This is yet another study confirming how criminal our FDA is, especially under the Regime of the Kenyan kommie.
This latest study published in the Journal of Public Health and Epidemiology by scientists at Sound Choice Pharmaceutical Institute is simply stated, jaw-dropping. What’s more, their findings are supported by the very fact that the FDA knew the potential dangers of the aborted fetal DNA inserting itself into vaccine recipients and the link of the contaminants to childhood cancers. We have included just one of the numerous publications by the FDA and highlighted some of their comments on page 2 of the press release. Please share this far and wide. Its time the FDA did something about this instead of trying to bury the truth.
New study in Journal of Public Health and Epidemiology correlates autism disorder increase and human fetal DNA, retroviral agents in vaccines
Even more alarming, Dr Theresa Deisher, lead scientist and SCPI founder noted that, “Not only are the human fetal contaminated vaccines associated with autistic disorder throughout the world, but also with epidemic childhood leukemia and lymphomas.”
States the Sound Choice Pharmaceutical Institute (SCPI):
So it should come as no surprise that the FDA has known for decades about the dangers of insertional mutagenesis by using the human fetal cell lines and yet, they chose to ignore it. Instead of conducting safety studies they regulated the amount of human DNA that could be present in a vaccine to no greater than 10ng. (www.fda.gov/ohrms/dockets/ac/05/slides/5-4188S1_4draft.ppt )
Unfortunately, Dr. Deisher’s team discovered that the fetal DNA levels ranged anywhere from 142ng – 2000ng per dose, way beyond the so-called “safe” level.
“There are a large number of publications about the presence of HERV (human endogenous retrovirus – the only re-activatable endogenous retrovirus) and its association with childhood lymphoma,” noted Dr Deisher. “The MMR II and chickenpox vaccines and indeed all vaccines that were propagated or manufactured using the fetal cell line WI-38 are contaminated with this retrovirus. And both parents and physicians have a right to know this!”
The WI-38 cell line was developed in July 1962 from lung tissue taken from a therapeutically [sic] aborted fetus of about 3 months gestational age. Cells released by trypsin digestion of the lung tissue were used for the primary culture. The cell morphology is fibroblast-like. The karyotype is 46,XX; normal diploid female. A maximum lifespan of 50 population doublings for this culture was obtained at the Repository. A thymidine labelling index of 86% was obtained after recovery. G6PD is isoenzyme type B. This culture of WI-38 is an expansion from passage 9 frozen cells obtained from the submitter.
Certainly these discoveries by SCPI should generate an immediate investigation by FDA officials, if not an outright ban on the use of aborted fetal cell lines as substrates for vaccine production. There are numerous other non-human FDA-approved cell lines that can and should be used.