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- STUDY GROUP AIDS THERAPY
- c/o Felix A. de Fries
- Eglistr. 7 CH-8004 Zürich, Tel. /FAX:
0041 1 401 34 24
- E-Mail: felix.defries@bluewin.ch
-
- Zurich, 1th
December 2005
-
“World AIDS-Day”
To people afflicted and their loved ones
To medical doctors and institutions
To the news media
HIV=AIDS, the continuing failure of a false medical
model
Dear Sir or Madam:
You may learn from the attached pages, which vitamins,
trace elements, amino acids and fatty acids are essential for
functional immunity. A lack in the daily doses of these substances
leads after a short time to immune deficiencies and functional
impairments in the detection and destruction of cells containing
viruses, fungi and mycobacteria, and in the defence against bacterial
infections by means of antibodies. If this lack occurs in childhood,
it leads to a malformation of the thymus gland and other organs
essential for the immune system, and later to immune weaknesses.
Furthermore, immune reactions are impaired not only by frequent
infections due to polluted drinking water and repeated tissue
injury, but also by industrial toxins in the environment, food and
drink, drugs (e.g.chemo-antibiotics and recreational drugs), and in
carrier substances of vaccines). When these immune deficiencies occur,
cells containing viruses, mycobacteria and fungi can no longer be
detected as abnormal and subsequently destroyed by killer cells. This
leaves an individual wide open to opportunistic infections and
cancerous changes.
The immune deficiencies which have been emerging since
1980 in developing countries and in particular risk groups (male
homosexuals, drug users and haemophiliacs) in Europe and the USA,
since 1984 were blamed on the "Human Immunodeficiency Retrovirus" HIV,
which has been postulated based on nonspecific proteins from
unpurified cellular particles that are expressed from immune cells
during overstimulation and oxidative stress reactions. The
HIV-antibody test, designed thereafter, declares persons with a higher
than normal rate (above an arbitrarily defined threshold) of
antibodies against these cellular proteins, to be carriers of this
HIV-retrovirus. Since then, this "new retrovirus", which is frequently
shown with virtual computer graphics, has never been approved as such
according to the rules for retroviral isolation defined in 1972
(electron microscope photos of particles that have been budding from
the cell membrane, centrifugal separation and purification of these
particles in a 1.16 g/ml sucrose-density gradient, the demonstration
of particle size and morphology typical of retroviruses, and the
subsequent transmission and cultivation of these particles in
uninfected control-group cells [see
http://aliveandwellsf.org/library.html#isolation
]). Furthermore, these protein tests are
proven to be cross-reactive in case of endemic tropical infections
such as tuberculosis, leprosy, etc.
Since the mid-Eighties, individuals who yield a
positive result on these HIV-antibody tests, and present with
illnesses that fall underneath the AIDS umbrella, (and in Africa after
the Bangui definition this can be simply be continuous diarrhea with
no blood test) have been treated according to the HIV=AIDS model with
high doses of nucleoside analogue drugs, which by their cytotoxic
effects cause life-threatening damage to the human organism and its
mitochondria.
After ten years of administering these nucleoside
analogue drugs, the dosage of these substances was reduced in 1995,
(with the effect of the immediate fall of the death rate in the people
treated!) and then were combined with synthetic protease inhibitors.
This combination therapy, since then the orthodox treatment of choice
in the USA and Europe, and in some developing countries, causes:
malaise, diabetes, kidney stones, fat abnormalities, osteoporosis,
bone necrosis, heart and/or liver failure; after a while, "resistance"
to the postulated HIV-retroviruses occurs, such that patients have to
be treated with a continuously changing formula of drugs (see Dr. H.
Kremer "The Perversions of AIDS-Medicine"
http://www.altheal.org/overview/pervmed.htm
)
Since 1988, it has been demonstrated in various
studies that both AIDS-patients and asymptomatic "HIV+" persons show a
persistent lack in glutathione, amino acids, antioxidant substances,
trace elements
and fatty acids. It has also been proven that by
administration of N-acetylcysteine (NAC) and other substances, the
lack in glutathione can be replenished with the effect that immune
deficiency and muscle
wasting are halted and reversed! As you may learn from
the text by Dr. H. Kremer: "The lifesaving knowledge on healing," ( http://aliveandwellsf.org/kremer/Kremer_Chapter_XI.pdf
) this treatment is founded upon numerous publications in
fundamental medical research.
These findings have been consistently ignored by AIDS
researchers and
by the national and international AIDS institutions,
as the orthomolecular substances involved cannot be patented and
therefore will not bring large financial profits. 17 years after the
first scientific publication on the role of glutathione deficiency in
AIDS, practically no patients are administered this highly effective
and non toxic therapy (see
http://aliveandwellsf.org/treatment_rec.html
)
To those who have carefully studied the available
data, it is evident that the illnesses which define the AID-Syndrome
are not caused by the postulated contagious HIV-retrovirus, but by
malnutrition, polluted water, poor living conditions and toxic
substances in food, drugs (pharmaceutical and recreational), and in
environment.
The HIV=AIDS model was formulated in 1984 on the basis
of presumptions that no longer hold water in regard to the basic
medical research gained since 1990 (in particular of the findings on
the role of nitric oxide in immune reactions). The HIV=AIDS model has
become a homophobic and sex-phobic racist ideology to allow human
trials for genetic medicine research and corporate profit; meanwhile
obscuring the ecological crises occurring in developed and developing
countries, and the continuing crisis of miserable poverty and famine
in developing countries.
Those who blindly promote and publicize this model in
medicine and science, bear the responsibility for the ineptitude and
unnecessary suffering that result from it. The truth about HIV and the
real causes of AIDS, (first of all the lack of nutrients essential for
the immune system in millions of people in developing countries) as
well as its effective treatment and prevention, can not be held back
any longer to the general public.
Felix A. de Fries David
Lowenfels
Study Group AIDS-therapy, Zurich
Alive&Well, San Francisco USA
Substances essential for the immune system:
substantial nutrients:
Vitamins
Biotin Calf
liver
Soybeen
Brewer’s yeast
Folic
acid Wheat
germ
Red beans
Spinach
Broccoli
B1
Brewer’s yeast
Pork
Ham
B2
Calf’s liver
Mushroom
Brewer’s yeast
B3
Calf liver
Peanut
Tuna
Chicken
B6
Calf liver
Potato
Banana
Lentils
B12 Calf
liver
Mussel
Solomon
Beef
C
Papaya
Broccoli
Brussels prouts
Orange
D
Tuna
Egg
E
Sunflower seed
Wheat bud
Potato
K
Spinach
Broccoli
White cabbage
Calf liver
Green tea
Trace Elements
Chromium
Lentils
Whole-grain bread
Sugarcane molasses
Chicken
Brewer’s yeast
Iron
(fe) Pork
liver
Oyster
Soya flour
Millet
Potassium Soya
flour
White beans
Lentils
Banana
Calcium Cheese
Sardines with bones
Soyabeans
Cabbage
Copper (cuprum)
Calf liver
Oysters
Lentils
Sunflower seeds
Magnesia
Soya meal
Rice with brain
Wheat bud
Sunflower seeds
Molybdenum Soya
flour
Red cabbage
White beans
Selenium
Tuna
Herring
Sardines
Calf liver
Soybeans
Zinc
Calf liver
Oysters
Lentils
Peas
Amino Acids
Arginine
Peanut
Soya beans
Hazelnut
Shrimp and Prawn
Lamb
Carnitine
Lamb
Beef
Pork
Chicken
Cysteine
/Methionine Salmon
Shrimp and Prawn
Chicken
Glutamine Chicken
Milk
Lysine
Pork
Beef
Soybeans
Taurin
Tuna
Mussels
Pork
Lamb
Fatty acids
Omega
6 Corn
Oil
Thistle Oil
Sunflower Oil
Flax/Linseed Oil
Omega
3 Fish
Oil
Wheat germ oil
Sunflower Oil
Flax/Linseed Oil
Soya Oil
Co-enzyme Q10
Soya Bean
Walnut
Almond
Sardines and Mackerel
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