I am not an ANTI-VAXXER — EXCEPT for what they put into it!
The Vaccination, that is!
A few years ago, Dr. Theresa Deisher, a PhD in Molecular and Cellular Physiology from Stanford University, the first person to discover adult cardiac derived stem cells, determined that residual human fetal DNA fragments in vaccines may be one of the causes of autism in children through vaccination.
She wrote, “It is possible that these contaminating fragments could be incorporated into a child’s genome and disrupt normal gene function, leading to autistic phenotypes.”
Since 2008, Sound Choice Pharmaceutical Institute (SCPI) has been researching what is causing so many DNA breaks and mutations in children.
Addressing DNA mutations, they wrote, “Have we created the perfect storm for DNA breaks, mutations, and regressive autism in our children? In 1979 we started injecting our children with vaccines that are contaminated with human fetal DNA fragments and a retrovirus, and autism began to rise. Then we added more jabs with aborted fetal vaccines and thimerosal, which can also cause DNA breaks, to vaccines in 1988, and autism rose more. Then in 1995, we added much more aborted fetal DNA contaminants to the chickenpox vaccine, and autism really rose. And now we have children born to older dads who have sperm with very breakable DNA. Aborted fetal contaminated vaccines plus thimerosal plus older dads result in more DNA breaks, thus more de novo mutations, in our children.”
Because drugs and vaccines are too large to produce in a test tube, SCPI states they must therefore be manufactured using cell lines, and the final products contain contaminants from the cell line used to manufacture the drug or vaccine.
SCPI points out when animal cell lines are utilized, our immune systems recognize those contaminants as foreign and eliminate them from our bodies.
However, when primitive human cell lines, such as aborted fetal cell lines, are used, such contaminants have the potential to trigger autoimmune diseases or genomic instability.
SCPI stated, “When we use human fetal produced vaccines or cosmetics, we are also injecting or transferring DNA and viruses from the human fetus used to create the cell line into our bodies.”
Due to these and other findings, SCPI hopes to end human exploitation in product development.
Despite this research and the dramatic rise in autism that seems to correspond with the methods used to manufacture vaccines, NCVIA, although passed over 30 years ago, protects vaccine manufacturers from liability.