HIV, the Human Immunodeficiency Virus, which causes AIDS is admittedly in some part iatrogenic, or man-made.
Here are some notable excerpt from Leonard Horowitz’s book (buy)(read) Emerging Viruses: AIDS and Ebola: Nature, Accident, or Intentional?
“Strecker’s first point was that AIDS was nonexistent in Africa
prior to 1975, and had it been the result of monkey bites
occurring in the 1940s, as some alleged, the epidemic should
have occurred in the 1960s and not late 1970s owing to the
twenty-year timetable for case incidence doubling.” (pg 17)
Strecker, an MD, had all of his claims checked by another Physician, Collin.
“In 1969 . . . [the] United States Defense Department requested
and got $10 million to make the AIDS virus in labs as a
political/ethnic weapon to be used mainly against Blacks. The
feasibility program and labs were to have been completed by
1974-1975; the virus between 1974-1979. The World Health
Organization started to inject AIDS-laced smallpox vaccine into
over 100 million Africans (population reduction) in 1977. And
over 2000 young white male homosexuals (Trojan horse) in 1978
with the hepatitis B vaccine through the Centers for Disease
Control/New York Blood Center….”
Collin, in his review, added: “Strecker remarks that it would be relatively easy to implant such viruses in the cow carcasses used to produce the smallpox vaccine. When the smallpox vaccine sera was recovered from the animal carcasses, animallymphotrophic viruses could be carried or mutated or incorporated in the vaccine…. [T]he epidemiology of multiple “contaminated” smallpox vaccines given in the early 1970s would provide exactly the right timetable for such a widespread AIDS epidemic in Africa today.” (pg 18)
SOURCE DOCUMENT [as quoted by Horowitz]: Department of Defence Appropriations Hearings for 1970 on the Development of Immune-System Destroying Agents for Biological Warfare:
The Soviet Union was far advanced to the U.S. in biological and chemical warfare at the time of this report. This report deals with the need of the U.S. to invest in the same technology.
“SYNTHETIC BIOLOGICAL AGENTS
There are two things about the biological agent field I would like to mention. One is the possibility of technological surprise. Molecular biology is a field that is advancing very rapidly and eminent biologists believe that within a period of 5 to 10 years it would be possible to produce a synthetic biological agent, an agent that does not naturally exist and for which no natural immunity could have been acquired.
Mr. SIKES: Are we doing any work in that field?
Dr. MACARTHUR: We are not.
Mr. SIKES: Why not? Lack of money or lack of interest?
Dr. MACARTHUR: Certainly not lack of interest.
Mr. SIKES: Would you provide for our records information on
what would be required, what the advantages of such a program
would be, the time and the cost involved?
Dr. MACARTHUR: We will be very happy to.”
He goes on to say a few things, the most damning of which is this –
“2. Within the next 5 to 10 years, it would probably be possible to make a new infective microorganism which could differ in certain important aspects from any known disease-causing organisms. Most important of these is that it might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease.” (pg 19-20)
This is shocking evidence. H.I.V. is exactly that – a virus that is “refractory” to the immune system of the human being.
The next part directly fingers the group who would be responsible for researching and producing this dreamy death virus.
“3. A research program to explore the feasibility of this could be
completed in approximately 5 years at a total cost of $10 million.
4. It would be very difficult to establish such a program.
Molecular biology is a relatively new science. There are not
many highly competent scientists in the field, almost all are in
university laboratories, and they are generally adequately
supported from sources other than DOD. However, it was
considered possible to initiate an adequate program through the
National Academy of Sciences – National Research Council
An excerpt from a video that Leonard Horowitz made about Robert Gallo, the man who “discovered” AIDS.
A physician named Alan Cantwell received an email from a California-licensed MD, Sue Arrigo, which detailed the creation of H.I.V. He put the letter online along with information about his medical credentials, other sources for the history of H.I.V., and Sue Arrigo’s credentials.
Here is the letter:
“Thank you for your courage and integrity in speaking the truth.
As an ex- CIA physician with high level access, I wrote a report for DCI Webster in about 1991 arguing for closure of all the US Bio-Warfare Labs. I did that after reviewing the Ft. Detrick and the CIA’s Langley Bio-Warfare Labs’s research, looking at their own documents. That review was authorized because Bush, Sr. had sold dangerous Bio-Warfare agents to Hussein, which I ended up having to recover from Iraq. Webster, as a former judge, willing to evaluate the evidence, allowed me to research the field and write a report for him of close to 100 pages and 1000 pages of supporting documents.
Although the focus of my report was why the Bio-Warfare Labs should be closed, the issue of the HIV virus developed by the Ft. Detrick lab formed about 18 pages of my report. At the time I wrote that report, the vaccine for HIV that had been developed in 6 months of work, had already been used by the Cabal since 1983.
It was a crime against humanity that the virus was unleashed on the world, and it continues to be a crime that the vaccine has been kept secret and for private use only. Meanwhile, the outer research to get to a vaccine is an exercise in how not to arrive at a solution before millions more die. The initial “hopes” for HIV per its designers was to be able to walk into Africa and take the resources from a ghost continent. They had hyped it as killing everyone there within a year, in their pre-release reports.
The research at the Labs addressed the fastest way to make vaccines to Bio-warfare agents, both in labs, at a front, and impromptu on a battlefield. That was a pressing concern and one that was researched using millions and millions of dollars.
Briefly, the consensus at the time was that
1) Any agent from a sick soldier left in a Waring Blender for 8 hours would be broken down well enough to not be infective in small doses ( ie. less than a 100 germs). The Labs had made an IgM set of antibodies to sediment out the human HLA antigens by centrifuging it. That allowed the supernatant to be used as a vaccine with little serum sickness problems. A physician in a war zone equipped with a Waring Blender, a blood specimen centrifuge, and a vial of the IgM could make a fast “fresh” vaccine and start inoculating soldiers. The labs tested that using a variety of agents and common cold agents. It was only if one wanted to store the vaccine in vials that one got into the problem of denaturing the proteins of the agent due to heat, chemicals,etc. That was where most of the problems of loss of effectiveness crop up.
2) The Labs found that causing a 1cm by 1cm abrasion until one got lymph and applying a drop of the “fresh vaccine” and a band aid, worked almost as well as an injection. The abrasion could be caused by three fast firm strokes of very fine sand paper over a template with a square of skin bulging through it. This method had much less serum sickness problem. The major problem was occasion keloid and scar formation and superficial infections.
3) The Labs also showed that it was possible to make a crude live vaccine as an emergency directly on the battlefield. The principle was that infection occurs when the body’s defenses are overwhelmed but that the body can usually fend off 10 to 50 organisms even of Bio-warfare agents. It was a simple dilution to get the agent into the right ballpark, starting with a secretion of a sick person. Then a drop of that dilute live agent would be placed on an abrasion. That was also tested during war games with colds etc. The diluted material can’t be stored for longer than an hour due to the risk of multiplying the agent. It was assumed that in the field it would not be known whether the agent was a virus or a bacteria. A bacteria that divided every 20 minutes could be 8 fold in quantity after an hour and risk causing the infection one was attempting to prevent. Of course, such a live agent could be extremely dangerous and except in an extreme emergency would not be used.
4) The issue of how to quickly sterilize a make-shift vaccine was also addressed in the research. The best method was to dry the agent, if time permitted. Second best was to preserve the agent in Vodka (40%), not gin, etc., and then to dilute it down to less than 2% alcohol before applying it to the abrasion.
That means that a simple vaccine for HIV can be made by virtually anyone in the world in a short period of time, though it would likely need to be repeated periodically to get and keep the titers up. But repeating it is a good idea anyway as that helps address the mutation problem. So, suppose one took 1 cc of secretions from each of 10 HIV patients in an area (without fungal infections preferably) and mixed them together to have a range of HIV agents. Then one could add 250 cc of Vodka and let it sit a week. Then one could remove a cc of that and add 20 cc of clean water to get a less than 2% alcohol solution. A drop of that could be applied to an abrasion. That, I believe, would give you about 60% protection. Repeating that at intervals of about 2 weeks to a month for 6 months and using new HIV secretions every 6 to 12 months, I think would give one fairly good protection in a person with a normal immune system to start with. Of course, that is a crude method and should be tested for efficacy etc. But it is simple enough to test on sex workers, if they were willing to volunteer. They are at such high risk that the likely benefits almost certainly outweigh the risks. The chief risk would still be sensitization with human HLA proteins. The beauty of using abrasions is that one can wash the vaccine off as soon as any untoward reaction is noticed.
If you know of people doing HIV research who are not controlled by the US govt, could you please pass this information on to them?
It would be good to get it out to those who could investigate this information with the intention of saving lives with it. Bio- warfare research is immoral and illegal. Unfortunately the US govt is accelerating that research and production of secret private vaccines.
Sincerely, Sue Arrigo, MD”
Here is an article from the London Times on May 1, 1987
Smallpox vaccine ‘triggered Aids virus’
By Pearce Wright, Science Editor
“The Aids epidemic may have been triggered by the mass vaccination campaign which eradicated smallpox. The World Health Organization, which masterminded the 13-year campaign, is studying new scientific evidence suggesting that immunization with the smallpox vaccine Vaccinia awakened the unsuspected, dormant human immuno defence virus infection (HIV).”
“But an adviser to WHO who disclosed the problem, told The Times: ‘I thought it was just a coincidence until we studied the latest findings about the reactions which can be caused by Vaccinia. Now I believe the smallpox vaccine theory is the explanation to the explosion of Aids.’ ‘In obliterating one disease, another was transformed.'”
“Further evidence comes from the Walter Reed Army Medical Centre in Washington. While smallpox vaccine is no longer kept for public health purposes, new recruits to the American armed services are immunized as a precaution against possible biological warfare. Routine vaccination of a 19-year-old recruit was the trigger for stimulation of dormant HIV virus into Aids.
This discovery of how people with subclinical HIV infection are at risk of rapid development of Aids as a vaccine-induced disease was made by a medical team working with Dr Robert Redfield at Walter Reed. The recruit who developed Aids after vaccination had been healthy throughout high school. He was given multiple immunizations, followed by his first smallpox vaccination.
Two and a half weeks later he developed fever, headaches, neck stiffness and night sweats. Three weeks later he was admitted to Walter Reed suffering from meningitis and rapidly developed further symptoms of Aids and died after responding for a short time to treatment. There was no evidence that the recruit had been involved in any homosexual activity.”
“The smallpox vaccine theory would account for the position of each of the seven Central African states which top the league table of most-affected countries; why Brazil became the most afflicted Latin American country; and how Haiti became the route for the spread of Aids to the US. It also provides an explanation of how the infection was spread more evenly between males and females in Africa than in the West and why there is less sign of infection among five to 11-year-olds in Central Africa.”
“Although no detailed figures are available, WHO information indicated that the Aids league table of Central Africa matches the concentration of vaccinations. The greatest spread of HIV infection coincides with the most intense immunization programmes, with the number of people immunised being as follows: Zaire 36,878,000; Zambia 19,060,000; Tanzania 14,972,000; Uganda 11,616,000; Malawai 8,118,000; Ruanda 3,382,000 and Burundi 3,274,000.
Brazil, the only South American country covered in the eradication campaign, has the highest incidence of Aids in that region. About 14,000 Haitians, on United Nations secondment to Central Africa, were covered in the campaign. They began to return home at a time when Haiti had become a popular playground for San Francisco homosexuals.”
“Dr Robert Gello, who first identified the Aids virus in the US, told The Times: ‘The link between the WHO programme and the epidemic in Africa is an interesting and important hypothesis. ‘I cannot say that it actually happened, but I have been saying for some years that the use of live vaccines such as that used for smallpox can activate a dormant infection such as HIV.”