READ THE BILL: The Colorado Vaccine Bill To Mandate Full CDC Schedule Passes Out of Committee https://www.ageofautism.com/2019/04/the-colorado-vaccine-bill-to-mandate-full-cdc-schedule.html
Yes, you heard that correctly.
If abortion became illegal, the current FULL CDC childhood vaccination schedule (which HB 1312 would mandate) would be IMPOSSIBLE to fill.
The original vaccine was a LIVING organism. Many still are. They need a home and food to multiply, JUST LIKE YOU AND ME. The laboratory virus' home is called a "petri dish medium." In the early '50's, "vaccinology" was primitive, and most of the ad hoc techniques were fueled by the government's biowarfare department. Time was of the essence to develop certain vaccines. Originally, cells taken from the organs of Rhesus monkeys ( and later African Green monkeys) became the "petri dish medium" to grow the polio virus in. OOPS! The Rhesus cells were contaminted by numerous Simian Viruses originally thought to only infect monkeys, NOT humans. Unfortunately, SV40, one of them, was found to be CARCINOGENIC in mice and SV40 has been identified in human brain and lung cancers ("SV40 and Cancer" https://www.nvic.org/nvic-archives/testimony/testimonyspetember102003.aspx ) If you had the sugar cube polio vaccine up to 1963, your body might harbor SV40 in tumors.
If you can't grow viruses safely in monkey cells, what can you use? Unborn baby tissue. Fibroblast cells. Now called "Human diploid cell strains" (HDCSs).
According to leading vaccine shill and vaccine patent owner Dr. Paul Offit, who reviewed the following:
"Varicella (chickenpox), rubella (the “R” in the MMR vaccine), hepatitis A, one version of the shingles vaccine, and one preparation of rabies vaccine are all made by growing the viruses in fetal embryo fibroblast cells. Fibroblast cells are the cells needed to hold skin and other connective tissue together. The fetal embryo fibroblast cells used to grow vaccine viruses were first obtained from ELECTIVE TERMINATION (emph. mine) of two pregnancies in the early 1960s. These same embryonic cells obtained from the early 1960s have continued to grow in the laboratory and are used to make vaccines today. No further sources of fetal cells are needed to make these vaccines. (Comment: THIS HAS NOT BEEN PROVEN TO THE PUBLIC. Cell lines evolve and change. This is why Merck is being sued by 2 of its own scientists. They claim the Jeryl Lynn mumps virus strain has evolved and weakened since it was licensed in the '60's. "Former Merck Scientists Sue Merck Alleging MMR Vaccine Efficacy Fraud" https://ahrp.org/former-merck-scientists-sue-merck-alleging-mmr-vaccine-efficacy-fraud/)
The reasons that fetal cells were originally used included:
Viruses need cells to grow and tend to grow better in cells from humans than animals (because they infect humans).
Almost all cells die after they have divided a certain number of times; scientifically, this number is known as the Hayflick limit, and for most cell lines it is around 50 divisions; however, fetal cells can go through many more divisions before DYING. (EMPH. MINE)
As scientists studied these viruses in the lab, they found that the best cells to use were the fetal cells mentioned above. When it was time to make a vaccine, they continued growing the viruses in the cells that worked best during these earlier studies."
https://www.chop.edu/centers-programs/vaccine-education-center/vaccine-ingredients/fetal-tissues
SOUNDS LIKE THE CELL LINES WOULD DIE OUT.
Vaccine King Dr. Stanley Plotkin was directly involved with working on aborted babies' tissue to create a "suitable, safe medium" to grow the viruses in.
HERE IS HIS DRAMATIC SWORN TESTIMONY:
"Stanley Plotkin - abortions for vaccines - 2018 deposition'
https://www.youtube.com/watch?v=PN7FQCkiBp8
MORE:
If you want to know the true history of modern vaccines, watch the 9 videos of top vaccine expert and inventor Dr. Stanley Plotkin's SWORN testimony. He wasn't expecting a 9 hour "discovery" under oath. Watch his expression and hand gestures. If you watch beginning to end in order, it all falls into place. You will also get to see a HIGHLY SKILLED attorney in action. He is BRILLIANT:
"Stanley Plotkin, Godfather of vaccines, UNDER OATH! - Part 1/9" https://www.youtube.com/watch?v=rGDNsqk0KR0YouTube
"Dr. Plotkin, who was an instrumental figure in the development of rubella, polio, rabies, varicella, rotavirus, anthrax, and other vaccines, traces the serendipitous beginnings of vaccinology in the 1700s to its flowering in the latter half of the 20th century. Additionally, he highlights the relationship of vaccinology to industrial and technological developments, as well as the special role of Philadelphia institutions and researchers in vaccine development. Especially interesting is a description of an exchange with Albert B. Sabin, MD, at a scientific meeting in the late 1960s, when Sabin objected to Plotkin's (and others') use of cell lines derived from human fetal tissue. Plotkin replied, "I must say that despite my great and sincere respect for Dr. Sabin, I think the statements he has made are strictly ex cathedra and without a factual basis. So my conclusion is that what we are dealing with here is theology, and you see, in theology it is very difficult to disprove the existence of ghosts. But this is not, to my mind, a basis for making intellectual decisions."" https://www.historyofvaccines.org/content/blog/video-four-centuries-vaccinology-stanley-plotkin-md
CDC/ SV40 contaminated vaccines
http://www.freerepublic.com/focus/f-news/1346894/posts
UPDATE: Will China's new HDCS, Walvax-2 be a potential replacement/competition for America's 1966 era MRC-5 Human haploid cell strain?
"We have developed a new HDCS, Walvax-2, which we derived from the lung tissue of a 3-month-old fetus. We established primary, master and working cell banks successfully from reconstituted frozen cells. Observations during the concurrent propagation of Walvax-2 and MRC-5 cells revealed differences in terms of growth rate, cell viability and viral sensitivities. Specifically, Walvax-2 cells replicated more rapidly than MRC-5 cells, with Walvax-2 cells attaining the same degree of confluence in 48 hours as was reached by MRC-5 cells in 72 hours. Moreover, Walvax-2 cells attained 58 passages of cell doublings whereas MRC-5 reached 48 passages during this period. We also assessed the susceptibility of these cells to rabies, hepatitis A, and Varicella viruses. Analysis of virus titers showed the Walvax-2 cells to be equal or superior to MRC-5 cells for cultivating these viruses."
https://www.ncbi.nlm.nih.gov/pubmed/25803132
SEE RECENT ARTICLE:
"New Fetal Cell Line from Live Abortion Emerges for Vaccine Production"
http://vaccineimpact.com/2015/new-fetal-cell-line-from-live-abortion-emerges-for-vaccine-production/
PROOF Edward Jenner, father of small pox vaccine, was an OPPORTUNIST and a QUACK!
https://ia802302.us.archive.org/34/items/storyofgreatdelu00whitrich/storyofgreatdelu00whitrich.pdf
HEAR TESTIMONIES AGAINST FORCED VAX BILL HB 1312 BY COLORADO PARENTS. HEARTBREAKING!
http://coloradoga.granicus.com/MediaPlayer.php?view_id=117&clip_id=14013
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[–] septimasexta [S] ago
Thank you Ginger Taylor, MS for standing against a forced vaccination bill in Maine! Ginger sent every member of the Maine Legislature this letter:
Dear Representative,
The religious and philosophical vaccine exemptions exist for very good reason.
There is a vaccine conversation that is upsetting for many, that must be had now. It is a discussion that the sponsors of vaccine exemption removal bills are unlikely to even know of, and is easily dismissed as internet rumor. I myself avoided this topic for the first 10 years of my 15 years of vaccine safety advocacy because I simply didn't want to face the reality of it. However, the topic is central to your deliberations on the removal of the religious and philosophical exemptions proposed by LD 798. Because some of those testifying on Wednesday will broach the subject, it is incumbent upon me to prepare you with the clinical facts at this time.
There are vaccines made with, and containing, materials that are morally and religiously objectionable to many Mainers. At the top of that list are the WI-38 and MRC-5 cell lines.
I have included the clinical information from the distributor on these two products in the links above. Please review the "General Information" carefully.
I am also including a video by Paul Offit of the Children's Hospital of Philadelphia, so that you may have confirmation on this matter from the principle vaccine industry spokesperson.
These WI-38 and MRC-5 cells are used to grow viruses in, and are destroyed in the manufacturing process, however the residual human blood products (human albumin) and DNA fragments remain in the final product as delivered. The passage of LD 798 will mandate the purchase and intake of these human derived products by Mainers who are vehemently opposed to this practice and who do not wish to do business with the industry that supplies these types of cell lines, in order to fully participate in society. (These cell lines have a shelf-life, so research into new cell lines, such as the new WALVAX-2, is ongoing.)
Further, there are other morally and religiously objectionable materials in vaccines that Mainers will be forced to inject to become educated Mainers. I have attached the full CDC vaccine ingredient list for your review.
As I am sure you can understand, many Mainers will find the use of bovine serum and porcine tissue religiously and ethically objectionable, and I hope you can agree that they have the right to refuse products using and containing human and animal biological material without coercion.
Because the MMR and Chickenpox vaccines contain all three of these substances, the purchase and injection of these objectionable materials will become required for full participation in public life. https://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf
"M-M-R ® II (MEASLES, MUMPS, and RUBELLA VIRUS VACCINE LIVE) DESCRIPTION M-M-R ® II (Measles, Mumps, and Rubella Virus Vaccine Live) is a live virus vaccine for vaccination against measles (rubeola), mumps, and rubella (German measles).
M-M-R II is a sterile lyophilized preparation of (1) ATTENUVAX® (Measles Virus Vaccine Live), a more attenuated line of measles virus, derived from Enders' attenuated Edmonston strain and propagated in chick embryo cell culture; (2) MUMPSVAX® (Mumps Virus Vaccine Live), the Jeryl Lynn™ (B level) strain of mumps virus propagated in chick embryo cell culture; and (3) MERUVAX® II (Rubella Virus Vaccine Live), the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts.{1,2}
The growth medium for measles and mumps is Medium 199 (a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum) containing SPGA (sucrose, phosphate, glutamate, and recombinant human albumin) as stabilizer and neomycin.
The growth medium for rubella is Minimum Essential Medium (MEM) [a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum] containing recombinant human albumin and neomycin. Sorbitol and hydrolyzed gelatin stabilizer are added to the individual virus harvests.
The cells, virus pools, and fetal bovine serum are all screened for the absence of adventitious agents.
The reconstituted vaccine is for subcutaneous administration. Each 0.5 mL dose contains not less than 1,000 TCID50 (tissue culture infectious doses) of measles virus; 12,500 TCID50 of mumps virus; and 1,000 TCID50 of rubella virus. Each dose of the vaccine is calculated to contain sorbitol (14.5 mg), sodium phosphate, sucrose (1.9 mg), sodium chloride, hydrolyzed gelatin (14.5 mg), recombinant human albumin (≤0.3 mg), fetal bovine serum (<1 ppm), other buffer and media ingredients and approximately 25 mcg of neomycin. The product contains no preservative." So a central question that will be posed is:
How do the sponsors of LD 798 justify removing First Amendment rights of Mainers to the free exercise of their religion by abstaining from the use of medical products made with WI-38, MRC-5, Bovine, Porcine and other objectionable materials?
These are just a few of the reasons that the removal of non-medical vaccine exemptions is unacceptable.
https://www.ageofautism.com/2019/04/a-difficult-discussion-wi-38-and-mrc-5.html