More Malicious Microorganisms

SV-40, SIV, and BSE aren't the only concern. Monkeys and cows, the preferred animals for making the polio vaccine, harbor thousands of viruses and potentially infectious microorganisms. Scientists have known since 1955 that monkeys host the “B” virus, foamy agent virus, haemadsorption viruses, the LCM virus, arboviruses, bovine immunodeficiency virus (BIV), and more.

In 1956, respiratory syncytial virus (RSV) was discovered in chimpanzees.

According to the controversial researcher Dr. Viera Scheibner, RSV viruses “formed prominent contaminants in polio vaccines, and were soon detected in children.” Allegedly, RSV caused “serious cold-like symptoms in small infants and babies who received the polio vaccine.”

By 1961, the link between RSV and respiratory tract illnesses became clear, as the virus was found in 57% of infants with bronchiolitis or pneumonia, and 12% of babies with a milder febrile respiratory disease.

Infected babies babies remained ill for three to five months. RSV was also found to be contagious, and soon spread to adults where it has been linked to the common cold.

According to the CDC, today RSV affects the majority of children by the age of two, and is the most common cause of bronchiolitis and pneumonia among children under one.

RSV remains highly contagious and results in thousands of hospitalizations every year; many people die from it. Ironically, scientists are developing a vaccine to combat RSV—the infectious agent that very likely entered the human population by way of a vaccine.

The Wikipedia page for RSV ends with this provocative statement: “The RSV is virtually the same as chimpanzee coryza virus and can be transmitted from monkeys to humans...the inactivated polio vaccine was reportedly contaminated with simian viruses, including Chimpanzee coryza, during 1955-1963.”

The two sources given for this statement are a 2005 study and, in the category of other simian viruses, Wikipedia provides a link to the now-deleted CDC page on SV40 contamination of the polio vaccine.

In 1996, at the Eighth Annual Houston Conference on AIDS, a microbiologist named Dr. Howard B. Urnovitz revealed that as many as 26 monkey viruses may have been in the original Salk vaccines, including the simian equivalents of human echo virus, coxsackie, herpes (HHV-6, HHV-7, and HHV-8), adenoviruses, Epstein-Barr, and cytomegalovirus.

Urnovitz maintains that contaminated Salk vaccines given to U.S. children between 1955 and 1961 likely set this generation up for immune system damage and neurological disorders.

He sees correlations between early polio vaccine campaigns and the sudden emergence of human T-cell leukemia, epidemic Kaposi's sarcoma, Burkitt's lymphoma, herpes, Epstein-Barr and chronic fatigue syndrome.

Indeed, as early as 1957 it was known that as many as eight “apparently new” viruses had contaminated the vaccine from using monkey-kindey tissue cultures.

Urnovitz challenged medical science to prove wrong his theory that the human immunodeficiency virus Type-1 (HIV-1) is a monkey-human hybrid that was created after 300,000 Africans were injected between 1957 and 1959 with quantities of experimental live oral polio vaccines contaminated with different monkey viruses.

Urnovitz also discussed “jumping genes”—normal genes that may recombine with viral fragments to form new hybrid viruses called chimeras. He believes that this is exactly what happened when monkey viruses and human genes were brought together during early polio vaccine campaigns.

And because the chimera “has the envelope of a normal human gene,” typical cures won't work. How do you develop a vaccine or other antidote against the body's own DNA?

For more information about autoimmune diseases and viruses, I recommend the following lecture available on Youtube: "The Exploding Autoimmune Epidemic: It's Not Autoimmune, you have Viruses." Here's a summary I put together of the important points mentioned in the lecture.