FETAL CELL USE IS ENFORCED SATANIC RITUAL MASS HUMAN SACRIFICE
Food and beverages, alcohol, GMO government produced medical marijuana cannabis, vape flavourings, drugs and medical products, perfumes, skin care, vaccines… most consumer products now contain live abortion-harvested human fetal cells. Unlike the human fat soaps and skin lampshades crafted from Nazi World War II concentration camp victims, the modern use of people is a multidisciplinary corporate enterprise, not visible to the human eye, or easily determined by reading product labels or online research: a clandestine agenda of mass satanic ritual abuse referred to in the Torah as “opening the matrix”, and is “the abomination in the temple”.
Fetal Parts in Daily Life
One might be committed to pro-life issues on every level, decry abortion and Planned Parenthood, yet through the use of food, drugs and products may be unwittingly cooperating in aborted fetal cell research by purchasing products that use aborted fetuses, either in the product itself or in its development.
A “Jane and John Doe” case in point: Jane takes Enbrel (Amgen) to relieve Rheumatoid Arthritis, and her husband John was given Zoastavax (Merck), a Shingles vaccine, at his annual physical. John’s mother with Type 2 Diabetes and kidney failure is prescribed Arensep (Amgen). Jane’s grandfather is given the blood product Repro (Eli Lilly) during an angioplasty. The local school district requires that their grandchildren receive the MMRII (the Merck Measles-Mumps-Rubella vaccine) before they are allowed to begin kindergarten. The entire family enjoys cookies, chocolates and flavoured coffee creamers and eats canned soups with artificial flavor enhancers (Senomyx/Firmenich) tested on artificial taste buds engineered from aborted fetal cells.
Because of the veiled trickery of Food and Drug Administration labeling, unless one has a background in chemistry and is proficient at reading pharmaceutical inserts as well as researching patents, it would be impossible to know that they were practicing human cannibalism on a daily basis – themselves and everyone they know! Without being expressly informed, consumer awareness of aborted fetal part use and ingestion is impossible.
The watchdog group Children of God for Life (COG), a pro-life public citizen group which tracks the use of aborted fetal parts. Under the leadership of Executive Director Debi Vinnedge, COG publishes a downloadable list of products that use aborted fetuses currently available in the U.S.
Products related to fetal material can be broken down into roughly three categories: ‘natural flavors’, daily use products and cosmetics, medicines (OTC as well as prescription) and vaccines
Food and Drink
The most opportunized disinformation tactic of the cabal’s governmental regulatory agencies is that food and beverages do not directly contain whole aborted fetal material, yet brutally murdered live-harvested babies are being used to affect both product performance, flavor and tastebud reactions. What biochemical slight of hand is this?
It has a technical term: INTENSATES
The American biotech company Senomyx developed chemical additives which enhance flavor and smell, the combination of which is taste. This is enabled by the laboratory fabrication of artificially formulated flavor receptors engineered from human embryonic kidney cells which can be identified by the designation HEK 293, from a fetal cell line popular in pharmaceutical research).1 These artificial taste buds can tell product developers which products the public will crave. The goal is to do a taste bud “sleight of hand,” creating low-sugar and low-sodium products that taste sweet or salty while actually using less sugar or sodium in the product.
The laboratory-created artificial enhancers do not have to be tested at length by the FDA because the Senomyx chemical “flavor compounds are used in proportions less than one part per million” and can be classified as artificial flavors.
In 2005, Senomyx had contracts to develop products for Kraft Foods, Nestle, Campbell Soup and Coca-Cola.2 However, when it was discovered in 2011 that PepsiCo was using Senomyx to develop a reduced sugar beverage, a boycott ensued that caused Kraft-Cadbury Adams LLC and Campbell Soup to cancel their contracts with Senomyx. In a 2012 letter to Children of God for Life, PepsiCo stated, “Senomyx does not use HEK cells or any other tissues or cell lines derived from human embryos or fetuses for research performed on behalf of PepsiCo.” To that effect, PepsiCo is working with Senomyx on two products developed with Sweetmyx 617, a new Senomyx sweet taste modifier. However, since this is an unregulated industry, who can believe anything these corporations state? Their agendas are dictated by the same top of the pyramid which gave humanity The Georgia Guidstones, Agenda 21, Agenda 2030, Agenda 2050, Operation Nano Domestic Quell, Operation Lockstep and Event 201, and the Eugenics depopulation agenda known as Planned Parenthood. Mind you the companies producing the most carcinocenic pesticides also produce the chemotherapy agents, a revolving door of profits from their governmentally-regulated death
In November 2018, the Swiss company Firmenich acquired Senomyx, Inc. Firmenich describes itself as “a global leader in taste innovation and expert in sweet, cooling and bitter solutions.”
Cosmetics: The fountain of youth comes from murdered babies.
Commercially, it’s known as Processed Skin Proteins (PSP), developed at the University of Lausanne to heal burns and wounds by regenerating traumatized skin. The fetal skin cell line was taken from an electively aborted baby whose body was donated to the university.
Neocutis, a San Francisco-based firm, was one of the first U.S.-based companies to use PSP in some of their anti-aging skin products. Their website claims the trademarked PSP “harnesses the power of Human Growth Factors, Interleukins and other Cytokines, to help deliver state-of-the-art skin revitalization.” Now it’s ubiquitous. And for the elite, bathing in human blood and drinking adrenochrome are ubiquitous too. It’s not a new thing, social media and memes have made this common knowledge.
Vaccines and Medicine: we now have human DNA in our vaccines and our drugs.
The Vaccine Card at the Sound Choice Pharmaceutical Institute (SCPI) website lists over 21 vaccines and medical products that contain aborted fetal cell lines. The Card is updated yearly, and also lists ethical vaccine alternatives when there are any. The morality of using these vaccines is a complicated issue; see this article for more detailed information.
SCPI is a biomedical research organization headed by Theresa Deisher, who has a PhD in Molecular and Cellular Physiology from Stanford, and holds 23 patents in the field to her name. Dr. Deisher, the first person to identify and patent stem cells from the adult heart, has an insiders understanding of genetic engineering having worked in the industry leaders such as Amgen, Genetech, and Repligen.3 Among other things SCPI “promotes awareness about the widespread use of fetal human material in drug discovery, development and commercialization.” No vaccine product is completely pure: “You will find contaminating DNA and cellular debris from the production cell in your final product. When we switch from using animal cells to using human cells we now have human DNA in our vaccines and our drugs.”3 The problem is three-fold. Aborted fetal parts are used for experiments, aborted fetal cell lines are used, and fetal cellular DNA debris are in vaccines and medicines. But it is not just human DNA that is left over, so are some of the chemical stabilizers that keep the product from degrading, as well as, stimulants to rev up the immune system.
Vaccines are a virus that have been put into a vial, in a liquid, which is the buffer, which we call excipients, and companies have put in stabilizers so that the virus won’t degrade and other things that kind of rev up your immune system so that they can use lower amounts of the virus and have a greater profit margin. And immune stimulants are things like aluminum and thimerosal, they are stabilizers but they rev up the immunes system, so all of these things are in the final product, including contaminates from the cell lines that are used to manufacture the vaccines.4
Why aren’t the contaminates removed? Because nobody wants a pediatric vaccine that costs a few thousand dollars.5 In finance, the yield is inversely related to the price. In chemistry, the yield is inversely related to purity. The price of inexpensive mass-produced vaccines is that the medical establishment accepts that the vaccines contain a high amount of fetal contaminates.
If they have purified out the containments from the cell lines, the yield would be so low that they wouldn’t make any money, or no one would pay a thousand dollars or ten thousand dollars for a vaccine. And so because of that case remnants from the cell lines, in that case, fetal cell lines are in the final product. And they are at actually very high levels. And in the chicken pox, the fetal DNA contaminates are present at twice the levels of the active ingredient which is Varicella DNA.4
The Fetal Tissue Marketplace: most research is done with fetal cells.
We know this because, for one, there’s a market for fetal parts. In a series of undercover videos, David Daleiden of The Center for Medical Progress exposed Planned Parenthood abortion clinics selling fetal parts to investigators posing as and medical researchers. And for his efforts his office was raided in 2016 by then California Attorney General Kamala Harris, now a Senator.6 Daleiden is currently being pursued in court by current California Attorney General, and former Democrat California Congressman, Xavier Becerra.
We already knew this was happening from the testimony of scientists themselves. On January 11, 2018, professor emeritus Dr. Stanley Plotkin, the lead developer of the Rubella vaccine for the Wistar Institute (Philadelphia) in the 1960s, was deposed as an expert witness on Vaccinology in a Michigan child custody case. Dr. Plotkin was asked how many aborted fetuses he has used in his experiments:
QUESTION: So in your, in all of your work related to vaccines throughout your whole career, you’ve only ever worked with two fetuses?
PLOTKIN: In terms of making vaccines, yes.
But after being presented with Exhibit 41 (Proceedings of the Society of Experimental Biology and Medicine), the two fetuses involved in his experiment grows exponentially to 76 aborted fetuses.
QUESTION: So this study involved 74 fetuses, correct?
QUESTION: And these fetuses were all three months or older when aborted, correct? PLOTKIN: Yes.
A true enough response. Fetal cells, for that matter all normal cells, have a finite capacity to replicate following the principle of cellular aging. The vaccine trail needed many cell lines in order to achieve its end. An interesting aside: during questioning Dr. Plotkin answered affirmatively that some of his subjects for experimental vaccine trials had been children of “mothers in prison,” the mentally ill, and “individuals under colonial rule” [Belgian Congo].
Dr. Theresa Deisher first became aware of the introduction of fresh aborted fetal material in drug discovery in 1996. Fresh fetal parts are a time-saver compared to the days spent washing and prepping animal tissue, like monkey hearts, for laboratory experiments. While it is not legal to sell aborted fetal tissue, it is still available in catalogues and comes with high prices for shipping and handling.
Stem cells are the unused better option
According to Dr. David A. Prentice Vice, President of the Charlotte Lozier Institute and Adjunct Professor of Molecular Genetics at the John Paul II Institute, adult stem cells are the benchmark for research that has led to actual cures for patients: “The superiority of adult stem cells in the clinic and the mounting evidence supporting their effectiveness in regeneration and repair make adult stem cells the gold standard of stem cells for patients.”
Then why are we still using embryonic cell lines when adult stem cells have become the ‘gold standard’? There seems to be little excuse for products that use aborted fetuses.
U.S. Policy on products containing aborted fetuses
On the 20th Anniversary of Roe v. Wade in 1993, President Clinton signed five abortion-related memorandums which included the reversal of the George H. W. Bush era moratorium on creating new fetal tissue for research, claiming at the time, “This moratorium has significantly hampered the development of possible treatments for individuals afflicted with serious diseases and disorders, such as Parkinson’s disease, Alzheimer’s disease, diabetes and leukemia.”
While a bio-ethics debate transfixed the country in 2006 as to whether the United States would allow the use of new aborted fetal stem cells in research [see White House Fact Sheet on Stem Cell Research Policy], the medical research community had already decided that the future lay with human-animal hybrids and new aborted fetal cell lines. According to a statement submitted to the President’s Bioethics Council:
Aborted human DNA in our vaccines is not the end, it is only the beginning, as the creation of human-animal hybrids demonstrates. A new aborted fetal cell line has been developed, called PerC6, and licenses have been taken by over 50 partners, including the NIH and the Walter Reed Army Institute, to use this cell line for new vaccine and biologics production. The goal of the company that created the PerC6 is to become the production cell line for ALL vaccines, therapeutics antibodies, biologic drugs and gene therapy.3
 Melanie Warner, “Pepsi’s Bizarro World: Boycotted Over Embryonic Cells Linked to Lo-Cal Soda.” CBS News Moneywatch. June 3, 2011.
 Melanie Warner, “Food Companies Test Flavorings That Can Mimic Sugar, Salt or MSG.” New York Times. April 6, 2005.
 Theresa A. Deisher, PhD. “Testimony on Conscience Rights Related to Biologic Drug Disclosure and Alternative Drugs.” President’s Council on Bioethics Archive. Georgetown University. September 8, 2008.
 “Dr. Theresa Deisher Guelph, Ontario Canada June 23, 2018.” Vaccine Choice Canada published on YouTube. August 2, 2018.
 The National Vaccine Injury Act was signed in 1986 so that manufactures wouldn’t raise the price of vaccines due to injury lawsuits. Robert Pear, “Reagan Signs Bill on Drug Exports and Payment for Vaccine Injuries.” New York Times. November 15, 1986.
 Paige St. John. “Kamala Harris’ support for Planned Parenthood draws fire after raid on anti-abortion activist.” Los Angeles Times. April 7, 2016.
“King of Vaccines Comes Clean!” The HighWire with Del Bigtree. Youtube. Published January 17, 2009.
Andrea Byrnes, “Products that use aborted fetuses”, April 23, 2019.