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Note: while each quote contains the word "genetic", not all have 'genetics' for a subject.

Two Quotes from: 'Lots of GREAT Vaccination Quotes'

"Autism may be a disorder linked to the disruption of the G-alpha protein, affecting retinoid receptors in the brain. A study of sixty autistic children suggests that autism may be caused by inserting a G-alpha protein defect, the pertussis toxin found in the D.P.T. vaccine, into genetically at-risk children." --Mary N. Megson, M.D.

"The medical authorities keep lying. Vaccination has been a disaster on the immune system. It actually causes a lot of illnesses. We are changing our genetic code through vaccination." --Guylaine Lanctot M.D. Canadian author of the best-seller 'Medical Mafia'.
See for a wonderful collection of Vaccine Quotes

Investigate Before You Vaccinate

The genetically engineered hepatitis B vaccine given to newborns and toddlers is very dangerous. According to the Association of American Physicians and Surgeons (AAPS), the risk of a serious reaction may be 100 times greater than the risk of the disease itself. The Centers for Disease Control (CDC) produced an internal memo suggesting a "possible association between the vaccine and multiple sclerosis." AAPS calls for a moratorium on hepatitis B vaccination, pending proper clinical studies. [The AAPS web site is:]

Neither vaccine profiteers nor government agencies have EVER conducted long-term studies on genetic damage and the probable cancer-causing effects of vaccines. Vaccine makers have no incentive to conduct expensive clinical control studies on vaccine safety since federal law protects them from liability if a child is severely injured or killed by a vaccine. Private insurance companies won't touch vaccine damage."

Basic Facts

1. Vaccines are toxic.
*Vaccines contain substances poisonous to humans (i.e. mercury, formaldehyde, aluminum, etc.) Vaccine package inserts contain this and other information required by law to be disclosed to the public. Although these inserts are produced for consumers, doctors do not make them available to their patients. *Vaccines are grown on and contain foreign tissue and altered genetic material of both human and animal origin.

Hepatitis B Information

The hepatitis B vaccine, Recombivax HB, manufactured by Merck and Co., is a recombinant DNA vaccine. It is produced by cloning the hepatitis virus, and then, adding the cloned virus to a yeast-based culture. This culture, as with all vaccine cultures, contains a variety of foreign proteins originating from other viruses and bacteria. In 1971, scientists in Geneva discovered that when viral proteins are injected directly into the bloodstream, they combine with human genetic material, causing DNA to mutate. 5
[5. "Vaccines and Production of Negative genetic Changes In Humans," Leading Edge Research Group, 1996-1998. See]
Since 1987, there have been at least 38 reports in international medical literature showing that the hepatitis B vaccine causes chronic autoimmune and neurological disease in both children and adults.11 Because it is genetically engineered, Recombivax HB can confuse the body's immune system into attacking itself resulting in an auto-immune response such as multiple sclerosis (MS).12 In 1997, while publicly defending hepatitis B vaccine, the CDC produced an internal memo suggesting a "possible association between the vaccine and multiple sclerosis."13
[11. "Hepatitis B, The Untold Story": a 16-page Report sent to 55,000 pediatricians by the National Vaccine Information Center in 1999.
12. "Ounce of Prevention, Pound of Misery?" Insight Magazine, March 22, 1999, In this article, Dr. Bonnie Dunbar, professor of cell biology at Baylor College of Medicine and an award-winning vaccine research scientist has stated that because the hepatitis B vaccine derives from a surface protein of virus molecules, the similarities between the antigen and proteins in human nerves and tissues may trick the autoimmune systems of the genetically susceptible into attacking themselves. Dunbar says it may take months or years for the auto-immune response to become obvious.
13. "Shots in the Dark," American Spectator Magazine, May 1999.
14. "Hep B Vaccine Linked Directly to Autoimmune Rheumatoid Diseases," From Doctor's Guide to Medical and Other News, ]

Medical Misdiagnosis

by Harold E Buttram, MD

In the opinion of this observer, the misdiagnoses in childhood autism come not in the diagnosis of the condition itself, something that is unmistakable once one has seen a few children with the condition, but from a failure to recognize autism as predominantly an environmental illness. (In this instance the term, "environmental illness," is used to include illnesses brought about by exposures to commercial chemicals and medical interventions as well infectious microorganisms and other exposures from the natural environment). This statement is based on a recent seminar on childhood autism held in the Washington D.C. area as sponsored by the National Institute of Health and other health agencies September 6th and 7th, 2001, at which the largest portion of the meeting was devoted to areas of genetics and neuropathology of autism. (3)
As related to childhood autism, it should be stressed that the field of genetics involves a susceptibility to autism but, except in rare instances, has nothing to do with its causes. The same could be said about virtually all epidemic-type diseases, in which there will be variability in genetic susceptibility. By their very nature, epidemics always arise from environmental sources of one type or another and not from genetic causes. Genetic changes take place very slowly in an evolutionary scale over a period of millennia and never with the rapid increases as seen today with autism.

VACCINES: New Plague for a New Era

by Karen Maidra

The burgeoning incidence of autism may also be correlated with rampant vaccine use. Although genetic factors are well accepted, there are variants of autism and it is known as an etiologically heterogeneous, or multi-causal, disorder. For some children, genetic vulnerability may interact with insults on the developing nervous system to lead to autism.(13) There is increasing evidence of immune system abnormalities in autism. A substantial number of reports on this subject have appeared in medical journals since the 1980s and most of these articles present data that appear to support the theory of a connection between immune system dysfunction and some cases of autism.(14)
One of the latest, and most frightening, developments in the vaccine arena is the edible vaccine. Information from WHO states that key genes are inserted into edible plants where they replicate -- producing vaccines at a fraction of the cost. There are a myriad of difficulties with this concept, some of which are already beginning to surface in its predecessor -- genetically engineered food. How will dosages be controlled? More importantly, how will the pathogens be kept from escaping into the food chain? Current practice is to insert plant or animal derived DNA into genetically altered foods but it is possible that synthetic DNA may be utilized which will contain bits of genetic code never occurring before in any species.(23) "Frankenfoods" are just the tip of the iceburg. What are they thinking? Irretractable damage to the ecosystem cannot possibly be justified by sheer profits.

Viral Vaccines

Viruses themselves are non-living pieces of nucleic acid surrounded by a coat of protein. When a virus enters a cell, it makes use of cellular enzymes and duplicates itself. They can be active or assume a latent, passive infective condition within the cell, waiting for the right conditions to activate. Viruses can remain undetected and latent for years within the body, only to suddenly manifest themselves explosively. Viruses can infect plants and animals, as well as bacteria. Duplication of the virus within a cellular structure often results in the death of the host cell, and viral particles are released through broken cell membranes and infect other cells. Viruses also have the capability to combine with the genetic material in the host cell chromosomes without killing the host cell. The nucleic acids RNA and DNA are spiral-shaped protein chains that express heredity codes transferred genetically and direct the formation of various protein substances. Nucleic acids contain individual packets of information which are species-specific.
Abnormal Viral Penetration By Injection

Viruses directly injected into the blood stream below the skin level avoids the proper immunogobulins and the naturally occurring oleic acid mantle, and are neutralized or blocked by circulating antibodies. We are talking about viruses that are not the result of genetic engineering. The body produced only one type, IgA, as the first line of defense, and this is against arthropod or insect-borne viruses which are carried by blood-sucking and stinging vectors injected directly into the blood or lymph. In other words, nature provides appropriate protection against predatory viruses as long as they attack through their natural routes. The problem comes in when viruses normally meant to run this gambit are injected, as when commercial immunizations are administered intramuscularly or subcutaneously.
Note: this article and 7 accompaning files were found on WWW.TRUFAX.ORG but unfortunately the link no longer works. So we ( are making them available at

Leading Edge Master Analysis of the Vaccination Paradigm V5

Several books have been written about pertussis vaccine, especially in combination with diphtheria and tetanus vaccine in a trivalent mixture dubbed 'DPT'. Most adverse reactions to vaccines reported to the National Registry involve reaction to DPT vaccines, and the DPT vaccine is estimated to cause some degree of minimal brain damage in all children, some more than others, and is ultimately the most significant vaccinal cofactor in the significant upswing of abberant behavior in the population for the past several generations, even modifying genetic structure. We discuss this progression in a special chapter in this book, and we will discuss DPT later in a separate section.
Note: this article and 7 accompaning files were found on WWW.TRUFAX.ORG but unfortunately the link no longer works. So we ( are making them available at

Smallpox Vaccine Adverse Effects Page

I am against a study of smallpox vaccine on children, or on anyone. Some good reasons we are heading in the wrong direction in this regard are below.

1. The authors of a study published in 1980 by "Mutation Research" came to the conclusion that smallpox vaccination has a "mutagenic effect" on human chromosomes. [Neil Z. Miller's 1999 book Vaccines: Are They Really Safe and Effective?, p. 46] "Viruses and viral vaccines are agents for the transfer of genetic imprints from one host to another. In other words, because they contain pure genetic material (DNA and RNA) from a foreign organism, once injected into a human recipient, the new genetic material is incorporated into the invaded cells." [Miller, p. 48] In the 1960s, Joshua Lederberg, Dept. of genetics, Stanford University School of Medicine, said that "live viruses are ... genetic messages used for the purpose of programming human cells". Lederberg said that "we already practice biological engineering on a rather large scale by use of live viruses in mass immunization campaigns." [Miller, p.49] "No one knows the long-term effects of tampering with the genetic codes and delicate structure of the human organism. However, the physical invasion of the human body by foreign genetic material may have the immediate effect of permanently weakening the immune system, setting in motion a new era of autoimmune diseases. For example, research indicates that psychotic disorders may be caused by viral infections. The incidence of schizophrenia is on the rise compared to earlier times, and studies now indicate that about one-third of all cases are autoimmune in nature. Once again, some authorities implicate the childhood vaccine programs." [Miller, p. 49]

Vaccines - Injections Of Death!
By Alan R. Yurko

Vaccines are contrary to God's protocols for health. They are unnatural, toxic blood contaminants and they are being pushed by a demonic force in an effort to attack and contaminate the blood of man, which, as the Bible records, is the life of the flesh (Lev. 17:11). Vaccines are not designed to protect and improve health despite claims to the contrary by the medical establishment. Vaccines disrupt and damage DNA, thus creating genetic disturbances and mutations in a healthy person, which eventually creates a cellular environment that is extremely susceptible to disease. Mass vaccination proarams are being pushed because the global elite are trying to implement a population control agenda. Just look at the destructive effects vaccines have had on the populations of Africa and how the AIDS epidemic is decimating this continent. In the book, Emerging Viruses, by Dr. Len Horowitz, he documents with convincing facts and figures that AIDS was a bioweapon developed by the U.S. government in collusion with several pharmaceutical firms and was administered through the Hepatitis B vaccine. When looking at their components and manufacturing process further, a spiritually enlightened person can easily understand that vaccines are nothing more than a demonic witches brew.

Flyers on Smallpox

The Defense Advanced Research Projects Agency (DARPA) lists 65 known biological warfare agents and an infinite number of organisms that can be created through genetic engineering.

5. Both old and new smallpox vaccines are experimental. The outdated Wyeth (Dryvax) and Aventis stocks dredged up by the CDC were made decades ago, using obsolete techniques and diseased cow (mad cow?) lymph. The new vaccines, to be made from human fetal tissue or monkey serum, will be recombinant at a time when many scientists believe that genetically engineered vaccines may be responsible for our nationwide epidemic of auto-immune and neurological conditions including autism, diabetes, chronic fatigue, rheumatoid arthritis, Lupus and MS-like illnesses.

7. A mass smallpox campaign could prove as disastrous as the government's recent anthrax vaccine disaster. Dr. Garth Nicolson, a world-renown cancer researcher and Nobel Prize nominee, told Congress in 2002 that contaminated anthrax vaccines administered to Armed Forces personnel are partially responsible for debilitating chronic illnesses now suffered by tens of thousands of them. Dr. Nicolson confirms that commercial vaccines are often contaminated with mycoplasma, causing symptoms associated with Gulf War Syndrome. When Dr. Nicolson examined the mycoplasma infecting sick Gulf War vets, he discovered that some strains had been genetically engineered with a portion of the HIV virus! Apparently this HIV-implanted mycoplasma was placed in Department of Defense vaccines for experimental purposes.

Mycoplasma: The Linking Pathogen in Neurosystemic Diseases

How the Mycoplasma Works

The mycoplasma acts by entering into the individual cells of the body, depending upon your genetic predisposition.

You may develop neurological diseases if the pathogen destroys certain cells in your brain, or you may develop Crohn's colitis if the pathogen invades and destroys cells in the lower bowel.

Once the mycoplasma gets into the cell, it can lie there doing nothing sometimes for 10, 20 or 30 years, but if a trauma occurs like an accident or a vaccination that doesn't take, the mycoplasma can become triggered.

Because it is only the DNA particle of the bacterium, it doesn't have any organelles to process its own nutrients, so it grows by uptaking pre-formed sterols from its host cell and it literally kills the cell; the cell ruptures and what is left gets dumped into the bloodstream.

by Viera Scheibner

Gupta et al. (1993) concluded that PT is too toxic to be administered to humans, but chemically detoxified or genetically inactivated PT may not exhibit the adjuvant effects comparable to the native PT.

The clonal selection theory, evolved by Burnett (1960), presupposes that the information requisite to the synthesis of the antibody is part of the genetics. While the body develops a wide range of clones of cells necessary to cover all antigenic determinants by random mutation during early embryonic life, those clones which are capable of reacting with antigens of the body ("self') are destroyed, leaving only those cells which are not oriented to self ("non-self'). Upon stimulation by a foreign antigen, the clones of the cells corresponding to the particular foreign antigen are stimulated to proliferate and to produce the antibody.

Other researchers demonstrated that there are at least four different antigens formed by descendants of a single cloned cell. By this mechanism, the information for antibody synthesis is contained in the genetic material of each cell (DNA) but is normally repressed. The antigen then assumes the role of a de-repressor and initiates (provokes) the RNA synthesis for a particular messenger, resulting in the corresponding antibody production. The antigen would instruct the genetically predisposed capability of multipotential cells as to which antibody to produce and might also command the cells to proliferate, resulting in clones of properly instructed cells.

Waksman (1962) proposed several mecnamsms of autoimmunisation, such as: 1.Vaccination with organ-specific antigens which are isolated from the lymphatic channels and bloodstream and are not recognised as self when brought into contact with the immunologic process. They are represented in the central and peripheral nervous systems, lens, uvea, testes, thyroid (thyroglobulin), kidneys and other organs.

2.Vaccination against constituents of tissues which have been altered antigenetically by various factors. These include myocardial infarction, X-irradiation, enzymatic or other chemical alteration, and changes induced by infectious disease agents or by drugs. Erythrocytes, platelets and leucocytes are the most affected cells. Various organs may also be affected.

Unvaccinated Children --Article by an MD

by Richard Moskowitz M.D.

The prophylaxis and treatment of measles varies somewhat from outbreak to outbreak, the genus epidemicus corresponding most closely to Pulsatilla in Hahnemann's series, Bryonia in Dr. Shepherd's experience, and probably other remedies in other times and places. In the U.S., largely because of mass vaccination programs, acute measles is now predominantly a disease of adolescents and young adults, undoubtedly involving some genetic interaction with the vaccine virus; and it will probably call for still other remedies. Pulsatilla remains the remedy most often recommended for prophylaxis, although my own experience is still too limited to confirm or refute it.

Leading Edge Master Analysis of the Vaccination Paradigm, V3

It is interesting to note, therefore, that since humans have been receiving animal viruses in vaccines, and viruses (including CMV) are present in immune deficiency syndrome ("aids") in humans, and known animal viruses and viral components are oncogenic (cancer-causing), and can cause all the "symptoms" of AIDS, and this has been going on since the 1940's (when polio vaccine cell cultures were first contaminated with simian virus 40 (used as a genetic carrier in all genetic biotech products having viral particle components), and this was well known in the medical field but suppressed from public knowledge, and ultimately the same people who politically control the pharmaceutical, biotech and vaccine companies also control the medical establishment, as well as benefit from fund-raising (i.e., American Cancer Society ,etc.) for "diseases" that never get resolved, you have a very large conspiracy that is worth trillions of dollars to keep from public scrutiny. That's the real bottom line. Research bears all of this out. You are now informed, and if you don't believe that something of this magnitude can be possible, do the research and you'll see that it is absolutely the case. If you comment on this without checking it out, which might involve a little work, there is nothing credible you can say. I haven't been putting in over 80 hours of research a week for more than a year for nothing in order to put this together.What is being done to the world population constitutes criminal negligence of genocidal proportions. Creating a clean biologically harmless, yet effective vaccine is not possible - it would be just too laborious and expensive, over and above the fact that the paradigm of vaccines is 19th century technology brought into a 20th century illusion. It is also fraud.


Rubella is a rather innocuous (benign) infectious disease caused by a virus. Most of the population contract this condition as a matter of course and develop a life-long immunity to the effect of the virus without recourse to the paradigm of synthetic immunity via injection of viral components. Side effects from naturally contracting the virus are extremely rare, although fetal development is subject to genetic deformity if a female contracts the virus during the first trimester of pregnancy. The fact that it can cause birth defects in newborn babies was seized as the justification for a rubella vaccine, which was licensed in 1969, even though there are indications that not all pregnant women exposed to the virus give birth to children with congenital defects. It is estimated that as of 1980, over 83,000,000 doses of rubella vaccine have been injected into the population. The number of cases seems to remain stable at about 30 to 40 per year, out of a population of 250,000,000. Despite the use of the rubella vaccine, the number of infections in women of childbearing age has remained the same, indicating a defective paradigm.

Polio --The Disease and the Vac from History

by Edda West -- 10/20/2001

Polio is in a class of eneteroviruses -- meaning they can colonize the gut. In a discussion paper on CFS (Chronic Fatigue Syndrome), Dr. William Campbell Douglas, MD says that many researchers view CFS as another form of polio. "Modern genetics has confirmed the genetic similarity between polio viruses, coxsackie, and another group called the echo viruses. Before the advent of the Salk and Sabin vaccines, there were only three polio viruses. Now, with the drastic alteration of the human gut over the years as a result of these vaccines, there are at least 72 viral strains that can cause polio-like diseases." (6)

"By the end of 1996, dozens of scientists reported finding SV40 in a variety of bone cancers and a wide range of brain cancers, which had risen 30 percent over the previous 20 years. Then, Italian researchers reported finding SV40 in 45 percent of the seminal fluid samples and 23 percent of the blood samples they had taken from healthy donors." This meant that SV40 was probably spreading through sexual activity, transmitted from mother to child, raising the possibility that the virus may now be incorporated into our genetic makeup. Another possibility is that, undetected by vaccine manufacturers, the virus continues to contaminate current stocks of polio vaccine. At a recent SV40 conference, it was revealed that funding has been granted to develop an anti-SV40 virus vaccine! (8) And so goes the disease merry-go-round: create more vaccines to target the diseases caused by vaccines in the first place. It is a very old game.

The Anthrax Vaccine Scandal

But even if the anthrax vaccine is safe and has nothing to do with Gulf War or other illnesses, is mandatory vaccination a smart policy? Alibek, for one, thinks not. Any errant Russian biowarfare expert with a briefcase full of germs could help any of a dozen states weaponize any of a dozen killers besides anthrax -- plague, Marburg, Venezuelan equine encephalitis, you name it. "If an enemy of the United States knows that our army is vaccinated against anthrax, they'll try to develop some other weapon -- they have many to choose from," Alibek said in an interview. What's more, the licensed anthrax vaccine "probably wouldn't work," he believes, against at least one strain of anthrax genetically altered by Soviet scientists.

One of the stories recounted in Alibek's book is the 1979 disaster at Sverdlovsk, now Yekaterinburg, in which a bungling technician at a germ factory failed to replace an air filter, releasing billions of anthrax spores into the night air. At least 66 people died in this, the worst confirmed germ warfare incident. The strain of anthrax released at Sverdlovsk -- Anthrax 836 -- was put into the tips of hundreds of Russian warheads. This virulent strain, Alibek notes, was itself a genetic mutant derived from sewer rats that contracted anthrax from a spill. When I asked Friedlander if his monkeys had been "challenged" with 836, he said, "We'd like to, but we can't get it [from the Russians]." He added, "We have tested 30 other strains, and have no reason to believe it is fundamentally different." Friedlander and others in the military have no convincing counter-argument, however, to the suggestion that U.S. enemies could easily use another germ agent. "If you use the anthrax vaccine, you're shutting down one of the enemy's capabilities," Friedlander says. Not a hugely reassuring statement.

With So Little Poliovirus Detected Around the World, What Is Causing Today's Outbreaks of Acute Flaccid Paralysis?
By Neenyah Ostrom

Dulbecco and Vogt"s claims, however, went further than they had evidence to support. They asserted not only that they had isolated poliovirus, but that, "Since each plaque stock originated from a single virus particle (as proved in the Discussion), these stocks constitute the purest lines of virus presently available."

How could they possibly know that a "single virus particle," something they had never seen or measured, was causing the growth of exactly one plaque in their cultures? The evidence Dulbecco and Vogt supplied to "prove" that a single virus particle produced each plaque is contained in a mathematical equation: They extrapolated the cell culture"s assumed "virus concentration" from the number of times the original fluid (for example, monkey spinal cord suspension) was diluted. The fewer times the fluid was diluted, the more plaques grew in laboratory cultures; the more times it was diluted, the fewer plaques grew. Dulbecco and Vogt"s mathematical model assumed this linear relationship between dilution of virus stocks and number of plaques formed and, when they reached the greatest possible dilution that still caused a single plaque to grow, they assumed that only one "virus particle" was present therein. And how did they prove that assumption, as promised? They provided their mathematical model. This is a perfectly tautological proof. Its most apparent flaw is that the mathematical model did not"could not"distinguish between a "single virus particle" and a biological complex that may have contained a single virus. This is made clear in Dulbecco and Vogt"s description of the plaque-forming "single virus particle" they claim to have isolated: "Having arrived at this point, it is now possible to define properly the characteristics of the virus particle detected by a plaque. Owing to its all-or-none effect, it has the character of a particle. It corresponds to a unit of the virus which is not further subdivisible at high dilution. From the property by which it is recognized, we call it a plaque-forming particle. We do not know its morphological or genetic properties. It might be a single elementary body, or a clump of them, provided that the clump persists indefinitely at high dilution...."9

It is puzzling, in retrospect, that Dulbecco and Vogt raised the possibility that they were detecting a "clump" of material, but thereafter ignored it. What if another type of virus was also included in these particles? Or, what if host genetic material attached itself to the particle to form a "clump"?

Leading Edge Master Analysis of the Vaccination Paradigm, V2

Serial Passage of Vaccine Components Through Animal Cell Lines

According to the vaccination paradigm promulgated by medical companies, the passage of viruses through animal cell lines is necessary in order to reduce the toxicity of the viruses to humans. This belief is contraindicated by historical evidence.

Back in the 1940's there was a campaign in French West Africa to immunize population groups to yellow fever virus. The virus was passed through mouse cell cultures 258 times, and the mice who were paralyzed had their brains ground up and dried, and this preparation was used to "innoculate" over 100,000 people in 1944. This resulted in over 100 cases of brain damage (meningioencephalitis) and 18 deaths.

The SV-40 Virus Contamination of Vaccine Cultures

In 1960 it was discovered that millions of polio vaccine doses produced in the early 1950's from monkey kidney cells were infected with simian virus 40 (SV-40), which was found in both Salk and Sabin polio vaccines. SV-40 is resistant to the "neutralizing effects" of the carcinogenic germicide formalin added to the vaccines, and was passed on to millions of people who now have SV-40 as part of their genetic structure. SV-40 is one example of a DNA polyoma virus. Polyoma (many tumor-causing) viruses cause prolonged infection where tissue is destroyed, integrate into the hosts genetic material, are capable of mutating a cell, may reproduce after coming into contact with a "helper" virus, enable the separate replication of the viral genome, can generate immune responses, and they can induce malignancy.

Scientists are amazed at how little genetic information these viruses carry in proportion to the damage they can cause. Also, with polyoma viruses, it becomes impossible to detect the viral genome once it has been integrated, and it may reappear if the transformed cells are fused to others which are naturally permissive for SV-40 or other polyoma viruses.There have not been many statistical studies done, for obvious reasons, to determine all of the long term effects of polio immunization; it is known that polio vaccines injected into humans before 1962 contained SV-40. This was documented in an article in 1969 in Science Magazine, a Journal Of The American Association for the Advancement of Science. It was an article by Dr. Joseph Fraumeni entitled "Simian Virus 40 in Polio Vaccine: Follow-up of Newborn Recipients". It stated that SV-40 virus was an unrecognized contaminant if virus vaccines prepared in monkey kidney cell cultures prior to 1962. However, the SV-40 virus was recognized by Dr. Hillman in 1960, which does not explain the two-year gap in "lack of recognition" and suppression of this information that followed. Legalese defines the word contamination, with respect to vaccines, as something external to the manufacturing process, and does not permit the public dissemination of the fact that the SV-40 virus already existed in the cultures used to prepare the "polio vaccine". SV-40 is an oncogenic (cancer-causing) virus.

According to the report, "from 1960 to 1962, polio vaccine in various forms and regimens was given to 1077 newborn infants at the Cleveland Metropolitan General Hospital, in a study to assess the feasibility of introducing active immunity to poliomyelitis in the presence of maternal antibodies. Normal term infants were assigned with parental consent to one of six study groups. An attenuated poliomyelitis vaccine was given orally to 925 infants; some received very high concentrations of S-40 within a few hours of birth. The remaining 152 children were injected with large doses of inactivated polio vaccine which had smaller concentration of SV-40 than the oral preparations. Later in infancy, all the chidden received "booster" injections of attenuated or inactivated polio vaccine, or both, which presumably contained SV-40. Since 1964, we have made periodic efforts to determine the death rate among the vaccinated children, who were from an urban, low socioeconomic, highly mobile, predominantly Negro population."

An analysis of the above reveals staggering gaps in logic that support the premise that it may well have been done deliberately to study the negative effects of the vaccine. The study purports to have been performed in order to "evaluate antibody formation" in newborn vaccines, but in defiance of the orthodox definition of an empirical study, no control group was used or selected so that such an evaluation could take place. Follow-ups were made to determine death rate and not state of health. The parental consent forms detailed no risks involved with the experiment that would bar the parents from signing. The health state of vaccines at the time of the report was not mentioned. Clearly, either total incompetence or negligence was involved, or the study was done to assess the known negative results to those vaccinated. Evidence points to the latter, and this constitutes a criminal act.

SV-40 is also a DNA virus. A study on DNA viruses was completed in 1966, and the results of the study were published in a 1967 edition of the American Journal of Pathology; the results clearly showed the known connection between such viruses and cancer: "A number of viruses containing DNA have been shown to induce tumors when inoculated into newborn animals. Members of the papovavirus group, mouse polyoma, and simian virus 40, all adenoviruses, are now recognized as oncogenic (cancer-causing) when tested by this method".

An article by M.A. Israel, "Molecular Cloning of Polyoma Virus DNA in E-Coli", published in Science Magazine in 1979 described the use of Polyoma DNA in molecular cloning into E.Coli for the purpose of ongenicity (production of a cancer-causing virus). It only takes 10 or 20 particles of polyoma per cell to cause malignancies. Matrix III volume one describes in detail the research done at the National Cancer Institute in producing cancer-causing viruses under the guise of cancer research.

Research indicates that there is an unusual feature to these viruses, in that the tumors they eventually cause appear to be virus-free, making it impossible to detect viral causation in tumors induced by these viruses. Over 500 million people have been inadvertently innoculated with SV-40.

SV-40 an Integral Part of genetically Engineered Products

When a genetically engineered product is manufactured, a probe, plasmid or vector is an essential part of the process; these can be defined as a specific kind of molecular structure that permits the passage and insertion of one type of DNA into the genetic material of the organism used to manufacture the genetically engineered substance. Some of the newest genetically engineered products for sale are those "vaccines" against "AIDS". Most of these vector probes contain SV-40 or portions of SV-40 as part of their structures, SV-40 being a very important active component in the process. Any review of the various symposia conducted on genetic engineering makes it clearly obvious that it is an important factor in recombining viruses and genetic material (recombinant genetic engineering). Due to the influence of the SV-40 base, various other viruses are eagerly assimilated. Sometimes, in genetic literature, SV-40 is called "plasmid pMV104, which uses SV-40 as its origin but hides the immediate relationship with SV-40 from public perusal. The action of the presence of Sv-40 material is analogous to that of DMSO, in that it acts like a "wheelbarrow" to carry other substances into an otherwise well-protected cellular body; this is the main reason why an individuals' subsequent reaction and susceptibility to environmental pollutants after injection with a vaccine.

Supporting these lines of thought, an article in the January 6, 1962 Science News- letter indicated that "common human viruses act as carriers in causing cancer by interacting with cancer-causing chemicals; this has been indicated by experiments which show that cancer-causing substances that are present in too small a quantity by itself will become active and create tumors when combined with single doses of virus. Malignant tumors appeared in five type of injected mice." The viruses mentioned were ECHO9, B-4, Coxsackie, and Poliovirus 2. The article further indicated that "viruses may also activate other cancer causing substances besides chemicals in the environment, such as DMBA, AF, and DBA."

The Use of Animal Cell Line Substrates for Human Vaccines

In our current cultural situation, medical drugs are generally dividied into three categories: (1) Pharmaceuticals, (2) Biologicals and (3) genetically Engineered Products, which now include sera (plural of serum), vaccines and blood derivatives. Most vaccines are manufactured using what are called continuous cell lines (CCL), usually animal tissue based, which provide the raw materials having specific biological properties which serve as the substrate for production of genetically engineered (biotech) drugs. In the past, vaccines were made solely from individual lots of animal tissues or human disease by products.The main aspect of CCL that is attractive to vaccine manufacturers is an infinite lifespan and a high growth rate, but the problems are "biochemical, biological and genetic variability in terms of the production of transforming proteins and potentially oncogenic (cancer-causing) DNA, contaminating viruses and predisposition to tumors in animals." J.B. Griffiths from the United Kingdom gave a presentation in 1988 in which he stated "it is now generally accepted that continuous cell lines are acceptable as substrates for the production of biologicals, provided that the manufacturing process yields no detectable risk attributed to the cell subtrate." Three French doctors in 1988 warned of hazards from introducing plasmid DNA into mammalian cells, "since part of the regulatory genetic elements used in the expression vectors (plasmids) is often virus-derived, and the presence of these DNA sequences in the final product represents a potential risk."

Known Simian Disease Epidemics

Since simians (monkeys) are the prime creature that is used for animal research, it is no surprise that the urge to perform experiments between species, a post Atlantean tendency, was due to fall on them. As a result, outbreaks of cancer occurred in primate laboratories worldwide. In one experiment documented in the Journal of the American Veterinary Association, human blood laced with leukemia was deliberately injected in gibbon monkeys under the guise of "malaria experiments", and watched as the speed of action and the severity of the virus increased with the program of infecting more and more animals. During a period between 1969 and 1973 a leukemia epidemic affected 900 inbred Hamadryas baboons at an experimental animal station in Soviet Georgia. These monkeys were then shipped to Litton Bionetics in Kensington, Maryland, a laboratory that had such a bad containment record that even the National Cancer Institute called it "grossly irresponsible", according to an article in a 1979 Science Journal. Other violations of containment were reported an another infamous laboratory run by Litton: the Frederick Cancer Research Center. In 1971 and again in 1973, researchers were "surprised" at the occurrence of two epidemics of leukemia in gibbons which happened "unexpectedly" at the Medical Research Lab of SEATO in Bangkok, Thailand.

From November 1969 to November 1982, a continuous AIDS-like illness was observed among primates worldwide. The illness had the following symptoms: diseased lymph nodes, enlarged spleen, fever, diarrhea, weigh-loss, and infection with microorganisms. These scientists were perfectly aware that transmission of a virus from a species that is a natural host to a species that is not, causes mutations and an increase in virulence, but did the experiments anyway, with total disregard for others in the society.

In the Primate Research Center in Beaverton, Oregon, the population of black macaque monkeys, between 1978 and 1983, contracted what scientists referred to as "simian AIDS". The high peak for the epidemic was in 1980, at the start of the Reagan-Bush administration. Of course, we all know about the Ebola Reston incident from the book The Hot Zone.

Vaccination and Genetic Change: Mobility of Genetic Material Between Life Forms

One of the indications that vaccinations may in fact be changing the genetic structure of humans became evident in September of 1971, when scientists at the University of Geneva made the discovery that biological substances entering directly into the bloodstream could become part of human genetic structure. Originally, Japanese bacteriologists discovered that bacteria of one species transferred their own specific antibiotic resistance to bacteria of an entirely different species. Dr. Maurice Stroun and Dr. Philip Anker in the Department of Plant Physiology at the University of Geneva, began to accumulate evidence that the transfer of genetic information is not confined to bacteria, but can also occur between bacteria and higher plants and animals. According to an article in World Medicine on September 22, 1971, "Geneva scientists are convinced that normal animal and plant cells shed DNA, and that this DNA is taken up by other cells in the organism."

In one experiment, scientists in Geneva extracted the auricles of frog hearts and dipped them for several hours in a suspension of bacteria. Afterward, they found a high percentage of RNA-DNA hybridization between bacterial DNA extracted from bacteria of the same species as that used in the experiment and titrated DNA extracted from the auricles which had been dipped in the bacterial suspension. Bacterial DNA had been absorbed by the animal cells. This phenomenon has been dubbed transcession. There is evidence that this kind of phenomenon is happening all the time within the human body. It is conceivable, for example, that heart damage following rheumatic fever could the the result of the immune system reacting to its own cells producing a foreign RNA complex after absorption of foreign DNA.

In Science magazine, November 10, 1972, bacterial RNA was demonstrated in frog brain cells after a bacterial peritoneal infection. In the April 1973 issue of the Journal of Bacteriology, transcription of spontaneously released bacterial DNA was found to be incorporated into cellular nuclei of frog auricles. Studies by Phillipe Anker and Maurice Stroun have indicated spontaneous release of DNA material from mammalian cells, spontaneous transfer of DNA from bacteria to higher organisms, spontaneous transfer of DNA between cells of higher organisms, release of RNA by mammalian cells, and biological activity of released complexes containing RNA.

Malignant Cellular Transformations Caused By Foreign DNA

There is evidence that freely circulating foreign DNA can cause malignancy. In a 1977 issue of International Review of Cytology, Volume 51, Anker and Stroun discuss the possible effects of foreign DNA causing malignant cell transformations. When foreign DNA is transcribed into a cell of a different organism, "this general biological event is related to the uptake by cells of spontaneously released bacterial DNA, thus suggesting the existence of circulating DNA. In view of the malignant transformations obtained with DNA, the oncogenic (cancer-causing) role of circulating DNA is postulated."

The discovery in 1975 that viruses causing cancer in animals had a special enzyme called reverse transcriptase makes the problem even more interesting. These kind of viruses are called RNA viruses. When an RNA virus has the reverse transcriptase enzyme within its structure, it allows the virus to actually form strands of DNA which easily integrate with the DNA of the host cell which it infects. Studies by Dr. Robert Simpson of Rutgers University indicate that RNA viruses which do not cause cancer can also fom DNA, even without the presence of reverse transcriptase. DNA formed in this way from an RNA virus is called a provirus. It is known that some non-cancerous viruses have a tendency to exist as proviruses for long periods of time in cells without causing any apparent disease. In other words, they remain latent. Some examples of common RNA viruses that do not cause cancer, per se, but have the capacity to form proviruses are influenza, measles, mumps and polio viruses. In the October 22, 1967 British Medical Journal, it was brought out by German scientists that multiple sclerosis seemed to be provoked by vaccinations against smallpox, typhoid, tetanus, polio, tuberculosis and diptheria. Even earlier, in 1965, Zintchenko reported 12 cases in which MS became evident after a course of antirabies vaccinations. Remember that millions of people between 1950 and 1970 were injected with polio vaccines containing simian virus 40 (SV-40) transferred from contaminated monkey kidney cells used to culture the vaccine. It is impossible to remove animal viruses from vaccine cultures. You are reminded that SV-40, the 40th virus to be discovered in simian tissue, is a cancer-causing virus.

Immunization programs against influenza, measles, mumps and polio are in fact seeding humans with RNA and forming proviruses which become latent for long periods in throughout the body, only to re-awaken later on. Post-polio syndrome is a good example of this problem. Other examples may include the so-called mesenchymal and collegen diseases, such as rheumatoid arthritis, multiple sclerosis and lupus erythmatosis, where antibodies are formed by the immune system against the person's own tissues - tissues which have been impregnated with foreign genetic material. According to a special issue of Postgraduate Medicine in May 1962, "although the body generally will not make antibodies against its own tissues, it appears that slight modification of the antigenic character of tissues may cause it to appear foreign to the immune system and thus a fair target for antibody production." Two years later in 1964, studies were conducted on the polyoma virus, a tumor-producing DNA virus. It was discovered that the persistent genetic DNA material in the polyoma virus brought about malignant transformations in hamster embryo cell cultures. This was reported in the November 23, 1964 issue of the Journal of the American Medical Association.

Even common non-tumor viruses, including those in smallpox vaccine and polio virus 2, can act as carcinogens. It was reported in Science on December 15, 1961 that these common viruses acted as catalysts in producing cancer when given to mice in combination with known organic carcinogens in amounts too small to induce tumors themselves. This means that some vaccinations will induce cancer, when combined with the growing problem of environmental pollution from toxic by-products of agriculture (pesticides on and in food) and industry. Of course, this information is hidden from the public, which is why the FDA, EPA and the agricultural industries can get away with "sanctioning" small amounts of pollutants in food, water and air. The connection has not been made public, much to the joy of the chemical industry, the National Cancer Institute and the growing cancer industry, which continues to fraudulently solicit public donations to justify its own existence. As an aside, it has alreadybeen admitted that polio vaccinations have caused 100% of all polio in the United States since 1980 and the predominant cases of all paralytic polio since 1972 (Science, April 4, 1977). It is suspected that the Salk and Sabin vaccines, made of moneky tissue culture, have also been responsible for the major increase in leukemia in the United States.

The use of viruses, bacteria and animal tissue cultures in mass immunization campaigns, considering that this information has been known for 20 years, constitutes an intentionally created hazard to humans. The global impact on the wide range of genotypes relative to human beings is difficult to assess, but the outcome is definitely negative, and permitting the seeding of latent proviruses in humans, knowingly, can have no other rationale other than future medical profiteering, and constitutes a criminal conspiracy of vast proportions which is tatamount to a genocidal policy against the population, further constituting crimes against humanity, which is internationally punishable by death. But, of course, especially in the United States, this fact is ignored and suppressed from public knowledge, despite a 1984 plea by some U.S. physicians to the United Nations in a report. The fact that this goes on with the full knowledge of the world medical community makes this an international conspiracy where the population has no recourse, given that vaccinations are becoming mandatory and a prerequisite for many social programs.

Persistence of long-term viruses and foreign proteins and their relationship to chronic and degenerative disease was also pointed out by Dr. Robert Simpson of Rutgers University in 1976, when he addressed science writers at an American Cancer Society seminar, saying "these proviruses could be molecules in search of a disease." Dr. Wendell Winters, a virologist at the University of California noted, "immunizations may cause changes in slow viruses and changes in the DNA mechanism." Although host cells containing latent viral particles operate more or less normally, they begin to synthesize viral proteins under the guidance of the viral DNA, eventually creating the circumstances for various autoimmune diseases, including diseases of the central nervous system, which unfortunately add to the growing load of aberrant social behavior patterns.
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Harold E. Buttram, MD; Susan Kreider, RN; Alan R. Yurko

"Unfortunately, efforts by scientists to explore fully the possible negative effects of vaccines mandated by public policy has been met with stiff resistance by public health agencies."
August 3, 1999
"My "agenda" is to tell the truth. Like the fact that, according to Centers for Disease Control (CDC) statistics, as many as 800,000 vaccine induced injuries have occurred every year in the United States since 1990."--Leonard Horowitz