Posted on 06/29/2020 1:25:04 PM PDT by ransomnote
OPEN LETTER TO LEGISLATORS REGARDING FETAL CELL DNA IN VACCINES
April 8, 2019
My name is Dr. Theresa Deisher. I am Founder and Lead Scientist at Sound Choice Pharmaceutical Institute, whose mission is to educate the public about vaccine safety, as well as to pressure manufacturers to provide better and safer vaccines for the public. I obtained my doctorate from Stanford University in Molecular and Cellular Physiology in 1990 and completed my post-doctoral work at the University of Washington. My career has been spent in the commercial biotechnology industry, and I have done work from basic biological and drug discovery through clinical development.
I am writing regarding unrefuted scientific facts about fetal DNA contaminants in the Measles-Mumps-Rubella vaccine, which must be made known to lawmakers and the public.
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 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), which can cause autoimmune attacks.
To illustrate the autoimmune capability of very small amounts of fetal DNA, consider this: labor is triggered by fetal DNA from the baby that builds up in the mother’s bloodstream, triggering a massive immune rejection of the baby. This is labor.
It works like this: fetal DNA fragments[i] from a baby with about 300 base pairs in length are found in a pregnant mother’s serum. When they reach between 0.46– 5.08 ng/mL, they trigger labor via the TLR9 mechanism[ii]. The corresponding blood levels are 0.22 ng/ml and 3.12 ng/ml. The fetal DNA levels in a child after being injected with fetal-manufactured vaccines reach the same level that triggers autoimmune rejection of baby by mother.
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 human fetal (primitive) non-self DNA to a child could generate an immune response that would also cross-react with the child’s own DNA, since the contaminating DNA could have sections of overlap very similar to 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]
Duke University demonstrated in a recently conducted 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, or triggers, introduced to the world around 1980 when autism first began to rise, must be identified and eliminated or reduced in the environment.
Injecting our children with human fetal DNA contaminants bears the risk of causing two well-established pathologies:
1) Insertional mutagenesis: fetal human DNA incorporates into the child’s DNA causing mutations. Gene therapy using small fragment homologous recombination has demonstrated that as low as 1.9 ng/ml of DNA fragments results in insertion into the genome of stem cells in 100% of mice injected[xii]. The levels of human fetal DNA fragments in our children after vaccination with MMR, Varivax (chickenpox) or Hepatitis A containing vaccines reach levels beyond 1.9 ng/ml.
2) Autoimmune disease: fetal human DNA triggers a child’s immune system to attack his/her own body.
An additional concern: retrovirus contamination.
Human endogenous retrovirus K (HERVK) is a contaminant in the measles/mumps/rubella vaccine[xiii].
The presence of both the high level contaminating fetal DNA as well as the HERVK contamination in the MMR vaccine is an unstudied risk with huge implications and dangers for individual and public health.
Solution: Pressure manufacturers to switch back to animal cell line derived rubella vaccines as was successfully done in Japan:
The MMR vaccine manufacturing process needs to be changed to address and eliminate the above risks for the public.
Thank you for your consideration. I will be happy to address any questions you may have concerning the above.
Sincerely,
Theresa A. Deisher, Ph.D.
END NOTES
[i] Lo et al. Am J Hum Genet. 1998 Apr;62(4):768-75
[ii] Enninga et al. Front Immunol. 2015 Aug 26;6:424
[iii] Deisher et al. Issues Law Med. 2015 Spring;30(1):47-70
[iv] Mostafa et al. 2014, J Neuroimmunol , Vol. 272, pp. 94–98; Mostafa et al. 2015, J Neuroimmunol , Vol. 280, pp. 16–20
[v] Dawson et al. Stem Cells Transl Med. 2017 May;6(5):1332-1339
[vi] Deisher et al. Issues Law Med, 2015 Vol. 30, pp. 25-46
[vii] https://www.cdc.gov/vaccines/pubs/pinkbook/rubella.html; Plotkin, SA. 2006, Clinical Infectious Diseases, Vol. 43, pp. S164–168;
[viii] https://www.cdc.gov/ncbddd/autism/data.html
[ix] Sebat et al. 2007, Science., Vol. 316, pp. 445-449; Sanders et al. 2011, Neuron, Vol. 70, pp. 863-885
[x] Series, WHO Technical Report. WHO EXPERT COMMITTEE ON BIOLOGICAL STANDARDIZATION 941; Deisher et al. Issues Law Med. 2015 Spring;30(1):47-70
[xi] Kramberger et al. Hum Vaccin Immunother. 2015;11(4):1010-21.
[xii] McNeer, N A et al. “Systemic delivery of triplex-forming PNA and donor DNA by nanoparticles mediates site-specific genome editing of human hematopoietic cells in vivo.” Gene therapy vol. 20,6 (2012): 658-69. doi:10.1038/gt.2012.82
[xiii] Victoria et al. J Virol. 2010, Vol. 84, pp. 6033-6040
[xiv] Lee et al. PLoS Pathog. 2007 3(1):e10; Dewannieux et al. Biologicals, Vol. 38, pp. 366-70
[xv] Taietal.9,Nov2008, Mult Scler, Vol. 14, pp. 1175-80; Dickerson et al. 2008, Schizophr Res. 2008 Sep;104(1-3):121-6, Vol. 104, pp. 121-6
[xvi] Hacein-Bey-Abina et al. J Clin Invest. 2008 Sep;118(9):3132-42
[xvii] Jpn J Infect Dis. 2016 May 20;69(3):221-3
+1
This is so creepy. I had also read several articles years ago that one of the worst side effects of the use of fetal stem cells was the causation of cancer. All fetal cells are programmed to reproduce vastly more rapidly than in babies, children and adults. I think that one article indicated that if a child continued to grow after birth at the same rate as the last month of gestation, the child would be something like 40’ tall. That is how fast cells need to reproduce to develop from a single cell to a 7 lb. baby in only 9 months.
That over production is a characteristic of cancer, uncontrolled cell reproduction. I’m wondering if the mmr vaccination has any relation to the incidence of cancer in children.
But if you are skeptical of vaccines you are automatically a conspiracy theorist. Furthermore if you are skeptical of vaccines, you are only concerned with yourself, hate humanity and want everyone to die.
Never mind that these vaccines may very well be killing us and our children.....
yup no good posting it here
the people here that are for vaccines don’t care if they hurt or kill you
they want you to take vaccines because it makes them feel better and safer and to hell with your own personal madical choices or you health, or your life
they’ve said it and admitted it, thats why they want you taking the vaccines - for THEM, NOT YOU
And youmsick phucks here who think that know who you are
The counter argument is;
$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$$
Now STFU!
At a glance, this is HUGE. Does it also explain the enormous uptick in allergies in kids?
Yes it does
And why my son was almost killed by MMR vaccine
Great point!
For the godless, babies (rather than Jesus Christ) have to die for them to live.
Thanks Ransomnote. I was able to download it, copy it and send it in a text to my dd so I could have a copy.
PING ME....saved for later...Great find, thank you
Bump
I read that Moderna DOES use aborted fetal cells on
https://cogforlife.org/
Here’s a website which will show you ethical vaccines:
https://cogforlife.org/ You can call them each year to find out if the flu vaccine is ethical. I checked with them a couple of times, and the flu vaccine WAS ethical those years. (Hopefully it always is.)
Moderna and Johnson and Johnson are two that use unethical vaccines for coronavirus. (But then Johnson and Johnson is bad news on many fronts.)
I was doing some reading on that matter. Wow! Chickenpox, Shingles, Hepatitis A, Rubella and other vaccines were also developed from cells from two fetuses in the early 1960s!
Sanofi Pasteur is using DNA from the cells of insects! Imagine what that could do to people!
And this, from the Vatican Pontifical Academy for Life in 2017 in favor of the fetal cell vaccines.
“In the past, vaccines had been prepared using cells from aborted human fetuses, however currently used cell lines are very distant from the original abortions ... today it is no longer necessary to obtain cells from new voluntary abortions, and that the cell lines on which the vaccines are based in are derived solely from two fetuses originally aborted in the 1960’s.”
What is the world coming to?
In regards to the bug cells, Sanofi Pasteur bought Protein Sciences and continued its work with those cells. Reminds me of the old movie, “The Fly.”
https://en.wikipedia.org/wiki/The_Fly_(1958_film)
At least there are ethical vaccines for some diseases, and https://cogforlife.org/ tells us the ethical ones. If you can’t readily find an ethical vaccine for a disease you might be interested in, you can always call them at the phone # on their website.
That statement from the Vatican Pontifical Academy for Life in 2017 also upset me. However, I am uplifted because bishops, and other pro-lifers, wrote a letter to the Health Dept. that it is disrespectful, etc. to use even old aborted fetuses. I’ll try to find the letter.
Personally, it gives me the creeps.
I did read something from years ago, that said if you can’t find an ethical vaccine, it is OK to use it, but you must first try to find an ethical one. Can’t remember it all, because I read this so long ago.
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