More on the AIDS scam.

[Guest guest]

<MedicalConspiracies (AT) googl (DOT) com>

 

(Another article that should be read. Please take a printout to read at

leisure.A question I wish to raise here, AIDS is perceived to be a major threat

in Africa, China and India. These three also happen to the most populous

regions. Another " coincidence " ?)

 

http://rense.com/general67/viru.htm

 

The Virus Cancer Program 1964-1980

The Birthplace Of AIDS And The Kaposi's Sarcoma Epidemic

By Alan Cantwell, MD

© 2005

9-27-5

 

 

The epidemic of HIV/AIDS and the epidemic of " gay cancer "

 

Kaposi's sarcoma (KS) is widely known as the " gay cancer " that often accompanied

AIDS when the first cases broke out in gay men in Manhattan in 1979. In 1994 a

new " human herpes-8 " virus was discovered that is now widely accepted as the

cause of all forms of KS. However, it is extremely important to note that the

new KS herpes virus (KSHV) is separate and distinct from the human

immunodeficiency virus (HIV), the virus that causes AIDS (Acquired Immune

Deficiency Syndrome). Therefore, it is now important to recognize that two new

viruses were " introduced " into gays that produced not only the epidemic of

HIV/AIDS, but also the new epidemic of KS ( " gay cancer " ).

 

Two new viral epidemics erupting exclusively in homosexuals is an unprecedented

event in medical science. Such a bizarre and unlikely scenario strongly suggests

to me that that the two epidemics of HIV and KS are more likely to have occurred

due to the deliberate or accidental " introduction " of new viruses into gay

men " -and not from two viruses suddenly appearing " out of Africa. "

 

The widely-held theory is that HIV originated in African primates in the African

bush. Somehow the monkey or chimpanzee virus " jumped species " into black

Africans to initiate the epidemic which has now killed 20 million people and

infected 40 million more. How this sexually-transmitted virus came from black

Africa to initially infect only young white gay men in Manhattan has never been

explained satisfactorily.

 

Furthermore, the epidemic in America erupted in the

late 1970s, at a time when AIDS in Africa was unknown. The AIDS epidemic in

Africa appeared in the autumn of 1982, at the earliest.

 

The man-made origin of HIV/AIDS

 

The man-made theory of AIDS is generally dismissed as " conspiracy theory. "

Nevertheless, AIDS researchers and writers like myself, Dr.Leonard G Horowitz,

Dr. Robert Strecker, Professor Robert Lee, and others have proposed for two

decades that HIV was seeded into gay men when they volunteered for the

experimental hepatitis B vaccine

experiment which took place in Manhattan, beginning in November 1978. Additional

similar hepatitis B experiments using gay men as guinea pigs continued in other

American cities until 1981 -the year the AIDS epidemic became official. Some of

the cities included Los Angeles and San Francisco which, along with New York

City, became the three big

epicenters of the epidemic.

 

My two books on the man-made origin of this disease: AIDS and the Doctors of

Death [1988] , and Queer Blood: The Secret AIDS Genocide Plot [1993], provide

documented evidence to support this theory. A Google internet search using the

key words -man-made origin of AIDS-has 246,000 citations to various websites

that explore this issue in detail. Despite all this, the man-made theory remains

totally ignored by the scientific establishment and the major media.

 

The origin of the new Kaposi's Sarcoma virus

 

Like HIV, the new KS herpes virus-8 discovered in 1994 is considered to be yet

another primate virus out of Africa with a suspected primate " viral ancestor "

hiding in the African jungle. We are expected to believe that two primate

viruses (a retrovirus and a herpes virus) jumped species in Africa at the same

time -and ended up exclusively in the blood of white gay American men to produce

a new immunodeficiency disease in 1979, now called AIDS. This proposed scenario

suggests to

me that such an unlikely African event has the markings of a

scientific fairy tale, and I remain stupefied that such nonsense can pass for

" science " in the twenty-first century.

 

The origin of Kaposi's Sarcoma

 

KS has a long history dating back to 1872 in Vienna, Austria, when dermatologist

Moriz Kaposi described five patients with red-purple skin tumors. Before the

AIDS outbreak, KS was a very rare disease affecting mainly elderly Jewish and

Italian men. It was never considered a contagious or sexually-transmitted

disease.

 

In the 1960s, it was discovered that KS was a common skin cancer tumor in blacks

in Central Africa, but the disease was never associated with the severe

immunodeficiency characteristic of AIDS, nor was there any evidence that KS in

Africa was sexually transmissible. KS was rarely,if ever, seen in

African-Americans. As a dermatologist for over 30 years I never saw a KS case in

a female; and KS in young men of any

race or sexual persuasion was as rare as hen's teeth before the " introduction "

of HIV.

 

KS is a medical enigma. How did a previously rare disease like KS in America

become a transmissible disease primarily affecting gay men? How did this herpes

KS virus escape detection during the first 15 years of the AIDS epidemic? Why

did the KS virus and HIV suddenly appear together in young gay men in 1979?

 

Further complicating this picture is the discovery of small bacterial forms

known as " mycoplasma " , and the even more recent discovery of extremely tiny

virus-like forms of bacteria called " nanobacteria " , as well as my published

reports of " cancer bacteria " as important etiologic agents in AIDS and KS. (For

details, Google: " alan cantwell "

+ cancer bacteria.) All these newer bacterial agents are generally ignored by

AIDS researchers, who focus exclusively on viruses.

 

I believe some of the answers to questions surrounding the origin of HIV/AIDS

can be found in the annual " Progress Reports " reports of the Virus Cancer

Program and the Program's relationship to animal cancer research, genetic

engineering of viruses, cancer vaccine research, and to covert biological

warfare research. These hard-to-find annual Reports were published by the

National Institutes of Health, Public

Health Service, U.S. Department of Health, Education, and Welfare, Bethesda,

Maryland.

 

The Virus Cancer Program (1968-1980)

 

The Virus Cancer Program had it roots in 1964 when Congress provided funds to

the National Institutes of Health (NIH) for intensive research into the possible

role of viruses in leukemia. In 1968 the Program, then titled the Special

Virus-Cancer Program, was enlarged to encompass all types of cancer. On July 1,

1973 the Special Virus Cancer Program was renamed The Virus-Cancer Program (VCP)

" to integrate the Program's research activities into the framework of the new

National Cancer Plan. "

 

The Program combined the talents of many of the nation's finest virologists,

biochemists, immunologists, molecular biologists, epidemiologists, and

physicians, in an attempt to uncover the viral cause of cancer. Two classes of

cancer-causing viruses were studied extensively: the RNA-type tumor

" retroviruses " (like HIV) and the DNA herpes-type viruses (like the KS virus).

 

The main goals were to collect various forms of cancer tissue and test them in

animals; to identify animal and human cancer-causing viruses; to grow large

amounts of " candidate human viruses " for testing purposes; and to develop

vaccines against these cancer viruses. In essence, the scientists wanted to

learn how to use viruses to make cancer - and to force " normal " cells to become

cancerous by subjecting to viruses.

I have studied the annual Virus Cancer Reports (VCP) covering the years

1971-1974 and 1976-1978. Each report is 300-400 pages, and the cumulative

volumes refer to thousands of animal cancer virus and genetic engineering

experiments.

 

Biological warfare research, monkey research, and the VCP

 

The annual VCP Reports must be studied with an awareness that the Program became

wedded to secret military biological warfare research in the early 1970s.

 

On October 18, 1971, as part of Richard Nixon's War on Cancer, the army's

biowarfare research laboratory at Fort Detrick, Maryland, was permanently joined

with the National Cancer Institute; and was re-titled . the Frederick Cancer

Research Center. Litton Bionetics was named as the military's prime contractor.

 

The primary task of the new Center was " the large scale production of oncogenic

(cancer-causing) viruses and suspected oncogenic viruses to meet research needs

on a continuing basis. " Special attention was given to primate viruses (the

alleged African source of HIV and the new KS virus)- and to the successful

propagation of significant amounts of " human candidate viruses. " Candidate

viruses were defined

as animal or human viruses that might cause human cancers. Later, the objective

was to determine if such viruses could induce (either alone or with other

co-carcinogens) human cancers (1977;58). Biowarfare scientists also had a keen

interest in the role of human and non-human primate viruses as " helper viruses "

in the production of cancer (1978;54).

 

A steady supply of research animals (monkeys, chimpanzees, mice, cats, etc. )

was necessary; and multiple breeding colonies were established for the VCP. For

example, a total of 2,274 primates from Africa and Asia were shipped to Litton

for military use in 1971.

 

Forcing cancer viruses into primates and other animals

 

To induce primates and other research animals to acquire cancer, their immune

system was deliberately suppressed by drugs, radiation, or cancer-causing

chemicals or substances. The thymus gland and/or the spleen were removed, and

cancer tissue and cancer viruses were injected into newborn animals or into the

womb of pregnant animals. Some animals were deliberately infected with malaria

to keep them chronically sick and immunodepressed.

 

The U.S. is the world's leading consumer of primates, and 55,000 are used yearly

in medical research. Primates (especially newborn and baby chimpanzees) are the

most favored lab animals because they are most similar biochemically and

immunologically to human beings. Humans share 98.4% of their DNA with

chimpanzees. Chimps were extensively used by the VCP because there would be no

official testing of cancer viruses on humans.

 

Robert Gallo, the discoverer of HIV in 1984, was a project officer of a primate

study contracted by Litton Bionetics that pumped cancerous human tissue, as well

as a variety of primate and other viruses, into newborn macaques (a small

species of monkey used as an animal model for human cancer).

 

The actual number and identity of all the primate viruses created and adapted to

human tissue during the 14 years of the SVCP is not known. In addition, some

primates were released back into the wild carrying lab viruses with them. This

fact is always ignored by molecular biologists searching for " viral ancestors "

in the African bush,

 

By the early 1970s, experimenters had transferred cancer-causing viruses into

several species of monkeys. Herpesvirus saimiri, a monkey virus discovered in

1967 in the squirrel monkey, has a close genetic relationship to the new KS

herpes virus. H. saimiri virus is harmless in the squirrel monkey, but when the

virus was forced in the lab to " jump species " into different animal species,

such as the owl monkey,

marmosets and rabbits, it produces cancer in the form of fatal

malignant lymphoma.

 

By 1971 Dharam V Ablashi of the NCI succeeded in transferring H. saimiri, into

various cell lines of human origin. (1971;35). Cancer-causing cat and hamster

viruses were also engineered into macaques and other monkey species.

 

By the early 1970s, it was recognized that forms of human leukemia and lymphoma

were associated with herpes-type viruses. Herpes saimiri, a DNA-type virus,

became the experimental model for the study of human leukemia and lymphoma.

" Thus far, the only DNA viruses associated with

natural cancer of animals and man are herpes viruses " (1973;15).

 

Luis Melendez of Harvard studied additional primate herpes viruses (H. ateles,

H. aotus, and H. saguinus) and determined their ability to induce cancer

(1973;247). Attempts were made " to find a suitable method for the large-scale

production of high-titer Herpesvirus saimiri " (1973;264). Researchers knew: " The

clinical and immunological picture of human lymphoma and leukemia is closely

approximated by the malignant disease induced in susceptible non-human primates

by H. saimiri. " (1973;265).

 

By 1976 it was also learned that H.saimiri could spread by " contact

transmission " between squirrel and owl monkeys in the laboratory.

 

A monkey virus injected into humans via polio vaccines in the 1950s

 

There are inherent dangers in vaccine production. Many vaccines are made on

living cells; and accidental contamination with bacteria, mycoplasma, viruses,

and newly-recognized " nanobacteria " are constant problems during the

manufacturing process. Laboratory additives (such as fetal bovine [cow] serum)

may also be a source of contamination.

Half the flu vaccine supply for 2004 had to be destroyed due to contamination

with disease-causing bacteria.

 

Some researchers believe that injecting living and killed viruses into the body

can result in these viruses combining with other viruses normally present in the

body, resulting in the formation of new viral disease-causing " recombinants. "

The dangers of vaccines are downplayed to assure the public that vaccines are

safe.

 

The possibility that cancer-causing primate viruses could have been " introduced "

into gays, via the experimental hepatitis B vaccine, cannot be dismissed as

paranoid fantasy. In this regard, we are told that HIV is the first primate

virus to " jump species " to produce an epidemic in millions of humans. But, in

truth, the AIDS epidemic is the second instance in which a monkey virus has been

transferred to humans.

 

A cancer-causing monkey virus called " simian virus 40 " (SV40) jumped species a

half century ago when virus-contaminated polio vaccines were injected into

millions of people, including half the U.S. population of that era. (For

details, see: www.sv40cancer.com) Government health officials insist there is no

proof that SV40 causes human cancer. However, independent research over the past

decade indicates SV40 is

clearly associated with rapidly-fatal cancers of the lung

(mesothelioma), bone marrow cancer (multiple myeloma), brain tumors in children,

and other forms of cancer.

 

A Washington Times report (September 21, 2003) states, " Some of the polio

vaccine given to millions of American children from 1962 until 2000 could have

been contaminated with a monkey virus that shows up in some cancers, according

to documents and testimony to be delivered to a House committee Wednesday. " The

SV40 story is detailed in the recently published, The Virus and the Vaccine: The

True Story of a

Cancer-Causing Monkey Virus, Contaminated Polio Vaccine, and the Millions of

Americans Exposed.

 

The VCP and links to bio-warfare and secret human experimentation

 

Every annual report of the VCP makes clear that human experimentation with these

newly created and genetically-engineered viruses would not be undertaken.

However, the 1972 Report (p 262) also states: " Since man will not be used as an

experimental recipient, it is necessary to gain proof of oncogenicity by other

means. "

 

It is well-known in science that medical doctors will not totally accept

laboratory findings in animals as absolute proof. An experimental finding in

animals must also be proven in humans. It cannot be assumed that covert human

testing of suspected cancer-causing viruses did not take place in the thousands

of experiments conducted under the auspices of the VCP, particularly with its

strong ties to covert biowarfare research. The U.S. military has a long history

of secret human experimentation. For proof, Google: secret human medical

experimentation.

 

Merck and Co, Inc. made most of the experimental hepatitis B vaccine that was

immediately followed by AIDS cases. Some of the experimental vaccine was

manufactured at the NIH. George Merck, who founded the drug company, was the

leading biowarfare advisor to President Roosevelt during WW2. He was a central

figure in creating the army's biowarfare laboratory at Ft. Detrick, Maryland,

which later became an integral part of the NCI.

 

Merck's role in the VCP was " to conduct investigations designed to develop

vaccines or other agents effective for the prophylaxis and therapy for human

neoplasia (cancer) of suspected viral etiology " (1972;139). Great interest was

taken in developing anti-herpes virus vaccines. Research involved a new type of

herpes vaccine using " purified viral protein vaccines " and a " subunit vaccine "

utilizing only a piece of the herpes virus (1977;135).

 

The Merck company declared: " Since live attenuated or killed virus vaccines for

potentially oncogenic viruses would not be acceptable for human use due to the

danger of transfer of functional genetic material, this project was initiated to

determine whether vaccines to purified viral antigens acceptable for use in

humans were of practical value. " (1977;160) (This proposed " purified " herpes

vaccine was similar in type to the experimental " purified " hepatitis B vaccine

injected into gays the following year.)

 

It is my contention that the introduction of HIV and the KS virus into gay

people, the most hated minority in America, was not an accident of nature due to

monkeys in the jungle.

Would scientists deliberately infect gay men with AIDS to finally prove that

animal cancer viruses cause cancer? In the January 1987 issue of MD magazine, an

Oklahoma internist wrote: " Homosexuality is a sin, deserving the death penalty. "

With that kind of mentality not rare in the medical and scientific world, the

answer to the question is, undoubtedly, yes.

 

The VCP and biohazards

 

The VCP was a biological disaster waiting to happen. What would happen if one or

more of these dangerous cancer and immunosuppressive viruses escaped from the

laboratory and produced a worldwide biologic holocaust?

 

The 1978 report from the Office of Biohazard Safety of the VCP states: " The

inadequate care and handling of animals during the past several years have

created a potential for the occurrence of infection of humans with simian

(primate) microorganisms and cross infection between species. Such interspecies

disease transmission may seriously compromise the integrity of the experiment as

well as the health of

the experimenter. Due to the magnitude of biomedical research

employing tissue cultures. Frequent evaluation of tissue culture

cross-contamination is very important. "

 

The yearly large-scale production of lethal cancer viruses

 

By the late 1970s the mixing of animal cancer viruses with human cells to

produce new " xenotropic " viruses was commonplace. The human cells in question

were placenta ( " afterbirth " ) cells from patients with immune disease, and cells

from leukemia (1978, p 192). Xenotropic viruses are viruses taken from one

species and transplanted into

another different species. All these experiments represent " species jumping "

performed in a laboratory.

 

By 1977 the Program was producing " approximately 60,000 liters (15,840 gallons)

of tissue culture-grown viruses, propagated in over 40 different cell lines, and

distributed in over 1250 shipments to over 250 participating laboratories

throughout the world. "

 

Also in 1977 Electro-Nucleonics Laboratories processed 8,044 liters (2,024

gallons) of virus-containing fluids harvested from several tissue culture

systems. About half this volume was concentrated xenotropic viruses. That same

year Pfizer drug company produced 28,000 liters (7,392 gallons) of virus harvest

fluids. The vast majority included primate viruses, such as the Mason-Pfizer

monkey virus, woolly monkey

sarcoma virus and baboon endogenous virus. (This baboon virus

contaminated Gallo's lab at the NCI). Litton produced 37,438 liters (9,984

gallons) of retrovirus material consisting essentially of four agents: mouse

mammary tumor virus, Raucher murine (rat) leukemia virus, Gross murine leukemia

virus and baboon leukemia virus.

 

The VCP made clear that: " Attempts are being made to chronically infect cell

cultures of human epithelial and fibroblast cells and similar cell cultures from

non-human primates (marmosets) with simian sarcoma virus, gibbon ape leukemia

virus and baboon endogenous virus " (1977;183). A few years later primates in the

African bush would be blamed for starting AIDS and the KS epidemics.

 

The VCP and the creation of an AIDS-like disease in chimps

 

In 1969 the military biowarfare experts predicted that a biological agent would

be developed within a decade that would have a devastating effect on the immune

system and for which there would be no treatment. (For details of this

congressional testimony, Google: Donald M MacArthur + biowarfare.)

 

The VCP had a keen interest in acquiring " information and materials from

carefully selected patients suffering from immunodeficiency diseases "

(1972;318). This is made clear in a 1973 Progress Report (p249) from the

University of Minnesota entitled, " The search for tumor virus related

information in human immunodeficiency patients with cancer " The researchers

proposed " continuation of studies linking immunodeficency, cancer, and oncogenic

viruses. "

 

As biowarfare expert MacArthur predicted, new cancer-causing monster viruses

(like HIV) were created by the VCP which had a deadly effect on the immune

system. In one experiment recorded in the 1973 Report (p169), later published in

Cancer Research in 1974, newborn chimps were taken away from their mothers at

birth and weaned on milk from cancer virus-infected cows. Some of the chimps

sickened and died with two diseases that had never been observed in chimpanzees.

The first was Pneumocystis carinii pneumonia (later known as the " gay pneumonia "

of AIDS); the second was leukemia, a cancer of the blood.

 

Cancer-Causing viruses and " helper " viruses

 

As the 1970s began it was clear that some cancer-causing viruses could not

produce cancer unless a " helper " virus was present. Certain chicken, cat and

mouse sarcoma viruses were found to be " defective " and unable to induce

cancerous changes. However, when a " helper " leukemia virus was added to the mix,

the sarcoma virus was able to induce cancer.

 

Mixing of a mouse sarcoma virus with a cat leukemia virus produced a " hybrid

virus " which could grow continuously in cat cells. Such a " hybrid virus " was

adapted to human embryonic (fetal) cells (1971, p22). Thus, it is obvious that

" species jumping " experiments were commonplace during the years of the VCP.

 

By the late 1970s it was known that " type C RNA viruses " (the

retroviruses connected with sarcomas and lymphomas and leukemias) existed

normally in cells as " endogenous viruses " within the cellular genomes of many

mammalian species. By 1977, the year the experimental hepatitis B vaccine was

being made, scientists in the VCP aimed " to determine the oncogenic potential of

putative human viruses " and " to begin viral vaccine (conventional or other)

testing and immunization

programs " (1977;32). The exact methods by which this was to be

accomplished was not stated.

 

Primate virus contamination of human cells

 

The possibility that animal cancer viruses could cause contamination of viral

laboratories and viral research was an accepted risk for the VCP. Primate virus

contamination problems have plagued the laboratories of the world's most famous

AIDS researchers, much to their embarrassment.

 

A decade before Gallo discovered HIV, he reported a " new " and " human " and

cancer-associated " HL-23 virus " that was eventually determined to be not one but

three contaminating primate viruses (gibbon-ape virus, simian sarcoma virus, and

baboon endogenous virus).

 

The baboon virus was discovered in the early 1970s at the Southwest Foundation

for Research and Education in San Antonio, Texas, which hosted a chimpanzee

breeding colony and produced simian viruses for research. The baboon virus

somehow made its way into the blood cells of a Texas women with leukemia. When

the infected cells reached Gallo's lab they were apparently joined with an

additional monkey virus and an ape virus. How these three viruses contaminated

Gallo's

lab is unknown. However, George Todaro, an equally famous virologist, was quoted

as saying, " You can get three viruses into a virus preparation easily just by

being sloppy, and Gallo had plenty of sloppy people. " (See John Crewdson's

Science Fictions: A Scientific Mystery, A Massive Cover-Up, and the Dark Legacy

of Robert Gallo, p20).

 

As late as 1986 Max Essex of Harvard " discovered " a new human AIDS retrovirus

that he found in the blood of healthy Africans. Eventually this virus also

proved to be a monkey virus that originated in a nearby primate colony. Somehow

the animal virus had worked its way into Essex's lab and blood samples.

 

Interestingly, both Gallo and Essex, the two foremost American AIDS researchers,

were the leading proponents of the African green monkey theory of AIDS. Now the

more widely accepted theory, proposed by Beatrice Hahn (who worked in Gallo's

lab when he proposed the green monkey theory), claims the virus traces back to

chimpanzees in the African wild. Hahn has never commented on the primate

contamination problems in Gallo's lab.

 

Could the primate " ancestors " of the RNA-type HIV retrovirus and the DNA-type

herpes saimiri-like KS herpes virus have accidentally -or deliberately-worked

their way into the experimental hepatitis B vaccine? The extremely high

incidence of both these " new " viruses in the gay men who volunteered for the

hepatitis experiments certainly provide enough additional circumstantial

evidence to make the man-made theory of AIDS as plausible as the monkey out of

Africa theory.

 

The gay hepatitis B experiments (1978-1981)

 

The experimental hepatitis B vaccine injected into gays was unlike any other

vaccine previously made. It was developed in chimpanzees and manufactured in a

year-long process of sterilization and purification of the pooled blood of 30

gay men who were hepatitis B virus carriers. During the first gay experiment

(November 1978-October 1979) at the New York Blood Center, there was great

concern that the vaccine might

be contaminated. According to June Goodfield's Quest for the Killers, p 86,

" This was no theoretical fear, contamination having been suspected in one batch

made by the National Institutes of Health, though never in Merck's. " The men

were given three inoculations of the vaccine over a period of time. The vaccine

was successful with 96% of the men developing protective antibodies against the

hepatitis B virus.

 

It has been assumed by some that these men were immunosuppressed due to their

promiscuity and history of venereal disease. Although the young men in the study

were indeed " promiscuous " (this was a requirement for entrance into the study),

they were in excellent health. Despite many previous sexual partners, these

volunteers had never contracted evidence of hepatitis B infection. Furthermore,

immunosuppressed people often do not respond to the vaccine.

 

The men in the Manhattan experiment had the highest rate of HIV ever recorded

for that time period (over 20% of the men were HIV-positive in 1981, and over

40% in 1984). Therefore, it must be assumed that many, if not most, of these men

eventually died of AIDS. The actual number of AIDS deaths among the men in the

experiment has never been revealed, nor have their medical records been studied.

Attempts to secure this information have been rebuffed due to the " confidential "

nature of the experiment.

 

The end of the VCP and the birth of AIDS

 

By 1980 the VCP came to an inglorious end with the inability to prove that

viruses were involved in human cancer. More than any other program it built up

the field of animal retrovirology, which led to a more complete understanding of

how cancer and immunosuppressive retroviruses caused disease in humans. The VCP

was the birthplace of genetic engineering, molecular biology, and the human

genome project. I am convinced the VCP (and not Africa) is the birthplace of

HIV/AIDS as well.

 

As the VCP was winding down in the late 1970s, the gay experiments began in New

York City, and continued in other cities, such as San Francisco and Los Angeles.

These cities would rapidly become the three primary epicenters of the new and

unprecedented " gay-related immune deficiency syndrome, " later known as AIDS.

 

The introduction of HIV and the KS herpes virus into gay men (along with some

" novel " and now-patented mycoplasmas discovered at the Armed Forces Institute of

Pathology) miraculously revived the career of Robert Gallo and made him the most

famous virologist in the world. And, of course, turned the " failure " of the VCP

into a triumph.

 

When Gallo's blood test for HIV became available in the mid-1980s, the New York

Blood Center's stored gay blood specimens were reexamined. Most astonishing is

the fact that 20% of the gay men who volunteered for the hepatitis B experiment

in Manhattan were discovered to be HIV-positive in 1980 (one year before the

AIDS epidemic became " official " in 1981). This signifies that Manhattan gays in

1980 had the highest incidence of HIV anywhere in the world, including Africa,

the supposed birthplace of HIV and AIDS. In addition, in 1982, in an AIDS trial

in New York City one out of five gay men (20%) tested positive for the new KS

herpes-8 virus when stored blood samples were re-examined by epidemiologists at

the NCI in 1999.

 

Rarely mentioned by AIDS historians is the fact that the New York Blood Center

established a chimp virus laboratory for viral vaccine research in West Africa

in 1974. One of the purposes of VILAB II, in Robertsfield, Liberia, was to

develop the hepatitis B vaccine in chimps. The lab also prides itself by

releasing " rehabilitated " (but virus-infected) chimps back into the wild.

 

Also conveniently forgotten in the history of AIDS is LEMSIP (The Laboratory for

Experimental Medicine and Surgery), the primate colony located outside New York

City. For many years, until disbanded in 1997, LEMSIP supplied scientists with

primates and primate parts (and unknown primate viruses) for transplantation and

virus research. Primate parts (and primate viruses) were experimentally

transplanted in human beings as early as the 1960s.

 

LEMSIP was also affiliated with New York University Medical Center, where the

first cases of AIDS-associated Kaposi's sarcoma were discovered in 1979.

Researchers at NYU were also heavily involved in the development of the

experimental hepatitis B vaccine used in gays. According to Leonard Horowitz,

author of Emerging Viruses: AIDS and Ebola, NYU Medical Center received

government grants and contracts

connected with biological warfare research beginning in 1969.

 

The evidence gathered here is a tiny fraction of the circumstantial evidence

supporting the man-made theory of AIDS. Scientists have a long and proven

history of covertly experimenting on people " in the name of science. " Anyone who

takes the time to study the reports of the VCP will recognize that human

experimentation with cancer viruses was undoubtedly considered and ultimately

desired. Is the fact that HIV/AIDS appeared within a decade of this dangerous

cancer virus

experimentation a coincidence? Should AIDS be blamed on human

sexuality, gays, blacks, and monkeys? I think not.

 

There is nothing wrong or unpatriotic or " conspiratorial " in

presenting the vast amount of evidence that connects out-of-control animal

cancer experimentation and biowarfare research with the birth of AIDS. What is

wrong, however, is the unwillingness of the scientific establishment and the

media and the public to look at it.

_____

 

Dr. Cantwell is a retired dermatologist and has written two books on the

man-made origin of AIDS; and two books on the infectious origin of cancer, all

published by Aries Rising Press, PO Box 29532, Los Angeles, CA 90029

(www.ariesrisingpress.com).

 

Email: alancantwell

 

Many of his writings can be found on www.google.com by typing in " alan cantwell "

+ articles. His latest book is Four Women Against Cancer: Bacteria, Cancer and

the Origin of Life. His books are also available on www.amazon.com and also

through

Book Clearing House @ 1-800-431-1579

 

Alan Cantwell M.D.

alancantwell

http://www.ariesrisingpress.com

FOUR WOMEN AGAINST CANCER

 

 

 

 

" Our ideal is not the spirituality that withdraws from life but the conquest

of life by the power of the spirit. " - Aurobindo.

 

 

 

 

 

 

 

What are the most popular cars? Find out at Autos

 

 

[Guest guest]

Interesting thought Jagannath - where does the US figure in this survey -

after all some of their cities are known to be inhabited by a predominantly

gay society?

 

I guess that this is encouraged now as a move away from the secure family

unit and population reduction in its own right? As well as a potential

pathway to the aids virus of destruction?

 

Regards

 

Jane

 

 

..A question I wish to raise here, AIDS is

> perceived to be a major threat in Africa, China and India.

> These three also happen to the most populous regions.

> Another " coincidence " ?)

>

> http://rense.com/general67/viru.htm