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."
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'
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
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."
SEE RECENT ARTICLE:
"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!
HEAR TESTIMONIES AGAINST FORCED VAX BILL HB 1312 BY COLORADO PARENTS. HEARTBREAKING!