives
of practitioners, suppliers and scientists
which applies different criteria for
traditional herbal remedies to those used
for conventional drugs. Until last month
herbalists in the UK have been consistently
assured that their rights under the
Medicines Act would be unaffected yet the
DoH is now rushing through these changes.
LICENSING OF HERBALISTS
A Herbal Practitioners Alliance has been
formed in the UK with membership of the
National Institute of Medical Herbalists
and other practitioner bodies. The HPA
has already started to meet with the DoH
to find ways of formalising the high
standards of training and practice which
have been established for herbalists here.
Such responsible initiatives towards
licensing of herbalists make no sense if
the DoH is to encourage the decimation
of herbal practice and the herb industry.
WHAT YOU CAN DO
Meanwhile there is lots to be done to
stop the threat to herbal medicines.
Please pass on this information to your
friends and relatives - anyone who uses
herbal remedies or might want to at a
future date.
Can you write urgently to your MP and
MEP and make the points above and ask
- why the rush?
- what about consultation?
- what about patients rights to choose
natural medicines?
Thank you for your help
Anne Stobart, NIMH
Consultant medical herbalist
21 Dean Street, Crediton, Devon EX17 3EN
The case is becoming even harder now. Many supplements that have been standard for our health are now classified illegal, and what will happen to you if you have them, is not pleasent, as you will see, from those who have been raided and held at gun point for 12 hours, including the elderly.
SUPPLEMENTS AT RISK FROM THE FDA
The FDA's battle against natural and alternative health care could produce the following casualties:
All Free Form Amino Acids:
These essential nutrients would be eliminated from the market to
be studied for "safety" and then handed over to medical
pharmaceutical corporations to be made into highly expensive
prescription-only drugs. Amino acids have been safely used by
consumers for over 20 years. The ban would include N-acetyl
cysteine (NAC) which is very promising in treatment for HIV and
has been used successfully to treat bronchitis.
Selected Herbs:
Many immune-boosting herbs and treatments for HIV and cancer may
be eliminated. All medicinal herbs are in jeopardy because the FDA
has never granted "generally recognized as safe" (GRAS) status to
any herbs used as medicines. Garlic, for example, is recognized as
safe when it is in food or as a flavor enhancer. But garlic as a
food supplement in a capsule or extract is not GRAS and is
therefore subject to FDA restrictions. Again, ALL medicinal herbs
are not recognized GRAS. The FDA can remove any herb from the
market which is in any way associated with health claims.
All Medicinal Claims For Herbs:
Since medicinal herbs cannot exist without claims, and claims put
an herb in the "unapproved drug" category, the FDA could and would
effectively *censor* much information regarding herbal treatments.
Consumers would be denied access to products and information.
Since the FDA has little respect or understanding for traditional
ethnic herbal treatment and folk remedies, the agency's judgement
with regard to the regulation of claims for products that have
been safely used for hundreds of years is suspect.
Breakthrough and "New Supplements":
As research mounts on newly emerging nutrients, natural compounds,
and herbs, promising treatments are denied to consumers because
the FDA does not understand that which it regulates. Products
which could be benefitting millions of people may become
unavailable because the FDA insists on defining these new products
as "unapproved food additives" or "unapproved drugs."
Cutting Edge Supplements in Jeopardy:
Co-enzyme Q10 All chinese herbs
Evening Primrose Oil Golden Seal Root
Black Currant Oil Selenium
Chromium
This is what we have already lost:
Chaparral Comfrey Stevia
L-Tryptophan Sassafras Pennyroyal
For more information, contact:
Citizens For Health
Natural Health Care Alliance Of San Francisco
1348 La Playa Avenue #2, San Francisco CA 94122
Telephone Michael at 415-292-4055
For those that offer viable solutions to cancer and the other multiple generated or amplified diseases due to the intensional insertion of chemicles and other deliberate factors, are discredited, and even eliminated. The Health industry is attacked and raided, and treated like criminals. The smallest victory here is soon smuged under the rug by ever more attacks and stories of failed hope alternative cases, when chemotherapy, and other medicinal drugs small percentage is never even whispered at, unless the new medicine arrives - costing lots, and bringing in reems of money. Here follows the clear evidence of A CORPORATE MEDICAL STATE, where health Professionals are raided, for the unsafety of things like blackcurrents OR VITAMIN E. Our fellow human beings, who were just trying to serve and help others, were subjected to guns, intimidated, smashed offices by the raiding troops, and loss of files. Hard to believe in this day and age, a silent war is harder to see - but these episodes are far from silent, only by manipulation of press. See for yourself.
THE FEDERAL DRUG ADMINISTRATIONS CRIMINAL RAIDS
ON THE HEALTH INDUSTRY
(A list of FDA raids From Life Extension Magazine)
...The FDA's strong arm tactics are used to intimidate and
terrorize Americans into toeing their police state party line on
healthcare and medicine. The FDA's purpose is not just to destroy
the business and lives of their targets but also to spread fear
and terror throughout the land so that others who may be tempted
to rebel against the agency will remain meek and submissive.
We urge you to let the FDA know how outraged Americans are at
their gestapo like raids. Call, write, or fax the seven FDA
officials listed at the end of this article. We've included the
FDA's Chicago office because they've been illegally seizing
products ordered by Americans from offshore companies.
When you voice your protests to these FDA officials, you can now
do more than just complain about the FDA's brutality, you can
tell them to obey the law! As discussed in the enclosed issue of
Life Extension Report, the new dietary supplement health and
education act demands that the FDA give anyone who they wish to
take enforcement action against at least 10 days notice and
opportunity to present their views, before taking action.
The FDA may be willing to ignore the constitution ....but they
may still be threatened by a law passed in 1994.
(Some of the information they printed on these raids are as
follows):
Raid: Traco Labs, Inc. - November, 1988
Address: 205 S Main St. Seymour, IL 61875
Phone: 1 (217) 687-2800 - Sid Tracy , President
Reason: FDA claimed that black currant oil was an unsafe
food additive.
Outcome: FDA seized two drums of black currant oil as well
as a large quantity of the capsulized product. On Jan. 28,
1993, the U.S. Court of Appeals ruled against FDA. The judge
said that FDA's definition of food additive is too broad
that even water added to food would be considered a food
additive.
Raid: Pets Smell Free, Inc. - Summer, 1988
Address: 350 W. 300 South, Salt Lake City, Utah 84101
Phone: 1 (801) 322-1221, Email Magnum@UTW.com - Mark Geiger
Reason: product designed to prevent pets from giving off
foul odor. (also sold for fishtanks) FDA called it an
unsafe, unapproved drug.
Outcome: Seized entire inventory and business records. PSF
won in court several times but in July, 1994 FDA won on
appeal, FDA wants PSF to sign consent decree but they have
refused.
Raid: The Life Extension Foundation - Feb 26, 1987
Address: PO box 229120, Hollywood, FL 33022
Phone: 1 (800) 333-2553 - John Hummell, Political Office
Reason: FDA alledged LEF was selling unapproved drugs
(vitamins in U.S.) and life extension drugs from overseas
companies.
Outcome :FDA seized $500,000 worth of vitamins, computers,
files, newsletters, personal belongings, phones riped out of
the walls, and terrorized empolyees. The foundations
leaders, Saul Kent and William Faloon, were indicted on 28
criminal counts (with Maximum prison time of 84 years in
November, 1991. Case is still pending.
Raid: Highland Labs - Fall, 1990
Address: Box 199 Mt. Angel, OR 97362
Phone: 1 (800) 547-0273 - Candy Scott
Reason: FDA claimed that product literature (with False
claims) was being shipped with products to customers. FDA
said these made COQ10 and GeOXY 132 unapproved drugs.
Outcome: After spending $250,000 in legal fees, defendent
was forced to, plead guilty to selling unapproved new drugs.
Six months house arrest. $5,000 fine.
Raid: Hospital Santa Monica - May 12, 1993
Address: 738 Design Ct., Chula Vista, Ca. 91909
Phone: 1 (619) 662-3010 - Kurt Donsbach
Reason: Hospital Santa Monica is an alternative cancer
hospital in Mexico that competes with mainstream hospitals
in the U.S. They were accused of distributing unapproved
drugs. More than 50 federal agents with guns drawn raided
the hospital office in San Deigo, seizing a tractor trailor
of business records, patient charts, and computers. They
also searched employees homes and seized $80,000 found in
the owners safe. Over $300,000 was taken from the bank
accounts of hospital and two vitamin companies.
Outcome: Friends kept the Hospital afloat with cash gifts.
The two vitamin companies were sold at a loss. Donsbach was
forced into bankruptcy. No charges have been filed.
Raid: Natures Way - June 30, 1992
Address: 1375 N. Mountain Springs Parkway, Springville, Utah
84663
Phone: 1 (800) 962-8873
Reason: The FDA seized a quantity of evening primrose oil,
both encapsulated and in bulk from this large manufacturer
during a routine inspection. They also seized a truckload of
primrose oil on the road. The FDA claimed it was an
unapproved food additive.
Outcome: Nature's Way filed a lawsuit to get their product
back, but was forced to remove the vitamin E from it because
the FDA asaid that Vitamin E has not been approved as a food
additive for evening primrose oil.
Raid: Family Acupuncture Clinic - Aug. 14, 1992
Address: 117 Granada, San Clememte, CA 92672
Phone: 1 (714) 361-3976 - Richard Lee, Ph.D., Director
Reason: FDA seized $15,000 worth of Hsaio Yao Tea Pills in
an attempt to strike back at acupuncturists who are taking a
lot of business away from conventional Drs. FDA ignored
California law, under which acupuncturists are licensed to
practice medicine. FDA also ignored the fact that many
insurance companies honor claims for acupuncture including
Aetna, Prudential, and Blue Cross.
Outcome: The seized herbs were shipped back to China by the
FDA after they had rotted. Dr. Lee is still in business.
Raid: Bursynski Research Clinic - Jul. 7, 1985
Address: 1200 Richmond Ave. #260 Houston, TX 77082
Phone: (713) 597-0111 - Dean Mouscher
Reason: Interstate shipping of antineoplastins (cancer
therapy) NCI, Aetna insurance and others pressured FDA into
raiding The Bursynski clinic.
Outcome: FDA seized 200,000 medical and research documents
forcing Burzynski to pay to make copies. No charges were
filed.
Raid: Solid Gold Pet Foods - Sep., 1989
Address: 1483 N. Cuyamaca, El Cajon, CA 92020
Phone: (619) 465-9507 (Sissy Harrington McGill, Owner)
Reason: FDA had been harassing McGill over labels on her
holistic pet food products. In March 1990, an FDA agent
seized products from her store without a search warrant and
shut down her store. On July 12, 1990, after being indicted,
she chose a jury trial. Upon appearing for her trial, she
was clapped into leg irons, put into a Maximum Security
Federal Prison for 179 days, and fined $10,000. While
incarcerated she suffered a near fatal stroke.
Outcome: McGill sued the Department of Justice and won a
victory on Feb. 20, 1992. She expects to file a $25,000,000
lawsuit against the FDA.
Raid: H.A. Lyons mailing Service - Oct. 16, 1990
Address: Driven out of business. Formerly in Phoenix, AZ
Reason: Mailing literature on behalf of vitamin companies
with no advance warning, 5 armed agents backed by an armed
policeman raided this home-based business run by a young
woman.
Outcome: The owner convinced the agents not to seize her
checkbook and cash. They did seize all her business records
and literature. No charges were filed.
Raid: Nutricology, Inc. - May 9, 1991
Address: 400 Preda Ave. San Leandro, CA 94577
Phone: (800) 545-9960 Stephen A. Levine, Ph.D. owner
Reason: FDA raided Nutricology, seized their bank accounts
and shut them down for 2 days, charging them with wire
fraud, mail fraud, selling unapproved drugs, unsafe food
additives, and misbranded drugs. Twelve armed agents
conducted an exhaustive search of the company's offices and
warehouse.
Outcome: On May 23, 1991 Federal Judge D. Lowell Jensen
denied the FDA's request for a Preliminary Injunction. On
Sep. 10, 1991, the FDA appealed to the 9th Circuit Court of
Appeals, but was again denied. On Sep. 23, 1993 Judge Jensen
denied the FDA's motion for summary judgement and granted
Nutricology's motion to eliminate the wire and mail fraud
charges.
Raid: Scientific Botanicals - Fall 1991
Address: 8003 Roosevelt Ave. NE 98115
Phone: (206) 527-5521
Reason: Alleged labeling violations. FDA seized herbal
extract products and literature sent to physicians. FDA
forced the company to stop using its patented trade names
lest they "mislead the consumer."
Outcome: FDA slowly released all seized products, forcing
the company to comply with all demands under threat of being
shut down. Company refuses to talk about their case for fear
of reprisal.
Raid: Thorne Research - Dec. 12, 1991
Address: 901 Triangle Dr. Sand Point, Idaho 83864
Phone: (208) 263-1337, Al Czap, Owner
Reason: FDA claimed that vitamin products sold by company
were "unapproved drugs." FDA agent and 3 U.S. Marshall's
seized the company's entire stock of $20,000 worth of
products and 11,000 pieces of literature intended for
physicians.
Outcome: Thorne initially notified District Court that it
would fight, but gave up as the expiration date on the
seized products was approaching and it became too expensive
to continue. The company no longer publishes any literature.
Raid: Tahoma Clinic, Dr. Jonathan Wright - May 6, 1992
Address: 24030 132nd Ave. S.E. Kent, WA 98042
Phone: (206) 631-9681, Harry Mills, P.R.
Reason: After L-tryptophan was banned, Dr. Jonathan Wright
continued to prescribe it. The FDA raided him and seized his
supply of tryptophan. Dr. Wright filed suit. The FDA
retaliated by storming into Wright's clinic with armed
sheriffs who terrorized employees and seized vitamins and
other natural therapies, allergy screening equipment,
computers, bank records, his mailing list, and medical
records.
Outcome: In Oct. 1992, Wright filed suit in district court
charging unlawful search and seizure and demanded his
property back. In response, the FDA convened a Federal Grand
Jury and subpoened Wright's clinic records. No charges have
yet been filed.
Raid: Ye Seekers - June 1992
Address: 1221 Blalock, Houston, TX 77055
Phone: (713) 461-0857 (Matt Malick, Vitamin Supervisor)
Reason: In Feb. 1992, Texas health authorities acting under
the direction of the FDA seized 50 products from several
health food stores in Texas including Ye Seekers. Then in
June, they seized more than 250 products including aloe
vera, zinc, flax seed oil, herb teas, vitamin C and coenzyme
Q-10.
Outcome: Although more than 410 products were seized, the
stores haven't filed suit for fear of reprisals. Ye Seekers
noted that Ginsana was seized from them at the same time it
was being advertised on the Larry King TV show.
Raid: Mihai Popescu - June 2, 1992
Address: Out of business - owner in Metro Detention Center
in LA.
Phone: (213) 933-6825 (wife) Leave message.
Reason: FDA claims that Gerovital (GH-3), which Popescu was
selling, is an "unapproved drug." Eight FDA and customs
agents raided Popesculs house with guns drawn, holding his
8-month pregnant wife and 83 year old grandfather at gun
point for 10 hours.
Outcome: They seized his computer and business records and
$5,000. worth of GH-3. Popescu has been in prison for 8
months and expects to be released in 3 months.
Raid: Natural Vision International (NVI)
Address: Driven out of business - formerly in Manitowoc, WI
Phone: Talked to an administrator at Holiday House at (414)
682-4663
Reason: Opticians and ophthalmologists pressured FDA into an
armed raid of NVI with two federal marshals to seize 17,000
pairs of pinhole glasses, which exercise and strengthen the
eyes. The charge was that NVI had failed to file a premarket
application with FDA. NVI notes that a pinhole is not a
lens.
Outcome: Despite the fact that NVI submitted hundreds of
testimonials from satisfied customers, the FDA drove them
out of business by not returning their stock of over
$200,000 worth of pin hole glasses.
Raid: Kirwin Whitnah - May 12, 1993
Address: Driven out of business. Formerly in Middletown, CA
Phone: (707) 928-1915
Reason: Whitnah was promoting the sale of deprenyl. The FDA
considered this "selling an unapproved drug." His house was
raided at gun point when he wasn't home, terrorizing a woman
staying at the house. They found no deprenyl. They seized
his computer, business records, mailing list, literature,
and $4,500 in money orders.
Outcome: No charges were filed, but Whitnah was driven out
of business.
Raid: Waco Natural Foods - May 14, 1993
Address: 1424 Lake Air Dr. Waco TX 76710
Phone: (817) 772-5743 (Tom Wiggins)
Reason: The FDA was looking for deprenyl citrate, a non
toxic supplement. They entered the store with a search
warrant wearing plain clothes. They searched for 4 hours and
seemed most interested in possible links to businesses in
the Seattle area.
Outcome: As soon as Mr. Wiggins, the owner, told the FDA his
attorney was a well known defender and prior District
Attorney in the WACO area, they apologized for the raid and
left with some documents. No charges were filed and the
store hasn't been raided since.
Raid: International Nutrition Inc - Jun 24 1993 and Aug. 3, 1993
Address: PO Box 1644 Santa Theresa, NM 88008
Phone: (800) 535-6442 (G.S. Odin)
Reason: Alleged "misbranding" of "illegal drugs" led 5 FDA
agents, a Federal Marshall, and a PR specialist to enter
with video cameras (instead of guns) in an effort to prevent
a public backlash. FDA seized $1,000,000 worth of vitamin
raw materials and products formulated by Dr. Hans Nieper of
Germany. Also seized were computers and business records.
Outcome: INI has lost 80 percent of its business since the
raid and had to lay off 80% of its work force. No court date
has been set.
Raid: Zerbo's Health Food Store - May 1993
Address: 34164 Plymouth Rd., Livonia, MI 48150
Reason: Reason for the raid was the alleged distribution by
78- year-old Mr. Zerbo of GH-3 to special customers. Armed
U.S. Marshall's and FDA agents cleaned off shelves of
coenzyme Q-10, selenium, carnitine, and GH-3. Mr. Zerbo and
his daughter Claire, who manages store, were indicted on
charges of "illegal drug trafficking."
Outcome: Claire Zerbo wanted to fight her indictment, but
chose not to do so because the FDA threatened her aging,
78-year-old father who has Parkinson's Disease with 7 years
in prison. Because of her fear that her father would die in
prison, they both pleaded guilty. Claire will likely receive
3 months probation. Her father is unlikely to go to prison
for more than 4 months.
November 15,1994 life extention magazine)
In 1993, the FDA announced that your right to purchase coenzyme
Q10, selenium, amino acids, herbals and high potency vitamins
would be taken away by the end of the year. Twenty-four million
Americans (including many of you) responded to the FDA's threat
by inundating Congress with letters, faxes and phone calls that
caused the FDA to back away completely from its proposed ban on
importation of these disease-preventing nutrients.
When you voice your protests to these FDA officials (and
Congress), ...you can tell them to obey the law..., the new
Dietary Supplement and Education Act requires that the FDA give
anyone who they with to take enforcement action against at least
10 days notice and the opportunity to present their views bafore
taking action.
Raymond Mlecko, District Dir.,
FDA Chicago District Office 312-353-5863; Fax: 312-886-3280
Jerome Bressler Compliance Dir.,
FDA Chicago Disrict Office 312-353-7382; Fax: 312-886-3280
David Kessler, FDA Commissioner 301-443-2410; Fax: 301-443-3100
Mitch Zeller, Special Assistant
For FDA policy 301-443-5004; Fax:301-594-6777
Gary Dykstra, FDA Deputy Assoc.,
Comm. for regulatory Afairs 301-443-2894; Fax:301-443-9767
Jim O'Hara, Assoc. Comm.
For Public Affairs 301-443-1130; Fax: 301-594-6004
Now that we have seen the present state of affairs in attempting to elliminate our awareness of nutrients for real solutions, let us embark on the easily available supplements, with which even some of the most drastic cases can be aided. Let us make sure that this knowledge is never lost, and continue to bridge to those who may require this knowledge, and yet do not know. Further, breaking down our knowledge, all the way upto the point where we can utilise the ellements around us to make these very remedies, should civilisation as we know it, collapse. As you will see some of this basic information is also included in the following compilations:
THE H202 OXYGEN SOLUTION
Hydrogen Peroxide Therapy
contents:
* What is Hydrogen Peroxide?
* How is Hydrogen Peroxide produced in nature?
* How else is Hydrogen Peroxide made?
* What grades of Hydrogen Peroxides are there?
* What are people using Hydrogen Peroxide for?
* Are the stabilized oxygen products as good as drinking dilute
solutions of H2O2?
* Where can I find Hydrogen Peroxide (H2O2)
* Are there storage and transportation guidelines of Hydrogen Peroxide
that I should be aware of?
* Should I store my Hydrogen Peroxide (H2O2) in the freezer?
WHAT IS HYDROGEN PEROXIDE?
Hydrogen peroxide is H2O2. You can think of it as water(H2O) with an extra
Oxygen atom (O1).
How is Hydrogen Peroxide produced in nature?
Hydrogen Peroxide is created in the atmosphere when ultraviolet light
strikes oxygen in the presence of moisture. Ozone (03) is free oxygen (02)
plus an extra atom of oxygen. When it comes into contact with water, this
extra atom of oxygen splits off very easily. Water (H20) combines with the
extra atom of oxygen and becomes hydrogen peroxide (H202).
How else is Hydrogen Peroxide made?
* Chemically - treat Barium Peroxide with Sulfuric Acid. Barium Sulfate
settles to the bottom and Hydrogen Peroxide is drained off. (To
concentrate, it is vacuum distilled.)
* Treat water with ultraviolet light.
* Electricity - silent, or open spark methods.
* Bubble Ozone (03) through cold water.
What grades of Hydrogen Peroxides are there?
3% Hydrogen Peroxide (Drug/Grocery Store Variety)
Made from 50% Super D Peroxide, Diluted. Contains stabilizers - phenol,
acetanilide, sodium stanate, tetrasodium phosphate among them.
6% Hydrogen Peroxide (Used by Beauticians for Coloring Hair)
Comes in strengths labeled 10,20,40 volume. Must have activator added to be
used as a bleach. Stabilizers used unknown at this point.
30% Re-Agent Hydrogen Peroxide
Used in medical research. Also contains stabilizers.
30-32% Electronic Grade Hydrogen Peroxide
Used for washing transistors and integrated chip parts before assembly.
Stabilizers unknown at this point.
35% Technical Grade Hydrogen Peroxide
Contains a small amount of phosphorus to neutralize any chlorine in the
water it is combined with.
35% Food Grade Hydrogen Peroxide (Also 50% Food Grade H2O2)
Used in food products like cheese, eggs, whey products. Also used to spray
inside of foil lined containers for food storage - known as the aseptic
packaging system.
90% Hydrogen Peroxide
Used by the military as a source of Oxygen at Cape Canaveral. Used as a
propulsion source in rocket fuel.
99.6% Hydrogen Peroxide
This was first made in 1954 as an experiment to see how pure a hydrogen
peroxide could be manufactured.
What are people using Hydrogen Peroxide for?
Food Grade (35%) Hydrogen Peroxide can be used in many different ways to
introduce oxygen into the body. Some of these include:
* bathing in dilute solutions of it
* drinking dilute solutions with distilled water
* spraying dilute solutions on your body after a hot shower
* gargle with it
* doctors are injecting dilute solutions of it into their patients using
IV
Are the stabilized oxygen products as good
as drinking dilute solutions of H2O2?
This is a very difficult question to answer. The stabilized oxygen
producers are very protective of their secrets, so we the consumer have no
real way of following up on their claims. Many say their product compares
to 20 drops of H2O2. When information is forthcoming from the manufacturers
as to how they substantiate their claims, this answer will be expanded.
By far, the stabilized oxygen products are more palatable, but they are
also much more expensive. Most people that have taken the products say they
feel the difference. Most are those that can no longer stomach the taste or
stomach upsets that are often associated with oral consumption of hydrogen
peroxide.
Mike Davis, who is a member of the OyxTherapy Mailing List did a comparison
using SuperOxy, Genesis 1000, and 35% Hydrogen Peroxide. See the results
below. Mike also updated this informaion on April 14, 1996 in OxyFile 360.
I have recently received some Quantofix peroxide test strips manufactured
by Macherey-Nagel from H202,Inc. They give a color indication of peroxide
concentration from 0-100 ppm. The test strip is said to also be sensitive
to organic and inorganic peroxides.
Sample Dilution Reading
SuperOxy Plain 1 ml:100 ml 10ppm(-)
Genesis 1000 1 drop:100 ml 10ppm(+)
35% H202 1 drop:150 ml 100ppm(+)
1 ml above:10ml 10ppm(+)
The SuperOxy is said to have twenty drops of 35% H202 per ounce, the 1 ml
sample should contain about .7 drop. The 35% was diluted with 150 ml water
to adjust for the drop amount. It still had to be diluted another ten times
to bring it into the range of the SuperOxy. The Genesis dilution was not
adjusted for drop size which might account for a slightly higher reading
than the SuperOxy. OxyToddy came out to 0 ppm at full strength.
I calculated the dilution of 35% to be 12ppm which agrees well with the
test figure.
This seems to indicate that in terms of peroxide activity as measured with
this technique 35% H202 is easily ten times stronger than either SuperOxy
or Genesis 1000.
Where can I find Hydrogen Peroxide (H2O2)
* You can try to located someone in your area on the H2O2 Sources Page
in Oxytherapy.com.
* You can check at your local health food store - they may carry it.
* You can contact either Crossroads or The Family News and they will
ship some to you wherever you are located.
* You can look in the yellow pages and look under chemical companies to
see if they carry it. Many chemical companies sell it (varying grades)
in large containers. If you plan on bathing in it, you will find this
the least expensive way means.
Are there storage and transportation guidelines of Hydrogen Peroxide that I should be aware of?
Absolutely. In the Oxyfiles Area, the ECHO Newsletter has many suggestions,
as well as the following Oxytherapy Mailing List has discussed it in the
following messages:
* http://www.oxytherapy.com/mail-archive/jul96/211.html
* http://www.oxytherapy.com/mail-archive/jul96/212.html
* http://www.oxytherapy.com/mail-archive/jul96/223.html
* http://www.oxytherapy.com/mail-archive/jul96/226.html
* http://www.oxytherapy.com/mail-archive/aug96/12.html
Oxidative Therapy
(Hydrogen Peroxide Therapy Part 2)
· What is Oxidative Therapy?
· What Chemicals are used in Oxidative Therapy?
· Is this a new form of Therapy?
· How does it work in the body?
· What has it been used to treat?
· How do I know if I would benefit from Oxidative Therapy?
· How is this therapy given?
· What about the safety or side effects of this therapy?
· Is this therapy expensive?
· Does Insurance pay for Oxidative Therapy?
· Can my Physician administer this therapy?
· How do I locate a Physician trained in Oxidative Therapy?
What is Oxidative Therapy?
Most biochemical reactions in the body are 'Balanced' through 'Redox'
mechanisms. Redox means (Red)uction (Ox)idation. Chemically, anytime
a substance is reduced (chemically changed) something else must be
oxidized (chemically changed the other way) for your body to stay in
balance. Oxidation, as an example, is the process which causes 'rust' on
metals (slow oxidation) or fire (rapid oxidation). In the body, some types
of oxidation is thought to be harmful (produces Free Radicals). We even
suggest people take Vitamin E (anti-oxidant) to help reduce Free Radical
formation. We know however, there could be no life if certain types of
oxidation did not occur. The body uses oxidation as its first line of defense
against bacteria, virus, yeast and parasites. Even breathing OXYGEN is an
oxidative process. Without oxidation we die very quickly. Without
OXYGEN for more than a few seconds, serious consequences follow.
Natural chemicals, found in the body, are used in 'OXIDATIVE
THERAPY' to encourage healthy oxidation in the cells and tissue.
What Chemicals are used in Oxidative Therapy?
A number of substances are known to cause oxidation in the body but the
most important of these is Hydrogen Peroxide. Hydrogen Peroxide, when
exposed to your blood or other body fluids, containing the enzyme
'Catalase', is chemically split into OXYGEN and water. Remember how
Hydrogen Peroxide foams when you put it on a wound? The foam is
OXYGEN being produced by the action of catalase on the Hydrogen
Peroxide. A small amount of Hydrogen Peroxide can supply large
amounts of OXYGEN to the tissue.
Is this a new form of Therapy?
Injections of Hydrogen Peroxide are nothing new. It was first reported by
Dr.T.H.Oliver in the British Medical Journal (Lancet) in 1920. Patients
with influenzal pneumonia were treated with Hydrogen Peroxide
infusions with very good results. The use of Hydrogen Peroxide
injections, to generate OXYGEN in the body, have been studied at many
major medical research centers throughout the world. Research reports
have come from Baylor, Yale, Harvard, UCLA, Boston, England, Japan,
Germany, Sweden, Russia, Canada, Nova Scotia and others. Today,
between 20 and 50 scientific articles are published each month about the
chemical and biological effects of Hydrogen Peroxide. More recently the
"Therapeutic Use of Intravenous Hydrogen Peroxide" was reported by Dr.
C.H. Farr at an International Medical Symposium in Czechoslovakia
attended by representatives from 26 different countries. Oxidative
Therapy, introduced by Dr. Farr, is the rediscovery of an old treatment
first reported almost 70 years ago.
How does it work in the body?
There are many theories about the function of Hydrogen Peroxide in the
body and a great deal of scientific material supports almost every one.
Hydrogen Peroxide is produced in the body in different amounts for
different purposes. It is part of a system which helps you use the OXYGEN
you breathe. It is part of a system which helps your body regulate all living
cell membranes. It is a hormonal regulator, necessary fot your body to
produce several hormonal substances such as estrogen, progesterone and
thyroid. It is important in the regulation of blood sugar and the
production of energy in all cells. It helps regulate certain chemicals
necessary to operate the brain and nervous system. It is used in the
defense system of the body against infections and has been found to be
important in regulating the immune system. Scientists are discovering
the function of Hydrogen Peroxide in the body is far more complex and
important than previously realized.
What has it been used to treat?
Oxidative therapy, using Hydrogen Peroxide, has been reported in the
scientific literature* and by physicians in the treatment of the following
conditions or diseases with varying degrees of success.
(*References available to professionals on request from IBOM)
Heart and Blood Vessel Diseases
· Peripheral Vascular Disease (poor circulation)
· Cerebral Vascular Disease (stroke and memory)
· Cardiovascular Disease (heart disease)
· Coronary Spasm (Angina)
· Cardioconversion (heart stopped)
· Heart Arrhythmias (irregular heart beat)
· Gangrene of Fingers and Toes
· Reynards Syndrome
· Temporal Arteritis
· Vascular and Cluster Headaches
Pulmonary Diseases
· Chronic Obstructive Pulmonary Disease (lung)
· Emphysema (lung disease)
· Asthma (allergy, lung)
· Bronchiectasis
· PCP (Pneumonia in AIDS)
· Chronic Bronchitis
Infectious Diseases
· Influenza
· Herpes Zoster (shingles)
· Herpes Simplex (fever blister)
· Systemic Chronic Candidiasis (Candida)
· Chronic Fatigue Syndrome (Ebstein-Barr Virus)
· HIV (AIDS) Infections
· Acute and Chronic Viral Infections
· Chronic Unresponsive Bacterial Infections
· Parasitic Infections
Immune Disorders
· Multiple Sclerosis
· Rheumatoid Arthritis
· Diabetes Mellitus Type II
· Hypersensitive Persons (Environmental and Universal Reactors)
Miscellaneous
· Parkinsonism
· Alzheimer
· Migraine Headaches
· Chronic Pain Syndromes (Multiple Etiologies)
· Pain of Metastatic Carcinoma
· Blood and Lymph Node Cancers
Physicians from around the world constantly share knowledge and
experience and the list of uses for Oxidative Therapy is growing every day.
Since Hydrogen Peroxide is a natural substance produced and used in
body chemistry, there will be discoveries about it's importance in
biochemistry for years to come.
How do I know if I would benefit from Oxidative Therapy?
Only a physician trained in the administtation of Oxidative Therapy can
answer that question for you. You may find your condition or illness
contained in the list above. If treatment of your condition or illness has
been unsatisfactory in the past you may wish to learn more about
Oxidative Therapy. The IBOM Foundation can supply you with the
names of recognized trained physicians in your area.
How is this therapy given?
Very weak, very pure Hydrogen Peroxide (0.0375% or less concentrations)
are added to a sugar or salt water solution, the same as used for
intravenous feeding in hospitals. This is given in doses from 50 to 500
mL, administered into a large vein usually in the arm. It is given slowly
over a period of 1 to 3 hours depending on the total amount given and
the condition of the patient. It is painless except for the very small needle
stick. Treatments are usually given about once a week in chronic illness
but can be given daily in patients with acute illness such as pneumonia or
flu. Physicians usually give 5 to 20 treatments, depending on the
condition of the patient and the type of illness, The patient is rechecked in
1 and 3 months to evaluate the benefits and determine if additional
treatements are indicated. Some patients, especially with chronic illness,
may need to take follow up treatments, in series of 5 to 10, or may need
maintaining indefinitely on a regular monthly schedule. As many as 50
treatments have been administered to several patients without
complications. Your experienced physician must decide how many
treatments are necessary in your individual case.
What about the safety or side effects of this therapy?
Over the past 50 years hundreds of patients have received Hydrogen
Peroxide without setious side effects. Early use of Hydrogen Peroxide was
reported to occasionally cause irritation of the vein being infused. This
troublesome side effect was eliminated after the concentration and rate of
infusion were adjusted downward. The IBOM Foundation publishes and
distributes a Protocol (How To Do It Booklet!) on the proper
administration of Hydtogen Peroxide. It is available to any IBOM trained
physician. A Protocol is the best way for physicians to properly learn about
any new therapy.
Is this therapy expensive?
Expense is a relative term. Persons with chronic diseases pay thousands of
dollars annually to physicians, pharmacies and hospitals for drugs and
therapies which do little more than maintain them at their current level
of sickness. If Oxidative Therapy could save you 1/2 to 3/4 of your current
expenses would you consider it expensive? The expense of any therapy
varies more with the type of illness than type of therapy. Persons with
serious complicated illnesses require more costly test to diagnose and
monitor than less ill patients. Much of todays medical cost is in the testing
rather than treatment. Don't be afraid to ask your physician, in advance,
about cost.
Does Insurance pay for Oxidative Therapy?
This usually depends on your insurance company and type of policy.
Generally, however, insurance companies will not pay for medical service
or care which may be classified as 'not usual and customary'. Usual and
customary simply means all physicians are providing the same service or
treatment for the same disease. Obviously, the average physician is not
using Oxidative Therapy and most are not even familiar with the therapy.
A qualified physician can more easily answer this question on an
individual basis.
Can my Physician administer this therapy?
Any licensed physician may administer this therapy. Only trained and
experienced physicians however are recognized by the IBOM Foundation.
Interested physicians can qualify for recognition by contacting the IBOM
Foundation for information regarding training seminars.
How do I locate a Physician trained in Oxidative Therapy?
For more information contact the IBOM Foundation.
International Bio-oxidative
Medicine Foundation
P.O.Box 61767
Dallas/Fort Worth
Texas, 75261 USA
817-481-9772
Note: The Doctors & Clinics List within this site also may be consulted.
AIDS AND CANCER CURED BY
HYPER-OXYGENATION
NOTE: The information presented in this article has been suppressed by
the medical community for decades due to the reprocussions it would
have on the pharmaceutical industry. First published in 1987, by the newsletter NOW WHAT issue #1 1987. Fortunately some doctors do
not feel the same as the general community and are using these
processes to cure people. Please copy a redistribute this article everywhere, to meet those who need it, half-way. This is service in action.
Several dozen AIDS patients have not only reversed their
death sentences, but are now back at work, completely free
of the disease. They destroyed the virus in their blood by
hyper-oxygenation, known in various forms as oxygen therapy,
bio-oxidative therapy or autohemotherapy. This is a simple,
inexpensive and very broad spectrum process that many feel
could force a complete overhaul of the medical industry.
The two basic types of oxygen therapy are ozone blood
infusion, and absorption of oxygen water (hydrogen peroxide)
at very low concentrations.
It turns out that the AIDS virus cannot tolerate high oxygen
levels in its victims' blood. Not only that, every other
disease organism tested so far has the same weakness. Even
cancer growths contract and disappear when the oxygen
saturation is sufficiently increased in the fluids
surrounding them, since they are anaerobic.
AIDS, herpes, hepatitis, Epstein Barr, cytomegalovirus and
other lipid envelope virus are readily destroyed by
hyper-oxygenating the patients blood with ozone. This was
demonstrated by among others Dr. Horst Kief in Bad
Hersfeld, West Germany. Dr. Kief has already cured a
number of AIDS victims by drawing blood, infusing it with
ozone and returning it to the patient, at regular intervals
until all the virus is gone. (He can be reached through
Biozon Ozon-Technik GmbH, An Der Haune #10, Bad Hersfeld,
D-6430, Federal Republic of Germany). Dr. S. Rilling of
Stuttgart and Dr. Renate Viebahn of Iffezheim are among the
growing number of physicians who have obtained similar
results with their patients. They are with Arztlich
Gesellschaft fur Ozonetherapie and JrJ Hansler GmbH,
respectively.
THE BASIS OF BIO-OXIDATIVE THERAPIES
For many years the health sciences have been seeking to
identify the primary physical cause of all diseases, and the
cure-all that this basic principal would yield. Now both
have been found, but their utter simplicity makes them
difficult to accept at first, since it seems like if it's
that easy, we should have been using them all along.
Our bodies are composed mostly of water, which is eight
ninths oxygen. Most nutritional studies tend to get caught
up in the small details of biochemistry and overlook our
most abundant and essential element, and the fundamental
role of its depletion in causing illness. Of all the
elements the body needs, only oxygen is in such constant
demand that its absence brings death in minutes.
The main difference, for healing purposes, between benign
microorganisms (including our own cells), and those which
cause disease, is that the later require much lower oxygen
levels. This is due to their more primitive evolutionary
origins, during the ages when free oxygen was far less
abundant. Now their descendants can only survive in low
oxygen environments such as accompany stagnation and decay.
To become a growth medium for such parasites, one has to
have allowed the oxygen saturation of the bodies fluids to
drop well below the optimum level for healthy cell growth
and function.
The simplest substances available for restoring one's oxygen
balance to a healthy range are ozone (O3), and hydrogen
peroxide (H2O2), which is much easier to obtain and use.
They are both highly toxic when concentrated, which has
tended to obscure their germicidal value except as a skin
antiseptic. But when diluted to therapeutic levels (for
H2O2, 1/2 of 1% or less), they are not only non-toxic but
uniquely beneficial.
OZONE BLOOD TREATMENT
Ozone overcomes the AIDS virus by a fundamentally different
process than usually attempted by drugs. Instead of
burdening the liver and immune system with more elaborate
toxic substances, ozone simply oxidizes the molecules in the
shell of the virus.
The treatment is remarkably simple. The ozone is produced
by forcing oxygen through a metal tube carrying a 300 volt
charge. A pint of blood is drawn from the patient and
placed in an infusion bottle. The ozone is then forced into
the bottle and mixed in by shaking gently, whereupon the
blood turns bright cardinal red. As the ozone molecules
dissolve into the blood they give up their third oxygen
atom, releasing considerable energy which destroys all
lipid-envelope virus, and apparently all other disease
organisms as well, while leaving blood cells unharmed.
It also oxygenates the blood to a greater degree than is
usually reached, what with poor air and sluggish breathing
habits. The treated blood is then given back to the
patient. This treatment is given from twice a week to twice
a day, depending on how advanced the disease is. The
strengthened blood confers some of its virucidal properties
to the rest of the patient's blood as it disperses.
The disease will not return, as long as the patient
maintains his blood in an oxygen positive state, through
proper breathing, exercise, and clean diet.
A Dr. Preuss, in Stuttgart, has written up ten case
histories of AIDS patients he has cured by this method. But
his and the other physicians' reports are all anecdotal
rather than in the form of "controlled studies", since they
could not be expected to treat some patients and deny
treatment to others just for the purpose of accumulating
evidence. Thus their results are not considered "proof" by
the US medical community. So the Medizone Company in New
York has taken on the task of doing the controlled studies
required for the treatment to be approved in the US for
general use.
MEDIZONE TESTING OZONE BLOOD TREATMENT
In the summer of 1986 Medizone obtained from the FDA an IND
(Investigative New Drug) Approval for ozone, which falls
under the heading of drugs even though it isn't. They
verified that ozone destroys the AIDS virus in vitro, and
completed their animal tests in the fall of 1986. The tests
demonstrated no indication of toxicity, at ten times the
equivalent amount that is proposed for human treatment.
The Medizone Co is at 123 E 54th St. Suite 2B, NY, NY
10022: phone is 212-421-0303. Medizone says that it has
obtained the rights to US patent #4,632,980, on "ozonation
of blood and blood products", from the company
"Immunologics", in exchange for Medizone stock shares. The
patent pertains specifically to inactivating lipid-envelope
virus. In humans, this includes AIDS, herpes, hepatitis,
Epstein Barr virus, and cytomegalovirus, among others.
Medizone obtained tentative FDA approval in April 1987 to
begin human testing, but for a variety of "bureaucratic
reasons" the FDA has postponed the actual start of the tests
eight times now, with requests for further data, some of
which had already been given to them.
Twenty months now have passed [as of December 1988], along
with several thousand AIDS victims, since the first
announced starting date was postponed. The Medizone staff
is hoping to finally begin in the spring of 1989, but are no
longer announcing expected starting dates with much
confidence. "There are no technical problems, but this is
the FDA we're dealing with, after all." As the Company's
future hangs on their decision, no one at Medizone wants to
risk antagonizing the FDA, by speculating about their actual
motives for stalling such a broad-spectrum cure.
All this can be done with virtually no publicity. The
official reason for is that the accepted procedure for
publishing medical breakthroughs is to complete all the
tests first, even though victims may die waiting for the
cautious, methodical testing procedure to run its course.
No one in the industry wants to raise false hopes, let alone
repeat the medical disasters that have resulted in the past,
from rushing approval on new treatments.
On the other hand, the enormously expensive and dubiously
effective drug AZT was widely publicized and many months
before it was approved in the US, as is ongoing research
into possible AIDS vaccines. In fact, FDA Commissioner
Frank Young has even announced a proposal to make
experimental drugs available to AIDS victims as swiftly as
possible, without waiting for full FDA approval procedure to
be completed. So there appears to be a sever double
standard involved here. It seems that highly profitable
"treatments" with serious side effects can be promoted
through massive news coverage, while an actual cure,
repeatedly demonstrated in Europe, with minimal cost and no
apparent harmful effects, must be delayed and kept quiet
while panic and deaths mount. Surely at this stage the
benefits of unauthorized publicity will outweigh the risks.
SAFE PURIFICATION OF BLOOD FOR TRANSFUSIONS
Ozone infusion also provides a simple method of purifying
stored blood and blood components, eliminating any
possibility of disease being transmitted by transfusion. It
also pre-oxygenates blood to be transfused, greatly reducing
the burden on the body receiving the blood.
This application alone, of the Medizone process has enormous
profit potential, and the treatment will have vast
international demand as the news spreads. This has not gone
unnoticed by various investment analysts. "Confidential:
report from Zurich", "Penny Stock Insider" and "Low-Priced
Stock Edition", among others, are urging their readers to
get in on Medizone now, comparing the opportunity to getting
in on Xerox, IBM, or Polaroid when they were still unknown.
Various physicians have independently discovered ozone to be
also effective against cancer, leukemia, arthritis, coronary
heart disease, arterial circulation disorders. colitis, gum
diseases, and assorted childrens' diseases. Some of these
findings have now been collected and published in the
volume, "Medical Applications of Ozone", available from the
International Ozone Association, 83 Oakwood Terrace,
Norwalk, Ct 06850.
Some of the medical uses of ozone have been appreciated for
years in Europe, Brazil, and elsewhere, as well as its
advantages over chlorine for water treatment (no toxic
residues, 5000 times more rapid disinfection) but its still
relatively unknown in the US.
OXYGEN WATER
A much simpler type of Oxygen Therapy uses hydrogen peroxide
(H2O2) which is what ozone (O3) forms on contact with water.
It can be taken orally if diluted with water to 1/200 or
less, absorbed through the skin by bathing in it (anywhere
from 1-8 pints of 3% H2O2 in a standard size bathtub half
full), or in severe cases it can be injected (250 cc of
.075% to .15% or roughly 1/1300 to 1/650). Injections
obviously require a physicians assistance, but self
treatment is possible with oral and skin applications.
The principle is the same as with ozone blood treatment.
All hostile micro-organisms prefer lower oxygen levels than
the bodies cells require to remain healthy. Boosting the
oxygen level revitalizes normal cells while killing virus
and other pathogens.
The domestic sales of hydrogen peroxide are rising at 15%
per year, as the news of this option spreads at the grass
roots level. The rapid expansion of the peroxide movement
is especially remarkable considering there has been almost
no media coverage, and in fact the FDA, American Cancer
Society and other enforcers of established medicine have
tried hard to discourage the practice.
Hydrogen peroxide is the only germicidal agent composed only
of water and oxygen. Like ozone, it kills disease organisms
by oxidation as it spreads through the patient's tissues.
This also destroys cancerous growths which are anaerobic.
Nobel prize winner Dr. Otto Warburg demonstrated over 50
years ago the basic difference between normal cells and
cancer cells. Both derive energy from glucose, but the
normal cell requires oxygen to combine with the glucose,
while cancer cells break down glucose without oxygen,
yielding only 1/15 the energy per glucose molecule that a
normal cell produces. This is why cancer cells have such a
huge appetite for sugar, and also why people who consume
excessive quantities of sugar tend to get cancer more often.
The anaerobic breakdown of glucose by cancer cells forms
large amounts of lactic acid as a waste product, the same
substance formed by fermentation of lactose, as in spoiled
milk. The liver converts some of this back into glucose,
in an attempt to salvage a food source from a toxic waste.
In doing this the liver uses 1/5 the energy per glucose
molecule than a normal cell can derive from it, but that's
three times the energy a cancer cell will get from it. The
more the weak, deranged cancer cell multiply, the more
energy is lost to the normal cells. Thus we find that low
levels of both oxygen and energy tend to occur where cancer
is present, and vice versa. This wasteful metabolism
becomes self-sustaining and dominant unless the oxygen
and/or energy levels are sharply increased, or the cancer's
food source is eliminated.
HEART TRANSPLANT
PIONEER RECOMMENDS OXYGEN WATER
Dr. Christian Bernard, who performed the first heart
transplant, said in march 1986 that he was taking peroxide
and water himself, several times daily to reduce arthritis
and aging, and he recommended it highly at the time. Since
then he has come under heavy attack by the medical
establishment for this position, and now states that he "is
not involved" with the peroxide movement. But he does not
retract his original endorsement, nor deny that he still
uses it personally.
Over a hundreds physicians are already curing a broad
assortment of "incurables" with this natural anti-microbial
agent. This includes some forty or more in the US. A
principal liaison to these free-thinking physicians is DR.
Charles H. Farr, who wrote "The Therapeutic Use of
Intravenous Hydrogen Peroxide". He directs the
International Bio-Oxidative Medicine Foundation, and
publishes the "IBOM Newsletter" which contains procedural
updates and technical refinements for physicians using
intravenous H2O2 therapy on their patients. By classifying
the treatments as experimental they can get around the FDA's
archaic restrictions for now, until massive public demand
and/or media exposure force official approval.
Dr. Farr summarizes the beneficial effects of H2O2 in
"IBOM" issue #2; these include killing bacteria, protozoa,
yeast, and virus, oxidizing lipids from arterial walls,
increasing oxygen tension intracellularly, stimulating
oxidative enzymes, returning elasticity to arterial walls,
dilating coronary vessels, and regulating membrane
transport. IBOM is at PO Box 61767, Dallas/Ft. Worth, TX
75261; 817-481-9772. Dr. Farr is at 1130 North May Ave,
Oklahoma City, OK 73120; 405-752-0070 and 799-8781.
H2O2 CAN BE SELF ADMINISTERED
The oral and skin applications offer the option of home
treatment, as no blood needs to be drawn, and hydrogen
peroxide is cheap and plentiful. Keep it diluted though; in
high concentrations it can irritate sensitive skin and
induce vomiting when ingested. (Veterinarians routinely
give common 3% H2O2 to animals that have swallowed poison,
to make them throw it up.)
The starting dosage is one ounce of .5% (1/200) H2O2 in
water, and some find they need to start with less. As the
peroxide contacts pathogens in the stomach it liberates free
oxygen, so those with high levels of virus and streptococcus
in their stomachs may feel slight nausea while the reaction
is occurring. The dosage is increased by an ounce per day,
up to five ounces on the fifth day, then finally up to five
ounces three times daily for a week (or until disease is no
longer present). Then the dosage is tapered back down over
a five week period.
Food-grade or Re-agent (these are 35%, dangerous if
undiluted) is better for internal use, since the common USP
3% H2O2 contains small amounts of chemical stabilizers and
other impurities. It can still be used if food-grade is
unavailable; it just isn't as pure.
An alternate dosage regimen uses three drops of 35% H2O2 in
a glass of water three times a day, which is then increased
by a drop per dose, per day, up to 25 drops per dose in
extreme cases. Candidiasis victims should start at one drop
per dose, and build their tolerance gradually. Some find
the taste rather bleachy and unpleasant, and may wish to
chase it with plain water. It can also be mixed with fruit
juice, and citrus juices in particular cover the taste
pretty well.
Adding seven drops of 35% H2O2 to a gallon of drinking water
and shaking well purifies it and gives it a pleasant
waterfall-like flavor.
For more dosage details and extensive
references on H2O2 taken internally, contact:
Walter Grotz, box 126, Delano, MN
55328; 612-972-2144. His progress report, "ECHO", costs $1.
He provided much of the material regarding H2O2 in this
article. Another source is father Richard Wilhelm, Box 18,
Union Rd, California KY 41007; 606-635-9297. These
gentlemen have continued the research initiated by Dr.
Edward Carl Rosenow (1875-1966). They have located over
4000 peer-reviewed medical articles on the applications of
hydrogen peroxide, some dating back to the 1800's. They
received the National Health Federation's Pioneer Award in
Medicine this year, for this ongoing research. Walter
Grotz, in particular, has been touring and lecturing
extensively on the benefits of self-administered H2O2,
literally saving lives wherever he goes, and bringing hope
to people who have been told there causes were hopeless.
Dr. Kurt W. Donsbach at the Bio-Genesis Institute in
Rosarita Beach, Baja Mexico (714-964-1535), has achieved a
remission rate exceeding 70% in over 300 patients, at last
count, most of whom had been previously told they were
beyond hope, and had "tried everything else". Bio-oxidative
therapies are now applied to all cases that arrive at this
clinic, and all respond except for those who arrive already
very close to death. The Guadalahara Medical School,
Mexico's largest, is initiating their own tests this summer,
and will add it to their curriculum upon verification.
As Dr. Donsbach has pointed out, no US clinic or
institution has ever tested intravenous H2O2 as a treatment
for cancer, so any claim that it is not effective is not
based on clinical trial, and amounts to willful
disinformation [This has now changed considerably, with major medical breakthroughs for i.v. treatment of cancer with H202 -Ananda].
The Gerson Institute and La Gloria Clinic in Mexico are also
using Hydrogen Peroxide therapies on their patients, after
the staff tested it on themselves and found it beneficial.
HYDROGEN PEROXIDE IN NATURE
Hydrogen peroxide occurs naturally in rain and snow, from
atmospheric ozone, and in mountain streams where rushing
water is continuously aerated. Most of us learned at an
early age to drink only from a stream only where the water
is running white, because that is where it gets cleansed of
germs. The reason is that H2O2 is forming there due to its
rapid agitation, and that's what kills any harmful microbes
present.
By just shaking a bottle of water vigorously for a while you
can tuck enough extra oxygen into it to form detectable
amounts of H2O2, improving its purity, flavor and vitality.
It turns out that the spring waters at Lourdes, France, long
recognized for their remarkable healing properties, are very
high in natural hydrogen peroxide. The spring is fed by
high altitude snow melt, so the snow apparently absorbs
unusually large quantities of ozone on its way from the
upper atmosphere. Other less-known high altitude springs
are said to be likewise effective.
Similar benefits can be obtained in a swimming pool or hot
tub, by discarding the chlorination system and simply
pouring in H2O2, or by bubbling ozone through the water.
One simple method of making pool-grade ozone is to pump air
past an enclosed ultraviolet lamp.
Raw, uncooked vegetables and fruits can contain natural
hydrogen peroxide. Cooking drives off the extra oxygen.
Fresh fruit juices are well known for their blood cleansing
and revitalizing capabilities, particularly when they are
not combined with other foods; this is largely due to the
H2O2 they contain. Reconstituted frozen juices have much
less and are no longer "alive", thus they are not nearly as
effective.
H2O2 IS THE HEART OF THE IMMUNE SYSTEM
Mother's milk contains a high amount of H2O2, especially
colostrum, the first milk secreted after birth, which
activates the newborns immune systems, and key to many other
metabolic processes.
Under conditions of optimum health, H2O2 is produced by the
body's immune system in whatever amounts are needed to
quickly destroy any invading hostile organisms. It is made
by combining water in the body with the free oxygen that is
supposed to be available. When the body is oxygen-starved,
it can't produce enough H2O2 to wipe out invading pathogens,
which can then get the upper hand and cause visible disease.
OXYGEN BOOST IS KEY TO OTHER HEALING METHODS
When penicillin is effective against infection, it is
largely due to the formation of bacterial amounts of H2O2,
when glucose is oxidized by O2 in the presence of penicillin
notatin. (General Biochemistry, Fruton & Simmonds 577.1
F944 p. 339)
Much has been made about the healing properties of
interferon, but it is unbelievably expensive. However, much
of its effectiveness is apparently due to the fact that it
stimulates the production of H2O2 and other oxygen
intermediates, which are a key factor in reactivating the
immune system. (Journal of Interferon Research Vol 3, #2,
1983 p. 143-151.) Thus Interferon may turn out to be simply
a very elaborate way to accomplish essentially the same
thing as H2O2 regimen.
Vitamin C (ascorbic acid) has long been recognized as
essential to the proper use of oxygen by the cells. Dr.
Linus Pauling has demonstrated that large doses of vitamin C
are effective against cancer. The mainstream medical
community still has not acknowledged this discovery, let
alone put it to use, despite Dr. Pauling's previous
credentials. As it turns out, vitamin C actually creates
extra H2O2 in the body.
Organic Germanium (bis-carboxyethyl germanium sesquioxide)
is gaining increasing recognition as a potent healing
substance, primarily through the work of Dr. Kasuhiko Asai.
This compound directly increases the body's oxygen supply,
as it contains a great deal of oxygen in a form that can be
easily assimilated. (See "Miracle Cure: Organic Germanium"
by Dr. Paul Asai, Japan Publications, Inc., Tokyo and New
York.)
Taheebo (aka Pau D'Arco or Lapacho Colorado) is a tree that
grows in the Andes and fixes high concentrations of oxygen
in crystalline form in its inner bark. The bark has been
used for centuries by the native peoples of the area to
prevent and reverse illness, and it is one reason, why they
do not get cancer. In recent years it has become popular in
the US, and it gets by the FDA as an "herbal tea" whose
distributors wisely make no medical claims for it. Again,
much of its effectiveness is apparently due to its high
oxygen content, released in solution when brewed as a tea.
CAUSES OF OXYGEN DEPLETION
There are several common practices that drop a person's
oxygen level far below what it should really be. At sea
level, 20% of the atmosphere is supposed to be oxygen, but
city air gets down as low as 10%, due to smog and removal of
trees. Air that tastes bad induces a tendency to breathe
shallowly, getting even less oxygen to the blood. So does
lack of exercise.
The carbon monoxide (CO) in smog does not normally occur in
nature in much quantity since it's formed by incomplete
combustion of carbon compounds. It is electrically
unbalanced, so it seeks to bond with any available oxygen to
form the more stable carbon dioxide (CO2). Those who
breathe too much carbon monoxide tend to die, fast or slow
depending on the concentration. It strips oxygen molecules
from the blood to form CO2, which the body can't use and
must exhale, at least until its oxygen runs out. The fact
that the body considers CO2 a waste product, by the way,
doesn't say much for carbonated beverages.
Tap water is very low in oxygen, having no opportunity to be
aerated during its journey through the pipes, and being
loaded down with chlorine and various contaminants. Since
cooking drives the extra oxygen out of vegetables, if one
diet is mostly cooked or processed foods, there's yet
another oxygen source lost.
EATING, FASTING AND OXYGEN BALANCE
Overeating is so common in the US it's considered "normal".
One cause is the widespread use of oral antibiotics. While
destroying the target germs, these drugs also kill off one's
intestinal flora, which are needed for healthy digestion.
With these friendly bacteria gone, digestive efficiency
plummets. As a result, the sensation of hunger comes more
often and lasts longer, as the body tries to compensate for
ineffective digestion by increasing the amounts consumed.
Even just eating daily, without ever giving the
gastro-intestinal tract a rest, loads down the blood with
toxins and impurities, especially uric acid crystals. Under
a microscope these resemble tiny coffin lids, interestingly
enough, another clue to our Creator's whimsical sense of
humor. When the waste products exceed the cleansing
capacity of the kidney's, the blood ends up just having to
haul it around the body and stash it wherever possible.
These toxins literally take up so much room in the blood
cells that the cells can't take on enough oxygen when they
pass through the lungs. The bloods primary function of
picking up and distributing oxygen gets blocked by overuse
of garbage-hauling function.
Fasting restores health by giving the overloaded blood cells
a chance to dump the toxins and inert matter through normal
organs of elimination at a rate they can handle, instead of
through the skin, as in acne, or other inappropriate places.
If the fast is long enough, accumulated residues in the body
are also scoured out and expelled, giving a considerable
spiritual resurgence once all the backlog is cleared away.
While the debris is flushed out, various toxic reactions may
come and go. Once the blood is cleansed the red corpuscles
have alot more room for oxygen molecules, the oxygen
saturation of the molecules is high, and health and energy
are boosted considerably. Each breath now gives more
life than it was able to in the bloods earlier state.
Most long-lived native peoples, who are not affected by our
more common diseases, either include fasting as a regular
part of their yearly food cycles, or eat much less overall,
than industrialized peoples.
Today many Americans are existing at such high levels of
toxicity, that their toxic reactions when attempting to fast
can seem intense enough to make them start eating again
before any serious cleansing can be accomplished.
Fortunately one can partially bypass the lungs and get the
blood level back up, by taking oxygenated water internally
and through the skin. Several weeks of detoxification of
this regimen will also make it much easier to fast without
discomfort, if one chooses. It reduces appetite, logically
enough, to a level more in line with the body's actual
needs.
The bacteria that aid digestion are not killed by oral use of H2O2, as long as it's diluted properly.
OXYWATER MAY EVEN CURE STUPIDITY
Perhaps the greatest potential benefit is the reversal of
the slight brain damage caused by long-term oxygen
depletion, which can be observed in the "average" human, and
is not always all that slight. It's well known that after
about nine minutes of no oxygen, from drowning or whatever,
you can kiss your brain good-bye. By the implications of
constant gradual oxygen starvation in our cities somehow
escape notice, despite the tiredness, depression,
irritability, poor judgement and health problems affecting
so many citizens.
Increasing the oxygen supply to the brain and nervous system
will reverse these conditions. The oxywater regimen
improves alertness, reflexes, memory and apparently
intelligence, and may offer the elderly a new weapon against
senility and related disorders. Alzheimer's and Parkinson's
are reported to be responding to it. Alcoholics who start
taking H2O2 soon loose interest in alcohol, and the thirst
does not come back. Look up what alcohol does to your blood
oxygen and your ability to use it, and you'll see why.
One possible spin-off of a coming major increase in the
blood oxygen supply to human brains is that various
short-sighted and oxygen-depleting activities such as
deforestation, and other intelligent practices, should fade
from the scene. Americans especially, will have an
opportunity to outgrow many stupid things.
It's strange that the common drug aspirin "stops pain" by
interfering with the nervous systems ability to use oxygen,
in the electrochemical reactions needed to transmit
impulses. Though maybe it's not that strange, considering
that the Bayer Company which originated it was a subsidiary
of IG Farben, the German chemical conglomerate that is
famous for, among other things, developing and
mass-producing the lethal gas Zyklon-B specifically for the
exterminations at nazi death camps.
ECONOMIC INERTIA
DR Terry McGrath, the CEO at Medizone, confirmed that
Hydrogen peroxide would in principle act much like ozone in
destroying AIDS virus, but pointed out that it's never
likely to be tested and proven in the laboratory. There's
simply no economic incentive, since it's an unpatentable
process and offers no commercial returns than most other
natural remedies. So it's completely up to individual
patients and concerned citizens to push these options out
into the open, immediately, before various companies get too
financially committed to the assumption that AIDS (or any
other disease) will continue to spread and be incurable.
This is a good place as any for the FDA-required disclaimer:
"Information given here is for research and educational
purposes only and is not intended to prescribe treatment."
VETERINARY AND AGRICULTURAL APPLICATIONS
Human's aren't the only life form to benefit from
compensation for their oxygen deficient air, water and/or
lifestyle. H2O2 in animals' drinking water, not enough to
taste unpleasant, knocks out a growing list of illnesses.
Locally, cats have gotten rid of their feline leukemia and
chlamydia, and are back to their old energetic slapstick
selves. Distemper in dogs has been reversed with H2O2, and
a growing number of farmers are applying it to their
livestock to cut losses from disease and infected wounds.
Plants grow better with an ounce of 3% H2O2 per quart of
water they're given. Spray the solution on their leaves as
well. Seeds germinate faster, with bigger sprouts, when
they are first soaked in 1 ounce of 3% H2O2 to a pint of
water. Instead of cutting trees that are diseased or
otherwise struggling, spray them with H2O2 and water (1 part
3% to 32 parts water).
WHY ISN'T IT ALREADY IN USE ?
The obvious question is, if hyper-oxygenation is so simple
and effective, why has it taken so long to discover it?
Ozone is hardly new and hydrogen peroxide has been on the
market for over a century. Why aren't all doctors already
using it ? How come this story isn't all over the major
news outlets?
Turning the question around helps clarify the problem. Jus
exactly what would happen if a cure was discoverer that was
completely effective against the vast majority of diseases,
ridiculously cheap and plentiful, and in most cases could be
self-administered without a physician?
Would the current medical establishment welcome a
breakthrough that could render 98% of all drugs, testing and
disease related surgery obsolete? What would the response
be of the pharmaceutical industrialists, hospital chain
owners, health insurance moguls, AMA, and FDA?
Would you expect to read or hear such an announcement from
any medical journal or media outlet owned by people
financially committed to the medical status quo, which is
practically all of them? How many want to make their own
occupation unnecessary?
And if the cure had already been suppressed once, wouldn't
the possible blame for allowing people to die without it
provide even more incentive continue keeping the whole thing
quiet?
All right then. This precisely the situation that exists,
and the cure has indeed been around for ages. It has been
independently reported effective against virtually every
disease at one time or another, in thousands of
public-domain medical articles, which had never been
collected or correlated untilrecently. And it is so simple
and basic that concealing it from physicians and the general
public has required a tremendous smoke screen of artificial
complications, narrow specializations, symptomatic
classifications and user hostile treatments.
If this is so, it follows that the more profit-fixed
elements of the medical establishment will not be too
thrilled about the recent surge in interest in oxygen
therapies. The drug industry has expanded enormously since
WWII, while America's level of health has dropped from the
world's highest to the lowest among the industrialized
nations. It does look as if the bottom line has been money
and not health, for a long time.
The battle for the future of medicine, between Nature's
truth and lucrative lies, is about to really heat up. We
can expect to see disinformation articles and newscasts with
persuasive medical experts, some of whom will even believe
what they're saying, warning of the dangers of hydrogen
peroxide, ozone and even regular oxygen. These reports will
attempt to blur the distinction between using therapeutic
dosages at safe dilutions, and the harmful effects of
excessive concentrations. Plenty of grizzly examples are
available, of what happens when various tissues are
over-oxidized.
Anti-oxygenation propaganda pieces will probably not mention
that over the years the FDA gas approved H2O2 as a skin
antiseptic at full 3% strength, as a hair bleaching agent at
6%, and for internal use as an additive for milk and in
antiseptic long-shelf-life packaging. Nor are they likely
to acknowledge that many European countries use ozone and
H2O2 in their cities' water supply, and that they enjoy much
better health than in the US. And they will be unable to
truthfully cite any examples of people who were harmed by
using H2O2 in the current demonstrated therapeutic
concentrations.
If not enough public move quickly to help spread the news of
this alternative, those who fear it could reduce their
economic power may go so far as to try to knock off someone
who promotes it, while trying to make it look like "too much
oxygen" is the cause. Also, product tampering has thus far
mostly targeted Bayer Aspirin's competitors, in case you
hadn't noticed, but drugstore hydrogen peroxide would not be
immune to such tactics. One approach might be to plant a
contaminated batch in a town where oral use is catching on
and the medical establishment is losing ground, so someone
gets hurt and the story gets nationwide coverage.
It is vital for Americans to realize that current economic
dynamics don't allow the businessmen in charge of health and
industry any incentive at all, to make people permanently
healthy and lose them as customers. It's the same reason
why the energy conglomerates do not encourage citizens to
become energy-self-sufficient, the Pentagon has no incentive
to stop wars, and the American Psychiatric Association sees
no advantage to ending mental illness.
Fortunately the majority of physicians really do want to see
their patients get well. They also wouldn't mind gaining
the respect and admiration with which physicians were once
widely regarded. When it comes down to choice between
saving lives and protecting profits, most will brave enough
to overhaul their medical belief systems, discard obsolete
methodologies, and basically tell the pharmaceutical
conglomerates to go shove it. The rest will simply get left
behind.
SOURCES FOR FOOD-GRADE HYDROGEN PEROXIDE
Most pharmacists have never heard of it, so it's usually a
waste of time to ask them. A number of chemical supply
houses have 35% H2O2 available; check your local directories
and call a few. Under FDA pressure, DuPnnt and possibly
other major chemical companies have recently issued warnings
to their distributors, not to sell hydrogen peroxide to
people who want it for healing purposes. So when you
inquire, if they ask what you want it for, it will
unfortunately be necessary to lie. If you say you want it
as a cleaning agent, that's at least pretty close to the
truth.
Several physicians quietly sell it through the mail, but
they aren't the same ones promoting its health properties,
for obvious FDA-related reasons. A good source in
California, though he can ship it anywhere, is Dr A J
McDonald, at PO Box 775, Lodi, CA 95240; 209-368-8681;
12$/pint.
Your best move would be to share this information with
owners of health food stores in your area. Call them and
ask if they have food-grade H2O2 (some already do) and tell
them you want it and how it works. Encourage them to carry
it and give them Dr McDonald's address if they don't seem
inclined to track down a local source.
Cleanroom-grade 30% H2O2 (used for cleaning in computer
rooms it is a powerful disinfectant and leaves no residue
when it evaporates) is reported to be just as pure as food
grade and much cheaper. Check with labs that make "water
fabrication" chemicals, or contact the manufacturers of
silicon chips and other computer parts, and the data
processing complexes that might use it in their cleanrooms,
and ask where they buy it. The more sources become known,
the harder it will be for anyone to make it unavailable.
GET THE WORD OUT
Write your elected officials, send copies of this
information, and point out what will happen to a politician
whose constituents learn he knew of a cure for cancer and
AIDS but didn't tell them about it. Call in on a radio talk
shows and share the good news, or send copies to their
reporters and program directors, especially at
listener-supported stations as these are less likely to
suppress it. Don't assume your local papers have already
heard of this; write letters to editors, and/or send copies
of this report. Tack it on every bulletin board you see,
and post it on all relevant computer bulletin boards.
If you know teachers, physicians, or health officials who
can still think for themselves, tell them about this and
give them the references. Notify your local police
officials that hyper-oxygenation gives them a way of making
sure they'll be safe from infection due to contact with AIDS
carriers. If you really feel bold, walk into the local
hospital cancer's wards and give a copy of this to anyone
who can still read, and slip out the back door before the
doctors walk in. Share it with anyone you know who has a
health problem, even a minor one; H2O2 apparently works on
everything from acne to warts.
Above all, stop buying the idea that cancer, AIDS, and other
"terminal" illnesses are automatic death sentences. When
you hear some celebrity is sick or dying from this or that,
look up their mailing address in Who's Who or whatever, and
mail them this information. If the address is for an agent,
which are notorious for blocking attempted communications to
their client, you might include a cover letter to the agent,
stating that the enclosed vital news is also being sent to
their clients family members, and that if he or she learns
through them that there was life saving information sent but
held up at the agent's, that agent will be out of a job.
Act like you have the clout it takes to make a difference,
and you soon will.
Major scientific breakthroughs go through three stages:
first they are ridiculed, then violently opposed, and
finally they are accepted for being self-evident all along.
Let's see if we can short cut those first 2 stages a bit,
OK?
FURTHER INFORMATION SOURCES:
"ECHO", a newsletter on Oxygen Therapy, is available from
Walter Grotz, Box 126, Delano, MN 55328, (1$, 8p);
612-635-9297) have extensive references and case histories
of successful treatments.
"The Peroxide Story" George L Borell, 3035 Rome Ave,
Anaheim, CA 92804; 60 pp, $4.95 plus $1 postage.
The International Bio-Oxidative Medicine Foundation (IBOM)
Newsletter contains technical updates for physicians using
H2O2 therapies on their patients. PO Box 61767, Dallas/Ft.
Worth, TX 75261; 817-481-9772.
Rex Research (PO Box 1258, Berkely, CA 94701) has five
folios on Ozone Therapy; #4 ($2, 10 pp) is specifically on
ozone treatment of AIDS; see also #1, ozone vs a wide
variety of conditions (6$, 55pp); #2, ozone vs herpes,
hepatitis, rheumatic diseases, also dental use ($4, 29pp);
#3, cardiovascular, ozone enrichment of blood prior to
transfusion (4$, 23 pp) and Ozone vs Cancer ($6, 55pp).
The International Ozone Association, 83 Oakwood Ave,
Norwalk, CT 06850; (203-847-8169) has available "Medical
Applications of Ozone" the largest single volume on the
subject, for 50$.
"Self-Treatment for AIDS: Oxygen Therapy" ($12.95, 100pp),
and home remedies for Candida" ($8.95, 112pp) consist mostly
of article reprints, compiled by Betsy Manning, 1600 Larkin
#104, S.F. CA 94109.
"Search for Health", APW, PO Box 3052, Iowa City, Iowa
52244. Tom Valentine, Editor. Includes info on other
oxygenating compounds for internal use, including AEROX,
which they sell, and which is reported to give the same
benefits as H2O2, but tastes better and is more stable,
though more expensive. (We have not yet obtained a sample
for testing.) APW also is a source for full-spectrum
health-enhancing KIVA lights.
Some of the formal medical articles on H2O2 include:
"Hydrogen peroxide mediated killing of bacteria", D P
Clifford and J E Repine, (Molecular and Cellular
Biochemistry 49, 143-149, 1982); Generation of H2O2 in
Biomembranes", T Ramasarma, (Biochemica et Biophysica Acta,
694, 1982, 69-93); "Removal of Cholesterol and Other Lipids
from Experimental Animal and Human Atheromatous Arteries by
Dilute Hydrogen Peroxide", James W Finney, Bruce E Jay, et
al, (Baylor University Medical Center, Dallas, Texas); also
a series on the role of H2O2 in immunity to malaria, in The
Lancet, 12/25/82 p 1431-1433, 1/29/83 p 234, and 2/12/83 p
359-360.
Medizone International, 123 East 54th St, Suite 2B, NY, NY
10022; 212-421-0303; issues shareholder reports updating the
stateside verification of ozone blood treatment. Hansler
ozone generators will also be available to licensed
physicians through Medizone.
Biozon Technik Co, in Bad Hersfeld, Federal Republic of
Germany, also makes ozone generators for medical use.
Reprinted from NOW WHAT, issue one; $4/issue, or $15/yr.
Order from Waves Forest, PO Box 768, Monterey, CA 93942 USA
If by this point anyone remains skeptical, and has not yet digested the Pharmaceutical and medical corporation conspiracy issues, raising questions such as "surely, if there has been a relevent degree of success, without serious side-affects, I would have seen this evidence in the medicle literature." Well, indeed, there has been such articles. But one must seek to find, it is not handed out on a platter. The following is thus an excellent, establishment article on H202:
Hyperbaric Oxygen:
More Indications Than Many Doctors Realise
---------by Eric P. Kindwall---------
from "British Medical Journal," August 28, 1993 v307 n6903 p515(2)
Subjects: Hyperbaric Oxygenation Therapeutic use
Full Text COPYRIGHT British Medical Association (UK) 1993
MORE INDICATIONS THAN MANY DOCTORS REALISE
Many British doctors are ignorant of the indications for
hyperbaric oxygen and sceptical of its benefits, according to a
recent survey of hyperbaric oxygen facilities. The survey, by the
BMA's Board of Science and Education, concluded that given the
present level of use then provision was sufficient, although
doctors may be underusing the treatment.[1]
They need to know for which conditions hyperbaric oxygen works
and refer accordingly. The telephone advisory service, run by the
Institute of Naval Medicine at Gosport (similiar to the National
Poisons Unit help line), should be better known.
Treatment with hyperbaric oxygen was introduced as an adjunct to
cardiovascular surgery before cardiopulmonary bypass techniques
and deep hypotheria became available. But when surgery in a
hyperbaric chamber was no longer necessary most of the original
researchers stopped studying it. Britain helped to pioneer the
use of hyperbaric oxygen to treat carbon monoxide poisoning,
refractory osteomyelitis,[2] and compromised skin grafts. But
with no formal training programmes and little funding, the
treatment now attracts little attention in Britian.
When administered at pressures greater than one atmosphere,
oxygen can assume properties more akin to a drug than a simple
support for metabolism. In carbon monoxide poisoning, for
example, it stops lipid peroxidation, which spares neuronal cell
membranes.[3]
It reduces odema by about 50% in post ischaemic muscle through
preserving adenosine triphosphate.[4] In acute burns it reduces
fluid requirements by 35% in the first 24 hours, thus reducing
oedema.[5-8] It reduces white cell adhesion to capillary walls
after ischaemic or traumatic insult, mitigating the no reflow
phenomenon.[9] Red cell flexibility is doubled in about 15
treatments.[10] White cell killing of aerobic bacteria and some
fungi is greatly enhanced at high oxygen pressures,[11]
facilitating control of osteomyelitis[12] and reducing the number
of operations and mortality in necrotising fasciitis.[13]
Extremely important is its stimulation of new capillary and
collagen formation in radiated tissue, normalising tissue oxygen
tensions to permit surgery, healing, and even bone grafting.[14
15]
Finally, it increases tissue levels of superoxide dismutase,
which counters the formation of free radicals after injury,
resulting in better tissue survival.[16] This is particularly
important in cursh injury, replants, and grafts, where free
radical formation is responsible for reperfusion injury.[17]
Although many doctors believe that good research on hyperbaric
oxygen is rare, the converse is true.[18-22] Over 3800 papers
have been published on the topic despite the relative scarcity of
chambers. The Undersea Medical Society began investigating the
claims being made for hyperbaric oxygen treatment in 1977. A
committee (which I chaired) considered 64 different allegedly
improved by treatment with hyperbaric oxygen. In most of them
there was insufficient evidence to warrant its clinical use.
In preparing out original report we consulted the largest private
insurers in the United States, Blue Cross/Blue Shield, and the
Federal Health Care Finances Administration. Since then the
report has been continually updated. At present only 12
conditions are approved by the society for reimbursement.[23]
Since 1977 the number of clinical chambers in the United States
has grown from 37 to nearly 300.
For inclusion on the approved list there had to have been
controlled studies or large clinical series indicating not only
the efficacy but also the cost effectiveness of treatment with
hyperbaric oxygen. In disorders for which prospective controlled
trials were impossible or unavailable, evidence adduced for the
efficacy of hyperbaric oxygen had to be at least as convincing as
that used to support reimbursement of other treatments routinely
paid for the insurers. The five major British centres for the
most part limit treatment to those disorders on the approved
list, despite there being no regulation to that effect.
This list can serve only as a guide. Though quite useful in
diabetic wounds, hyperbaric oxygen is only part of a programme of
total wound care. For some diabetic wounds hyperbaric oxygen is
inappropriate if the large vessels distal to the trifurcation at
the knee are occluded or severely stenotic. Crush injury and
impending compartment syndrome need to be treated immediately if
any worthwhile result is to follow. Late referral, which gives
time for oedema, reperfusion, and injury; free radical damage;
and the no reflow phenomenon to do their work, makes the
treatment largely a waster of time and money. For some surgical
patients the potential dangers of further trauma to the wound
during transportation will militate against the use of hyperbaric
oxygen. Experience has shown, however, that patients with severe
carbon monoxide poisoning can be transported safely over long
distances in a properly equipped ambulance or helicopter.
Before transfer a critically ill patient is contemplated it
should be ascertained that the receiving chamber facility can
deliver the necessary level of intensive care. Whenever the use
of hyperbaric oxygen is considered, consultation with the
physician in charge of the hyperbaric oxygen facility is
mandatory to ensure that referral is appropriate. The timing of
hyperbaric oxygen in relation to surgery is also critically
important. For example, in necrotising fasciitis, surgery is the
accepted primary treatment, with hyperbaric oxygen used as a
follow up. With gas gangrene, however, the hyperbaric chamber is
used before surgery (other than for fasciotomy). In the treatment
of radionecrosis the patient should be treated at least 20 to 30
times in the chamber, to induce the formation of new capillaries,
before elective surgery is performed if healing is to be
expected.
NOTES
[1] BMA Board of Science and Education. Clinical hyperbaric
medicine facilities in the UK London: BMA, 1993.
[2] Perrins DJD, Maudsley RH, Colwil MR, Slack WK, Thomas DA. OHP
in the management of chronic osteomyelitis. In: Brown IW, Cox BG,
eds. Proceedings of the third international conference on
hyperbaric medicine. Washington, DC: National Academy of
Sciences, National Research Council, 1966:578-89. (Publication
1404.)
[3] Thom SR. Antagonism of carbon monoxide-mediated brain lipid
peroxidation by hyperbaric oxygen. Toxicol Appl Pharmacol
1990;105:340-4.
[4] Nylander G, Lewis D, Nordstrom H, Larsson J. Metabolic
effects of hyperbaric oxygen in post-ischemic muscle. Plast
Reconstr Surg 1987;79:91-6.
[5] Cianci P, Leuders HW, Lee H, Shapiro RL, Sexton J, Williams
C, et al. Adjunctive hyperbaric oxygen therapy reduced length of
hospitalisation in thermal burns. J Burn Care Rehabil
1989;19:432-5.
[6] Nylander G, Nordstrom H, Eriksson E. Effects of hyperbaric
oxygen on oedema formation after a scald burn. Burns
1984;10:193-6.
[7] Stewart RJ, Yamaguchi YT, Cianci PA, Knost PM, Samadani S,
Mason SW et al.The effects of hyperbaric oxygen on adenosine
triphosphate in thermally injured skin. Surgical Forum
1988;39:87-90.
[8] Wells CH, Hinton JG. Effects of hyperbaric oxygen on post-bur
plasma extravasation. In: Davis JC, Hunt TK (eds). Hyperbaric
oxygen therapy. Bethesda, Maryland: Undersea Medical Society,
1977:259-65.
[9] Zamboni WA, Roth AC, Russell RC, Graham B, Suchy H, Kucan JO.
Morphological analysis of the microcirculation during reperfusion
of ischemic skeletal muscle and the effect of hyperbaric oxygen.
Plast Reconstr Surg 1993;1110-23.
[10] Mathieu D, Coget J, Vinckier F, Saulnier A, Durocher ET,
Wattel F. Red blood cell deformability and hyperbaric oxygen. Med
Subaquatique Hyperbar 1984;3:100-4.
[11] Mader JT, Brown GL, Gluckian JC, Wells CH, Reinarz JA. A
mechanism for the amelioration by hyperbaric oxygen of
experimental staphylococcal osteomyelitis in rabbits. J Infect
Dis 1980;142:915-22.
[12] Davis JC, Heckman JD, DeLee JC, Buckwold FJ. Chronic
non-hematogenous osteomyelitis treated with adjuvant hyperbaric
oxygen. J Bone Joint Surg [Am] 1986;68:1210-7.
[13] Riseman JA, Zamboni WA, Curtis A, Graham DR, Konrad HR, Ross
DS. Hyperbaric oxygen therapy for necrotising fasciitis reduced
mortality and the need for debridements. Surgery 1990;108:847-50.
[14] Marx RE, Johnson RP. Problem wounds in oral and
maxillofacial surgery: the role of hyperbaric oxygen. In: Davis
JC, Hunt TK, eds. Problem wounds: the role of oxygen. New York:
Elsevier Science Publishing, 1988:65-125.
[15] Marx RE, Johnson RP, Kline SN. Prevention of
osteroradionecrosis: a randomised prospective clinical trial of
hyperbaric oxygen versus penicillin . J Am Dent Assoc
1985;111:490-554.
[16] Kaelin CM, Im MJ, Myers RA, Manson PN, Hoopes JE. The
effects of hyperbaric oxygen on free flaps in rats. Arch Surg
1990;125:607-9.
[17] Manson PN, Anthenelli RN, Im MJ, Bulkley GB, Hoopes JE. The
role of oxygen-free radicals in ischemic tissue injury in island
skin flaps. Ann Surg 1983;198:87-90.
[18] Davis JC. Hyperbaric oxygen therapy. Intensive Care Med
1989;4:55-7.
[19] Goulon M, Barois A, Rapin M, Nouilhat F, Grosbuis S,
LaBrousse J. Intoxication oxycarbonee et anoxie aigue par
inhalation de gaz de charbon et hydrocarbures. Am Intern Med
1969;120: 335-49.
[20] Hart GB, Lamb RC, Strauss MB. Gas gangrene 1: a collective
review. J Trauma 1983;23:991-5.
[21] Kindwall EP. Uses of hyperbaric oxygen therapy in the 1990s.
Cleve Clin J Med 1992;59: 517-28.
[22] Strauss MB, Hargens AR, Gershuni DH, Greenberg DA, Crenshaw
AG, Hart GB, et al. Reduction of skeletal muscle necrosis using
intermittent hyperbaric oxygen in the model compartment syndrome.
J Bone Joint Surg [Am] 1983;65:65-62.
[23] Thom SR. Hyperbaric oxygen therapy: a committee report.
Bethesda: Undersea Hyperbaric and Medical Society, 1992.
Physiological Effects Of Tissue Oxygenation
On Wound Healing
-----------by JoAnne D. Whitney-----------
in "Heart and Lung" Sept 1989 v18 n5 p466(11) - ABSTRACT ONLY
Subjects:
Wounds and injuries Care and treatment
Skin Wounds and injuries
Oxygen in the body
Physiological aspects
Wound healing Physiological aspects
Reference #: A8868463
Abstract:
The availability of oxygen to tissues plays an important role in
the process of wound healing. When skin is damaged, swelling
occurs, fibroblasts (a type of cell) grow, and blood vessels and
connective tissue begin to grow.
During the early inflammatory phase, the process of wound repair
begins with the activation of enzymes and white blood cells which
destroy bacteria and cause blood clot formation. Macrophages
(cells that engulf debris) clear the wound of destroyed cellular
material. The blood flow to the injured area increases, bringing
nutritive substances to the damaged tissue.
Macrophages also stimulate fibroblasts to secrete collagen, a
type of protein that strengthens the tissues. New blood vessels
are formed to continue the supply of nutrients to the wound.
Although the mechanism is not well understood, the wound then
begins to contract and tissue forms from the wound's edge.
Within one to two days, the epithelial cell layer begins to form.
Nutrition, the immune system, oxygen, blood volume, infection,
immunosuppression (caused by drugs or disease) and a decrease in
red blood cells are all influential factors in wound healing.
Oxygen affects the production of collagen, epithelial cell
growth, and the growth of blood vessels. A decrease in the volume
of circulating blood and the concentration of red blood cells can
compromise the amount of oxygen available for wound healing.
Interventions to improve oxygenation and enhance wound healing
include replacing reduced blood volume, monitoring fluids,
watching for signs of infection, and monitoring the overall
healing progress.
- (Consumer Summary produced by Reliance Medical Information, Inc.)
HEALING FOR PEANUTS
Amadis's Two Cents
Oxygen Therapies are a political and medical hot-potato. Ask your doctor
what Ozone Therapy is, and he/she will probably respond "Never heard of
it!" You might even hear the words "If there was something to it, I would
have heard about it."
Oxygen Therapies have been around for many years, and range from the use of
hydrogen peroxide to Ozone Therapy.
Ozone is by far the most aggressive of all the Oxygen Therapies, and
perhaps the most controversial. Accepted in 16 countries, Ozone Therapy has
met with much resistance in the United States. The FDA does everything in
its power to quell the acceptance of it, but it is slowly gaining
acceptance. The FDA would like people to believe that Ozone is a form of
pollution found in the air, but Ozone in relation to Oxygen Therapies is
produced using high quality Ozone generators from Medical Grade Oxygen.
The main thrust behind the suppression of Ozone appears to be
pharmaceutical based. Only Ozone delivery methods are patentable, so there
is not much money to be gained by pursuing it clinically. On the other
hand, the money that the pharmaceutical companies stand to lose because of
Ozone is where the problem begins. If Ozone Therapy were to eliminate the
use of even 50% of pharmaceutical drugs, billions of dollars are at stake.
I am fortunate to live in Canada where Ozone Therapy is allowed (the
legality of it remains a gray area), but still not widely known. The Former
Deputy Surgeon General of Canada feels that there is something to Ozone
Therapy, as does Canadian National Defence. Many doctors are skeptical of
it, but I feel this is because of a lack of education. Results speak
wonders, and if doctors are truly concerned with patients good health, they
will have no choice but to listen.
I use Ozone Therapy and other Oxygen Therapies for general maintenance of
my health. I do this with some degree of acceptance from my doctor. I have
seen it do wonders on many immune-suppressive disorders. Unfortunately,
many turn to this type of therapy after their bodies have been ravaged by
traditional medical methods (toxic drugs, chemotherapy, radiation, etc.)
and expect miracles. Oxygen Therapies will try to clean up the toxic mess,
but sometimes it is just too late.
I have talked to people that say, "I tried it, but it didn't work for me",
or, "I knew someone that tried it, and it didn't help them." When you get
into an in depth conversation with the person, you find out that proper
protocols using an ozone generator that outputs proper concentrations were
not used.
-Amadis (Dave)
As todays skin care and beuaty products, are extensions of the silent war, being emulsed in petrolium products, such as the propyl alchohol, which enters the immune system within 30 seconds, and allows the intestinal fluke and other parasites the ability to enter the thymus gland, and eat it up etc, clearly it is time for a new skin care awareness to emerge. Oxygen again offers a key. For true long term beauty, not several year beauty's, at the expense of rapid unset of ugliness, disease, and damaged image. Oh do 02.
Oxygen Emuslion: The basics
by Ted Kalli
Vice President
AURA Research
291 Mercer Avenue
Marmora, NJ 08223
U.S.A.
This article will mainly concentrate on the various aspects of
the use of oxygen, as related to skin care. To do this, we must
have a basic understanding of one of life's basic elements,
Oxygen. This requires some knowledge of Bio-Chemistry, the
anatomy and physiology of the skin, nutrition, effects of the
environment, etc.
While some of us are not medical professionals, our industry is
getting more medically oriented. The tremendous reception The
Advanced Dermatologics News has received in both the beauty
industry and medical community is a direct result of this trend
and is a prime example of the thirst for knowledge, expressed by
professionals throughout the industry. Therefore, we must obtain
a clear understanding of many terms and procedures common to both
the medical profession and skin care industry.
Educational opportunities abound at trade shows, seminars,
conferences and even with manufacturers. Why manufacturers, all
they want is to sell their product line! Whether or not you use
the products is your professional decision. But, how can you make
this decision without full understanding?
It is up to you can to make your purchasing decision based on the
facts presented. I have attended classes offered by esthetic and
pharmaceutical manufacturers and have found many of them to be
very informative and well worth my time.
In my column much of my text will be direct quotes from reliable
sources. All sources will be listed so you can obtain the
complete text. And now on to Oxygen.
Webster's Medical Dictionary defines oxygen as: an element that
is found as a colorless, tasteless gas in the atmosphere of which
it forms about 21% or combined in water, in most rocks and
minerals, and in numerous organic compounds, that is capable of
combining with all elements, except the inert gases, is active in
the physiological processes and is involved esp. in the
combustion processes. To understand the definition, lets talk
about how oxygen is used in the body.
The following are some excerpts from a consumer information
brochure by International Bio-Oxidative Medicine Foundation
(IBOM). IBOM is a Not for Profit Educational and Research
Foundation. It contains a good description of oxidation.
Most biochemical reactions in the body are 'Balanced' through
'Redox' mechanisms. Redox means (Red)uction (Ox)idation.
Chemically, anytime a substance is reduced (chemically changed)
something else must be oxidized (chemically changed the other
way) for the body to stay in balance.
Oxidation, is the process which causes 'rust' on metals (slow
oxidation) or fire (rapid oxidation). In the body, some types of
oxidation is thought to be harmful producing free radicals. We
now suggest individuals take vitamin E (an anti-oxidant) to
reduce free radical formation. However, there could be no life if
certain types of oxidation did not occur. The body uses oxidation
as its first line of defense against bacteria, virus, yeast and
parasites. Even breathing OXYGEN is an oxidative process. Without
oxidation we die very quickly. Without oxygen for more than a few
seconds, serious consequences follow.
Before I go any further I would like to address Free Radicals.
Dr. Kurt W. Donsbach D.C., Ph.D, in his book O2 O2 O2, gives an
excellent explanation addressing this issue.
The Free Radical Flap
The most misunderstood aspect of hydrogen peroxide is the
contention that it is a free radical. This is false. First of
all, let's define a free radical.
It is an element or compound which has an unpaired or unmatched
electron. This lack of balance causes this substance to have a
very reactive character.
However, it must be noted that these free radicals are very short
lived. Usually in the one ten-thousandth of a second range,
during this short time, these free radicals can cause damage by
joining with other body chemicals and changing their character.
Sometimes they produce a chain reaction by creating new free
radicals.
That is the negative side. There is also a beneficial side to
free radicals, but let us see what happens to hydrogen peroxide
when it first enters the body through the blood stream (or the
skin).
Hydrogen Peroxide + Catalase = Water + O
When hydrogen peroxide enters the blood stream, an enzyme
catalase which is very prevalent in the human body almost
immediately breaks it down to water and atomic oxygen, also
called singlet oxygen or free radical oxygen.
O + O = O2
In less than one ten-thousandth of a second, the atomic oxygen
has become stable O2 oxygen by pairing with another atomic
oxygen. O2 is the kind of oxygen the human body uses constantly.
There is no time for the unstable atomic oxygen to attack a cell and cause any damage.
As mentioned before, there are beneficial free radicals. One of
them is atomic oxygen released when hydrogen peroxide is formed
in the white blood cell (leukocyte) known as a macrophage. This
has a special area called a peroxisone which produces hydrogen
peroxide, breaking down to water and atomic (reactive or free
radical) oxygen which will kill an invading bacteria allowing the
macrophage to engulf and destroy harmful organisms.
Another example of free radical benefit is carbon monoxide (CO),
a deadly form of gas which can kill the human organism if inhaled
in large enough quantities. It can be inhaled but not exhaled,
accumulates in the blood stream reducing the amount of stable
oxygen carried to the cells, where it is needed. To decrease the
amount of carbon monoxide in the blood stream, it must be changed
to carbon dioxide (CO2) a form of gas which is readily exhaled.
This is accomplished by the simple mechanism of adding a singlet
oxygen to the carbon monoxide.
Well, I hope this clears up the free radical issue and we can
concentrate of the beneficial use of oxygen emulsion products in
skin care. To do this we must know something about hydrogen
peroxide, since it is where we get the oxygen and water.
Hydrogen peroxide has been around since the 1870's. It is made up
of hydrogen and oxygen. In fact, hydrogen peroxide is 94 %
oxygen. Whenever hydrogen peroxide comes in contact with the
enzyme, catalase, it always breaks down to oxygen and water. This
is true whether it is on the skin or in the blood stream. It
should be noted that many of the references I will be using
pertain to the oral and infusion use of hydrogen peroxide. Yes,
people do drink very diluted hydrogen peroxide, but not the kind
you buy in the supermarket or drug store. The are several
different grades of hydrogen peroxide. The different grades are
as follows:
3% Hydrogen Peroxide (Drug/Grocery variety)
Made from 50% Super D Peroxide, diluted. Contains stabilizers -
phenol, acetanilide, sodium stanate and tetrasodium phosphate
among them.
6% Hydrogen Peroxide (used by Cosmetologists)
Comes in strengths labeled 10, 20 and 40 volume. Must have an
activator added to be used as a bleach.
30% Reagent Hydrogen Peroxide
Used in Medical research. Also contains stabilizers.
30 - 32% Technical Grade Hydrogen Peroxide
Used for washing transistors and integrated chip parts before
assembly. Stabilizers contained are unknown.
35% Food Grade Hydrogen Peroxide
Used in food products like cheese, eggs, whey products. Also used
to spray inside of foil lined containers for food storage - known
as aseptic packaging system. The product of choice in most
applications using hydrogen peroxide.
90% Hydrogen Peroxide
Used as a source of Oxygen at Cape Canaveral. Used as a
propulsion source in rocket fuel.
The 35% Food Grade Hydrogen Peroxide, greatly diluted, is what is
consumed by humans by choice. This is not widely practiced in the
United States, but there has been a great deal of research on the
subject. Dr. Donsbach's book, O2 O2 O2 lists 32 such studies in
his bibliography. Many of these studies were done in the United
States at the Mayo Clinic and Baylor University. If you
interested in further information on this subject, look for
Oxygen Therapies, Ed McCabe, Energy Publications, 1988.
This writer is concerned about the external use of hydrogen
peroxide.
Hydrogen peroxide in it's aqueous form is not very stable. When
it is in the emulsion, it is very stable.
In 1990, I introduced oxygen emulsion skin products to the United
States. It was a new concept and many professionals were
skeptical about it. But, in less than two years "oxygen emulsion"
had become a popular industry buzzword.
Why and how does it work? The facts are, very simple. The enzyme
catalase exists in the skin, as well in other parts of the body.
When hydrogen peroxide comes in contact with the skin, it always
breaks down to oxygen and water. In the aqueous form, which is
commonly used as an antiseptic, most of the oxygen escapes to the
atmosphere. This is the 'bubbling' that is often seen on the
surface of the skin.
The oxygen emulsion, which is an oil-in-water emulsion of
hydrogen peroxide, also breaks down to water and oxygen. But, the
oil phase of the emulsion does not allow the oxygen to escape to
the atmosphere. This creates a pressure and the skin becomes the
path of least resistance. When hydrogen peroxide changes from a
liquid to a gas (which happens instantaneously), it increases in
volume 22.4 times. This increase in volume is what causes the
pressure and why it penetrates the skin. The oxygen becomes a gas
only during this instantaneous reaction. When it penetrates the
skin, it is dissolved in the extracellular water and in the
capillary plasma. Molecular oxygen (gas) can only exist in the
lungs. The presence of the oxygen in the plasma of the blood can
be measured using medical monitoring equipment manufactured by
Kontron, a division of Hoffman-LaRoche. "Before and after"
measurements using this equipment will show a dramatic increase
in the partial pressure after application of the oxygen emulsion.
When the oxygen penetrates the skin it acts as a 'vehicle.' It
propels water and other ingredients with it when it penetrates the
skin, if they are of the correct molecular
size. When combined with beta-caroten, the oxygen carries
the beta-caroten with it. Once the beta-carotene penetrates
the skin, its is converted by the body to vitamin A acid. This conversion is well
documented by many published papers on the activity of beta-carotene and other carotenoid.. So in addition to oxygen and
water, we have all the benefits of retinoic acid, without the
adverse side effects.
References
1. Webster's Medical Desk Dictionary, Merriam-Webster, 1986
2. O2 O2 O2, Dr. Kurt W. Donsbach D.C., Ph.D,
Wholistic Publications, 1991
3. Oxidative Therapy, International Bio-Oxidative Medicine Foundation,
P.O. 610767, Dallas/Ft. Worth, TX 75261
4. Hyperbaric oxygen therapy, Grim, Pamela S.; Gottlieb, Lawrence J.;
Bobbie, Allyn; Batson, Eric, JAMA, The Journal of the American
Medical Association, April 25, 1990 v263 n16 p2216(5)
5. Hyperbaric Oxygen; More Indications than Many Doctors
Realize.(Editorial), Kindwall, Eric P., British Medical Journal,
August 28, 1993 v307 n6903
6. Hyperbaric Oxygen Therapy for Foot Ulcers. (includes related
articles), Cianci, Paul; McCarren, Marie, Diabetes Forecast, June
1993 v46 n6 p57(5)
7. Breathing New Life into Oxygen Therapy.(includes related
articles), Newson, Lesley, New Scientist, Nov 23, 1991 v132 n1796
p50(4)
The Mechanics of O3 in Medicine
Why? Because even among all the ozone doctors, only a few rare
souls understand the back-away-and-look-at-the-whole-thing
concept. The concept is simple: the human body is 66% water. In
a 150 pound man, there would be 100 pounds of water. It divides
up like this:
Percentage of water making up tissues, organs, fluids and bone
in the human body.
Brain 75%
Heart 75%
Lungs 86%
Muscle 75%
Liver 85%
Kidney 83%
Bone 22%
Blood 83%
Saliva 95%
Perspiration 95%
Some are conditioned to think of ozone as "another drug". It
would be useful to take a minute and forget the idea of putting
a little drug in the body to bring about changes, and instead
look at out task of cleaning up 100 pounds of water as if you
were not a doctor, but an engineer approaching a mechanical
problem. Away from the human body, how would you physically
completely detoxify and completely purify 100 pounds of dirty,
disease-laden water? You would micro-bubble a lot of strong
ozone through it for a long time while running it through
filters. This would rid out 100 pounds of water of any
bacteria, viruses, fungi, pathogens, and any other toxic
contamination.
Take your thoughts back to the human body. How are you going to
purify 100 pounds of body water? By putting 10cc's of low
concentration ozone in a muscle? Of course not. That may bring
about minor blood chemistry changes, but complete purification?
No. You must *flood* the body with oxygen long enough to purify
it, and at a rate slow enough so that the filters (organs of
elimination) won't clog. The only way to achieve optimum
purification or healing using ozone.
Our 150 pound man with 100 pounds of water has approximately 12
pints of blood in him. His blood is 83% water, so in our case
therefore, about 10 pounds of water. Even if you completely
purify the bloodstream, you are only purifying 10% of the dirty
water problem. The blood circulates through the body 12 to
twenty times per minute, but what about the lymph?
Here's what the AMA said in a "Today's Health" article
(December 1964) by J. D. Ratcliff.
"The Lymph .... as vital as the main bloodstream, the intricate
and all but invisible lymphatic network ... it is one of the
world's rivers of mystery - sluggish, largely unmapped, many
miles long. The Lymphatic system has puzzled physiologists
since early Greek times ... our health, even our lives depend
upon how well this complex system functions.
In contrast to the bloodstream, which follows a swift flowing
closed circuit from arteries to capillaries to veins and then
back to the arteries, the lymphatic system flows slowly in a
single direction. Its initial rivulets - microscopic in
dimension - originate in intercellular space. Fluid gathered
here passes through ever-enlarging ducts until it reaches the
lower neck region, where it empties into veins leading to the
heart to be mixed back into the blood. (Note: it takes 24 hours
for the lymph to completely circulate through the body.)
Much of the mystery surrounding the lymphatic system traces to
the fact that most of its ducts are so fragile that they are
almost invisible - the smallest have walls of only one wall
thickness. And the fluid they carry is ordinarily almost as
clear as water. Moreover, at the touch of a probe, all but the
largest lymphatic vessels collapse, as they do in death.
Exploring such a gossamer stream has called for supreme
ingenuity. In many respects the body is like a vast swamp. Its
trillions of fluid-bathed cells live an aquatic life. The
lymphatic network provides an all-important drainage system."
So, when you're up to your neck in alligators (facing terminal
disease) it is hard to remember that your original objective
was to drain the vast swamp. To purify the water, all of it,
beyond the blood, into the lymph, into the gossamer
passageways, through the organs, within the cell walls
themselves, even the aquatic life surrounding the DNA, how are
you going to do it?
The German clean a pint or more of blood three times a week.
Pioneers in the U.S. inject several syringes of oxygen/ozone
into the bloodstream once a day for six weeks and get great
results, but are we even close to what is needed? Blood and the
lymph eventually carry oxygen to every cell, but what about the
hidden backwaters of the swamp. Maybe the present eventually
carry oxygen to every cell, but what about the hidden
backwaters of the swamp? Maybe the present methods work, but
can we improve the delivery system?
There are four devices now on the market to answer the call of
approaching total purification:
OZONE BODY BAGGING
Plastic or ripstop nylon bags with drawstrings at the neck and
cuffs, some with legs, some without. The patient takes a shower
and while still wet with the pores "open", he completely covers
his body, except his head, within a big bag. The bag is pumped
full of ozone made from pure oxygen.
THE AQUACIZER
The patient reclines in a large "clamshell" chamber with head
protruding outside while micro-nozzles spray warm ultra-pure
water homogenized with pure oxygen ozone into the body. The
skin capillaries dilate and discharge toxins into the very
hungry 10 megohm ultra-pure water, and absorb ozone into the
skin, lymph and bloodstream at the same time.
HYPERBARIC CHAMBERS
Patients lie or sit in a pressurized oxygen atmosphere. The
oxygen pressure on their whole body harmlessly forces oxygen
through their skin and deep into the most hidden body cavities.
THE POLYATOMIC APHERESIS UNIT
This has to be the most advanced medical ozone delivery system
to date. The patient lies in a reclined chair while blood is
withdrawn out of one arm, ozonated at slight pressure
continually, and pumped back into the other arm. A one hour
treatment alone is superior to any other ozone delivery method.
Recent clinical trials had a few patients circulating in the
chair for over eight hours! Imagine the volume of blood, lymph,
and organ purification in an eight hour treatment. Now combine
Polyatomic Apheresis with The Aquacizer and hyperbarics. Total
purification inside and out.
A little ozone can clean the blood up so well that an immediate
blood test will show a state of health, but unless all the
little gossamer ducts are cleaned up, after a few days of the
lymph recirculating, doing its job of picking up debris and
remixing with the blood, a person could test positive again for
a virus. The original PCR HIV test sensed one viral particle in
one thousand units, now it detects one particle in two million.
To be and remain totally PCR or any virus negative -
All the patient's body water must be totally purified.
As we relay elswhere in this book, negative ions dramatically increased Extra Sensory Perception scores that were made in double blind faraday studies by Dr. Andrija Puharich. He also found an immense increase in the healing capability of the body, as negative ions increased the 8 hz bi-hemespheric synchronisation of the two brain halves. It is this 8 cycles per second rhythm, which Dr. Puhrich measured being emitted from the hands of successful healers, and also has been repeatedly demonstrated to be the frequency, at which water electrolysed, actually produces the COHN set of proto-life - this findings were conclusive, and replicated by many. The negative ion increase, allows the body to be flooded by electrons, which then fill in the eight electron orbital positions of the atoms, in the polysacharide cells, forinstance. This changes the cellular charge polarity, and allows only harmoni 8Hz life giving waves to enter into the cells. Here, breathe therapy, and the importance of oxygen takes another dimension. Following are other points for negative ion consideration:
Why Are Negative Ions
So Healthy?
Lenard (1915) found that when water is atomized (e.g. on impact of a
water droplet), negative and positive charges are SEPARATED.
Molecules which are torn from the surface of the water bear a
NEGATIVE charge (small negative ions) whereas large drops or the
entire mass of water are POSITIVE.
This provided an unexpected explanation for the refreshing,
invigorating effect of residences close to a waterfall or spring, or
even after rain.
Some of these reactions which IMPROVE WELL-BEING and physical and
mental capacity have since become known.
Negative ions produce an INCREASE in hemoglobin/oxygen
affinity so that the partial oxygen pressure in the blood
rises but the partial carbon dioxide pressure DECREASES.
This results in REDUCED RESPIRATORY RATE and ENHANCES the
METABOLISM of water-soluble vitamins.
In addition, negative ions produce an INCREASE in PH and, in
particular, an INCREASE in the SECRETORY performance of the MUCOSA
with an INCREASE in CILIARY MOVEMENT in the airways.
According to the studies of Fleischer and Pantlitschko, negative
ions probably also IMPROVE BLOOD FLOW by increasing the release of
proteolytic enzymes with fibrinolytic activity.
Wordens studied the adrenals of golden hamsters kept under the same
experimental conditions. The adrenals of animals treated with
POSITIVE ions weighed 33% LESS than the adrenals of animals treated
with normal respiratory air.
On the other hand, the weight of the adrenals from golden hamsters
treated with NEGATIVE ions was 29% HIGHER.
Olivereau found a 30% ENLARGEMENT of adrenals in rats after 20 days
of treatment with NEGATIVE ions. This finding suggests that the
ability of the adrenals to produce glucocorticoids is REDUCED by
POSITIVE ions and INCREASED by NEGATIVE ions.
Considerable INCREASE in VITAL CAPACITY were observed by M.A.
Vytchikova and A. Minkh in 1959, with the maintenance of blood sugar
and blood oxygen levels.
Thus, in a group of 9 sports students, Minkh found that ergometer
endurance was INCREASED by 260% in 32 days compared with a normal
control group following the INHALATION for 15 minutes DAILY of air
enriched with 1.5 million NEGATIVE small ions per centimeter.
Even before the 1976 Olympics, air ionization in the sleeping
quarters of team members was used to improve performance in sports
centres in the USSR and the GDR [M. Jokl, Prague].
Studies by Altmann in 1975 clearly show that the performance of
school children can, for example, be CONSIDERABLY INCREASED by
changing the electrical conditions of the rooms. Comparable effects
have also been achieved by the use of IONIZED AIR.
According to the latest information in the fields of medicine,
biology and meteorology, it can be definitively established that
atmospheric ions have a biological effect.
Atmospheric electrical factors are a component of our environment
and we humans are clearly affected by ELECTRO-IONIC MICROCLIMATES to a far greater extent than previously imagined.
This finding acquires particular significance since, as a result of
artificial air conditioning (e.g. atmospheric pollution, buildings,
air-conditioning units, heating, electrical installations,
plastics), civilized man spends 50-100% of his time in an
UNNATURALLY CHARGED ELECTROCLIMATE.
In cities, in closed rooms and in cars, etc., the proportion of
small negative ions in the atmosphere is markedly reduced compared
with undisturbed nature.
An atmosphere with an EXCESS of NEGATIVE ions, such as frequently
arise under open sky, usually INDUCES a complete VEGETATIVE TURN-
AROUND within twenty days.
In the curative phase of this total turn-around, the vegetative
nervous system is normally RESTORED and the course of infectious
diseases is essentially ATTENUATED (weakened) and (healing is)
ACCELERATED.
--------------------------
VANGARD NOTES:
The information in this paper provides more than sufficient
evidence that negative ion generators can only be a good
investment. The small decorative water fountains which cascade
or spray are not only visually appealing, but also provide the
pleasing sound of moving water. Now with the explanation of
the negative charge from the rupturing of the water molecule,
we can see how the atomizing process is a highly desirable
effect to bring about.
Many of the electronics magazines have ads in the back for
companies which sell surplus. We have seen small plastic
impeller pumps which could easily be built into a fountain or
waterfall. The cost is minimal, something on the order of $5
to $25 for the pump, plastic, plaster of paris, concrete,
fiberglass or earth all can be used to build the fountain.
A very neat and healthful project, in fact, something which
could make money for all you entrepeneurs. Many people would
buy such devices if they were available for a reasonable price.
One in the bedroom, where face it, we spend at least 6 hours
per day, one in the living room or den, where we spend up to 4
hours or more per day. There are lots of possibilites.
For that matter, the atomizer does not have to be decorative,
just a way to moisturize the air with the negatively ionized
droplets. Incidentally, most modern cooling systems use
refrigerated air which means the air is essentially
recirculated and the majority of the moisture is REMOVED.
Have fun and good health to you!
The Father of Oxygen Therapies
The reason so many people have been turned onto Oxygen Therapies is due to the daring and pioneering work of Ed McCabe. For years he has been at the forefront of the public making strides in introducing these cheap solutions, and was struck numerous times by the threatened Medical corporate state. In 1992 he published: O2xygen Therapies - A New Way of Approaching Disease. Many consider the doctor to be the father of Oxygen Therapies. For over nine years now, Ed has dedicated his life to furthering the cause, traveling the world in an attempt to get the word out.
ED McCABE BIOGRAPHY
Ed is an investigative journalist and leading international author, speaker, and
expert on the subject of oxygen therapies. His ongoing involvement with advanced
healing modalities encompasses a span of over 25 years. He holds a degree in
Educational Media from the University of Massachusetts, and he became expert on
the subject of oxygen therapies since focusing solely upon them as a research
journalist during 9 years of intensive study, investigation, experimentation,
interviews, and travel.
Although several oxygen therapies have been in use for over 100 years, Ed is the only
person to date who has undertaken a worldwide investigation and publication of
their effectiveness. To do this, he interviews thousands of patients and hundreds of
doctors, and regularly visits many of the major oxygen therapy centers worldwide.
Although oxygen therapies are stated by many experts to be highly effective, before
Ed's published works and his extensive lecturing, these therapies remained mostly
unknown to the general public, and the professional organizations promoting them
were in danger of floundering. The patents on most of the oxygen therapies had
expired years ago, so there had been little interest by the pharmaceutical houses and
the media in promoting them, and almost no advertising had been done to let
people know of their existence. Ed has daily spent the last 7 years of his life actively
changing this situation in order to lessen the all too common and unnecessary
suffering of people with serious diseases. The legion of converts to these therapies
grows daily, and the manufacturers and professional organizations surrounding
them are now flourishing, in very large part because of Ed's focusing the public's
attention on them. He created the Oxygen Therapy movement where there was none
before!
Ed has publications, tapes, and videos which have over 40 distributors in seven
countries, including the largest U.S. health book distributors. Now in its 40th
printing, his best-selling classic book Oxygen Therapies was the first publication in
history to detail all known ways of using special forms of oxygen to oxygenate the
body. Now millions know that the use of oxygen therapies is of prime importance in
order to maintain health and in the treatment of disease.
Ed writes a syndicated newspaper column and numerous national magazine articles
appearing in "Aids Patient Care," "Health Freedom News," "Health Consciousness,"
"Explore!," and "New Perspectives" magazines. He has been a very popular guest on
over 1,200+ radio and television stations and speaking platforms in the U.S.,
England, Scotland, Australia, Canada, Mexico, and New Zealand, including the U.S.'s
"Maury Povich" national television talk show on April 21st, 1993, which devoted a
whole show to the oxygen therapy work surrounding Ed and his associates.
Ed is the Executive Director of The Foundation For The Advancement Of Oxygen
Therapies, a not for profit public service organization. The Foundation is dedicated
to oxygen therapies research, education, and the spreading of the good news about
oxygen therapies through the media.
Ed is also a recipient of The International Bio-Oxidative Medicine Foundation's
prestigious "Special Recognition" and "Distinguished Speaker Awards."
Ed's publications and tapes can be ordered through:
Crossroads and Family Health News 1-800-635-5823]
Books
* O2xygen Therapies - A New Way of Approaching Disease
* Oxygen, Oxygen, Oxygen
* Hydrogen Peroxide, Medical Miracle
* The Use of Ozone in Medicine - 2nd Revised Edition
* Hydrogen Peroxide Therapy - Newly Revised 11th Edition
* The Un-Medical Miracle - Oxygen
* Oxygen Healing Therapies
* The Story of Ozone
* Ozone - Purifier of the Earth and Cleanser of all Living Beings
* Art of Breathing
* Super Power Breathing for Super Energy
O2xygen Therapies - A New Way of Approaching Disease
Product No: K989 Disease $15.00
By Ed McCabe
In this book Ed McCabe reveals:
* Current popular methods of increasing cellular oxygenation.
* Formulas, patents and ongoing lab scientific and medical studies.
* Anecdotal and medical case histories of former AIDS and other
degenerative disease victims, who were treated with oxygenation
methods by health professionals, and are now viral free.
This book is a virtual encyclopedia of all known ways of oxygenating the
body.
Oxygen, Oxygen, Oxygen
Product No: K463 $3.95
By Dr. Kurt Donsbach
DR.DONSBACH TELLS YOU WHAT YOU NEED TO KNOW ABOUT OXYGEN.
Spokesperson who has earned the respect and admiration of his colleagues
with his on target approach to nutritional care and preventive health
philosophy.
In this book Dr. Donsbach answers your health questions as he guides you
the intricacies of the human body.
* Understand the physiology of various conditions.
* Assist the body with nutrition oriented measures.
* Avoid health problems with good prevention.
* Apply proper dietary habits for specific conditions.
Hydrogen Peroxide, Medical Miracle
Product No: B01 $12.95
By Dr. William Campbell Douglass
No other chemical compound comes even close to hydrogen peroxide in its importance to life.
H2O2 is involved in all of life's vital processes. It is truly the wonder
molecule. The cells in the body that fight infection, called granulocytes,
produce H2O2 as the first line of defense against every type of invading
organism - parasites, viruses, bacteria and yeast. The presence of this
amazing substance is required for the metabolism of protein, carbohydrates,
fats, vitamins and minerals. It must be present for the immune system to
function properly. Join Dr. William Campbell Douglass as he reveals how
this fascinating, miraculous healer works to rid the body of disease. Dr.
William Campbell Douglass is a fourth generation physician. His family has
been serving the state of Georgia since 1850. He is a graduate of the
University of Rochester, New York; the University of Miami School of
Medicine; and the United States Naval School of Aviation and Space
Medicine. Dr. Douglass travels the world giving lectures, doing radio and
TV talk shows and gathering information that is not covered by our press.
Dr. Douglass was voted Doctor of the Year in 1985 by the National Health
Federation, and was a founding member and state president of the Florida
American College of Emergency Physicians.
The Use of Ozone in Medicine - 2nd Revised
Product No: B02 Edition $33.95
By Renate Viebahn
Part 1 is devoted to the history of ozone/oxygen therapy and to
its biochemical, technical and clinical applications.
Part 2 presents a selection of ozone equipment, safety precautions and
shows how to treat lesions, burns, virus infections such as herpes and
hepatitis, circulatory disturbances or rheumatic/arthritic complaints with
ozone.
A special yellow-pages section provides the therapist with an alphabetical
listing of indications and applications (e.g. acne, allergy, bathing
therapy with ozone, cancer, intramuscular injection, the use of ozone in
dental and veterinary medicine, use of ozonized water, wound healing) and
with guidelines for the treatment of each case.
Part 3 offers a comprehensive bibliography of European literature on
ozone/oxygen therapy and other useful information about organizations and
their publications, equipment and its manufacturer. It also offers a sample
of the brochure distributed to patients by the Medical Society for Ozone
Therapy.
Hydrogen Peroxide Therapy - Newly Revised 11th
Product No: K361 Edition $3.95
By Conrad LeBeau
Includes:
* Bio-oxidative Formulas you can make at home.
* Hydrogen Peroxide and Cancer - the scientific evidence.
* The historical use of ozone in the treatment of AIDS, by Dr. John
Pittman, M.D.
* New immune rebuilding diet plan
The Un-Medical Miracle - Oxygen
Product No: T663 $12.95
By Elizabeth Baker
Demand for the truth, for information, for help, is making The Un-Medical
Miracle - Oxygen by Elizabeth Baker a best seller with over 10,000 copies
in print. Now in a new updated version this book has even more to offer
those who need help and support for their health. Expanded and with more
practical and timely information concerning our greatest resource --
OXYGEN, it is a must reading for all concerned with the critical health
issues of today. The book plays a vital role in understanding the nature of
the therapies available to all of us for combating diseases. The safe and
natural element, oxygen is available to each and every one of us at a
fraction of the cost of standard contemporary medicine. Oxidation is life,
without it we would cease to exist.
A primary aspect of The Un-Medical Miracle - Oxygen is to make readers
aware that the therapies mentioned are not new. They have been around for
the better part of this century and are well documented, not only in the US
but around the world. Why should we let someone else decide the state of
our health and wellness when it is within our own power to do so? Oxygen is
nutrient number one, readily available to help us rebuild and recover, to
heal and not harm.
Elizabeth Baker has given us a book to do just that. It is a book inspired
by a woman who has known the suffering of disease and the road to recovery.
It's Elizabeth's great joy to share the knowledge and information gathered
from her research. Her own experience has proven the worth of her words.
Elizabeth devotes her life to helping others through nutrition and
alternative health therapies. She continues to travel around the world,
making available her wit and expertise on the subject of health and
nutrition in classes, lectures and on radio and television.
This book is the perfect follow up to the UN-MEDICAL BOOK in offering
people the best opportunity for optimal health. Elizabeth has given years
to the study of rejuvenation of health. A mostly raw food diet was a key
turning point in her quest to conquer Addison's Disease, colon cancer,
arthritis and a weakening immune system.
Oxygen Healing Therapies
Product No: 1306 $12.95
By Nathaniel Altman
Scientists recognize that most disease states - including heart
disease, cancer, immune disorders such as candida and infections
related to HIV - are caused by oxygen starvation at a cellular level. We
receive most of our oxygen from the air around us, but breathing isn't
always enough. With the new bio-oxidative therapies you can actually
generate more oxygen in your body to achieve optimum health and longevity.
OXYGEN HEALING THERAPIES is the only book on the subject to place
bio-oxidative therapies in the context oh holistic health. Assembled here
is the latest, most reliable and most accessible information about the
therapies, how they work and what to do to promote the healing process. The
author also shows how you can enhance the effectiveness of the treatment
through diet and the use of minerals, herbs, exercise and visualization.
Nathaniel Altman traveled to Germany and Cuba and interviewed scientists
from Russia, France and the United States to obtain documented scientific
evidence and clinical findings. He demystifies the terms "antioxidants" and
"free radicals", describes oxygen's role as a detoxifying agent and
explores various bio-oxidative therapies that can help restore oxygen to
the immune system at a cellular level and increase vitality.
The Story of Ozone
Product No: B03 $10.00
By Plasmafire International
THE STORY OF OZONE contains a collection of several articles, stories and
letters covering the medical history ozone therapies, uses of ozone
therapies and many different applications of ozone therapies. Some of the
authors include; Saul Pressman, Fritz Schellander, Dr. Kurt Donsbach, Alive
Magazine and the Canadian Government.
Ozone - Purifier of the Earth and Cleanser of all Living Beings
Product No: B04 $71.95
By H. E. Sartori, M.D.
This book, the result of over 40 years of experience with all
aspects of ozone, is perhaps the most complete listing of
applications of ozone compiled so far. It offers detailed protocols for the
effective treatment of degenerative diseases including cancer, AIDS,
rheumatoid diseases, multiple sclerosis, Alzheimer, Parkinson, allergies
and immune diseases, infectious diseases, cardiovascular disease,
rheumatoid arthritis and systemic lupus erythematosus, diabetes mellitus,
impotence, cataracts and many other conditions. It also discusses
veterinary ozone applications, sterilization of blood and blood products
with ozone, preservation and enhancement of topical with ozone, as well as
a comprehensive system of environmental cleanup including toxic waste,
destruction transmutation of radioactive wastes, metal separation and
beautification of ecoparks.
Throughout the work, a comprehensive holistic approach is stressed whereby
ozone, in most cases, is the only part of a comprehensive treatment program
which includes diet and lifestyle, specific nutrients, herbal treatments,
homeopathy, EDTA - Chelation, neural therapy, electromagnetic therapies,
cell and thymus therapies and other complementary methods.
Art of Breathing
Product No: T1779 $9.95
By Nancy Zi
Progressive exercises, specific applications, and mental imagery drills
teach the oni yi method of controlled breathing.
Super Power Breathing for Super Energy
Product No: B641 $6.95
By Paul Bragg & Patricia Bragg
Formerly titled: "super brain breathing". Revised and expanded to better
teach readers how to resist disease by using their lungs to the fullest
capacity.
Breathing deeply' calms the nerves' and fully energizes the body and can
fill us with peace so that we can experience a longer, healthier, more
youthful life.
The next nutrient we now introduce from various perspectives and viewpoints, is the Aloe Vera plant. In addition to its rich nutrients, it also harbours superconductive mono atomic ellements (re Dr. David Hudson's special analysis). Thus it may well be related to the White Lion of alchemy, and certainly provides the body with more mega herz of life force, and thus light. Its other affects are equally astounding.
Digestion & the Immune System
& Aloe Vera MPS
--------By Dr. John C. Pitmann, M.D.--------
Poor digestion results in two primary problems:
1. Food is not broken down into the elemental building blocks necessary
for the body to rebuild itself and generate energy for metabolism. At
a cellular level, toxins are not removed from the cells, sufficient
nutrients are not moved in to the cell, and not enough energy is
produced for cell functioning. This effects all cells including the
immune system cells such as white blood cells, which then lack the
fuel and the oxygen to carry out their normal function.
2. Even more significant is that maldigestion results in food remnants in
the gut causing several pathological reactions. First, there is
irritation of the intestines, causing increased permeability of the
cells in the intestinal wall. Undigested protein can then leak across
into the lymph system and then into the general circulation, with the
immune system reacting to contain the foreign invaders. The immune
system becomes overtaxed and runs down. Oxygen and fuel gets used up;
the immune cells wear out faster and do not reproduce in sufficient
numbers.
Undigested food remnants can also become a breeding ground for candida and
several types of parasites. Candidiasis produces toxins that cause
increased digestion dysfunction, food allergies, fatigue and a host of
other problems. Ultimately, this causes the immune system to become even
further depressed.
The inflammation in the intestines causes further damage by causing
reactions that produce oxidative free radicals as waste by-products. Then
negatively charged oxygen molecules begin to chop holes in cell membranes
in an attempt to grab a positive charge. This results in further damage to
the intestinal walls and ever increasing permeability. The leaky gut
syndrome increases with more food particles going into the blood.
Research has shown that Aloe mucopolysaccharides have a remarkable ability
to normalize all of these damaging processes, which has the effect of
enhancing the immune system function through improved digestion. Aloe
mucopolysaccharides act as a potent anti-inflammatory agent, stopping the
damage and leakage of the intestinal wall, thereby taking the stress off
the immune system.
Aloe mucopolysaccharides have direct ant-bacterial, anti-viral,
anti-fungal/yeast and anti-parasite effects. Chronic yeast growth can be
controlled so the normal, healthy flora can then thrive more easily.
Furthermore, the macrophages, monocytes, antibodies and T-cells are
stimulated. Phagocytosis (when large white blood cells engulf particles) is
dramatically increased to ingest foreign proteins, such as the HIV virus.
Aloe mucopolysaccharides increases the number and intensity of all immune
cells in the body.
The key to integrating healthy digestion with a healthy immune system is
the oral ingestion of Aloe mucopolysaccharides.
Aloe Vera Saves A Doctor's Life
By Dr. David Wheeler , D.C.
Published In The March/April 1996 Issue Of "To Your Health"
In May of 1995 I believed I was going to die. I was so sick that every living
moment was an agony. I had no idea that I was actually about to undergo
a powerful and unforgettable healing experience.
I had been ill for three years--ever since a trip to India where I came down
with bacterial and amoebic dysentery. Tropical medicine specialists had
prescribed potent drugs, but even so I continued having recurrent nausea,
fatigue, cramping, and bloody stools. Each time the dysentery came back, I
took another course of toxic medication.
In January of 1995, when I took the final course of drugs, the side effects
were devastating. My immune system literally crashed. My throat became
so sore I could barely swallow, my joints hurt unbearably with arthritis,
and lumps appeared in my neck that ultrasound tests indicated were
tumors.
I had been trained in Network Chiropractic (a gentle and powerful system
of chiropractic developed by Donald Epstein, D.C., and practiced around
the world), and out of this developed my own energetic system of body
work. I am actually able to see energy patterns. Disease appears to me as
energetic patterns of different colors and densities. I had always believed
in the innate healing potential of the human body, so to help heal myself I
left Manhattan to rest in Hood River, Oregon. I believed that rest alone
would heal me.
But even in a setting of sylvan beauty my health continued to deteriorate
rapidly. I returned to New York and my wife was shocked at my
appearance: the swelling in my throat made me look like a bullfrog. She
sent me to a holistic doctor in Toronto who gave me almost every
alternative treatment in the book: ozone, vitamin and botanical injections,
special herbal and nutritional supplements, life crystals, deep thermal
therapy, radionics and more. Nothing had any significant impact. I
returned to Oregon, and began to suffer from brief blackouts.
One morning when I woke, I had severe vertigo, roaring in my ears, and
hearing loss. I sensed I was close to dying. My faith in healing, the whole
edifice upon which I built my practice as a chiropractor--was deeply shaken
and I became so emotionally fragile that I was unable to withstand any
stress at all.
My wife, Meeta, suspended her Manhattan healing practice to fly out to
me. She put me on a diet of raw vegetables and fresh juices. It helped my
joint pain, but other symptoms raged on. My life funneled down to one
single pleasure: Sleep.
MY LAST CHANCE
My wife and I drove to a bookstore in Portland specializing in alternative
healing. There we happened to see a poster advertising an all-day seminar
by David Hudson, a researcher I'd heard about in Toronto. Hudson had spent
huge sums of money researching a truly wild premise: the idea that there
were elements in the periodic table that consisted of only a single atom
per molecule. He called them monatomic elements.
According to complex scientific literature cited by Mr. Hudson, these
elements could actually generate photons (light particles), and in the body
this transmission of light would allow the body to heal itself. (The theory
behind this supposition involves superconductivity research carried out by
the U.S. Navy on actual living cells, as well as an understanding of how
RNA and DNA communicate.)
There were 11 of these monatomic elements, Hudson claimed, and at a
laboratory in Arizona he had been working with a world famous metallurgist,
Dr. Sicafoose, who had developed methods to study them. Monatomic elements
exist in relatively high concentration in certain plants.
Aloe Vera is one of these plants. According to Hudson, monatomic elements
exist within the structure of the mucopolysaccharide molecules in pure Aloe
Vera gel. The mucopolysaccharide molecule is a complex carbohydrate, which
is many sugar molecules linked together. Mucopolysaccharides have been
demonstrated to have a wide range of healing effects.
The long chain sugars have been isolated and extracted by a laboratory in
Texas, which has developed a freeze dried extract of the pure
mucopolysaccharides, classified by the FDA as an investigational new drug.
However, the lab also manufactures the same extract in a powder that
contains 60% of the pure freeze dried sugars, and remarkably, this is
allowed by the government to be sold as a nutritional supplement.
OVERNIGHT HEALING
Was it a lucky coincidence? In Toronto I had purchased capsules of the
mucopolysaccharides, but I hadn't taken them. I went home and emptied
thirty capsules into water, drank the mixture all at once, and within
twenty minutes felt a profound and incredible energy shift. I could
actually watch the light as it began to flow down my arms and legs and
saturated my thymus gland and heart area. Drenched in Light, I sat down and
meditated.
Within three days of taking the supplement, I was feeling so much better
that I was actually able to go swimming in a river and hike a few miles
with my wife. MY vertigo, cramps, pain, fatigue, depression had decreased
dramatically. And the lumps in my neck began to shrink.
I could hardly believe that I had stumbled upon the answer to my health
crisis. I immediately began to research the scientific literature about
Aloe, and discovered that the plant has different lengths of the long chain
sugars, which correspond to different healing effects (according to Dr.
Ivan Danhof, M.D., Ph.D.). Think of the many different lengths as
necklaces. Some of the necklaces have as few as sixty beads, the longest
have thousands. The kind of Aloe gel and juice that is typically available
in the healthfood store contain only shorter "necklaces" because of a
natural enzyme on the aloe leaf that breaks down these log chain
muccopolysaccrides unless it (the enzyme) is properly deactivated. The
benifits of these shorter lenght chains is limited to anti-inflammatory
properties which is one of the reasons why they're effective in healing
burns and sunburns.
Aloe also contains medium size muccopolysacchride "necklaces" that can help
regulate blood sugar in diabetes, and fight bacteria and viruses. The
longest "necklaces" are the ones that can actually boost the immune system.
The freeze dried powder that I took contains all the different lengths of
the sugar "necklaces." Interestingly enough, only 2 parts per thousand of
the Aloe plant is composed of mucopolysaccharides!
I took 1,000 milligrams--or 1 teaspoon--of the powder a day for four
months, then raised the dosage to 4 teaspoons a day for six weeks, and then
dropped to a maintenance dose of a quarter of a teaspoon daily.
These dosages were based purely on intuition and sensing the changes in my
body: When I first took the powder, I went through a detoxifying phase, and
could not tolerate more than a teaspoon a day. Now, because I am much
healthier, I don't need more than the maintenance dose, and in fact, if I
take more, I don't feel right.
I recently asked my wife what her impressions were at the time I was at my
sickest. She said, "What frightened me was how fast you became ill. You
went in a downward spiral that just got worse and worse. Before that, you
were so vital and involved in life. After you took the Aloe powder I saw
such a dramatic change in your health."
Making The Freeze-Dried Aloe Vera MPS Available
I have decided to distribute the product myself at a reduced price in its
pure powder form, rather than in the capsules.
Now, through word of mouth, individuals from around the country are
contacting me to purchase the product, which I have named, MPS-GOLD. I have
started a company, Light Resources Unlimited. to distribute this product.
A woman in South Fallsburg who was diagnosed with AIDS and had a chronic
fungal infection for several months took the product; within two weeks the
infection was gone. A Vermont woman had suffered from ulcerative colitis
for many years, within a few weeks of taking the product she called me to
tell me 90% of her debilitating symptoms had vanished.
I recently heard from a Lyme's Disease victim who said on the first day she
took MPS-GOLD her energy level improved dramatically. A man from Texas who
has been diagnosed with pancreatic cancer is feeling much better and has
weight gain after only two weeks of taking the product.
I've found that MPS-GOLD is effective for spiritual healing as well. It's
as if light works on all levels. A man came to me after meditating in an
ashram in India for eight years. He had returned to New York in good
health, but the stress of living in the city had caused his health to
collapse. He told me that as soon as he took the product this energy field
expanded and he returned to good health.
I believe that the Aloe plant holds great healing potential. I hope to
offer other individuals the opportunity to experience similar healing
breakthroughs.
---------------------------------------------------------------------------
David Wheeler, D.C. is a Network Chiropractor. He can be reached at 20 West
20th Street, Suite 803, NY, NY 10011 (212)741-8187
Fundamentals of Aloe Vera
Mucopolysaccharides (MPS)
----DR. Ivan Danhof, M.D., Ph.D.----
The Aloe Vera mucopolysaccharide (MPS) is a long chain sugar molecule
composed of individual mannose and glucose sugar molecules connected
together. There is wide range in the size of the mucopolysaccharide
molecule.
The varying sizes determine their healing properties:
1. Small/50-600 molecules. Reduces inflammation--which is involved in
such diseases as ulcerative colitis, arthritis, and gastric reflux.
Also helps with the reduction of blood sugar with both type I and II
diabetes.
2. Medium/up to 1500 molecules. Where as vitamins and minerals can only
function outside the cells, mucopolysaccharides are very effective
intracellular antioxidants and free radical scavengers--very important
in preventing and treating arteriosclerosis, heart disease and
Parkinson's disease. With the ever increasing pollution on the planet
and loss of nutrients in the soil, the increase in free radicals and
loss of cellular oxygen will only become worse with time. This makes
Aloe Vera mucopolysaccharides even more important than ever.
3. Large/up to 5,000 molecules. Has a direct anti-bacterial and
anti-viral effect. Important with all the new infectious diseases
cropping up and the older ones becoming more virulent from long term
use of antibiotics.
4. Very large/up to 9,000 molecules. The very large molecules are immune
modulating, which have a powerful healing effect on AIDS, cancer and
many different immune system disorders. It is also this large molecule
that causes the body to produce a natural chemical, tumor necrosis
factor, that functions to shut off the blood supply to tumors.
The mucopolysaccharide molecule is very fragile. When the leaf is cut,
enzymes in the plant are released which breaks down the long chain sugars
of the mucopolysaccharide into simpler sugars, which then results in a loss
of the different healing properties. There are very few products on the
market that can claim to contain stabilized mucopolysaccharides.
Stabilization requires extraction of the mucopolysaccharides in a freeze
dried form; but also the process must include a way to deactivate the
enzymes released in the plant when it is cut. Furthermore, the high
concentration of mineral salts found in Aloe Vera gel must be separated
from the final extract because they are very irritating to the gut. An Aloe
product must be very soothing to the gut to promote healing.
Synergism is a property that many of the large Aloe companies tout who do
not have the patented technology to extract stabilized mucopolysaccharides.
In other words, many of these companies claim that all 200 of the various
ingredients found in Aloe Vera must be present for healing to occur. But
none of these claims have any basis in scientific research, while there is
abundant scientific research to prove that the mucopolysaccharide is the
sole ingredient responsible for all the healing properties attributed to
Aloe.
REMEMBER IT IS THE POLYSACCHARIDE CELLS WHICH REACT TO NEGATIVE IONS. IT IS THEIR PEREPHERY CHARGE WHICH IS CHANGED, CREATING THE FARDAY AFFECT TO THOSE GIVEN CELLS SATURATED BY THE 8 POSIBLE ELECTRONS (ECSTASIS). ALLOWING ONLY 8 HZ WAVES IN (COHERENCE: LOVE: HARMONY), AND ALLOWING ACCESS TO THE SUPERCONDUCTIVE INFORMATION OF THE CELLS. HERE ALOE VERA OFFERS SOME CLUES.
ALOE & Cancer Research
Research by the immunologist Ian Tizard, Ph. D. and virologist Maurice
Kemp, Ph.D. from Texas A&M led to the discovery that Aloe
mucopolysaccharide is taken into a special leukocyte, the macrophage, and
this cell is stimulated to release messenger molecules called cytokines
(interferons, interleukines, prostaglandins, tumor necrosis factor and
stem-cell growth factors.)
Tumors release a chemical that attracts blood circulation so that malignant
cells have a supply to the tumor and it therefore dies. All of the immune
modulating effects from Aloe contribute greatly to the prevention and
healing of malignant cells.
Colitis and Crohn's Disease
In 1986 there was an initial FDA sanctioned clinical pilot study for
treating ulcerative colitis and Crohn's disease with Aloe
mucopolysaccharides, with very encouraging results. In 1993-94 a six center
clinical study was conducted with Vanderbilt Medical Center
Gastroenterology Department. The results were encouraging enough to
continue with a second phase that began in 1995.
Proven Non-Toxic
The Aloe Vera mucopolysaccharide molecule is a complex carbohydrate, a food
chemical, and is totally non-toxic. Gallen Marshall, M.D., Ph.D., professor
of immunology and allergy at the University of Texas Health Science Center
in Houston injected 50 medical students in 1993 with Aloe
mucopolysaccharides, with FDA approval, and confirmed that there were no
toxic side effects (no toxicity in the liver, bone marrow, kidneys and
cells in general).
Composition:
MPS-GOLD is a freeze dried powder, extracted by a special patented process
from freshly harvested, organically grown Aloe Vera leaves. It is composed
of approximately 60% stabilized longchain mucopolysaccharides and 40%
inactive (inert) plant substances. It contains no added fillers or
preservatives.
Comparisons:
Only two thousanths of one percent (.2 or 2 parts per thousand) of commonly
available (store bought) Aloe Vera gel is long chain stabilized
mucopolysaccharides. It takes approximately 7 gallons of these Aloe Vera
gels to make the equivalent - in terms of long chain muccopolysaccharides -
of one ounce of MPS-GOLD!
To Order by Visa or Mastercard Call:
1-800-760-3530
or 212-741-8187 outside of the US
If you would like to order MPS-GOLD refer to price list below for the
quantity you desire. For powerful healing effects, higher doses are
recommended. At three grams a day, one ounce will last a month. For general
healing or maintenance, lower doses are sufficient. At one gram a day, an
ounce lasts about four months.
Included with each order are dosage instructions tailored to specific
healing needs, a review of the scientific literature and a special audio
tape on Aloe mucopolysaccharides by the foremost expert, Ivan Danhof, M.D.,
Ph.D.
PRICES:
* 1/4 ounce: $75.00
* 1/2 ounce: $99.00
* 1 ounce: $170.00
* 3 ounces: $400.00 (equals $133.33 per ounce)
* 6 ounces: $775.00 (equals $129.67 per ounce)
* 12 ounces: $1500.00 (equals $125.00 per ounce)
Shipping Charges:
* One to three ounces $10.00
* Four to twelve ounces $14.00
* Over 12 ounces$16.00
New York residents please add 8.25% percent sales tax.
Make Checks or Money Orders payable to:
Light Resources Unlimited.
20 West 20th Street
Suite 803
New York, NY 10011 USA
VITAMIN C, SEE, SEA C# 261
One of the major nutrient, albeit enzymes, which the human race is an anomaly not to produce themselves, is ascorbate, or Vitamin C. Literally, every animal produces upto 15 gms a day of Vitamin C, and human beings produce ZERO. We are the only beings to be in such a position on Earth (it almost appears to be a deliberate editorship, along with our other anomolies). Vitamin C has overwhelming evidence for stopping most virus's, and even stopping cancer on one injection, and furthermore, literally shrinking tumours. In this domain especially, one can proove a conspiracy is at hand. As even Dr. Linus Pauling, the only single man ever to have won the Nobel Prize two times, was attacked a ridiculed for the rest of his life, for his adament exposures on the evidence for ascorbate treatment against cancer and other diseases, despite his absolute genius, to include the discovery of the single Helix of the DNA, before Francis Cricks double Helix. With the latest research and evidence, this evidence is now even more overwhelming. What follows now is the amunition you may need at hand, in order to defend youself against the silent war, and with which you can actually step beyond the unconscious war programmes inculcated into your doctor, via the Rockefeller and Rothschilde sponsorred education programmes. Millions do not need to die or suffer, if the following would be known and implemented cheaply by them, without side-affects. Millions of dollars could be saved and placed into solutions for a planet that is in dire straits for solutions. WAKE UP HUMANITY and C.
VITAMIN C:
THE NONTOXIC, NONRATE-LIMITED, ANTIOXIDANT FREE RADICAL SCAVENGER
(C) Robert F. Cathcart, III Allergy, Environmental, and Orthomolecular
Medicine 127 Second Street, Los Altos, California 94022, USA Telephone
415-949-2822. Medical Hypotheses, 18:61-77, 1985.
ABSTRACT
The amount of oral ascorbic acid that a patient can tolerate without
diarrhea, increases somewhat proportionately to the "toxicity" of his
disease. Clinically, in a disease ameliorated by ascorbate, there is a
suppression of symptoms only with very high doses and approximately to that
extent which a nonrate-limited,_antioxidant_free_radical_scavenger, might
be expected to affect that disease process if all harmful free radicals and
highly reactive oxidizing substances were quenched. In most pathologic
processes, the rate at which free radicals and highly reactive oxidants are
produced, exceeds the rate at which the ordinary rate-limited antioxidant
free radical scavenging mechanisms can quench those free radicals and
oxidants. When ascorbate acts as a scavenger, dehydroascorbate is formed;
but if the ascorbate/dehydroascorbate (AA/DHA) ratio is kept high (the
redox potential kept reducing) until the unstable dehydro- ascorbate
undergoes hydrolysis or can be reduced back to ascorbate, the
dehydroascorbate will do no harm. Since even at very high doses, ascorbate
is virtually nontoxic, it may be given in the enormous doses necessary to
quench almost all unwanted free radicals and oxidants. The wide spectrum of
infectious diseases ameliorated by massive doses of ascorbate indicates
some common pathologic processes in these diseases.
INTRODUCTION
Based on my experience with over 11,000 patients during the past 14 years,
it has been my consistent observation that the amount of ascorbic acid
dissolved in water which a patient, tolerant to ascorbic acid, can ingest
orally without producing diarrhea, increases considerably somewhat
proportionately with the "toxicity" of his illness. A person who can
tolerate orally 10 to 15 grams of ascorbic acid per 24 hours when well,
might be able to tolerate 30 to 60 grams per 24 hours if he has a mild
cold, 100 grams with a severe cold, 150 grams with influenza, and 200 grams
per 24 hours with mononucleosis or viral pneumonia. The clinical symptoms
of these diseases and other conditions previously described, are markedly
ameliorated only as bowel_tolerance dose levels (the amount that almost,
but not quite, causes diarrhea) are approached (1-6).
TABLE I - USUAL BOWEL TOLERANCE DOSES (4)
GRAMS PER NUMBER OF DOSES
CONDITION 24 HOURS PER 24 HOURS
normal 4 - 15 4 - 6
mild cold 30 - 60 6 - 10
severe cold 60 - 100+ 8 - 15
influenza 100 - 150 8 - 20
ECHO, coxsackievirus 100 - 150 8 - 20
mononucleosis 150 - 200+ 12 - 25
viral pneumonia 100 - 200+ 12 - 25
hay fever, asthma 15 - 50 4 - 8
environmental and
food allergy 0.5 - 50 4 - 8
burn, injury, surgery 25 - 150+ 6 - 20
anxiety, exercise and
other mild stresses 15 - 25 4 - 6
cancer 15 - 100 4 - 15
ankylosing spondylitis 15 - 100 4 - 15
Reiter's syndrome 15 - 60 4 - 10
acute anterior uveitis 30 - 100 4 - 15
rheumatoid arthritis 15 - 100 4 - 15
bacterial infections 30 - 200+ 10 - 25
infectious hepatitis 30 - 100 6 - 15
candidiasis 15 - 200+ 6 - 25
There was a remarkable lack of systemic difficulties in these patients that
could be directly related to the massive doses of ascorbate. The majority
of these patients, ill with some acute or chronic disease, were able to
take massive doses of ascorbic acid orally without difficulties. Minor
complaints about ascorbic acid such as it causing gas, diarrhea, or acid
stomach, while common in well persons even at low doses, were rare in very
sick patients. Low or moderate doses (doses substantially below bowel
tolerance) usually had no noticeable immediate beneficial effects, but high
doses (doses just below the amount that would produce diarrhea in a patient
tolerant to ascorbate) would have the effect of markedly suppressing
symptoms as the high dose levels were reached. This sudden effect is often
quite dramatic clinically and is not usually obtained even partially at
lower doses. It is as if a threshold were reached at which point the
ascorbate becomes very effective.
Mixtures of mineral ascorbates (calcium, magnesium, potassium, zinc, and
sometimes sodium) are used in certain circumstances to increase bowel
tolerance for even more clinical effectiveness but do not clearly
demonstrate the increasing bowel tolerance phenomenon being discussed here.
Knowledge of the known vitamin functions of ascorbate would not have
allowed one to predict these beneficial results. The lack of serious
difficulties with these massive doses is surprising.
EFFECT OF ASCORBATE
DETOXIFICATION DRAMATIC IN SELECTED GROUP:
Part of the unexpected benefit at the high dose levels is frequently a
feeling of well-being. This feeling of well-being, especially with the more
toxic conditions, is despite the gas and diarrhea sometimes produced. If
the malaise from the basic disease is great (e.g. mononucleosis, acute
hepatitis, viral pneumonia, etc.), the obvious benefit from ascorbic acid
is usually so great that the patient usually cares little about the minor
gastrointestinal disturbances. Lowering dose levels too soon before bowel
tolerance decreases, results in the return of the malaise and other acute
symptoms of the disease.
The_clinical_sensation_experienced_with_the_massive
doses_of_ascorbate_is_one_of_"detox- ification"_as_a_threshold_is_reached.
By raising and lowering the doses, the symptoms of "toxicity" can be
readily turned off and on rapidly by some skilled patients.
I cannot emphasize enough that in "selected" patients (selected only by
excellent tolerance to ascorbic acid, good understanding of the principles
of determining the flexible bowel tolerance doses, and the willingness to
follow directions in fine detail), this effect is invariable, dramatic, and
unmistakable. The patient most likely to experience this effect is the
psychologically stable, not suggestible, practical, not liking to be sick
patient, with a "cast iron stomach." Children and teenagers, much as they
may hate the taste of ascorbic acid in water, make particularly good
patients once they experience the ameliorating effects of these massive
doses. Infants, upon receiving very large intramuscular or intravenous
injections, frequently "detoxify" in minutes to the astonishment and marked
relief of their parents.
These feelings of well-being experienced by tolerant patients from the
ingestion of massive doses of ascorbic acid are definite clinical
indications that no acidosis or other acute toxic metabolic effect is
resulting. Massive intravenous doses of sodium ascorbate are even more
impressive than oral ascorbic acid, because the beneficial effects are even
more dramatic and gastrointestinal gas and diarrhea are not produced.
Patients who ordinarily would be relatively incapacitated, can usually
remain functional and sometimes even participate in athletics if frequent
and massive ascorbate doses are maintained.
Patients must be encouraged to take these massive doses. Patients taking
vitamin C on their own, seldom take doses high enough to discover this
effect. I do not want to give the impression that this method is easy to
use; the mechanics of taking these doses can be very difficult for many
patients. Nevertheless, when properly instructed, the majority of patients
are able to achieve these effects. If a patient is relatively intolerant to
oral ascorbate only because of gastrointestinal complaints, and if his
disease is one that usually responds to oral ascorbate in tolerant
patients, and if the severity of the condition warrants the inconvenience
and expense, then intravenous ascorbate is indicated.
Such effects of these large doses of ascorbate cannot be readily explained
from its known vitamin functions. The spectrum of diseases affected by
massive doses of ascorbate is a wonder in itself, but also gives some hint
at the probable mechanisms involved. The sudden detoxifying effect
experienced clinically only at the very high threshold doses, suggests that
ascorbate is participating in chemical reactions where a critical
concentration of ascorbate is necessary, or where a certain ratio between
ascorbate and certain other reactants must be achieved. The concept that
free radicals and other highly reactive oxidants are a frequent factor in
pathologic processes (7,8) and that ascorbate is an antioxidant free
radical scavenger, could explain much of this.
THE RATE LIMITATIONS OF ANTIOXIDANT FREE RADICAL SCAVENGERS, A CAUSE OF MANY PATHOLOGIC PROCESSES
Chemical reactions involving free radicals and highly reactive oxidants are
necessary in the normal metabolism of cells. Metabolic processes utilizing
oxygen (aerobic metabolism) which release energy are important examples.
Ordinarily, these reactions occur in conjunction with appropriate enzymes
or in the proper places within the cells. While it has been documented that
potentially harmful reactants leak from their normal cellular confines and
are potentially toxic (9), these rates of leakage are usually low enough
for the natural antioxidant, free radical scavenging mechanisms to handle.
One of the causes of natural aging may be that some (albeit small) portion
of stray free radicals inevitably escape quenching (10). While the human
body does contain many free radical scavenging mechanisms for the purpose
of mopping up free radicals, I hypothesize that in_pathologic
processes_these_rate-limited,_mechanisms_are_acutely_inadequate_t
o_neutralize the_volume_of_free_radicals_produced. A threshold is reached
where these additional free radicals produced, initiate an inflammatory
cascade, can cause immune suppression, and can result in degenerative
diseases.
EXAMPLE OF A RATE-LIMITED, ANTIOXIDANT
FREE RADICAL SCAVENGING PATHWAY
In general free radical scavenging occurs through complex metabolic
pathways involving many steps which are rate-limited. Deficiencies of
nutrients, vitamins and minerals, which make up the enzymes and coenzymes
of these systems can slow down or halt certain pathways.
It is apposite to describe one of these rate-limited, free radical
scavenging mechanisms, to give the impression of its complexity and why it
is rate-limited. The example chosen involves the glutathione pathway which
is possibly one of the most important pathways.
When, for example, a superoxide radical must be destroyed, superoxide
dismutase can catalyze its conversion to O2 and H2O2 (11). Ascorbate,
nonenzamatically, also converts superoxide to H202 but is oxidized in the
process to the ascorbate free radical and dehydroascorbate. The ascorbate
free radical and the dehydroascorbate are reduced back to ascorbate either
by NADH (catalyzed by semidehydroascorbate reductase and forming NAD) or
reduced glutathione (GSH) (catalyzed by dehydroascorbate reductase and
forming oxidized glutathione (GSSG)) (12). Some of the peroxide can be
converted to oxygen and water by catalase but most will be destroyed by a
glutathione-requiring enzyme system. GSH (catalyzed by glutathione
peroxidase) reduces the peroxide to water but in the process is oxidized to
GSSG. The resulting GSSG is reduced by NAD(P)H (catalyzed by glutathione
reductase). The resulting NAD is reduced back to NADH by way of the Krebs
cycle or resulting NADP is reduced back to NADPH by the hexose
monophosphate (HMP) pathway. It is thought that commonly the rate-limiting
step in the last series of reactions is that catalyzed by glutathione
peroxidase and its cofactor selenium, but other substances which could
limit all this are the vitamin E, vitamin C, vitamin B2, vitamin B3,
cysteine, etc. Note: the ascorbate used in this example is as in the
vitamin C sense; the small amount available is oxidized to dehydroascorbate
and then must be reduced back to ascorbate by the pathway described, to be
reused as ascorbate. One can easily see how this mechanism and similar
mechanisms could be overwhelmed by a toxic pathogen liberating free
radicals or by an inflammatory cascade regardless of its cause.
FREE RADICAL SUPPRESSION OF THE IMMUNE_SYSTEM, COMMON
TO MOST INFECTIOUS DISEASES, NEUTRALIZED BY ASCORBATE
I further hypothesize that the pathogens of most acute infectious diseases
depend upon free radical toxicity to defend themselves against immediate
destruction by the immune system. If a pathogen produces free radicals at a
rate sufficient to exceed the rate at which the host can produce free
radical scavengers to protect the immune system, the pathogen will be free
to invade and multiply. The more toxic pathogens produce more free radical
toxins than just necessary to suppress the immune system. The spill over of
free radicals reaches a threshold where an inflammatory cascade in the
tissues affected, is initiated.
Neutrophils liberate free radicals and highly reactive oxidants both
intracellularly and extracellularly in their attempt to destroy pathogens,
in the process termed the respiratory burst (13-18). The respiratory burst
consumes NADPH which must be continually restored if the respiratory burst
is to be maintained. Restoration of NADPH supplies is accomplished by way
of the HMP pathway, by various rate-limited enzymatic mechanisms.
I suggest that if rate-limited enzymatic processes or the limited
availability of the antioxidant free radical scavenging mechanisms of the
leukocytes, superoxide dismutase (18), catalase (20), glutathione
peroxidase, and glutathione (21-23), fall short of being able to contain
and direct free radicals and reactive oxidants toward the pathogen, that
failure causes the free radicals to backfire, damage the host itself, and
initiate an inflammatory cascade.
If a critical tissue concentration of free radical scavenger could protect
the immune system from the free radicals produced by the pathogen, and
would assist the leukocytes in modulating their own free radical
generation, the immune system might be expected to prevail and destroy the
pathogen rapidly by direct phagocytosis. If such a scavenger were found to
be effective in large numbers of infectious diseases, it could imply that
there was a common mechanism of free radical suppression of the immune
system operative in all these diseases. Until such a free radical scavenger
were recognized to exist, the commonality of such a mechanism to all these
diseases might be overlooked. I hypothesize that ascorbate is, in fact,
such a free radical scavenger when used in the doses being discussed. Its
effectiveness in a wide spectrum of infectious diseases is evidence of the
common mechanism many pathogens have of sup- pressing the immune system.
By neutralizing virtually all unwanted free radicals and toxic oxidants,
massive doses of ascorbate can be made to protect the immune system to such
a degree that early in acute viral diseases, the immune system can usually
destroy the pathogen within hours. When used later in the course of an
acute viral disease where the pathogen has established itself
intracellularly in significant numbers of cells, massive doses of ascorbate
can protect the immune system, suppress most symptoms, and prevent
secondary complications until the immune system destroys the pathogen by
secondary means such as with antibodies.
I have found that massive doses of ascorbate work synergistically with
appropriate antibiotics when used against acute bacterial diseases, and
broaden the spectrum of the antibiotics considerably. I have not been able
to explore thoroughly the extent to which ascorbate can be used alone in
bacterial diseases, but I have had some serendipitous clinical evidence
that certain bacteria do very poorly in the face of massive doses of
ascorbate even where antibiotics were not used.
Conditions involving indolent bacterial infections such as chronic
bronchitis, sinusitis, otitis media, tonsillitis, osteomyelitis,
nonspecific urethritis, etc., are frequently cured by massive doses of
ascorbate.
I_hypothesize_that_probably_induced_localized_scurvy_plays_a_deci
sive_part_in
a_pathologic_equilibrium_set_up_between_the_chronically_infected_
tissue_and_the pathogen. When the induced scurvy is eliminated by driving
tissue levels of ascorbate up above a certain threshold, the immune system
usually rapidly eliminates the infection and the affected areas heal.
Where allergies in combination with infections play a major role, massive
doses of ascorbate are helpful but continuing maintenance doses will be
required. In this situation, continuing blockade of the
allergically-induced inflammatory cascade must be maintained.
With recurrent herpes virus infections, very high maintenance doses of
ascorbate seem to prevent some attacks, and bowel tolerance doses will
shorten and reduce the severity of attacks. A topically applied ascorbate
paste (ascorbic acid or sodium ascorbate and water) (24) appears to be
particularly effective on herpes simplex. In chronic hepatitis, ascorbate
may not cure the condition; nevertheless, massive doses of ascorbate will
usually ameliorate the condition; and I have evidence that shedding of the
virus may stop. I have not determined whether the patient will resume
shedding of the virus if large doses of ascorbate are discontinued. In
conditions where a virus has become well established intracellularly, there
are some limitations on the ability of ascorbate to assist the immune
system.
ASCORBATE IN AIDS
More recently, I have found ascorbate useful in the management of the
acquired immune deficiency syndrome (AIDS). The AIDS patient who has
already suffered a marked suppression of helper T-cells, presents a
clinical problem of management similar to a bubble baby. If, in addition to
the other measures described in my previous reports (24,25), the patient
takes bowel tolerance doses of ascorbic acid orally almost every hour
(intra- venously in emergencies), he may remain clinically well despite the
continuing severe suppression of the helper T-cells. All this must be
started before multiple infections riddle the patient's body with excessive
sources of free radicals. There have been suggestive anecdotal cases which
indicate that in the prodromal period, before the destruction of the helper
T-cells, there might be avoidance of the development of the AID syndrome by
this program. Confirmation of this possibility awaits long- term laboratory
follow-up. There is evidence that a retroviral infection in cats, the
feline leukemia virus, can be cured in the prodromal stage with large oral
doses of ascorbate used in combination with other nutrients (26).
ASCORBATE, A NONRATE-LIMITED, ANTIOXIDANT
FREE RADICAL SCAVENGER
It is my hypothesis that what makes ascorbate truly unique is that very
large amounts can act as a nonrate-limited antioxidant free radical
scavenger.
Clinically, ascorbate is virtually nontoxic (27,28,4). But as ascorbate
acts as an antioxidant free radical scavenger in the body, it is oxidized
to dehydroascorbate. There are animal experiments that indicate that
dehydroascorbate is toxic (29-31). However, dehydroascorbate is not
administered directly to humans as it was in the animal experiments.
Whatever dehydro- ascorbate comes to exist in the human body, comes by way
of the oxidation of ascorbate, as the ascorbate is utilized to reduce free
radicals or other reactive oxidizing substances. The potential of the
dehydroascorbate to do damage should be less than the harmful potential of
the substances it reduces to become dehydroascorbate (the oxidizing redox
potential has been diminished). Therefore a patient should not be expected
to be more toxic from the dehydroascorbate formed than he was from the
original disease unless there is some peculiar specific sensitiv- ity to
dehydroascorbate (see discussion of G-6-PD deficiencies below).
Used in the doses I suggest, there is an even more important mechanism
which prevents toxicity from dehydroascor- bate. I take advantage of a
combination of the facts that even in enormous doses, ascorbate is not
clinically toxic, and that dehydroascorbate is only toxic when there is a
low AA/DHA ratio.
EFFECTIVE REDUCING REDOX POTENTIAL
AT A HIGH TISSUE THRESHOLD
Several (32-36) have hypothesized and reviewed many of the biochemical
advantages of large doses of ascorbate. Of particular interest are Lewin's
calculations and hypotheses (34) that high tissue concentrations of
ascorbate to dehydroascorbate can directly reduce various substances (e.g.
the disulfides). I doubt that tissue levels of ascorbate achieved with
doses much below bowel tolerance are sufficient to significantly accomplish
these reductions under pathological circumstances. Clinically however,
something very dramatic happens as bowel tolerance is approached. I
hypothesize that as a certain threshold ratio of ascorbate to
dehydroascorbate is reached, certain direct reductions of substances such
as oxidized glutathione and adreno- chrome by ascorbate begin. When a
patient is sick or experiencing much stress, the amounts of these
substances which can potentially and beneficially be reduced, increases
greatly. If ascorbate is not available to reduce these substances, those
that escape reduction to nontoxic derivatives by the rate-limited,
antioxidant free radical scavenging mechanisms, damage the patient and
cause symptoms. Under these circumstances, when made available, large
amounts of ascorbate are utilized for these direct reducing purposes. These
ascorbate reductions are not rate-limited, and therefore quench the harmful
oxidants and free radicals almost instantly.
When the potential need for ascorbate for these purposes is satisfied, the
blood level of ascorbate rises and retards the absorption of ascorbate from
the gut. Soon, sufficient amounts of ascorbate reach the rectum to produce
diarrhea.
Based on clinical evidence, I hypothesize that ascorbate can maintain this
reducing redox potential under very adverse circumstances, but that the
doses necessary to do this are enormous by any other standards. This
antioxidant free radical scavenging effect of enormous doses of ascorbate
seems not particularly contingent upon other nutrients. However, vitamin
functions of lower doses of vitamin C are frequently potentiated by and
work in conjunction with vitamin A, zinc, selenium, bioflavonoids, and
other nutrients which play roles in various defense mechanisms.
Chayen has discussed the significance of redox couples and has emphasized
that whether a reaction will proceed left to right, or in reverse, depends
upon the ratio of the oxidized to the reduced members of a redox couple. He
suggests designing "redox drugs" as a possible way of treating imbalances
of oxidation-reduction potentials of critical intracellular systems (37).
WIDE SPECTRUM OF BENEFITS FROM ASCORBATE MATCH EXPECTATIONS FOR A NONRATE-LIMITED, ANTIOXIDANT FREE RADICAL SCAVENGER
I would anticipate that if it were possible to eliminate the vast majority
of stray free radicals and highly reactant oxidative substances, the usual
inflammatory cascade would not occur following injury or surgery. Pain,
complications, and recovery times would be reduced. In conditions resulting
from combinations of mechanical derangements, nutritional deficien- cies,
immune dysregulations, hemorrhage with release of free radical generating
iron and copper atoms, and then secondary inflammatory cascades (e.g.
degenerative disc disease, degenera- tive arthritis, rheumatoid arthritis,
ankylosing spondylitis, blunt trauma of the spine, etc.), therapeutic
effects could be expected proportional to what might result from blocking
of the free radicals and the inflammatory cascade. Reversal of the
mechanical and nonfree radical injury could not be expected, although
certain healing mechanisms might be enhanced.
Toxic substances, whose mechanisms of action involve free radical
generation, e.g. toxic poisons such as snake bites and spider bites,
certain drugs, such as barbiturates, chemotherapeutic agents, narcotics,
and powerful oxidizing pollutant chemicals, might be neutralized.
Conditions triggered by allergic reactions and perpetuated by the
inflammatory cascade might be expected to be partially alleviated.
Psychological symptoms resulting from oxidative products such as
adrenochrome and noradrenochrome (38), would be expected to be ameliorated
to a degree.
Tumors invading the body or holding off the immune system by way of free
radical toxicity might be expected to respond to varying degrees. As an
increasing number of human cancers are recognized as probably being caused
and possibly maintained by infectious organisms (e.g. Kaposi's lesions by
the CMV (39), some adult T-cell lymphomas by the HTLV (40), certain
cervical and vaginal cancers by the papilloma virus (41,42)), it should not
be surprising if such tumors would respond in various degrees to ascorbate.
Since any treatment of cancers by a physician with nutritional substances
is incredibly a felony in California in 1984, it may be practical to
recognize early that a tumor caused by a virus should no longer be
considered a cancer (e.g. Kaposi's lesions).
If, to these diseases, we add conditions benefitted which could be caused
or aggravated by actual dietary deficiency of vitamin C, or from an acute
induced deficiency of vitamin C, there is a very close approximation to the
clinical spectrum of disease conditions which in the experience of those
actually using such doses (4,26-28,32,33,43,44), appear to be beneficially
affected. In a rough way, these conditions are ameliorated to the degree
that one might anticipate if this ideal mechanism of being able to quench
all stray free radicals and highly reactant oxidative substances, were
actually accomplished.
GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G-6-PD) DEFICIENCIES
There is fear that ascorbate given in large amounts to patients with G-6-PD
deficiencies would cause hemolysis (45,46). In a case where a black man
with G-6-PD deficiency who sustained a burn of one hand was given 80 grams
of ascorbic acid intravenously on each of 2 consecutive days, the patient
subsequently suffered hemolysis, renal failure, a stroke, coma, and then
death (46). There are available for intravenous use, solutions of actual
ascorbic acid rather than sodium ascorbate; ascorbic acid, in my opinion,
should never be used in any large amount intravenously. It must be buffered
to reduce the acidity. There are also preparations labelled vitamin C that
contain preservatives which also should never be used. It was not clear
from the article what preparations had been used.
The sequence of reactions whereby certain drugs cause hemolysis with G-6-PD
deficiency is poorly understood. It appears that G-6-PD deficient cells
lack a mechanism to regenerate reduced glutathione (GSH) from oxidized
glutathione (GSSG) and that this lack may result in several biochemical
alterations, the final result being hemolysis of the red cells. The
maintenance of glutathione in the reduced state (GSH) is probably the most
important function of the HMP pathway. It may be that the hemolysis caused
by certain drugs is initiated by the drug forming either free radicals or
hydrogen peroxide. When peroxides are reduced back to water, GSH is
oxidized to GSSG, a reaction catalyzed by glutathione peroxidase.
Ordinarily the GSSG is reduced back to GSH by NADPH, a reduction catalyzed
by glutathione reductase. The resulting oxidized NADP is reduced back to
NADPH in the first step of the HMP pathway, as glucose-6- phosphate is
oxidized to 6-phosphogluconolactone. This critical reaction is catalyzed by
G-6-PD. G-6-PD deficient cells may be expected to accumulate peroxides
which could then oxidize other red cell components (see review in 47).
As discussed previously, if the AA/DHA redox potential is kept reducing
enough by high enough concentrations of ascorbate, it should directly
reduce the GSSG to GSH. I hypothesize that this mechanism should compensate
for the lack of G-6-PD; but I would offer some words of caution. I have no
clinical experience with this condition. It is apparent, however, that in
the case reported that the redox potential was not kept consistently on the
reducing side throughout the course of treatment and that there might have
been variables not appreciated at the time which were very important.
With the increasing millions of persons taking large doses of vitamin C, it
is inevitable that individuals with G-6-PD deficiencies will take these
doses. Serendipitous data should be collected. I would appreciate receiving
any well documented case histories.
It is important to understand that G-6-PD deficiencies have a wide range of
clinical severities. Severe deficiencies are rare and found in
Mediterranean and Asian groups. Blacks have a milder form but with higher
frequency of occurrence. There is substantial decrease in the activity of
G-6-PD with aging. The possibilities exist that in certain individuals with
various degrees and forms of G-6-PD deficiencies that: 1) vitamin C has no
deleterious effect; 2) vitamin C has a peculiar effect on that person such
that any significant amount causes hemolysis; 3) vitamin C in low or
moderate amounts will produce hemolysis, while massive amounts maintaining
a continuing reduced redox potential will not cause hemolysis and will
prevent the hemolysis from other causes. (This last possibility will not be
determined unless those administering the ascorbate are very aggressive and
do not let up the doses until whatever was the cause for which the
ascorbate was given in the first place, is completely passed.)
As the immense value of ascorbate in the doses I am describing becomes
entirely apparent in normal people, the theoretical possibility of
preventing hemolysis in G-6-PD deficient persons subjected to pathologic
oxidative stress, which would result in massive hemolysis of blood cells
anyway, may be recognized. Meanwhile,
I_advise_that_large_doses_of_ascorbate
not_be_given_G-6-PD_deficient_patients. I suggest the possibility that all
this may apply to G-6-PD deficiency only to stimulate the collection of
data and to suggest research on the subject.
Calabrese has suggested that megadoses of ascorbic acid might pose a
hemolytic risk to persons with sickle cell trait and sickle cell anemia
because their erythrocytes possess more copper than normal persons and that
ascorbic acid markedly enhances copper induced hemolysis (48). Again I
suggest that it is possible that if ascorbate is given in large enough
amounts during a sickle cell crisis, it may keep the redox potential of the
various problem systems reducing. Vitamin E might futher facilitate
beneficial effects (49).
OTHER POSSIBLE DIFFICULTIES
One might remain unnecessarily cautious in the use of ascorbate because of
my qualification about "tolerant" patients. Any real problems have been
rare. I cannot recall any patient who has been damaged by large doses of
ascorbate (other than the topical effect of the acid on tooth enamel). Some
preexisting gastrointestinal tract difficulties, such as peptic ulcer or
colitis, may have been aggravated by topical effects, but advice on these
is difficult to give because more frequently the same conditions may be
benefitted. All these topical difficulties are circumvented by using
intravenous ascorbate.
A high percentage of persons with food and/or chemical sensitivities may
have nuisance difficulties with vitamin C. However, attempts to have these
sensitive patients take ascorbate should be made because great benefits can
often be obtained, particularly from calcium, magnesium, and potassium
ascorbate, in many of these patients. Frequently, after the administration
of selenium, ascorbate is better tolerated by chemically allergic patients.
Levine has suggested that chemically allergic patients frequently benefit
from selenium because selenium augments the glutathione peroxidase activity
(8). I have had some clinical evidence that certain chemically allergic
patients who force through nuisance problems of low doses of ascorbate, can
derive benefits from consistently taken large doses. It may be that
chemically allergic persons accumulate dehydroascorbate more readily than
others because of a deficiency of glutathione per- oxidase. I had one
chemically allergic patient who responded well to intravenous ascorbate
until an hour after it was discon- tinued. She then developed a severe
headache that lasted several hours. In retrospect, it seems possible that
the intravenous ascorbate was able to maintain a reducing redox potential,
which then returned to the oxidizing side after the intravenous ascorbate
was discontinued.
True allergic reactions seem always traceable to substances from which the
ascorbate is made, or chemicals used in its manufacture, and not to the
ascorbate itself.
OXALATE KIDNEY STONES
Oxalate kidney stones have been suggested as a theoretical problem, in that
oxalate is one of the breakdown products of ascorbate (50). In my
experience clinically, ascorbate in these doses not only does not cause
kidney stones but seems to prevent stones in patients who have had them
previously. The slight increase in the acidity of the urine from ascorbate
(51,52), and the slight diuresis (53) solubilizes calcium salts. I think
that high concentrations of ascorbate, by being bacteriostatic in the
urine, should prevent many of the niduses of infection around which oxalate
stones frequently form. The increased ascorbate concentration complexes
Ca++ and thereby decreases the amount of Ca++ available to complex with
oxalate (34). Here again is the paradoxical situation where with small
doses of vitamin C, it is possible that where most of the nutrient is
oxidized to dehydro- ascorbate and then some to oxalic acid, it is
theoretically possible that there could be a slight increase in tendency to
form stones. However, I find it difficult to believe that if this were the
case, that this tendency would not have been noticed with the millions
taking small doses of vitamin C. I hypothesize that by using the bowel
tolerance method of determining the dosages of ascorbate to be taken, that
no matter how much dehydroascorbate is formed and hence oxalic acid, the
spill of ascorbate in the urine will be kept very high and should prevent
oxalate stones.
ANASCORBEMIA AND ACUTE INDUCED SCURVY
I suggest that the enormous draw on ascorbate for free radical scavenging
purposes, can exhaust the vitamin C available for known housekeeping
functions of the vitamin. I term this condition acute_induced_scurvy. This
deficiency starts in the tissues directly involved in the disease; then
blood levels of vitamin C drop (anascorbemia); and then tissues distant
from the primary focus of the disease become involved. Secondary
complications occur which can be averted by fully satisfying the increased
need for ascorbate (4).
A very important part of these very large doses of ascorbate being able to
assist the immune system against pathogens is likely that serum levels and
leukocyte levels of ascorbate are raised enough to drive ascorbate into the
depths of infected tissues. The amount of ascorbate needed to satisfy the
enormous potential utilization of ascorbate as an antioxidant free radical
scavenger in the depths of the diseased tissues is provided. The shut down
of vitamin C dependent housekeeping functions of affected cells and the
shut down of vitamin C dependent immune system functions are prevented.
SUDDEN INFANT DEATH SYNDROME
I think that many crib deaths are caused by this acute induced scurvy even
before it is evident that the infant is sick with some infectious disease.
Kalokerinos (28) has demonstrated the value of vitamin C in preventing crib
deaths. I have seen enormous increases in bowel tolerance to ascorbate in
adults several hours before there was any outward sign of their getting
sick. It is easy to imagine certain vital centers in an infant failing when
suddenly deprived of vitamin C by the ascorbate being used up for acute
free radical scavenging purposes. For_many_reasons, it is unfortunate that
the free radical scavenger ascorbate is the same substance as vitamin
C. Infants tolerate ascorbate well. In addition to substantial maintenance
doses of vitamin C, even infants should be given large doses of ascorbate
when ill. Amounts should be given sufficient to relieve fever,
irritability, and other outward signs of toxicity (4).
CONCLUSIONS
While it is not denied that there could be very rare serious complications
associated with the use of massive doses of ascorbate, fear of this
possibility should not retard use of the substance in patients with normal
metabolism. In my experience, the margin of safety (therapeutic index or
selectivity) for massive doses of ascorbate as related to significant
complica- tions is greater than aspirin, antihistamines, antibiotics, all
pain medications, muscle relaxants, tranquilizers, sedatives, diuretics,
etc. Not only is the margin of safety of ascorbate extremely favorable but
when used with most of these drugs, the combination frequently acts
synergistically and has a margin of safety greater than with the drug
alone. While ascorbate may block the effects of some sedatives and
narcotics, massive doses of ascorbate frequently alleviate the need for
those substances.
Clinically, ascorbate in the very large doses described is very effective
and safe as part of the treatment of a wide variety of conditions,
especially infectious diseases. It is my hypothesis that this clinical
effectiveness when a critical threshold is reached, as indicated by bowel
intolerance to ascorbic acid in the form of diarrhea, occurs both because
massive doses of ascorbate can act as a nonrate-limited, antioxidant free
radical scavenger and because acute induced scurvy is avoided. When high
enough tissue levels are reached in tissues directly affected by the
disease processes, the redox potential of the AA/DHA system in those
tissues is kept reducing; substances such as oxidized glutathione are
directly reduced; and stray free radicals are rapidly quenched.
This effect of ascorbate is rate-limited only by the lack of courage of
those administering ascorbate or the tolerance of the patient taking it. I
hope to increase that courage by pointing out the observed lack of toxicity
clinically and the theoretical reasons for that lack of toxicity.
This effect, when understood, opens up a wide range of opportunities to
understand certain pathological processes. It is especially important in
the case of infectious diseases because of the probable common mechanism of
free radical toxicity that many pathogens have of suppressing the immune
system. The increasing bowel tolerance to ascorbic acid can be used as a
fairly accurate measure of the "toxicity" and activity of certain disease
processes.
In toxic conditions, the use of ascorbate by the body for these scavenging
purposes, results in such a localized and systemic deficiency of vitamin C
that there is not enough of the nutrient remaining for vitamin C dependent
housekeeping functions. I call this condition acute_induced scurvy. This
condition can be induced by any stress and is responsible for a high
percentage of the secondary complications of many diseases. The magnitude
of this scavenging drain on ascorbate is enormous as revealed by the
increasing bowel tolerance to ascorbic acid somewhat proportional to the
toxicity of the disease process. Only the doses discussed can fully satisfy
this need.
I think that most crib deaths are due to acute induced scurvy.
I have hypothesized here that massive doses of ascorbate may paradoxically
be of benefit in G-6-PD deficiency, but have urged caution until more data
is obtained. Ascorbate, when used with care, can be of great benefit in
chemically allergic patients.
Rinse ascorbic acid and carbonated ascorbates off the teeth as prolonged
exposure may cause damage to the enamel.
ACKNOWLEDGEMENTS
Partly supported by the Burton Goldberg Foundation. The author appreciates
the comments of Stephen A. Levine and Parris M. Kidd.
REFERENCES:
Dr. Cathcart
Bibliography
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Medical Hypotheses 7:1359-1376, 1981.
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42. zur Hausen H. Human genital cancer: Synergism between the
two virus infections or synergism between a virus infection
and initiating events? Lancet 1:1370-1372, 1982.
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45. Mengel CE, Green HL, Ascorbic acid effects on
erythrocytes. Ann Intern Med 84:490, 1976.
46. Campbell GD, Steinberg MH, Bower JD. Ascorbic acid-induced
hemolysis in G-6-PD deficiency. Ann Intern Med 82:810, 1975.
47. Beutler E. Glucose-6-phosphate dehydrogenase deficiency. In
Stanbury JB et al (Eds.) The Metabolic Basis of Inherited
Disease, McGraw Hill Book Company, New York, 1983.
48. Calabrese EJ. Does consumption of mega-doses of ascorbic acid
pose a hemolytic risk to persons with sickle cell trait and
sickle cell anemia. Med Hypostheses 9(6)647-649, 1982.
49. Natto CL, Machlin LJ, Brin M. A decrease in irreversibility
sickled erythrocytes in sickle cell anemia patients given
vitamin E. Am JClin Nutr 33:968-971, 1980.
50. Burness LA. Safety considerations with high ascorbic acid
dosage. In Second Conference on Vitamin C, King CG, Burns JJ
(Eds) Ann NY Acad Sci 258:523-527, 1975.
51. McDonald DF, Murphy GP. Bacteriostatic and acidifying effects
of methionine, hydrolysed casein and ascorbic acid on the
urine, New England J Med 261:803-805, 1959.
52. Murphy FJ, Zelman S. Ascorbic acid as a urinary acidifying
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Biochem J 31:339-342, 1937.
Content (C) 1995 and prior years, Dr. Robert F. Cathcart.
Dr. Cathcart 415-949-2822
-----------------------------------
--- Dr. Robert F. Cathcart, M.D. ---
--- Allergy, Environmental, and ---
----- Orthomolecular Medicine -----
------- Orthopedic Medicine -------
--- 127 Second Street, Suite 4 ---
--- Los Altos, California, USA ---
---- Telephone: 415-949-2822 ----
---- Fax: 415-949-5083 ----
-----------------------------------
The Third Face of Vitamin C
Dr.CATHCART,
J. of Orthomolecular Medicine, 7:4;197-200, 1993.
ABSTRACT:
Bowel tolerance to orally ingested ascorbic acid increases
with the toxicity of diseases. Bowel tolerance with a disease
such as mononucleosis may reach 200 or more grams per 24 hours
without it producing diarrhea. A marked clinical amelioration or
cure is achieved in many disease processes when threshold doses
near bowel tolerance are given. In a sense, it is the reducing
equivalents carried by free radical scavengers that quench free
radicals, not the free radical scavengers themselves. Ascorbic
acid can be dramatically useful in quenching free radicals
because it is usually tolerated in amounts necessary to provide
the reducing equivalents necessary to quench almost all the free
radicals generated by severe disease processes. Vitamin C
functions are incidental at these dose levels; the benefit is
from the reducing equivalents carried. To the extent that free
radicals are either essential to the perpetuation of a disease or
just part of the cause of symptoms, the disease will be cured or
just ameliorated. These effects are even more dramatic from
intravenous sodium ascorbate.
Keywords: vitamin C, ascorbate, acute induced scurvy, bowel
tolerance, titrating to bowel tolerance, the ascorbate effect,
free radical scavengers, reducing equivalents.
INTRODUCTION
A clinical experience prescribing doses of ascorbic acid up
to 200 or more grams per 24 hours to over 20,000 patients during
the past 23 year period has revealed its clinical usefulness in
all diseases involving free radicals. The controversy continues
over the value of vitamin C mainly because inadequate doses are
used for most free radical scavenging purposes. Paradoxically,
the non controversial use of minute doses of vitamin C in the
prevention and treatment of scurvy has set the minds of many
against more creative uses.
I have found vitamin C exceptionally useful in a very high
dose range. Its usefulness is in three such distinct realms that
I will describe them as the three faces of vitamin C.
1. vitamin C to prevent scurvy
(up to 65 mg/day.)
2. vitamin C to prevent acute induced scurvy (, )
and to augment vitamin C functions
(1 to 20 grams/day.)
3. vitamin C to provide reducing equivalents
(30 to 200 or more grams/day.)()
One might criticize the wisdom of my use of these massive doses but Klenner
had successfully utilized them previously (, , , ). The works of Irwin
Stone (, , ), Linus Pauling (, , ), and Archie Kalokerinos () have
supported many of my observations. It was apparent that in all the studies
yielding negative or equivocal results, inadequate doses were used. In some
studies, doses barely bordering on adequate, tease the investigator with
statistically significant but not very impressive beneficial results.
My early discovery was that the bowel tolerance to ascorbic acid of a
person with a healthy GI tract was somewhat proportional to the toxicity of
their disease (). Bowel tolerance doses are the amounts of ascorbic acid
tolerated orally that almost, but not quite, cause diarrhea. A patient who
could tolerate orally 10 to 15 grams of ascorbic acid per 24 hours when
well, might be able to tolerate 30 to 60 grams per 24 hours if he had a
mild cold, 100 grams with a severe cold, 150 grams with influenza, and 200
grams or more per 24 hours with mononucleosis or viral pneumonia (1, 2).
Marked clinical benefits in these conditions occur only at the bowel
tolerance or higher levels. I named the process whereby the patient
determined the proper dose as titrating to bowel tolerance. These increases
in bowel tolerance in the vast majority of patients normally tolerant to
ascorbic acid (perhaps 80% of patients) are invariable. The marked clinical
benefits are noted only when a threshold dose, usually close to the bowel
tolerance dose, is consumed. I call this benefit the ascorbate effect.
Most patients are started at first with hourly doses of ascorbic acid
powder dissolved in small amounts of water. Later, after the patient has
learned to accurately estimate the dose necessary to achieve the ascorbate
effect, comparable doses of tablets or capsules are also used. Where
patients are intolerant to adequate amounts of ascorbic acid orally and the
severity of the disease warrants it, intravenous sodium ascorbate is used.
Failures are related to individual difficulties in taking the proper
adequate doses. I now have had 22 years to gather clinical experience and
to reflect on this phenomenon (, , , ).
I want to emphasize the importance of this increasing bowel tolerance with
increasing toxicities of diseases. The sensation of detoxification one
experiences at these doses is unmistakable.
The effect is so reliable and dramatic in the tolerant patient as to make
obvious the fact that something very important, that has not been widely
appreciated before, is going on.
THE THREE FACES
Vitamin C probably always functions by being an electron donor. At the
lowest dose level (the first face), it is necessary as a vitamin to prevent
scurvy. It is essential for certain metabolic functions which are well
described and mostly non controversial.
At a second level (the second face) vitamin C is still used as a vitamin
but larger doses are necessary to maintain its basic vitamin C functions
because the vitamin is destroyed rapidly in diseased or injured tissues
where there is an overabundance of free radicals. I described the resulting
state of deficiency, if the vitamin C is not replaced, as acute induced
scurvy (1, 2). There is ample evidence of this depletion of vitamin C by
stress and disease as recently reviewed in the literature ().
Additionally, the recent extensive research on vitamin C has concerned
itself with certain functions that may be augmented by higher than minimal
doses of vitamin C (20). Strangely, any usefulness of these larger than
minimal doses of vitamin C remain mostly neglected by clinicians. This
level is from about 1 to 20 grams a day. Benefits vary from person to
person.
At this second level, as in studies reviewed by Pauling (11) and more
recently by Hemil" (20), there may be expected a slight decrease in the
incidence of colds but a more significant reduction in the complications
and the duration of colds. Personally, I am impressed by the number of
patients (but certainly not all) who tell me that they have not had a cold
for years since reading Pauling's book and taking vitamin C. Patients with
chronic infections frequently have those infections cured for the first
time. Antibiotics work synergistically with these doses. A surprising
number of elderly persons benefit from doses of this magnitude and may
indeed have what Irwin Stone described as chronic subclinical scurvy (10).
The third level of doses (the third face) is virtually undiscussed in the
literature but is the most interesting. These doses range usually from 30
to 200 grams or more per 24 hours. The most important concept to understand
is that while incidentally at these dose levels the vitamin C performs all
the functions of levels one and two, it is mostly thrown away for the
reducing equivalents it carries (3). With these doses it is possible to
saturate the body with reducing equivalents, neutralize the excessive free
radicals, and drive a reducing redox potential into involved tissues.
Inflammations mediated by free radicals can be eliminated or markedly
reduced. In many instances patients with allergies or autoimmune disease
have their humeral immunity controlled while their cellular immunity is
augmented (19). To the extent that free radicals are either essential to
the perpetuation of a disease or just part of the cause of symptoms, the
disease will be cured or just ameliorated.
The list of diseases involving free radicals continue to grow. Infections,
cardiovascular diseases, cancer, trauma, burns both thermal and radiation,
surgeries, allergies, autoimmune diseases and aging are now included. It is
more difficult to think of a disease that does not involve free radicals.
Progressive nutritionists routinely give vitamin C, vitamin E, beta
carotene, selenium, NAC, etc. to counter free radicals. I certainly agree
with this practice. However, there is one important concept neglected.
In the spirit that if you throw a bucket of water on a fire, it is the
water that puts the fire out, not the bucket; it is the reducing
equivalents carried by the free radical scavengers that quench the free
radicals, not the free radical scavenger itself.
Most of the reducing equivalents utilized by non enzymatic free radical
scavengers do not come from the ingested free radical scavengers but come
through glycolysis, the citric acid cycle, NADPH, FADH2, glutathione, etc.
Dietary free radical scavengers carry in on ingestion only a small
percentage of the total reducing equivalents carried by those scavengers
during their lifetime in the body. After their first pass neutralizing free
radicals, the free radical scavenger must be recharged with reducing
equivalents made available in the mitochondria.
Consider the following: Early in this study a 23-year-old, 98-pound
librarian with severe mononucleosis claimed to have taken 2 heaping
tablespoons every 2 hours, consuming a full pound of ascorbic acid in 2
days without it producing diarrhea. She felt mostly well in 3 to 4 days,
although she had to continue about 20 to 30 grams a day for about 2 months.
Subsequently, all my young mononucleosis patients with excellent GI tracts
have responded similarly and have had equivalent increases in bowel
tolerance during the acute stage of the disease.
I believe that the loose stools caused by excessive doses of ascorbic acid
orally ingested is due to a resulting hypertonicity of ascorbate in the
rectum. Water is attracted into the rectum by the increased osmotic
pressure and results in a benign diarrhea. With toxic illnesses, the
ascorbate is destroyed rapidly in the involved tissues resulting in a rapid
absorption from the gut. Of the ascorbate, what does not reach the rectum,
does not cause diarrhea. Intravenous sodium ascorbate does not cause
diarrhea and, in fact, increases bowel tolerance to orally ingested
ascorbic acid while the IV is running. With hypertonicity of the ascorbate
both in the blood and in the rectum, the osmotic pressure of the ascorbate
is more equal on both sides of the bowel wall so no diarrhea results. If
the diarrhea was cause by other metabolic processes, diarrhea would be
caused by intravenous ascorbate.
It should be noted that in some cases of pathological diarrhea, ascorbic
acid stops the diarrhea. Presumably in these cases some of the increased
destruction of ascorbate is from free radicals in the bowel. However, in
most toxic systemic diseases there is no reason to believe that the
destruction of the additional ascorbate occurs directly in the bowel, so it
is a safe hypothesize that this increased destruction occurs in the
interior of the body.
The increased tolerance to ascorbic acid orally provides an interesting and
somewhat useful measure of the toxicity of a disease. Probably it is
somewhat a measure of the free radicals involved in a disease. I describe a
cold that at its maximum makes it possible for a patient to just tolerate
100 grams of ascorbic acid orally without diarrhea, a "100 gram cold."
Patients, appearing to be well, who have a tolerance over 20 to 25 grams
per 24 hours probably have some subclinical condition which is being hidden
by their own free radical scavenging system.
Patients with chronic infections (and a normally strong stomach) can ingest
enormous amounts of ascorbic acid. One of my chronic fatigue patients is
functional only because of his ingestion of 65 pounds of ascorbic acid in
the past 12 months. In 22 years, I, personally, have ingested approximately
361 kilos ( 797 lbs ) ( 4.3 times my body weight ) of ascorbic acid because
of chronic allergies and perhaps chronic EBV.
Considering the reducing equivalents carried by such amounts of ascorbic
acid, one can only guess at the turnover rate of the non enzymatic free
radical scavengers in a patient acutely ill with a 200 gram mononucleosis.
However, one gains the impression that all the non enzymatic free radical
scavengers would have to be rereduced many times a day.
AN ANALOGY
Suppose you owned a farm and on one end of the property there was a barn
and on the other end of the property there was a water well. One day the
barn catches fire and neighbors come with buckets to set up a bucket
brigade between the water well and the barn and are putting out the fire
when the well goes dry.
My use of ascorbate is like thousands of neighbors coming from miles
around, each with a bucketful of their own water, throwing their own water
on your fire once, and then leaving.
CONCLUSION
Because of the invariable (in patients tolerant to ascorbic acid)
increasing bowel tolerance to ascorbic acid in patients roughly in
proportion to the toxicity of their disease, there has to be something
happening to ascorbate in the sick patient other than its being used as
vitamin C in the classic sense. The amelioration or sometimes cure of
different diseases appears related to the importance of free radicals in
the perpetuation of the paticular disease.
The sudden marked benefit in many disease processes which is achieved at
doses near to the bowel tolerance level suggests that a reducing redox
potential is forced into the affected tissues only at those dose levels.
This ascorbate effect only at the high dose levels is also suggestive that
something other than classic functions of vitamin C is involved. This
ascorbate effect is more compatible with principles of redox chemistry.
Only a small percentage of the total reducing equivalents donated by non
enzymatic free radical scavengers to neutralize free radicals, come in on
the ingested nutritional free radical scavengers. Ascorbate is unique in
that the body can tolerate doses adequate to supply the necessary reducing
equivalents to quench the free radicals generated by severely toxic disease
processes. The vitamin C is thrown away for the reducing equivalents it
carries. Only in this way can the large amounts of free radicals generated
by the most toxic disease processes be rapidly quenched.
REFERENCES
Dr. Cathcart Bibliography
1. Cathcart RF. The method of determining proper doses of
vitaminC for the treatment of disease by titrating to bowel
tolerance. J Orthomolecular Psychiatry 1981; 10: 125-32.
2. Cathcart RF. Vitamin C: titrating to bowel tolerance,
anascorbemia, and acute induced scurvy.
Medical Hypotheses 1981; 7:1359-76.
3. Cathcart RF. A unique function for ascorbate.
Medical Hypotheses 1991; 35: 32-7.
4. Klenner FR. Virus pneumonia and its treatment with vitamin C.
J. South. Med. and Surg. 1948; 110: 60-3.
5. Klenner FR. The treatment of poliomyelitis and other virus
diseases with vitamin C.
J. South. Med. and Surg. 1949; 111:210-4.
6. Klenner FR. Observations on the dose and administration of
ascorbic acid when employed beyond the range of a vitamin in
human pathology. J. App. Nutr. 1971; 23: 61-88.
7. Klenner FR. Significance of high daily intake of ascorbic
acid in preventive medicine.
J. Int. Acad. Prev. Med. 1974; 1:45-9.
8. Stone I. Studies of a mammalian enzyme system for producing
evolutionary evidence on man.
Am. J. Phys. Anthro. 1965; 23:83-6.
9. Stone I. Hypoascorbemia: The genetic disease causing the human
requirement for exogenous ascorbic acid.
Perspectives in Biology and Medicine 1966; 10: 133-4.
10. Stone I. The Healing Factor: Vitamin C Against Disease.
Grosset and Dunlapp, New York, 1972.
11. Pauling L. Vitamin C and the Common Cold.
W.H. Freeman and Company, San Francisco, 1970.
12. Pauling L. Vitamin C, the Common Cold, and the Flu.
W.H.Freeman and Company, San Francisco, 1976.
13. Pauling L. How to Live Longer and Feel Better.
W.H. Freeman and Company, New York, 1986.
14. Kalokerinos A. Every Second Child.
Keats Publishing, Inc., New Canaan, 1981.
15. Cathcart RF. Clinical trial of vitamin C. Letter to the
Editor, Medical Tribune, June 25, 1975.
16. Cathcart RF. Vitamin C in the treatment of acquired
immunedeficiency syndrome (AIDS).
Medical Hypotheses 1984; 14(4): 423-33.
17. Cathcart RF. Vitamin C: the nontoxic, nonrate-limited,
antioxidant free radical scavenger.
Medical Hypotheses 1985; 18:61-77.
18. Cathcart RF. HIV infection and glutathione (Letter to editor
concerning Vitamin C tolerance in AIDS).
Lancet 1990; 335(8683);235.
19. Cathcart RF. The vitamin C treatment of allergy and the
normally unprimed state of antibodies.
Medical Hypotheses 1986;21(3): 307-21.
20. Hemil H. Vitamin C and the common cold.
Br J Nutr 1992; 67:3-16.
Content (C) 1995 and prior years, Dr. Robert F. Cathcart.
DHEA is presently being attacked by the corporate establishment. It is listed as a drug in Germany, yet it is throughout nature in Saw Palmetto tree, and when our DHEA levels come down to a certain range, we all would get cancer naturally. With DHEA supplementation, we can expect to expand human lifespan 125 years.
The Cognitive Enhancement Research Institute
DHEA
by Ward Dean, M.D., and Steven Wm. Fowkes
Dehydroepiandrosterone (pronounced
dee-hi-dro-epp-ee-ann-dro-stehr-own), or
DHEA as it is more often called, is a steroid
hormone produced in the adrenal gland. It is
the most abundant steroid in the
bloodstream and is present at even higher levels in brain tissue. DHEA levels are
known to fall precipitously with age, falling 90% from age 20 to age 90. DHEA is
known to be a precursor to the numerous steroid sex hormones (including estrogen
and testosterone) which serve well-known refunctions, but the specific biological
role of DHEA itself is not so well understood. It is difficult for searchers to separate
the effects of DHEA from those of the primary sex steroids into which it is
metabolized. The apparent lack of any direct hormone action for DHEA has
prompted the suggestion that it may serve the role of a "buffering hormone" which
would alter the state-dependency of other steroid hormones. Although the specific
mechanisms of action for DHEA are only partially understood, supplemental DHEA
has been shown to have anti-aging, anti-obesity and anti-cancer influences. In
addition, it is known to stabilize nerve-cell growth and is being tested in Alzheimer's
patients.
Our understanding of the specific mechanisms of DHEA in metabolism has recently
been advanced by the publication of The Biologic Role of Dehydroepiandrosterone
(DHEA), edited by Mohammed Kalimi and William Regelson [1990]. This book
presents 24 chapters from scientists around the world who are conducting DHEA
research. The breadth of the work is impressive. As Drs. Regelson, Kalimi and Loria
stated in their introductory remarks, "DHEA modulates diabetes, obesity,
carcinogenesis, tumor growth, neurite outgrowth, virus and bacterial infection,
stress, pregnancy, hypertension, collagen and skin integrity, fatigue, depression,
memory and immune responses." With this wide range of potential clinical uses, it
is amazing that more books about DHEA have not been written.
The introductory chapter, by the editors and Roger Loria, briefly reviews DHEA's
biochemistry, endocrinology, and potential clinical uses. They contend that it is
perhaps the most significant endocrine biomarker known, and further postulate that
all of its effects may be explained by its action as a precursor hormone which
provides "a host of steroid progeny with which to maintain the broad balance of host
response related to species and individual survival."
DHEA and Cancer
Early reports from England [Bulbrook, 1962, 1971] suggested that DHEA was
abnormally low in women who developed breast cancer, even as much as nine years
prior to the onset or diagnosis of the disease. Of the 5000 women followed in the
study, 27 developed cancer. Most of the 27 had abnormally low levels of DHEA. If
low DHEA levels contributed to breast cancer, might the opposite be true? Many
years later, Dr. Arthur Schwartz of Temple University found that supplemental
DHEA significantly protected cell cultures from the toxicity of carcinogens. Cell
cultures usually respond to powerful carcinogens with mutations (changes in DNA),
transformations (changes in cell appearance), and a high rate of cell death. But when
Schwartz added DHEA along with the carcinogen, all three of these effects were
significantly diminished.
Subsequent studies [Schwartz, 1979] identified powerful protective effects of
supplemented DHEA for breast-cancer-prone mice. The results of the experiment
was clear after 8 months. The control animals were "getting cancer left and right"
while the DHEA animals had no tumors. In two later studies with different strains of
mice, Schwartz found 75% and 100% reductions in tumor incidence at 8 months of
age and 50% and 75% reductions at 15 months of age [Schwartz, 1981; 1984]. DHEA
has demonstrated protective effects for cancers of the skin, lungs, bowel, breast and
liver. According to William Regelson, "Whenever [DHEA] has been tested in a
model of carcinogenesis and tumor induction, DHEA has preventative effects."
Although DHEA is now beginning to be tested in human cancer, it is still to early to
know whether the successes achieved in animals will be realized in humans.
The Anti-Obesity Factor
At about the same time that Schwartz was investigating the anti-cancer properties of
DHEA, Dr. Terrence T. Yen was studying the effect of DHEA on genetically obese
mice. Although the DHEA-treated mice ate normally, they remained thin -- and they
lived longer than control mice. This "leanness" effect was also conspicuously noted
by Dr. Schwartz. In another experiment, Dr. M. P. Cleary found that even
middle-aged obese rats lost weight when fed DHEA-supplemented food. Diabetes, a
typical complication of obesity, was also dramatically decreased.
DHEA and Glucose Metabolism
Investigators have shown that DHEA inhibits glucose-6-phosphate dehydrogenase
(G6PDH), an enzyme that breaks down glucose. There are two glucose-metabolizing
pathways in the body, the catabolic, energy-yielding pathway and the anabolic,
biosynthetic pathway. G6PDH happens to be the first enzyme in the biosynthetic
pathway, the one which results in the synthesis of fatty acids and ribose (the sugar
used in making deoxyribonucleic acid, or DNA). In simple language, G6PDH turns
glucose into fat.
DHEA's inhibition of G6PDH may redirect glucose from anabolic fat-production into
catabolic energy metabolism, thus creating a leaner metabolism. This function of
DHEA is well reviewed by Arthur Schwartz and colleagues in their chapter on "The
Biological Significance of Dehydroepiandrosterone" in The Biologic Role of
Dehydroepiandrosterone. They assert that DHEA-mediated reductions in
ribose-5-phosphate activity may be centrally responsible for the anti-tumor
promoting, anti-tumor initiating, and possibly the anti-atherogenic properties of
DHEA. They also note that DHEA 1) produces hepatomegaly (liver enlargement), 2)
stimulates liver catalase activity (a protective antioxidant enzyme), and 3) causes
proliferation of peroxisomes (cellular organelles which specialize in oxidative
processing and the decomposition of hydrogen peroxide). The absence of such
influences with synthetic analogs of DHEA (like 16-alpha-fluoro-5-androsten-17-one)
prompts Schwartz and colleagues to recommend that such analogs be considered for
clinical applications in humans. Toxicity factors still need to be assessed.
DHEA and Appetite
In different experiments, DHEA supplementation has resulted in increased,
decreased and unchanged food consumption. Dr. Schwartz found that it is the level
of dietary fat influences food consumption. DHEA-treated rats on a high-fat diet ate
less food than control rats while those on a low-fat diet ate more.
Since DHEA inhibits G6PDH activity and suppresses the body's ability to synthesize
fat from carbohydrate, dietary sources of fat become more important. This can affect
changes in appetite. But despite possible increases in food intake, DHEA-treated
animals consistently weighed less than control animals. In other words, increases in
appetite, when indulged, did not negate the anti-obesity property of DHEA.
DHEA and Aging
The body's production of DHEA drops from about 30 mg at age 20 to less than 6 mg
per day at age 80. According to Dr. William Regelson of the Medical College of
Virginia, DHEA is "one of the best biochemical bio-markers for chronologic age." In
some people, DHEA levels decline 95% during their lifetime -- the largest decline of
an important biochemical yet documented.
In animal studies, DHEA extends rodent lifespans up to 50%. The animals not only
lived longer, they looked younger. The graying, course-haired controls could easily
be distinguished from the sleek, black-haired, DHEA-treated animals.
DHEA levels are directly related to mortality (the probability of dying) in humans. In
a 12-year study of over 240 men aged 50 to 79 years, researchers found that DHEA
levels were inversely correlated with mortality, both from heart disease and from all
causes. This finding suggests that DHEA level measurements can become a standard
diagnostic predictor of disease, mortality and lifespan. Furthermore, if animal results
hold true, supplemental DHEA may prevent disease, reduce mortality, and extend
lifespan in humans.
Enhancing Brain Function
DHEA may also be intimately involved in protecting brain neurons from
senility-associated degenerative conditions, like Alzheimer's disease. Not only do
neuronal degenerative conditions occur most frequently when DHEA levels are
lowest, but brain tissue contains many times more DHEA than is found in the
bloodstream. One of the scientists at the forefront of this field of research is Dr.
Eugene Roberts who found that very low concentrations of DHEA were found to
"increase the number of neurons, their ability to establish contacts, and their
differentiation" in cell cultures. He also found that DHEA also enhanced long-term
memory in mice undergoing avoidance training. It may play a similar role in
human brain function.
Drs. Roberts and Fitten report initial research on "Serum steroid levels in two old
men with Alzheimer's disease before, during and after oral administration of
DHEA" in the book The Biologic Role of Dehydroepiandrosterone. Roberts' and
Fitten's data are the best we've seen regarding acute and chronic changes in
numerous hormone levels following various oral doses of DHEA (see adjacent
graphs). Because of the short peak duration of DHEA (heavier line in illustration),
they recommend that future studies or therapeutic trials use time-release capsules or
transdermal patches to provide more uniform delivery of DHEA.
Levels of pregnenolone and 17-alpha-pregnenolone, the direct precursors to DHEA,
were too low to be measured in the two patients illustrated, but Roberts and Fitten
present data from three other Alzheimer's patients. Their data indicate that in all
three patients, "control values for pregnenolone and 17-alpha-pregnenolone not
only were below the means for the population controls, they were lower than the
lowest values." In other words, the highest of the Alzheimer's patients was lower
than the lowest of the population controls. When they were administered 400 mg of
DHEA, all three experienced decreased levels of 17-alpha-pregnenolone.
Pregnenolone levels increased in two patients and fell in the third. In the two
patients experiencing increased pregnenolone and decreased 17-alpha-pregnenolone
in response to DHEA, levels of 17-alpha-pregnenolone rebounded strongly at 24
hours. Roberts and Fitten suggest that "a prolonged inhibition of 17-alpha
hydroxylation occurred as a result of continued DHEA intake."
DHEA and Immune Function
DHEA is known to enhance general immune response. Oral and subcutaneous
DHEA has been observed to protect rodents against the lethality of RNA and DNA
viruses, and lethal bacterial infections. Drs. Loria, Regelson and Padgett report in The
Biologic Role of Dehydroepiandrosterone (DHEA) that a single subcutaneous dose of
DHEA is considerably more effective in protecting against infection than oral dosing.
Intraperitoneal [within the abdominal cavity] injections were completely ineffective.
Dr. Loria and colleagues noted that subcutaneous dosing did not result in the typical
weight loss observed with oral DHEA. Presumably it works by a different
mechanism. DHEA has been reported to counteract the thymic involution
[shrinking of the thymus gland] and immuno-suppression caused by corticosteroids.
But the special role of skin tissues in the immune facilitating properties of DHEA
suggest a different mechanism is involved. Cutaneous immune cells, such as
Langerhans cells and keratinocytes, are believed to play a role in "immune
surveillance" and "antigen presentation." These cells may be a site of DHEA's action.
Subcutaneous injection of DHEA results in the "formation of a local deposit leading
to a relatively prolonged exposure to the lymphoid system." DHEA skin patches
might provide a similar exposure.
The delay in protective effect of subcutaneous DHEA has prompted Loria and
colleagues to postulate that a DHEA metabolite is involved in cutaneous immune
enhancement. In a recent paper [Loria and Padgett, 1993], they advance
androstenediol [5-androsten-3-beta-17-beta-diol] as the active metabolite, the
production of which is predominantly localized in the skin and brain. They found
that androstenediol was significantly more effective than DHEA (10,000 times more
with coxsackievirus B4!).
Neither DHEA nor androstenediol have any direct (in vitro) antiviral activity. The
amount of viral load in heart, spleen, pancreas, liver and blood tissues was
unaffected by either DHEA or androstenediol administration. The effect of these
steroids appears to be strictly mediated through stimulation of lymphocytes,
lymphoid organs, and immune-modulating cytokines [immune hormones].
DHEA: The Buffering Steroid?
DHEA may be unique among hormones for it's lack of specificity for hormone
receptor sites. Just as vitamin E has never been shown to have a specific metabolic
role (it is only proven essential as a general antioxidant), DHEA may serve an equally
general purpose. "DHEA is the first example of a buffer action for hormones that I
know of," states William Regelson. "It is a broad-acting hormone that only
demonstrates itself under a specific set of circumstances. In that way, it is like a buffer
against sudden changes in acidity or alkalinity. That is why when you get older,
you're much more vulnerable to the effects of stress. As DHEA declines with age,
you are losing the buffer against the stress-related hormones. It is the buffer action
that [helps prevent] us from aging." The decrease of DHEA with age may result in
gradual decline of a system for suppressing enzyme systems responsible for creating
the building blocks of new cells, like lipids, nucleic acids (RNA and DNA) and sex
steroids. The resulting rise in enzymatic activity in advanced age may be responsible
for the proliferative events (cancer) and degenerative disease that become more
frequent in advanced age. In this respect, DHEA might be best considered to be an
anti-hormone, which might "de-excite" steroid-sensitive receptors that would
otherwise lead to enhanced metabolic activity.
Dosage
Exact dosages for humans have not been clearly determined. Daily dosages vary from
5 to 10 mg to as much as 2000 mg, with 5, 10, 25 and 250 mg being the range for typical
tablet and capsule sizes. DHEA is usually split into 2-4 daily doses, especially at the
higher dosage levels.
We recommend that dosage be adjusted to bring blood DHEA and DHEA-S
measurements towards young-adult levels. These blood tests can be ordered by your
physician (don't forget to get your first test before you start taking DHEA).
Conclusion
Because of its generally universal function in human metabolism, DHEA is being
associated with numerous human maladies. For example, DHEA has recently been
found to have a highly statistically significant correlation with vertebral bone density
in postmenopausal women suggesting that DHEA (and other weak androgens) may
protect against osteoporosis. This, and its low toxicity, may tend to give DHEA the
same panacea stigma that the antioxidants vitamin E and C suffer.
Regulatory Difficulties
In Europe, DHEA is already available as a drug in 5 and 10 mg doses (although it has
been hard to obtain). It is used primarily for the treatment of menopause. In the
United States, DHEA must first be approved as a drug by the FDA before it can be
marketed for medical purposes. Unfortunately, this is an adversarial process (the
drug companies advocating for the drug and the FDA demanding proof of efficacy
and safety) which takes up to 100 million dollars and a decade to accomplish.
Without a patent to restrict competition, prices cannot be raised high enough to
recover the investment in the approval process. DHEA is an unpatentable substance.
References:
Barrett-Connor E, Khaw KT and Yen SS. A prospective study of
dehydroepiandrosterone sulfate, mortality, and cardiovascular disease. New England
Journal of Medicine 315(24): 1519-24, 11 December 1986.
Bulbrook RD, Hayward JL and Spicer CC. Abnormal excretion of urinary steroids by
women with early breast cancer. Lancet 2: 1238-40, 1962.
Bulbrook RD, Hayward JL and Spicer CC. Relation between urinary androgen and
corticoid excretion and subsequent breast cancer. Lancet 2: 395-98, 1971.
Chen TT, et al. Prevention of obesity in Avy/a mice by dehydroepiandrosterone.
Lipids 12: 409-13, 1977.
Cleary MP and Fisk JF. Anti-obesity effect of two different levels of
dehydroepiandrosterone in lean and obese middle-aged female Zucker rats.
International Journal of Obesity 10(3): 193-204, 1986.
Coleman DL, Leiter EH and Applezweig N. Therapeutic effects of
dehydroepiandrosterone metabolites in diabetes mutant mice (C57BL/KsJ-db/db).
Endocrinology 115: 239-43, 1984.
Coleman DL, Leiter EH and Schweizer RW. Therapeutic effects of
dehydroepiandrosterone (DHEA) in diabetic mice. Diabetes 31: 830-33, 1982.
Coleman DL, Schweizer RW and Leiter EH. Effect of genetic background on the
therapeutic effects of dehydroepiandrosterone (DHEA) in diabetes-obesity mutants
and in aged normal mice. Diabetes 33: 26-32, 1984.
de Peretti E and Forest MG. Pattern of plasma dehydroepiandrosterone sulfate levels
in humans from birth to adulthood: Evidence for testicular production. J Clin
Endocrinol Metab 47: 572-77, 1978.
Kahn, Carol. Beyond the Double Helix: DNA and the Quest for Longevity, Times
Books, 1985, page 143. A thorough and highly readable "inside" account of DHEA
research.
Loria RM, Regelson W and Padgett DA. Immune response facilitation and resistance
to virus and bacterial infections with dehydroepiandrosterone (DHEA). In: The
Biologic Role of Dehydroepiandrosterone (DHEA), Mohammed Kalimi and William
Regelson [Eds], page 107-130, Walter de Gruyter, New York, 1990. ISBN 3-11-012243-X.
Loria RM and Padgett DA. Androstenediol regulates systemic resistance against
lethal Infections in mice. Annals of NY Academy of Sciences 685: 293-95, 1993.
Nyce JW, Magee PN, Hard GC and Schwartz AG. Inhibition of
1,2-dimethylhydrazine-induced colon tumorigenesis in Balb/c mice by
dehydroepiandrosterone. Carcinogenesis 5: 57-62, 1984.
Orentreich N, Brind JL, Rizer RL and Vogelman JH. Age changes and sex differences
in serum dehydroepiandrosterone sulfate concentrations throughout adulthood. J
Clin Endocrinol Metab 59: 551-55, 1984.
Pashko LL and Schwartz AG. Effect of food restriction, dehydroepiandrosterone, or
obesity on the binding of 3H-7,12-dimethylbenz(alpha)anthracene to mouse skin
DNA. J Gerontology 38: 8-12, 1983.
Schwartz AG. Inhibition of spontaneous breast cancer formation in female
C3H(Avy/a) mice by long-term treatment with dehydroepiandrosterone. Cancer
Research 39: 1129-32, 1979.
Schwartz AG, Hard GC, Pashko LL, Abou-Gharbia M and Swern D.
Dehydroepiandrosterone: An antiobesity and anti-carcinogenic agent. Nutrition and
Cancer 3: 46-53, 1981.
Schwartz AG, Nyce JW and Tannen RH. Inhibition of tumorigenesis and
autoimmune development in mice by dehydroepiandrosterone. Mod Aging Res 6:
177-84, 1984.
Schwartz AG, Fairman DK and Pashko LL. The Biological Significance of
Dehydroepiandrosterone. In: The Biologic Role of Dehydroepiandrosterone (DHEA),
Mohammed Kalimi and William Regelson [Eds], Walter de Gruyter, New York, 1990.
Yen TT, Allan JA, Pearson DV, Acton JM and Greenberg MM. Prevention of obesity
in Avy/a mice by dehydroepiandrosterone. Lipids 12: 409-13, 1977.
Cancer Chemoprevention With The
Adrenocortical Steroid Dehydroepiandrosterone
& Structural Analogs
Author(s): Schwartz AG; Pashko LL
Address: Fels Institute for Cancer Research and Molecular Biology, Temple
University School of Medicine, Philadelphia, PA 19140.
Source: J Cell Biochem Suppl 1993;17G:73-9
Abstract: Dehydroepiandrosterone (DHEA) is an adrenocortical steroid that produces
broad-spectrum cancer chemopreventive action in mice and rats. In the mouse
two-stage skin tumorigenesis model, DHEA treatment inhibits tumor initiation, as
well as tumor promoter-induced epidermal hyperplasia and promotion of
papillomas. There is considerable evidence that DHEA exerts its anti-proliferative
and tumor-preventive action through the inhibition of glucose-6-phosphate
dehydrogenase and the pentose phosphate pathway, which generate NADPH
(required for mixed-function oxidase activation of chemical carcinogens, as well as
for deoxyribonucleotide synthesis) and ribose 5-phosphate (also required for
deoxyribonucleotide synthesis). Long-term DHEA treatment of mice also reduces
weight gain (apparently by enhancing thermogenesis), and appears to produce many
of the beneficial effects of food restriction, which have been shown to inhibit the
development of many age-associated diseases, including cancer. Using the mouse
two-stage skin tumorigenesis model, we found that adrenalectomy completely
reverses the anti-hyperplastic and antitumor-promoting effects of food restriction. It
is not unlikely that food restriction stimulates enhanced levels of adrenocortical
steroids, such as the anti-inflammatory glucocorticoids and DHEA, which in turn
mediate the tumor-inhibitory effect of underfeeding
Smart Basics March 1996 IntelliScope
Precursor Hormones That
Feed The Tree of Life
In April Smart Basics announced that we now carry DHEA
(dehydroepiandrosterone) in 10, 25 and 50 mg. capsules. This is pharmaceutical-grade
DHEA, assayed at 101% purity. The extra 1% is an artifact of the laboratory assay
procedures. We prefer to be painfully truthful when we say our DHEA is 99.8% pure
(the difference reflecting the slight amount of pregnenolone precursor used as the
base). Smart Basics DHEA should not be confused with the Dioscorea (Wild Yam)
extracts that have been on the market for some time now. While Wild Yam products
have been marketed as potential precursors for the body's production of DHEA, we
have yet to see a single study where DHEA-S levels have been elevated by one of
these products.
We've also recently introduced PREGNENOLONE, a naturally occurring metabolite
of cholesterol that acts as a precursor to DHEA and other steroid hormones. Animal
research indicates that pregnenolone possesses memory enhancing activity
approximately 100 times higher than that of other compounds with similar effects.
Used in the 1940's for the treatment of arthritis, pregnenolone has a long history of
use in humans without toxic side effects.
DHEA, or dehydroepiandrosterone, is produced by the adrenal glands, and is the
most abundant, naturally-occurring hormone in the human body. DHEA is often
referred to as the "Mother Hormone" because our body can convert it upon demand
into a host of other necessary health-enhancing hormones such as estrogen,
testosterone, progesterone, and corticosterone. DHEA blood levels reach their peak
around age 20, then decline in a linear fashion, making it one of the most reliable
markers for measuring biological aging. By age 80 DHEA blood levels have declined
as much as 95%, signaling the onset of the aging process.
"DHEA is most abundant in the human bloodstream. Research has found it to have
significant anti-aging effects. DHEA levels naturally drop as people age, and there is
good reason to think that taking a DHEA supplement may extend your life and make
you more youthful while you're alive. Additionally, DHEA may be an important
player in cognitive enhancement."
- Dr. Ward Dean, M.D.
More than just a precursor for the synthesis of other hormones, scientists have also
identified specific body cells designed to bind to DHEA. This receptor function
indicates that DHEA plays a far more direct role in human health than was
previously recognized. There have been over 2,500 published papers documenting
DHEA's multiple benefits, but the most recent paper studied the quality of life
enhancing effect of this natural hormone: "DHEA will improve the quality of life
over a longer period and will postpone some of the unpleasant side effects of aging,
such as fatigue and muscle weakness." The report also stated that those patients
receiving DHEA supplements slept better, had more energy and were better equipped
to handle stress compared to the placebo group not receiving the DHEA.
The potential benefits of DHEA have been known to the scientific community for
over 20 years, but this is the first placebo controlled human study conducted that
sought to assess the therapeutic benefits of DHEA replacement therapy. We'll have
more on this and other studies next month.
" DHEA is currently being investigated as an anti-aging hormone. New evidence
suggests this hormone is so beneficial that it may turn out to be the most important
advance of the decade."
- Dr. Alan R. Gaby, M.D.
To offer a more balanced view of DHEA, especially in light of the many "miracle"
effects commonly attributed to this supplement, Jim English recently had the
opportunity to interview Steven Wm. Fowkes of CERI, (Cognitive Enhancement
Research Institute). In addition to being the director of CERI, Mr Fowkes also edits
the monthly newsletter, Smart Drug News. Steve has consistently been on the
forefront of nutritional science and supplement development, and in the following
interview addresses many questions regarding the use of supplemental DHEA and
Pregnenolone, bringing a balanced view to the topic. We hope the following
information will help to cut through the usual marketing hype to aid our clients in
assessing not only the possible benefits, but the potential risks associated with these
supplements.
Jim: Steve, thank you for taking the time to speak with us. To start out, what exactly
is DHEA?
Steve: DHEA is a metabolite of cholesterol that acts as a precursor to the sex
hormones estrogen and testosterone. DHEA is an important raw material from
which the body manufactures hormones which are very important to normal
physiological functions. DHEA levels normally decline markedly with age, so we're
interested in knowing if supplemental DHEA may have health-enhancing or
anti-aging properties.
Jim: You're referring to the body's natural production of DHEA?
Steve: Yes. The enzymes that convert cholesterol into pregnenolone limit the
amount of sterols and steroids the body produces. Furthermore, these enzymes
decrease with age.
Jim: So, pregnenolone is actually a precursor to DHEA?
Steve: Exactly, and all other steroids. If you think of the steroid synthesis pathways as
a tree, cholesterol is the root system, pregnenolone is the trunk of the tree, and
DHEA is one of the main branches.
Jim: And the other sex steroids?
Steve: Estrogen and testosterone-and the corticosteroids-would be the crown of the
tree, the leaves. Dihydrotestosterone is maybe one of the leaves that has turned
yellow and is about ready to fall off the tree (laughs).
Jim: It needs to be pruned-that's a rather pastoral picture.
Steve: There's also aldosterone, which is used to regulate sodium and blood pressure
in the body. Another main branch off the trunk would be progesterone, from which
the corticosteroids are produced.
Jim: Isn't progesterone another precursor to the main sex hormones?
Steve: It can be, although typically it doesn't go that way. You can think of it as a
place where the tree branches and then rejoins, but that rather stretches the tree
analogy a bit.
Jim: Can you define some of the more common age-related health problems that can
occur from a decline in the body's production of DHEA.
Steve: Well, we don't really know at this point in time what primary function DHEA
has in the body. We know it has a precursor function, but there may be other direct
effects that DHEA can have in and of itself. DHEA doesn't just sit there, inert,
waiting to be converted into something else; it has an effect. Some of the effects that
we know about are relatively indirect. For example, DHEA provides nutritional
support for the body's repair mechanisms. In this case it has an anti-cortisol effect, so
it moderates the potency of cortisol to minimize the damage that may be caused by
stresses.
When you get injured or suffer stress, your body produces cortisol, and unrestrained
cortisol levels can have a profound effect not only on our healing ability, but the
immune system overall. If you get stressed-out, your body produces cortisol, and the
degree to which we lose control of cortisol production can interfere with our
immune system, the body's natural repair mechanism. In a sense, elevated cortisol
levels cause accelerated aging and aggravate control of free radicals.
DHEA is also important for the modulation of estrogen. And because DHEA can
produce estrogen and testosterone, there may be a downside for people who
over-convert DHEA into estrogen or dihydrotestosterone. I think that's the real
concern with high-dose DHEA. If you are merely taking a physiological replacement
dose of DHEA in the range of 10-30 milligrams, then the DHEA may not go gushing
down those other pathways. In other words, I don't think high DHEA levels are in
themselves much of a risk, but the enzymes that can convert DHEA into other
steroids could go into overdrive and cause problems. DHEA dosages in the hundreds
of milligrams range could cause dramatic increases in dihydrotestosterone or
estrogen levels, and that's why it's important to have medical supervision with
high-dose DHEA.
Jim: Would someone taking DHEA in 25 milligram doses specifically need to test
blood serum levels to measure their increase in DHEA levels?
Steve: I don't think it's absolutely necessary, but I think it's wise. Even at 25
milligrams, there could be significant increases in dihydrotestosterone or estrogen
that could be aggravating factors in people with benign prostrate hypertrophy (BHP)
or risks of cancer.
Jim: Particularly breast cancer which we know is estrogen respondent.
Steve: And estrogen in men should not be ignored; men get breast cancer, too. In my
opinion, you don't have to measure DHEA or DHEA-S for safety reasons. DHEA
itself is minimally toxic. Even an acute dose of 10-20 grams would probably would
have minimal toxic effects on people. Natural DHEA levels vary dramatically
between people, maybe even by a factor of 20 in people of the same age. If you
compare teenagers and elderly adults, you're going to find them straddling a huge
range. So DHEA itself is not a toxic agent that we need to be concerned about. We do
assume that DHEA and DHEA-S levels indicate to some degree the appropriate
amount, that as long as we do not push it way above normal, we are not going to
have downstream effects. But that may not be true. We may, at fairly moderate levels
of DHEA, convert too much of it into testosterone and other steroids. That
conversion process could vary widely among people, and that's really what we
should be looking at!
Using the tree analogy, we shouldn't be looking at the diameter of the DHEA branch,
we should be looking at the growth of the crown of the tree. Although it is a more
difficult process to measure all of the steroids, I think that it is clinically warranted
when high-dose DHEA is indicated.
We shouldn't be prejudiced by sex stereotypes. Women make testosterone and men
make estrogen. So it's important to look at all the hormones to know what's going
on. For women, a little extra testosterone increases their libido and their enjoyment
of life, and that's often a good thing. But if women take 50 or 200 mgs, too much
testosterone can make them uncomfortable libido-wise or can produce masculine
characteristics, like a deepening voice or facial hair growth. So women should
definitely be careful of those issues. There are significant biological consequences of
taking DHEA, and just because some of them are beneficial does not mean it should
be used like candy.
Jim: Most people I've spoken with want to increase their energy levels to those closer
to those they experienced as adolescents. Are there any specific guidelines people
should follow?
Steve: One factor is how far back you want to push it. The radical approach is to push
DHEA back to age twenty. My advice is to push it back ten to twenty years younger-so
if you're 50, you might want to shoot for a 30-year-old DHEA level-because there may
be downstream problems. In other words, the way in which the body converts DHEA
into testosterone, dihydrotestosterone and estrogen may change with age, so it may
be the case that as we get older we have more of a tendency to produce
dihydro-testosterone and estrogen and less of a tendency to produce testosterone.
Jim: And that could exacerbate the kinds of problems we were talking about earlier.
Steve: Like BPH in men, and endometriosis and breast cancer in women. We don't
have enough experience with DHEA to say absolutely that there is no risk in
humans.
Jim: What would you recommend as a dosage for a normal, healthy individual
starting out taking DHEA?
Steve: One 25 mg capsule first thing in the morning (or right before bed) is the
standard recommendation. For those getting medical supervision, they may want to
do it at both times. There may be some usefulness in exploring 5-15 mg dosages.
Jim: Is there any problem with taking DHEA with food?
Steve: It's best to take it on an empty stomach. The liver gets rid of 50% to 90% of
DHEA, and I think that taking it with food tends can increase the percentage of loss. I
think it's best taken on an empty stomach first thing in the morning or right before
bed.
Jim: Personally I find DHEA to be pleasantly stimulating so I would likely avoid
taking it right before bedtime.
Steve: Not everybody has that reaction. That's one difficulty with DHEA; you can't
really tell people what they should expect. Some people don't notice anything at all -
I'm like that. A fair number of people notice some hard-to-define feelings of
improved well being.
Jim: Now lets talk a bit about pregnenolone, which you mentioned earlier as the
direct precursor to DHEA.
Steve: Pregnenolone probably has more pronounced cognitive effects. Pregnenolone
and progesterone are produced in fairly large quantities in the central nervous
system, which is unusual given that it could be transported from the liver or adrenal
glands. The brain must have a special need for pregnenolone. Amounts are fairly
large when we're young and our brains are rapidly growing. Also, this may account
for Dr. Eugene Roberts observations that even minute quantities of pregnenolone as
small as a few hundred molecules have a very potent effect on the ability of mice to
learn and navigate mazes1. That's an exceedingly small amount of material.
Jim: Would this increase memory in a person taking other cognition enhancing
products such as piracetam or hydergine?
Steve: There's research that suggests that's the case with piracetam, (2-4) and I suspect
it would be the same with the other cognitive enhancing products. I suspect that this
is one of the reasons that Alzheimer's studies using piracetam have not been
fruitful. Alzheimer's is known to be characterized by exceedingly low sterol and
steroid levels. Therefore, you would expect that this would undercut the piracetam
mechanism. Also, we might expect the combination of piracetam and pregnenolone
would be worth trying.
Jim: When dealing with pregnenolone, would you also recommend that one get
tested by a doctor to establish a baseline to measure one's progress?
Steve: Yes, because your dealing with the same pathways. Pregnenolone is amazingly
safe. I think Dr. Ray Peat recounted an episode where he took a heaping tablespoon
of pregnenolone - and nothing happened. So I would worry only about the
downstream effects.
The advantage that pregnenolone has is that your not "nesting" in only one side of
the tree. Pregnenolone is not committed to any specific steroid pathway. As long as
your body doesn't have some kind of screwy imbalance in terms of the way that
steroids are metabolized, you're feeding everything with pregnenolone. Unless I
know otherwise, I would trust the wisdom of the body to balance it out.
Jim: So basically the body can determine the best use of pregnenolone as it
disseminates it throughout the body.
Steve: And you can measure it by measuring before-and-after DHEA levels. When
you are taking pregnenolone, DHEA is a downstream hormone.
It's important to realize that sex steroids are hundreds of times more potent
biologically - in terms of dose - than pregnenolone or DHEA. That's why I think we
need to pay more attention to what's going on with these end hormones.
Jim: Should someone who is in their 40's, 50's or 60's feel at high risk from taking a
10 mg capsule of pregnenolone or 25 mg of DHEA? What I'm trying to determine is
how necessary is it to go out and get the blood studies, especially if you have a doctor
who doesn't really know what you're asking for.
Steve: I think the risks are minimal when you're dealing with replacement dosages,
i.e., less than the amount your body would produce if it were healthy. When the
DHEA and pregnenolone levels are within the normal range of what the body would
be producing at one's general state of age, that's a fundamentally benign state of
affairs. When you start dealing with dramatic increases in DHEA and/or
pregnenolone, then the issue changes dramatically.
Jim: I know of people that are taking 600 mgs of DHEA a day; that strikes me as
exceedingly high.
Steve: It is. I know people who take from 500 to 2,500 milligrams a day, but they are
typically HIV positive with abnormally low DHEA levels who are dealing with
serious immune system dysfunction. It is not clear to what degree this benefits or
harms them. I believe that estrogen is very counter-productive in HIV positive
people and that it has an immunosuppressant effect. It has, at the same time,
cognitive enhancing effects because of it's neurotoxicity, so it stimulates neurons and
makes people more awake and more alert, but in doing so causes damage like that of
cysteine or MSG would do in excess.
Jim: In other words, you're getting a temporary benefit but your accelerating the
damage at a much higher rate.
Steve: At least causing stress, even if no overt damage is done. I don't know the
mechanism of that excitotoxicity, but I believe it is direct. I've looked into aspartame
excitotoxicity and how it relates to pyroglutamate and piracetam, but I haven't
researched estrogen yet.
Jim: Lets take a little side step here because you raise the interesting issue of
aspartame. We have one or two products which contain very small amounts of
aspartame. Some of our customers are very concerned. They won't take aspartame in
any amount.
Steve: It's a choice. As long as people are informed of the potential risks, that's fine.
My experience is that aspartame sensitivity varies dramatically from person to
person. There are people who can take it with minimal immediate consequences.
Others take it and have immediate overt symptoms, like headaches, blood pressure
changes, ringing in the ears, vision problems or seizures. They just have to stay away
from it, period.
1. Floor, J.F., Morley, J. E.,and Robers, E,. Memory-Enhancing Effects In Male Mice Of
Pregnenolone And Steroids Metabolically Derived From It. Proc. Natl. Acad. Sci.
USA 89: 1567-71, March 1992.
2. Burov YV et al. Castrated rats: Influence of amiridine, tacrine and piracetam on
passive avoidance response and brain biochemical parameters. Biological Amines
9(4): 327-35, 1993.
3. Mondadori C, Bhatnagar A, Borkowski J and Hausler A. Involvement of a
steroidal component in the mechanism of action of piracetam-like nootropics. Brain
Research 506(1): 101-8, 1 January 1990.
4. Mondadori C and Hausler A. Aldosterone receptors are involved in the mediation
of the memory-enhancing effects of piracetam. Brain Research 524(2): 203-7, 6 August
1993.
Contact Us To Place Orders, Speak With Customer Service
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Last modified: June 3, 1996
The following is an abstract written by the inventor of CellFood--Everett L. Storey.
Even Albert Einstein gave recognition to Storey for his work with the hydrogen and
oxygen molecule.
CELLFOOD... THE COMMON COLD... VIRUSES & CANCER
by Physical Chemist & Microbiologist Everett L. Storey
In the list of 78 essential elements, the only elements with more than one tenth of 1% volume are oxygen, hydrogen, carbon and sulfur. Concentration is Not a key to success in Advanced Medicine. Greater dilutions seem to provide more electron and deuteron activity of the constructive type.
With this array of useful elements, the human body can be revitalized. Damaged tissues can, with proper exercise and a nutritional diet, be effectively and safely rebuilt. Cancerous tissue wilts and disappears, flushed away with other dead cells due to the fluid rich with magnesium and nascent oxygen released into the bloodstream.
The mind takes control of body functions induced by the electrical currents moving through the fully conductive nervous system.
Just as weight control calls for a new lifestyle... the fight against the common cold...viruses and malignancies must be fought each day with full resources and all-out dedication. Unfortunately cold germs and viruses feed the very conditions from old injuries to system congestion, drawing extra power from any toxins or contaminants found in the bloodstream.
The combinations of elements that might normally result in toxic compounds cease to be threatening in the presence of Deuteron activity. Harmful compounds are broken down into their constituent-free elements on a measured time release pattern. Immune antibodies can be formed as required as well as catalysts, enzymes and vitamins.
It Is time for general acceptance of the concept that even in some terminal cases, our bodies can, given essential building blocks, repair and reconstitute every living cell within a span of 11 months.
Each cough, sneeze, sniffle, sore throat, sore muscle or congestive pain should serve as a warning signal that our glandular, gastro-intestinal, pulmonary, neurological or cardiovascular systems will in some way become or may be under stress or actual attack.
When in doubt, call in an allergist. Time, study and patience can often solve the most baffling problems.
General Practitioners and family-oriented Physicians can aid with the patient's own self-discipline teaching that everyone must become his own body's best friend. No matter how crushed with work, the sincere Physician or Surgeon must push or at least nudge his patient into either mental or physical exertion simply because life generates more life and thus feeds the electrical process of revitalization.
In summary, the winding road to health leads ever uphill from some form of hydrogen, probably Deuterium, its most versatile isotope which is about to be recognized as the creative and sustaining, force of all life.
Physicians and Surgeons by monitoring the progress along life's highway with a view to keeping peopleaway from the exits and moving ever forward can perform the most worthwhile service in the world.
CELLFOOD
Cellular Food for Advanced Nutrition
The Premier Oxygen Product
The inventor of CELLFOOD Everett L. Storey, was an author, physical
chemist, microbiologist and humanitarian. After more than 24 years of
research and development, CELLFOOD was developed as a broad spectrum,
highly energized liquid. CELLFOOD {Deuterium Sulfate [D2SO4]} is a
proprietary secret formulation, developed from a di-base solution.
Contained in this di-pole formula are "Aerobic" proteins, 17 amino acids,
34 enzymes, 78 major and trace elements and deuterons , electrolytes, and
disolved oxygen.
CELLFOOD has the unique ability to dissociate the water molecule into
nascent hydrogen and nascent oxygen. This "splitting" of the water molecule
results in the release of nascent hydrogen and oxygen gases simultaneously
in a chain reaction that only involves about one five-hundred thousandth of
the available moisture at one time. This results in an additional source of
oxygen available from the water molecule. Some of the benefits of a
mineral-rich and oxygen-rich diet include: high energy levels; better
assimilation and utilization of the food we eat and the supplements we
consume; and the creation of enzymes that are necessary for vitamins to
function, increasing their effectiveness four to five times in the body.
When a body is deficient in oxygen, hydrogen, trace minerals, enzymes,
amino acids and water, it does not have the ability to repair and maintain
itself. It is said to be in a state of disease (dis-ease). Since the
elements in CELLFOOD are suspended in liquid form and are broken down into
an ionic state, they are absorbed at a much greater rate than the same
elements in a tablet form.
CELLFOOD flows throughout the entire body, cleansing and energizing the
system. This highly effective, unique formula may be used for specific
purposes or as an enhancer.CELLFOOD has antitoxic, antiviral and
antibacterial properties. It is also a powerful detoxifier and will help
digest and eliminate toxins from the bowel, such as remains of undigested
foods. CELLFOOD creates an environment in which harmful bacteria and
viruses can no longer thrive. It allows the body to maintain and produce
its own vitamins, catalysts and enzymes, thus helping the body to function
more efficiently while removing waste materials. With the proper
elementals, the body can repair itself, naturally. It also enhances the
natural vital force in the body. It is a nontoxic
oxygen/mineral/enzyme/amino acid formula, which has been developed using
the most advanced scientific methods available. CELLFOOD is a blend between
science and traditional medicine..
Many satisfied clients have claimed that CELLFOOD has helped in the
following conditions:
Arthritis Bladder infection
Cancer Candida
Chronic Fatigue Syndrome Common Cold
Diabetes Eczema
Gout Heart Diseases
Herpes simplex Lung conditions
HIV Hypertension
Impotence Menstrual Problems
Nervous system disorders Post Polio Syndrome
Psoriasis Sickle Cell Anemia
Shingles Viruses
And many more
CELLFOOD:
From The Desk Of Ed Mccabe, "Mr. Oxygen"
For over twelve years, I have researched various forms of oxygen [Image]
therapies available worldwide. I have lectured throughout the world
sharing thousands of accounts of amazing health and healing benefits from
increasing the oxygen levels in the body. Perhaps you have attended one of
my lectures, listened to my audio tapes, or watched my video.
If you recall reading my book,Oxygen Therapies: A New Way of Approaching
Disease, you know that our bodies were designed by the Creator to function
on nearly 50% more oxygen than is available in today's atmosphere. By
living in an oxygen deficient environment, and not feeding our cells the
proper oxygen and nutrients needed for clearing wastes, our body fluids and
blood can become toxic. In today's toxic world, nearly everyone can benefit
from increased oxygenation at the cellular level. There is an easy and
effective way to supplement your body's need for increased oxygen: Oxygen
for Life's new product CELLFOOD.
During my numerous appearances on TV and radio, I have consistently
repeated that after twenty-five years of private research, I noted exactly
which supplements people responded to--quickly and with the best results.
Here they are--the five most important things the human body needs in
today's toxic world to regain or maintain health. The five crown jewels of
health are: Lots of cellular OXYGEN, the body cleanser and immune booster;
COLLOIDAL MINERALS, the building block of everything your body is made up
of; ENZYMES, the scavenger / catalysts; good clean WATER, the cleanser and
transport mechanism, and a moral and spiritual BALANCE.
In my experience, from the thousands of interviews I personally conducted,
I have seen amazing results consistently and quickly in people who have
properly applied just oxygen supplementation, or just colloidal minerals,
or just enzymes. Each one has proven to be a powerhouse all by itself. Now,
imagine your level of wellness if you combine all three.
That's exactly why I'm writing to tell you that the folks at Oxygen for
Life have done exactly that. Their new product CELLFOOD actually combines
three of my five crown jewels of health in just one product. CELLFOOD
supplies your body with a diet of OXYGEN, MINERALS and ENZYMES all at once!
CELLFOOD has been refined by brilliant scientists over many years in order
to optimize its synergistic action. The main properties of CELLFOOD are
amazing. It increases the bioavailability of oxygen in the water or juice
you place it in and I believe that this means it also releases oxygen into
the body by taking just a little bit of your body's water (most of you have
over one hundred pounds of water in your body--two thirds of your body is
water) and then, since water is made of oxygen,CELLFOOD safety generates
oxygen right from your internal water and releases it to the cells! Pretty
neat, huh? You know how good oxygen is for you. Just a little bit of
CELLFOOD every day, with consistency, and the cleansing and building
process begin and then continue.
Although CELLFOOD already has enzymes and colloidal minerals in it, to be
sure you're getting optimum nutrition, I would strongly suggest taking
digestive enzymes along with the new CELLFOOD product. Then you will be
sure to have enough basic oxygen, minerals, and enzymes.
OFL DIGESTIVE PLANT ENZYMES are full spectrum replacements for the natural
enzymes that are supposed to be in our food but have been destroyed by the
usual commercial food processing, and the decline of bodily enzyme
production from aging. Without enough enzymes, our bodies cannot properly
digest food, and undigested food particles putrefy in the body and create
an unhealthy fluid environment that disease microorganisms love, People who
take digestive enzymes (including me) report their digestion improves, like
they used to have when they were children. Remember?
The minerals in CELLFOOD are absolutely necessary for 95% of your body's
daily functions. Commercial farming has caused our soils to become mineral
depleted. Due to poor crop rotation and the loss of valuable top soil from
flooding and over-irrigation, much of the natural minerals and trace
minerals has been lost from today's food supply, When a body is lacking
minerals, vitamins have little or no effect. Because CELLFOOD's pristine
sea source and ancient plant source minerals are suspended in a liquid
form, they are more readily absorbed and utilized by the body than minerals
in tablet or capsule form, An easy and effective way to supplement your
body's need for minerals is by using CELLFOOD.
Oxygen for Life's premier liquid nutritional supplement is CELLFOOD. For
optimum cellular nutrition, and ease of detoxification, follow the label
direction. CELLFOOD IS POWERFUL--A LITTLE GOES A LONG WAY.
A months supply of CELLFOODcomes in a 8 ounce bottle and cost only $32.00
retail. And a month's supply of DIGESTIVE PLANT ENZYMES cost only $28.00
retail.
* [All products can be ordered directly from Oxygen for Life. To
receive a 10% discount please e--mail Timothy M. Sanders, D.D.S.
(Oxygen@wwns.com) and use the word's "Order Only" in your request.
Ordering information will be provided. It's simple to order
CELLFOOD If you wish to buy CELLFOOD at at the wholesale
distributor price please request a complete information pack from
Timothy M. Sanders, D.D.S. (Oxygen@wwns.com) An information pack
plus an immediate ordering number will be provided. Use the word
"CellFood Pack" in your request.]
Remember that CELLFOOD has been tested and used daily for years. It is a
proven product and OFL has received hundreds of positive reports. The OFL
ongoing CELLFOOD research project team would like to tally your personal
results from addi ng CELLFOOD to your diet on a regular daily basis.
Oxygen for Life and I would be most appreciative if you dropped them a note
at the following address:
CELLFOOD PROJECT
11555 Rancho Bernardo Rd,
San Diego, CA 92127-1441
Sincerely yours, and Happy Oxygen!
Ed McCabe
CELLFOOD
ENZYME CONTENT TRACE MINERALS
Hydrolyses, Carbohydrases Actinium
1. Maltase Antimony
2. Sucase Argon
3. Emulsin Astatine
Nucleases Barium
1 Polynucleotidase Beryllium
2. Nucleotidase Bismuth
Amidase Boron
1. Urease Bromine
Peptidases Calcium
1. Aminopolypeptidase Cadmium
2. Depeptidase Carbon
3. Prolinase Cerium
Esterases Cesium
1. Lipase Chromium
2. Phosphotases Cobalt
3. Sulfatases Copper
Iron Enzymes Dysprosium
1. Catalase Europium
2. Cytochrome oxidase Fluorine
3. Peroxidase Gadolinium
Copper Enzymes Gallium
1. Tyrosinase Germanium
2. Ascorbic acid oxidase Gold
Enzyme containing Coenzymes 1 and/or 2 Hafnitim
1. Lactic Dehydorgenase Heliumn
2. Robison Ester Dehydrogenase Holmium
Enzymes which reduce cytochrome Hydrogen
1. Succinic Dehydrogenase Indium
Yellow Enzymes Iodine
1. Warburg's Old Yellow Enzymes Iridium
2. Diaphorase Iron
3. Haas Enzyme Krypton
4. Cytochorme C reductase Lanthanum
Hydrases Lithium
1.Fumarase Lutetium
2. Enolase Magnesium
Mutases Molybdenum
1. Aldehyde Mutase Neodymium
2. Glyoxalase Neon
Desmolases Nickel
1. Zvmohexase (adlolase) Niobium
2. Carboxilase Nitrogen
Other Enzvmes Nobelium
1. Phosphorvlase Osmium
2. Phosphohexisomerase Oxygen
3. Hexokinase Palladium
4. Phosphoglumutase Phosphorus
AMINO ACIDS Platinum
Alanine Polonium
Argenine Potassium
Aspartic Acid Praseodymium
Cystystine Promethium
Glutamic Acid Rhenium
Glycine Rhodium
Histidine Rubidium
Isolentine Ruthenium
Lysine Samarium
Methionine Selenium
Thenylalanine Silicon
Proline Silver
Serine Sodium
Threonine Sulfur
Tryptothan Tantalum
Tyrosine Technetium
Zaline Tellurium
Terbium
Thallium
Thorium
Tin
Titanium
Tungsten
Vanadium
Xenon
Ytterbium
Zinc
Zirconium
THESE PRODUCTS CARRY A 100% 60 DAY MONEY BACK GUARANTEE SO ORDER NOW!!
FOR A FREE AUDIO TAPE ON CELLFOOD WITH COMMENTS FROM ED MCCABE
Please e-mail your Federal Postal Address and the word "CellFood" to:
Oxygen@wwns.com
To receive a 10% discount when you order call Oxygen for Life at
1-800-619-6994 and tell them that you wish to order as a Preferred Customer and that your distributor is (SANDENT ID # 409-03-7547) . To order at full wholesale you must enroll as a distributor. I recommend that you convince yourself that these products work by trying them first as a Preferred. Customer before you enroll as a distributor. For distributor details e-mail Oxygen@wwns.com or call at 1-615-890-2806 or 1-615-896-8301 or fax at 1-615-890-2806.
THE CHEMISTRY OF CELL FOOD
Cell Food is a proprietary, super energized, complex concentrate of 78
trace elements, 34 enzymes, 17 amino acids and dissolved oxygen held in a
colloidal suspension. A colloid is a minute particle which is suspended in
a liquid solution. Since most of the bodily fluids (blood, lymph and CSF)
are colloidal in nature and negatively charged, the similarity between Cell
Food and the bodily fluids increases the bioavailibility of the nutrients
contained in CellFood to every cell in the body. This increased availabilty
of nutrients allows the body to function more normaly.
Cell Food is unique due to its ability to create nascent oxygen. Nascent in
Latin terms means newly born. In biochemical terms it refers to this newly
born singlet oxygen as O- that has not yet entered into biochemical
reaction. Free radicals (which many biochemists now believe are a primary
cause of the aging process and degenerative disease) are positively charged
ions of singlet oxygen, O+. Nascent oxygen is negatively charged O-. The
opposite charge of these ions cause them to attract each other, forming
simple pure Oxygen O2. Nascent oxygen "seeks out" and neutralizes dangerous
free radicals, combining to form pure oxygen in the process!!!
(O- nascent oxygen & O+ free radical ion= O2 stable oxygen.)
Cell Food is developed from a di-base, di-pole solution. Cell Food has the
ability to dissociate H2O>O- & H-. simultaneously in a chain reaction that
involves only 1:0005000 available moisture at one time >which yields an
additional source of oxygen to the body. "Splitting" of the water molecule
is performed by means of weakening the bonding electrons (Ionic Transfers).
1. DI-POLE: In the H20 molecule, the density of the electron cloud is
located around the Oxygen atom; the bonding electrons are shifted toward
Oxygen and away from Hydrogen. CellFood allows the bonds in the electron
distribution to be unsymmetrical (Polar). The hydrogen molecule can then be
described as DI-POLE with the Oxygen atom acting as a negative pole and the
Hydrogen as a positive pole.
2. DI-BASE: Generally dissociate in solution into one Hydrogen ion and the
residue of the molecule, the second replacable Hydrogen atom not splitting
off as an ion until the greater quanity of the first has been removed.
Questions And Answers
Q. Does CellFood contain oxygen?
A. CellFood is able to generate oxygen from "splitting" the water molecule.
The concentrate is added to water and at that time begins to generate
oxygen. CellFood itself does not really contain large amounts of oxygen.
Q. What stops the generation of oxygen and hydrogen?
A. Simply stated, when the body needs oxygen, it utilizes the oxygen
needed. Since Cellfood utilizes only one five-hundred thousands of the
available moisture at one time, there is usually plenty more there
available to release if needed. (Note: you will not explode with an excess
amount of oxygen or hydrogen as it is not released until needed).
Q. What is the shelf life of CellFood?
A. The shelf life of CellFood is almost indefinate. Sample batches from 25
years ago have been tested and have actually improved with time (similar to
fine wines).
Q. Can CellFood be used to purify water?
A. Yes. CellFood can be used to purify water that you are somewhat
uncertain about (such as from a river or stream). Simply add 3 drops of
CellFood to 1 pint of water. It will even take the "smell" out of the water
and improve the taste. In earthquake areas (such as CA) CellFood should be
kept available to make sure that stored water that is kept around for
several months can be purified. (Note: It is suggested that CellFood not be
added until ready to use).
Q. How is CellFood used Topically?
A. Mix CellFood with at least 20 parts of water and use this solution for
soaking or dabbing onto the cut, burn or affected area. (Company owners use
a small amount of CellFood in a spa and have experienced tremendous results
with softening skin and other side benefits as well as keeping the spa
water clean and clear).
Q. What is the function of Trace Elements in Cell Food?
A. Trace elements are needed as cofactors for specific enzymes and for a
wide variety of other critical functions such as acid-base balance. Each
enzyme is specific in that it will catalyze only one type of reaction.
There are thousands of chemical reactions that take place within the body,
and therefore we have thousands of enzymes, each with its own shape and
active site.
The ability of enzymes to function may be limited or destroyed by changes
in the intracellular or extracellular fluids in which they are found.
Changes in blood pH and temperature are especially crucial for enzymatic
functions. Acid-base balance must be maintained in order for enzymatic
reactions to proceed normally. CellFood helps maintain this balance.
Q. What is the function of the Amino Acids contained in CellFood?
A. There are aproximately 80 amino acids which are found in nature: only 20
are necessary for human metabolism and growth but, the ones that must be
provided by supplementation are called essential. Amino acids are necessary
for protein metabolism and muscle energy (ATP). CellFood supplies these
needed Amino Acids.
IN CONCLUSION
The combinations of elements that would normally result in toxic compounds
cease to be threatening in the presence of deuteron activity. Harmful
compounds are catabolized into the constituent free elements on a measured
time release pattern. Immuno antibodies can be formed as needed as well as
catalyst enzymes and vitamins.
Since catabolism (destructive phase of metabolism- the process of reducing
complex substances to simple substances with a release of heat) feeds on
lack of oxygen, we must provide ample nascent oxygen and hydrogen to every
cell. As well, some bodily processes require hydrogen, we must provide a
means of dissociating water yielding nascent hydrogen and oxygen to
continue this life giving chain reaction.
THE BEST MEDICINE IS HEART ECG COHERENCE, In Plane terms Compasionate Love Heals. Remember to breath, and keep looking up.
This section will be expanded.