Toxic Vaccines

Dr Sundardas   December 2, 2009   No Comments on Toxic Vaccines

To most people, vaccines sound medically harmless. “They’re good for you!” say the doctors and drug companies, but they never really talk about what’s in those vaccines. There’s a good reason for that: If people knew what was really in those vaccines, they would never allow themselves to be injected with them.

Vaccine production is a disgusting procedure. To begin, one must first acquire the disease germ — a toxic bacterium or a live virus. To make a “live” vaccine, the live virus must be attenuated, or weakened for human use. This is accomplished by serial passage — passing the virus through animal tissue several times to reduce its potency. For example, measles virus is passed through chick embryos, polio virus through monkey kidneys, and the rubella virus through human diploid cells — the dissected organs of an aborted fetus! “Killed” vaccines are “inactivated” through heat, radiation, or chemicals.

The weakened germ must then be strengthened with adjuvants (antibody boosters) and stabilizers. This is done by adding drugs, antibiotics, and toxic disinfectants to the concoction: neomycin, streptomycin, sodium chloride, sodium hydroxide, aluminum hydroxide, aluminum hydrochloride, sorbitol, hydrolyzed gelatin, formaldehyde, and thimerosal (a mercury derivative).

Aluminum, formaldehyde, and mercury are extremely toxic substances with a long history of documented hazardous effects. Studies confirm again and again that microscopic doses of these substances can lead to cancer, neurological damage, and death. Yet, each of them may be found in childhood vaccines.

In addition to the deliberately planned additives, unanticipated matter may contaminate the shots. For example, during serial passage of the virus through animal cells, animal RNA and DNA – foreign genetic material — is transferred from one host to another. Because this biological matter is injected directly into the body, researchers say it can change our genetic makeup.

Undetected animal viruses may jump the species barrier as well. This is exactly what happened during the 1950s and 1960s when millions of people were infected with polio vaccines that were contaminated with the SV-40 virus undetected in the monkey organs used to prepare the vaccines. SV-40 (Simian Virus #40 — the 40th such virus detected since researchers began looking), is considered a powerful immunosuppressor and trigger for HIV, the name given to the AIDS virus. It is said to cause a clinical condition similar to AIDS, and has been found in brain tumors, leukemia, and other human cancers as well. Researchers consider it to be a cancer-causing virus.

The Food and Drug Administration (FDA) Modernization Act of 1997 called for the FDA to review and assess the risk of mercury containing food and drugs. In line with this review, U.S. vaccine manufacturers responded to a December 1998 and April 1999 FDA request to provide more detailed information about the thimerosal content of their preparations which include this compound as a preservative. Thimerosal has been used as an additive to biologics and vaccines since the 1930’s.Some but not all of the vaccines recommended routinely for children in the United States contain thimerosal. As a result.some children could be exposed to a cumulative level of mercury over the first six months of life that and there is the riskof neuro-developmental effects

The Public Health Service, the American Academy of Pediatrics, and vaccine manufacturers agree that thimerosal-containing vaccines should be removed as soon as possible. Similar conclusions were reached in 1998 in a meeting attended by European regulatory agencies, the European vaccine manufacturers, and the US FDA which examined the use of thimerosal-containing vaccines produced or sold in European countries.

A 1994 study found that children diagnosed with asthma (a respiratory ailment not unlike SIDS) were five times more likely than not to have received pertussis vaccine. Another study found that babies die at a rate eight times greater than normal within three days after getting a DPT shot. The three primary doses of DPT are given at two months, four months, and six months. About 85% of SIDS cases occur at one through six months, with the peak incidence at age two to four months.

In a recent scientific study of SIDS, episodes of apnea (cessation of breathing) and hypopnea (abnormally shallow breathing) were measured before and after DPT vaccinations. “Cotwatch” (a precise breathing monitor) was used, and the computer printouts it generated (in integrals of the weighted apnea-hypopnea density — WAHD) were analyzed. The data clearly shows that vaccination caused an extraordinary increase in episodes where breathing either nearly ceased or stopped completely. These episodes continued for months following vaccinations. Dr. Viera Scheibner, the author of the study, concluded that “vaccination is the single most prevalent and most preventable cause of infant deaths.”

In another study of 103 children who died of SIDS, Dr. William Torch, of the University of Nevada School of Medicine at Reno, found that more than two-thirds had been vaccinated with DPT prior to death. Of these, 6.5 percent died within 12 hours of vaccination; 13 percent within 24 hours; 26 percent within three days; and 37, 61, and 70 percent within one, two, and three weeks, respectively He also found that SIDS frequencies have a bimodal-peak occurrence at two and four months — the same ages when initial doses of DPT are administered to infants.
Aside from the dangerous ingredients many people already know about (like squalene or thimerosal), one of the key ingredients used in flu vaccines (including the vaccines being prepared for the swine flu pandemic) is the diseased flesh of African Green Monkeys. This is revealed in U.S. patent No. 5911998 – Method of producing a virus vaccine from an African green monkey kidney cell line. (http://www.patentstorm.us/patents/5…)

As this patent readily explains, ingredients used in the vaccine are derived from the kidneys of African Green Monkeys who are first infected with the virus, then allowed to fester the disease, and then are killed so that their diseased organs can be used make vaccine ingredients. This is done in a cruel, inhumane “flesh factory” environment where the monkeys are subjected to a process that includes “incubating said inoculated cell line to permit proliferation of said virus.” Then: “harvesting the virus resulting from step (c); and… (ii) preparing a vaccine from the harvested virus.”
Vaccines anyone?

be well
Dr Sundardas

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