Aborted Fetal DNA in Vaccines

Larry A. Law

We've been talking a lot about the coronavirus vaccines lately. There are grave concerns about them, but they aren't the only concerns we have when it comes to vaccines. For instance, the CDC has long maintained that vaccine ingredients do not cause autism. They say that vaccine ingredients cannot induce disease. But they mislead the American public by shifting the focus away from the preservatives and adjuvants in vaccines. A common preservative in many vaccines is thimerosol (mercury). Mercury is probably the most harmful substance known to man. Yet it is injected into the bodies of children and adults in far greater amounts than what the FDA warns us about when eating tuna fish. Adjuvants like aluminum are used to inflame the immune system. Aluminum is highly toxic and destructive to health, but the CDC insists vaccine manufacturers require it so the vaccine will work better. It is only by keeping the public ignorant of these ingredients that another generation of children is at risk of getting sicker and sicker.  

Dr. Theresa Deisher has recently suggested there is also another possible mechanism for vaccine-induced autism: the aborted fetal tissue used in vaccine development. Many studies have noted a strong correlation between autism and de novo mutations (new genetic mutations). These genetic mutations or changes in the DNA suddenly show up anew in the autistic child and are not present in ​either parent's DNA. Hundreds of mutations have been identified in over 1,000 autistic individuals. Dr. Deisher believes these mutations are linked directly to the presence of contaminant DNA in vaccines which use aborted fetal cells. A study published in 2013 demonstrated that doses as low as 1.9 ng/mL of foreign DNA were sufficient to cause gene modifications in the recipient's DNA. 

This new DNA is being inserted into the host's DNA, resulting in these de novo mutations. Vaccines made using aborted fetal cells are the source of this foreign DNA. The DNA from fetal cells cannot be purified out of the final vaccination and remain as a contaminant. The contaminated DNA can be as high as 350 ng/mL which is over 180 times the genetic threshold for gene mutation! Since the contaminating DNA is human DNA (not animal), it is readily assimilated into the DNA of the vaccine recipient and creates genetic mutations. Thus, the genetic makeup of the recipient is no longer just based on their own mother and father, but now includes the DNA of a third individual, the aborted fetal baby. 

It is well known that retrovirus contaminants exist in the MMR vaccine. Such viruses are able to reverse transcript or insert foreign DNA into the individual's genome. This is a form of genetic engineering the vaccine recipient is unaware of and the ramifications can be quite serious. Autism, cancer, autoimmune, degenerative, and neurodenerative diseases are all possible results associated with foreign DNA genetic mutations.

The following vaccines on the CDC's recommended schedule are made using aborted fetal cell lines: chickenpox (Varivax and Varilrix), hepatitis A (Vaqta, Havrix, Avaxim, Epaxal), hepatitis A & B (Twinrix), measles/mumps/rubella (MMR, Priorix), measles/rubella (MR, Vax, Eolarix), mumps/rubella (Biavax II), rubella (Meruvax II), measles/mumps/rubella/chickenpox (ProQuad/MMR-V, Priorix Tetra) polio (Poliovax, DT PolADs, Polio Sabin), DTaP/polio/Hib (Pentacel, Quadracel, Infanrix-IPV-Hib), and a number of the candidates for the SARS-CoV-2 vaccine like those produced by Johnson & Johnson, Moderna, AstraZeneca, Beijing Institute of Biotechnology, and Inovio Pharmaceuticals.

To get a good handle on key components for strengthening immune function see my book, There's An Elephant in the Room--Exposing Hidden Truths in the Science of Health. Hope for avoiding the toxic contaminants and foreign DNA found in these vaccines lies in knowing the risks. We need to trust and allow our immune systems to do the job they were designed and created to do.