The U.S. Special Virus Program made HIV/AIDS, weapons of mass destruction(March 5, 2002)

"....There is a reason the 'establishment' does not want you to see the experiments and contracts of this federal weapons program of ethnic mass destruction...." - Boyd E. Graves, J.D. March 5, 2003

SAN DIEGO - The federal lawsuit for "full disclosure" of the secret virus development program was served on President Bush Saturday March 1, 2003. {See, U.S. federal court docket, case no.: 02 CV 02396, Southern District of California, filed December 6, 2002 (Graves v. U.S.)}

"There is a reason the 'establishment' does not want you to see the experiments and contracts of this federal weapons program of ethnic mass destruction," Graves said referring to the formerly secret virus development reports issued annually under the auspices of The U.S. Special Virus Program.

The Office of the President of the United States is compelled to respond to Graves' AIDS bioengineering allegations and demand for the review of the U.S. Special Virus Program by May 1, 2003.

Extracts from "Full Disclosure"

Extracts from the book "Full Disclosure" by Dr Gary Glum, published in 1994, but obstructed from bookshop distribution by the US government ever since.In late July 2001, Dr Glum invited free distribution of the book through Internet at: , but two months later that location is no longer active.

Dr Gary Glum is also well known as the author of the book "Calling of an Angel", which describes the life-long work of Rene Caisse to provide a North American (Ojibwa) herbal recipe that she called Essiac to thousands of terminally ill cancer patients during her life time, resulting in thousands of testified cures.

AIDS was the result of a decades-long research program carried out in Chemical and Bacteriological Warfare labs in this country (USA) and others. For those involved, it is a triumph of science and the answer to what they regard as the planet's most pressing problem: population control. AIDS is the perfect biological weapon. It can be confined with some degree of success to certain specific groups, and since the incubation period can be more than seven years, millions can be infected before the first person in the chain displays any symptoms. (Chapter 1)

Freeze-dried and microencapsulization techniques developed by the U.S. Army (primarily at Fort Detrick and Los Alamos) since 1967 were successful in creating a product that reduces toxicity to the agent handling the material and allows dissemination on impact and a sustained release. Using these techniques, the U.S. government now has the capability of delivering any virus to any unsuspecting person or group. (Chapter 2)

It's all happened very fast. Except in a few top secret, carefully guarded laboratories, AIDS did not exist in the United States before 1978—not in stored , not in humans, not anywhere. No American was infected with AIDS. (Chapter 5)

I don't know when the virus that would kill by destroying the human immune system was first conceived in some scientist's brain. But intelligence reports indicate that the actual laboratory experiments—at Fort Detrick, Los Alamos and Cold Spring Harbor—began during the 1960s. How were the experiments conducted? According to intelligence documents, under the heading "Common Genetic Alterations of RNA," virologists mixed and ured a combination of bovine leukemia virus and sheep maeda-visna virus. (chapter 6)

The bovine and sheep viruses were repeatedly injected into human tissue in the Fort Detrick labs until they actually mutated by incorporating human genes. (chapter 6)

Here is how Dr. Seale described their invention: "The AIDS virus (human immunodeficiency virus or HIV) is a lentivirus—a little-studied sub-family of the retroviruses. It is highly pathogenic to man, but it differs profoundly from any other virus of humans. It is the first virus to have appeared in mankind for many centuries which is entirely new, highly lethal and spreading steadily from person-to-person worldwide." (chapter 6)

This was a project coldly calculated to discover whether a new virus could be created that would decimate a population in a seemingly "natural" plague. The experiments were concluded in 1967. Thus was born the AIDS virus. (chapter 6)

Blacks were more likely than whites to become infected with the virus. They would also have a shorter incubation period before showing symptoms and earlier . The British report found that people with a certain Gc 1 gene were predisposed to the HIV virus, while a Gc 2 gene offered some protection. As one intelligence report said, "Extensive research by the British team came up with the conclusion that blacks and mulattos have Gc 1 genes while whites have Gc 2 genes. (chapter 6)

The cover for the introduction of AIDS into Africa and Brazil—with its large black population—would be the World Health Organization's massive "humanitarian" campaign to "eradicate smallpox for once and for all." It was perfect. It even matched the surest way to pass the virus: injection. The WHO smallpox vaccines would be contaminated with the AIDS virus. (chapter 6)

A WHO advisor who disclosed the problem told The Times, 'I believe the smallpox vaccine theory is the explanation to the explosion of AIDS…The greatest spread of HIV infection coincides with the most intense immunization program.' (chapter 6)

Haiti was targeted next. But the Haitian experiment was not racial; it was aimed at homosexuals. . . . . After the CIA experiment in Haiti, small numbers of AIDS cases began to be reported among homosexuals who had vacationed on the island. The first recorded case of this new disease in America was in March 1980. (chapter 7)

The doubling time for the numbers of people infected every 14 months in relation to the first reported cases in Africa and Brazil and Haiti proved beyond any reasonable doubt that a very substantial number of people had to have become infected with the AIDS virus, all more or less at the same time. (chapter 7)

In Kenya, Uganda and Zaire, (AIDS) wiped out the population—all age groups—of whole villages and towns, where there was much less crowding and sanitary conditions were better. The AIDS virus in Africa was not caused by increased heterosexual activity; the very idea is preposterous. Why would an increase in heterosexual activity spread an epidemic that was confined to homosexuals and abusers in Western countries? (chapter 8)

Intelligence reports on the Fort Detrick research indicate that the virus is able to hide in "immunologically privileged sites, where T-cells do not penetrate, typically in the brain and bone marrow." The implications of that simple statement are profound. It means that it is possible that the virus will not always show up in tests. People carrying the virus could test negative. Yet the same test done three months later could show positive. Footnote 14: It is an established fact that the virus can ride the macrophages through the -brain barrier. Once inside the brain, the infected cells emit enzymes toxic to neurons and immediately begin a toxic reaction. In Virology, second edition, it is proved that the AIDS virus directly infects the neuron and glial cells in exactly the same manner as it infects monocytes and T-4 cells. The same work proves that the GP-120 protein of the AIDS virus envelope inhibits the growth of nerve cells. (chapter 10)

Current tests are quite reliable at showing infection that is more than three months old. But they are not one-hundred percent reliable. With the possibility of the virus hidden in the brain, there is a small chance of a false negative. "It might be as long as fourteen years before seroconversions show up in tests," the same intelligence report concluded. (chapter 10)

A study at Walter Reed Hospital threatened the conventional wisdom, noting ample documented evidence that the HIV virus has a neurotropic tendency, attacking the brain at a very early stage of infection, long before immune deficiency symptoms appear. Specifically, the study concluded that neurological problems—a persistent headache, lack of concentration and a general malaise which are usually chalked off to stress—are present prior to symptoms of immunodeficiency in about eighty-six percent of cases of those infected with the newest HIV virus. (chapter 10)

In the final analysis, people do not die of AIDS. They die of diseases they contract because AIDS has destroyed the ability of their immune systems to fight them off. The AIDS retrovirus goes straight for the central nervous system, as well as the lungs, and it attacks the brain, causing AIDS virus encephalopathy—also known as dementia. There are three clearly definable stages of AIDS infection. Stage one is the Asymptomatic Carrier Stage. The person may look well and feel well. No sign of AIDS is detected. Stage two begins with sudden drenching night sweats, persistent diarrhea, chronic fatigue, severe weight loss, candidas and psychogenic disorder. These are called AIDS Related Complex (ARC) or the pre-AIDS syndrome. The virus has now settled in the brain, kidneys, lungs, liver—even the eyes—and multiplied until its dread presence can no longer be hidden. . . . . In Stage three, the terminal stage, the brain becomes dysfunctional, causing loss of muscular control, chronic memory loss, dementia, seizures and the inability to speak in a coherent manner. These symptoms appear in rapid succession, and they are accompanied by often severe psychiatric disorders. (chapter 11)

What makes AIDS such a lethal epidemic is that stage one, the asymptomatic stage, can last for years—five years and more is not uncommon. Such persons appear to be in good health, and even remain in good health for varying periods. With nobody sensing danger, they may infect any of their friends or family—or even strangers—because their body begins "shedding" the AIDS virus through bodily secretions, including sweat and tears. (chapter 11)

There is a great deal of informed speculation—too much to ignore—that Cold Spring Harbor labs are currently engaged in molecular research to develop a virus with even greater ability to infect people who have the most melanin in their skins. Black and "colored" skin has substantially more melanin than white skin. British microbiologists at the CAB research unit at Porton Downs are believed to have successfully developed a virus with a ninety percent selective capability. (chapter 13,footnote 18)

What AZT's victims are not aware of is that they are using the most toxic ever considered, let alone approved, by the government. So horrific is AZT's toxicity that only about half the AIDS patients can tolerate it. The other half must be taken off it—or they die. . . . . AZT is highly toxic, severely damaging kidneys and liver, bone marrow, causing muscle-wasting, dreadful nausea and violent bouts of vomiting as the body tries to rid itself of the poison. It destroys the immune system, leads to leukemia through the destruction of cells and causes cancer. Even the FDA issued a bulletin admitting that AZT is "a potential carcinogen." The fact is that AZT will hasten the onset of AIDS, not delay it, because of the 's depressive effect on the human immune system. (chapter 15)

They are still working to shorten the "symptom-time," the time between the arrival of the virus in the body and the onset of symptoms. One experiment of this new fast-acting AIDS has already been conducted in a remote area of Liberia, bordering on Sierra Leone. The results, I'm told by someone who knows, were "disastrous." (chapter 16)

Biological intrusions by new artificially created viruses will be made that much easier with genome study. The "profound differences" could be exploited as a weapon of destruction—even against entire races—that are no longer wanted. Any disease could be manufactured in laboratories having the genome history of a specific person—or group. A genetic print-out would reveal changes that could be made in a person's enzymes—to create better health or illness. It wouldn't be difficult. The average human typically carries dozens of diseases—which remain dormant, but when properly aroused would cause immediate or slow . (chapter 16)

The right questions must be asked —and honest answers demanded. Any solution to the AIDS epidemic must begin with the public learning the truth about two questions: What caused it? How does it spread? (chapter 18)

In the African country of Ghana, Nanan Kofi Drobo was an herbalist who attracted AIDS sufferers from all over the world, particularly Europe. They came to him because of his amazing record of success in healing AIDS cases, using only herbal compounds. Drobo was a man who knew what the Western pharmaceutical companies did not know—or pretended they didn't know. He knew how to stop AIDS in its tracks with herbal compounds. His success in treating AIDS patients sent fear coursing through the medical and pharmaceutical establishments. Drobo's work was not sanctioned by the Ghanian government, which was under pressure from the International Monetary Fund (IMF) and powerless to disobey the IMF's orders to destroy Drobo's work. In the end, Drobo grew so renowned that he had to be killed. This heinous crime has been officially classified as % by means of self-inflicted gunshot wound." The weird part is that all of Drobo's herbal compounds—and his formula and notes—were missing from his home when he was found. What happened to them? So far, the Ghanian authorities are not saying. (chapter 19)

In September of 1983, one hundred and fifteen virologists from around the world met in secret sessions at Cold Spring Harbor. Not one single word from that conference has ever been published, but according to intelligence sources, the role of viruses was fully discussed in relation to biological warfare against the civilian population. It was stressed that an organism as simple as a virus could threaten the very existence of all human life on earth.

Here is the first sketchy outline of what those virologists secretly shared with each other at Cold Spring Harbor in 1983:

HIV genetic information is filed in the form of ribonucleic acid (RNA), the opposite of most other organisms which have genetic material comprising deoxyribonucleic acid (DNA.) DNA carries the information, strung together like molecular beads, that is critical to the organism. Scientists were now finding out that molecules are made of matter, whose origin the proponents of the "big-bang" theory cannot explain; these molecules being the building blocks of the universe.

The sequence of molecular "beads" are then mirrored in plants and animals. The "mirrored" image is in fact RNA, and in it are the information codes needed to make proteins—the life- giving component of living organisms. The strings are then "beaded" with smaller molecules called amino acids. In this manner most organisms produce their own proteins, but this does not happen in the case of viruses, which are parasites and must have a host to live off.

At the Cold Spring Harbor conference, it was stated that viruses do not have a life-like bacteria; a virus is an incomplete cell, because its genetic material is incomplete and is covered by a hard shell of protein. Before a virus can "live," it has to latch onto and invade living cells. When it penetrates the host cell, it then comes alive and begins to replicate. In the case of the HIV virus, the replication process is extremely rapid.

AIDS-HIV viruses have RNA as their genetic material. By inserting its RNA into the host cell, the cell is deceived into stepping up its manufacture of viral proteins. Part of these proteins are the enzymes needed to synthethize more viral DNA. It is from this process that the term "Retro" (backward) was coined because the host cell is deceived, like the mother bird who feeds the baby cuckoo in her nest. The host cell is blinded into believing it must convert viral RNA from the invader virus back to DNA. Ordinarily the cell would make RNA from DNA, but here the process is reversed. This goes on until the cell "blooms" or "flowers" with its packed HIV parasites, and the component parts burst out into the stream, infecting it with millions more HIV viruses.

When the HIV virus and the healthy cell come together, the HIV receptor fuses with the membranes of the cell it is taking over. The enzyme released is known as a reverse transcriptase. This is unique to retroviruses and is totally absent in human cells. The viral RNA then enters and integrates itself in the DNA of the cell it has taken over. Once inside, the viral DNA becomes dormant, which is the period we know as the latency period. This latency period in AIDS is known to last up to ten years, but in the case of blacks and Hispanics, the HIV virus seems to have a far shorter latency period and acts in a more virulent manner toward the host cell.

At some time during the latency period, the virus will be triggered. Russian scientists had

apparently perfected a technique using electromagnetic signals on the same wavelength as the virus, which, when "radiated" by the signals, would spring to life. A viral "Manchurian Candidate," so to speak. More common causes are believed to be repeated occurrences of infections, such as of Hepatitus B or herpes, for example.

The manufacture of viral proteins and viral DNA—the two main components of HIV—is

stimulated. Next comes the "flowering" or "budding." At this point, the victim will be at great risk and a danger to all who come into contact with him or her. With "budding," the HIV virus takes part of the outer fatty cell membrane and its glycoprotein (molecules of sugar) and swallows them up.

What's most diabolical about HIV is that it prefers to attack cells in human bodies assigned the task of protecting the body from any and all foreign invaders, the so-called T-4 cells.