One of the problems scientists tried to solve when developing vaccinations was how to weaken a virus so that it wouldn’t hurt or kill humans but it would still be strong enough to initiate an effective immune response. They discovered that viruses often become more benign when they jump between species. They began to pass viruses through other tissue to weaken them. Max Theiler won a Nobel Prize for developing a yellow fever vaccine by passing the virus through mouse brain tissue. Unfortunately, in the process the vaccine can pick up unknown latent viruses from the mouse that may prove deadly to humans. Polio vaccines used between 1955 and 1963 were contaminated with a virus called simian virus 40 (SV40). It was picked up from monkey kidney cells used to grow the vaccine. Today it is suspected of causing non-Hodgkin lymphoma (NHL) in 50% of all U.S. patients.
An unknown fact most people are unaware of is that some vaccines are grown in aborted fetal tissue. Varicella, rubella, and hepatitis A vaccines involve growing the viruses in “human cell culture.” Two aborted fetuses from the 1960s provide the human cell lines needed to produce these vaccines. Most people are never informed by their doctor that this is the case. It seems unethical to withhold this information. A vegan would demand the right to know that the food they were offered contained meat. Shouldn’t people who are for or against abortions have a right to know they are being injected with a substance grown via an aborted fetus?
Dr. Theresa Deisher, founder and Chief Scientist at Sound Choice Pharmaceutical Institute, received her doctorate in Molecular and Cellular Physiology from Stanford in 1990 and has extensive experience in the drug and biotechnology industry. She wrote an open letter to legislators on April 8, 2019 regarding fetal DNA contaminants in the Measles-Mumps-Rubella vaccine. Merck’s MMR II vaccine (and chickenpox, Pentacel, and all Hep-A containing vaccines) are manufactured using human fetal cell lines which are heavily contaminated with human fetal DNA from the production process. Levels in our children can reach up to 5 ng/ml after vaccination, depending on the age, weight and blood volume of the child. That level is known to activate Toll-like receptor 9 (TLR9—a glycoprotein) which can result in autoimmune attacks.
She describes the power of fetal DNA using an example everyone is familiar with. When a certain amount of fetal DNA accumulates in a pregnant mother, labor starts and triggers a “massive immune rejection” of the baby. This is a natural process we call labor and delivery. The same level of fetal DNA fragments causing labor are contained in these vaccines! If fetal DNA can trigger labor (a naturally desired autoimmune reaction), then those same levels in vaccines can cause autoimmune reactions within a vaccinated child. Fragments are 215- 300 base pairs in length and blood levels reach 0.46-5.08 ng/ml. These levels were previously claimed to be ‘low, innocuous amounts’–nothing to worry about. But science has now proven that statement is absolutely false. That level of fetal DNA fragments represent a very strong pro-inflammatory trigger.
Children with autism have antibodies against human DNA in their circulation that non-autistic children do not have. This research now establishes a clear link between vaccines grown in aborted fetal tissue and those antibodies. A study conducted at Duke University demonstrated autism was not due to genetic issues. It had to be environmental. They treated autistic children with “banked autologous cord blood” and observed significant improvements in their behaviors. This was the blood saved from their birth placenta. Because their original blood helped cure them, it proved that something had happened to them since their birth–some environmental cause (not genetic) had happened to them. Is it just coincidence that the FDA approved the manufacturing switch for rubella virus from animal cells (duck embryo) to aborted human fetal cells (WI-38) in 1979? Prior to 1980 autism was very rare. Afterwards, autism began to skyrocket. It continues today on an exponential growth curve. The rubella portion of the MMR vaccine contains 175 ngs of human derived fetal DNA contaminants which is more than ten times the World Health Organization (WHO) threshold of 10 ngs per dose. The FDA never conducted toxicity profiling on the MMR vaccine and is, therefore, clueless about these hazards. No other drug has ever been permitted to enter the market without this type of testing.
Scientists know that injecting foreign fetal human DNA causes DNA mutations. The human body can incorporate that foreign DNA resulting in DNA mutations in the injected child. These mutations are a known cause of cancer and autoimmune diseases. Amounts as low as 1.9 ng/ml were proven to cause DNA mutation in 100% of mice injected. Merck vaccines reach levels well above 1.9 ng/ml.
In addition, retrovirus contamination is another huge problem. Human endogenous retrovirus K (HERVK) is a known contaminant in MMR vaccine. This retrovirus can reactivate within humans and transcribe its DNA into the host DNA. HERVK codes for a protein (integrase) which specializes in integrating DNA into the human genome. This just adds fuel to the fire as HERVK is associated with several known autoimmune diseases. It is no wonder that autoimmune diseases have increased in number over the same time period.
Dr. Deisher recommends that at a minimum the U.S. switch back to a rubella vaccine derived from animal cell lines. This was done in Japan because of concerns about the Merck combination MMR. Using single, separate doses of MMR (not the combination vaccine) still offers people vaccine protection but without the risk of aborted fetal cell contamination. Of course, the problem will be fighting Merck who has the patent on the combination MMR and not the single dose version. Merck will try to bury this science. If they succeed, you will know that money and profit won out again over vaccine safety. This is exactly what happened to Dr. Andrew Wakefield in Britain when he proposed British parents opt out for the single dose MMR instead of the combination MMR. Maybe it will be different this time. We can only hope Dr. Deisher doesn’t get Wakefielded. For more information on vaccines, see my book, There’s An Elephant in the Room–Exposing Hidden Truths in the Science of Health.
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