Danke
Top Rated Influencer
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Last I checked? Why?
'cause the ingredients have changed.
Last I checked? Why?
The science behind them is to expose your immune system to a weakened, killed, or partial pathogen like for instance polio for your body to develop antibodies against without actually acquiring the disease. Once your immune system learns how to make antibodies against it, if you are ever exposed to the actual disease then you can fight it off before it can infect you or before it overwhelms your defenses. This is also why breast milk is so important, it is full of the mothers antibodies from all of the illnesses she has an immunity for, when the baby drinks it these antibodies are transferred to the baby and will protect him from disease, one way is by coating the inside of his mucus membranes like the nose and throat killing any pathogen that they come into contact with when inhaled.
'cause the ingredients have changed.
The Polio vaccine and SV40 (Simian Virus 40)? They knowingly knew that SV-40 would give people cancer and they continued allowing it to be put in. That should give anyone pause who think vaccines are good for them and that Big pHARMa is looking out for our best interest!
Deep sequencing – which identified a viral contaminant of the rotavirus vaccine Rotarix - could have revealed the presence of simian virus 40 (SV40) in the poliovirus vaccine, had the technique been available in the 1950s. Exposure of over 100 million Americans to SV40, and many more worldwide, could have been avoided, as well as the debate about the role of this monkey virus in human cancer.
SV40 was discovered by Maurice Hilleman in 1960 as a contaminant of poliovirus vaccine. It was present in batches of both the Salk and Sabin poliovirus vaccines produced and distributed from 1954 to 1963. The source was the rhesus and cynomolgous monkey kidney cells used to produce the vaccine. Even more troubling was the observation that SV40 could cause tumors in hamsters. By 1963 screening procedures were instituted to ensure the absence of SV40 in poliovirus vaccines. Ironically, monkey cells were used for poliovirus vaccine production because it was feared that human cells might contain unknown human cancer viruses.
SV40 does not cause tumors in its natural host – monkeys – because it kills infected cells. However, in the wrong host- such as a hamster – the viral replication cycle is incomplete and virions are not produced. At a very low frequency, pieces of the viral DNA become integrated into the host chromosomal DNA. Problems arise if these viral DNA fragments encode the viral T (tumor) antigen. This protein is essential for lytic replication (which takes place in monkey cells) because it kick-starts cellular DNA synthesis. The cellular DNA synthetic machinery is then co-opted for replication of the viral DNA. When only T antigen is present, the cells divide without stopping – they are transformed, and on the way to becoming a tumor. SV40 does not need to cause tumors as part of its life cycle; they are an aberrant result of having T antigen push the cells to divide. SV40 T antigen can transform human cells, and therefore in theory the virus could cause human tumors.
The results of epidemiological studies initiated in the 1960s through the 1970s, in which thousands of poliovirus vaccine recipients were studied, indicated that this population did not have an increased risk of developing cancer.
Then you have Contaminants like SV40 that is still in the polio vaccines1.
It is true that simian virus 40 was in some polio vaccines but at the time there was no way of knowing that it was there or to test for it. Once a test was developed it was removed and hasn't been found in any vaccines since 1963 and no cases of cancer have been traced to it. If that video included the entire interview, that would have been explained.
http://www.virology.ws/2010/04/13/poliovirus-vaccine-sv40-and-human-cancer/
As noted in that article, internal Lederle documents indicate that the company has not been able to document that it tested all vaccine seeds to confirm the absence of SV40 contamination. Therefore, statements in Nelson's article, such as “[p]eople most likely to have received contaminated vaccines were born from 1941 through 1961,” are inaccurate and potentially misleading.
The absence of confirmatory testing of the seeds, as well as testimony of a Lederle manager, indicate that this claim of removal of SV40 and the testing for SV40 in all the seeds cannot be fully substantiated.
These legal documents and testimony indicate that the scientific community should not be content with prior assumptions that SV40 could not have been in the oral polio vaccine. Only further investigation by outside scientific and independent researchers who can review the test results claimed in the January 1997 meeting and who can conduct their own independent evaluations by testing all the seeds and individual monovalent pools will assure that SV40 has not been present in commercially sold oral poliovirus vaccine manufactured by Lederle.
but that the
vaccine regulators who are charged with keeping our families safe, have
known all along that SV-40 was never removed from vaccines.
"Whether SV40 was removed from Sabin Oral Polio Virus strains remains a
serious and unanswered question," writes Kops, who has represented several
plaintiffs in polio vaccine products liability cases.