Dr. Theresa Deisher received her Ph.D. in Molecular and Cellular Physiology from Stanford University and has spent over 20 years in commercial biotechnology.
In her Open Letter to Legislators, she warns that vaccine products contain DNA fragments from fetal tissue that cannot be filtered out. Research conducted suggests that using foreign, human DNA fragments is having unintended consequences.
To illustrate the autoimmune capability of very small amounts of fetal DNA, consider this: labor in childbirth is triggered by fetal DNA from the baby that builds up in the mother’s bloodstream, triggering a massive immune rejection of the baby when it is time. This is [normal] labor. (source)(source)
Regarding DNA In MMR, Hep-A
Merck’s MMR II vaccine (as well as the chickenpox, Pentacel ,and all Hep-A containing vaccines) is manufactured using human fetal cell lines and are heavily contaminated from the production process [and are] known to activate Toll-like receptor 9 (TLR9), which cause autoimmune attacks.
Anyone who says that the fetal DNA contaminating our vaccines is harmless either does not know anything about immunity and Toll-like receptors or they are not telling the truth.
If fetal DNA can trigger labor (a naturally desired autoimmune reaction), then those same levels in vaccines can trigger autoimmunity in a child. Fragmented fetal DNA contained in vaccines is of similar size, ~215 base pairs.[iii]
This is direct biological evidence that fetal DNA contaminants in vaccines are not in low innocuous amounts. They are a very strong proinflammatory trigger.
Administration of fragments of non-self human fetal DNA to a child (as in shots), could generate an immune response that would also cross-react with the child’s own DNA.
Children with autistic disorder have antibodies against human DNA in their circulation that non-autistic children do not have. These antibodies may be involved in autoimmune attacks in autistic children.[iv]
It Appears, Children are Not Born with Autism
Duke University demonstrated in a recent study that significant improvements in behavior were observed when children with autism spectrum disorder were treated with their own banked autologous cord blood[v]. This treatment clearly shows that most children with autism are not born with it since genetic diseases like Down syndrome or muscular fibrosis cannot be treated with autologous stem cells. Therefore, an environmental trigger(s), introduced to the world around 1980 when autism first began to rise, must be identified and eliminated or reduced in the environment.
- Strong change-point correlation exists between rising autism rates and the vaccine manufacturing switch from animal-derived cell lines for rubella vaccine to human aborted cell lines in the late 70s[vi].
- The earliest change point for Autistic Disorder (AD) was preceded by a switch in the manufacturing process:
- In 1979, the FDA approved the manufacturing switch for the rubella virus from animal based (grown in duck embryo cells) to the human fetal cell line WI-38 using the RA27/3 virus strain[vii]. Both the newly approved monovalent rubella vaccine and the MMR vaccine utilize the WI-38 fetal cell line for manufacturing of the rubella portion.
Dr. Deisher testifies on the connection between vaccines and rising rates of autism…
Dr. Plotkin’s Admits aborted fetal tissue and DNA used to develop vaccs and in the ingredients
Dr. Stanley Plotkin, dubbed the “Godfather of Vaccines”, has contributed to the development of a number of vaccines during his long career. (source)
In the deposition below, you’ll hear Plotkin admit that 76 abortions took place in just a single study during the development of these vaccines. He confirms in his statement that these experiments involved tissue taken from the pituitary gland, lungs, skin, kidney, spleen, heart and other body parts of these healthy babies who were aborted (and other heinous admissions).
Below this video, there is a full outline of where in the video he admitted something that until now it was hard to verify!
Ex. 7:50:35 Did you use orphans and mentally retarded children to test an experimental disease?
Full 9 hour deposition under oath recorded on 1/11/18.
1:21:00 I don’t do it for the money
1:24:00 Would you remember if you were paid 6 million dollars?
2:44:00 Rotavirus conflict of interest
3:17:50 Is 5 days long enough to detect adverse reactions in this study? No control group in the study
3:20:00 Why such a long list of adverse reactions? 10+ minutes worth
3:32:00 There was no placebo group?
3:45:20 The package insert for MMR2
3:59:20 So within 3 years of vaccinating, every child in this country will experience a serious adverse event!
4:24:20 The GARDASIL/Saline Placebo Control
4:48:00 “Double-blind works if you want to be certain, but…”
5:33:00 Do vaccines cause autism?
5:43:00 Shouldn’t you wait until you know that vaccines do not cause autism?
6:05:00 We’ve been asking for 30 years
6:09:00 The only placebo vs. vaccine study results
7:05:30 What kind of antigens are in vaccines?
7:11:33 Calf serum, guinea pig cells, and cow’s milk
7:39:20 Does Alum bind to cells?
7:43:10 How many fetus’ have you worked with?
7:48:25 Aborted fetal tissue and DNA used in development and in the ingredients of vaccines
7:53:20 “Better to perform experiments on those less likely to contribute to society like mentally handicapped”
7:54:02 The letter to the editor of Ethics of Human Experimentation – “Its unlike Nazi philosophy”
7:56:00 The 1959 experiments on over 1 million people under Colonial Rule in the Congo, Leopoldville, Burundi
8:02:50 Do you take issues with Religious beliefs?
8:18:30 Are you asking me if I’m launching AIDS?!
8:31:00 How do you define an Anti-Vaxxer?
8:47:30 Harvard’s Study of VAERS Vaccine Adverse Events Reporting System finds less than 1% are reported
- Strabismus, Facial & Spinal Asymmetry Occurring Post-Vacc: Look For It
- What I’d Tell You Over Coffee If You Asked Why We Didn’t Vaccinate
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Thanks for reading!