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 http://www.vaclib.org/basic/quotes.htm 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: www.aapsonline.org]
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.
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, www.pslgroup.com/mednews.htm. ]
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.
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
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 (vaclib.org) are making them available
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 (vaclib.org) are making them available
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!
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.
By Alan R. Yurko
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
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
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.
ADVERSE EFFECTS OF ADJUVANTS IN VACCINES
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.
by Viera Scheibner
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
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
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
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.
Note: this article and 7 accompaning files were found on WWW.TRUFAX.ORG but
unfortunately the link no longer works. So we (vaclib.org) are making them available
VACCINES AND GENETIC MUTATION by
Off site links
Harold E. Buttram, MD; Susan Kreider, RN; Alan R. Yurko
THE NEED FOR VACCINE SAFETY http://www.protectmedicalfreedom.com/vac-safety.html
"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
WRITTEN TESTIMONY OF DR. HOWARD B. URNOVITZ
August 3, 1999
COMMITTEE ON GOVERNMENT REFORM AND OVERSIGHT
http://www.whale.to/vaccines/damaged.html VACCINE DAMAGE
"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