Tag Archives: DNA

Study Links Autism To Vaccines Using Aborted Fetus Cells

A new study shows vaccines that come from human fetal cell lines can contribute to autism.

The study uses data from the U.S., U.K., Denmark and Australia.  It was complied by the Sound Choice Pharmaceutical Institute.

“Not only are the human fetal contaminated vaccines associated with autistic disorder throughout the world, but also with epidemic childhood leukemia and lymphomas,” said Dr. Theresa Deisher of SCPI.

The study showed that in most cases, the amount of fetal DNA in the vaccines was significantly above the levels considered safe.  No more than 10ng should be in a dose, yet in some cases the levels were as high at 2000ng per dose.

“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 report comes on the heels of a CDC report that was withheld showing an increase among African American boys and autism when vaccinated prior to 36 months.

Scientists Alter DNA To Cure Disease

A genetic disease has been cured in an adult animal for the first time in history.

Scientists at MIT have recorded using a procedure where they edit the DNA of a live adult animal to replace a defective gene that causes liver disease.  The scientists say the procedure, known as Crispr, allows them to edit a single “letter” in the genetic alphabet.

“We basically showed you could use the Crispr system in an animal to cure a genetic disease, and the one we picked was a disease in the liver which is very similar to one found in humans,” said Professor Daniel Anderson.

The MIT team believes because the DNA is so similar, they should be able to begin testing of the Crispr protocol in humans within the next few years.

The process would have to be altered, however, to carry the mutations into the human body via harmless adeno-associated viruses.