‘This Week’ With Mary + Polly: You Can’t Sweep Deaths Under the Rug + Free Pot With Your COVID Shot? + More
In “This Week” with Mary Holland, Children’s Health Defense vice chair and general counsel, and Polly Tommey, co-producer of “Vaxxed,” Mary and Polly discuss the growing reports of injuries and deaths from COVID vaccines … and more.
Some “fantastic” news: Massachusetts rescinded its flu vaccine mandate. “This is the power of the courts.”
More exciting news: A group of scientists convinced the National Institutes of Health to no longer recommend against the use of Ivermectin to treat COVID. “It’s very exciting that this cheap, effective treatment is no longer being withheld from patients.”
A new peer-reviewed study from Stanford University says there’s no benefit to COVID lockdowns. “There are lawsuits against these in virtually every state.”
Despite a big push to get nursing home workers to get the COVID vaccine, some are pushing back. A Wisconsin nursing home said it will lay off employees who refuse the vaccine. “We believe any attempt for an employer to mandate a vaccine that hasn’t been licensed by the FDA is illegal. Under federal and state law, no one can be forced to participate in this experiment.”
The Telegraph reported that Germany’s eastern state of Saxony says it could put people who violate COVID quarantine rules in detention centers. “Human rights lawyers say this won’t fly, but we have to be very concerned about these detention centers.”
Forbes reported this week that a group calling itself “Joints for Jabs” is offering free marijuana as an incentive to get the COVID vaccine. “What I find most disturbing about this article is this quote: ‘If you believe in the science that supports medical cannabis, you should believe the science that supports the efficacy of the vaccine.’ Science isn’t something you ‘believe,’ it’s something that’s proven.”
If you see something disturbing, as in evidence of “quarantine camps” or attempts to bully people into getting the vaccine, or if you or someone you know experiences an adverse reaction, please contact CHD@childrenshealth.org. “These messages don’t go into a black hole, we react to all of them.”
Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. CHD is implementing many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured. Your support is essential to CHD’s successful mission.
(Please note that I have excerpted a good deal of the text which is available at the link below)
Sausage Making at FDA: How Human Cancer Cells Got Into Vaccines
In a 2012 meeting, the FDA voted to allow the use of human fetal cells and adult human tumor cells in vaccines, despite acknowledging the many risks, including that vaccine recipients might later develop cancer.
“If the American people knew some of the things that went on at the FDA, they’d never take anything but Bayer aspirin.” — Len Lutwalk, FDA scientist
“The FDA, by spinelessly knuckling under to every whim of the drug companies, has thrown away its high reputation, and in doing so, forfeited our trust.” — Drummond Rennie, deputy editor of JAMA
Vaccines and related biological products advisory committee today
Today — Thursday, Dec. 10 — the Vaccines and Related Biological Products Advisory Committee (VRBPAC), which is the U.S. Food and Drug Administration’s (FDA) internal panel that licenses new vaccines as “safe and effective,” will meet to consider Pfizer’s COVID vaccine. VRBAC will meet in one week, Dec. 17, to consider approval of the Moderna vaccine.
The damning safety studies in Pfizer’s late release clinical trial data dump, and the severe (life-threatening) allergic reactions that bedeviled the vaccine’s UK rollout, have raised red flags and public anxiety about the safety of the companies’ mRNA vaccines. Anthony Fauci has addressed growing skepticism about COVID vaccines and the Operation Warp Speed program, by reassuring the public that “VRBPAC” is an “independent panel of leading experts” whom the public can absolutely trust to assure vaccine safety.
How FDA originally approved use of fetal cells in vaccines
FDA allows both human fetal cells and adult human tumor cells in vaccines. Both types have cancer risks. While both Pfizer and Moderna tested their mRNA vaccine using fetal cells, there are no fetal cells, cell debris or DNA in their final products.
However, according to company documents, Johnson and Johnson (Janssen) and Altimmune’s COVID vaccines are manufactured in the human fetal cell line PER-C6, and thus the final vaccine products will contain cellular debris and DNA fragments from these cells. Researchers harvested these cell lines from the eyeball of an 18-week-old human fetus aborted in 1985, and then rendered them immortal by making them cancerous.
The AstraZeneca, Cansino, Gamayela, Vaxart, LongComm and Upitt vaccines are manufactured in the human fetal cell line HEK293, and thus the final vaccine products will contain cellular debris and DNA fragments from the fetal HEK-293 cell line. Scientists harvested this cell line from the kidney of a female Dutch fetus legally aborted in 1973 and then immortalized the cells by rendering them cancerous.
Normal primary cells, which are unable to replicate indefinitely, ultimately die. Immortalized cell lines are derived from known malignant cancer cells such as those obtained from Henrietta Lacks (HeLa) or created in the laboratory by introducing viral oncogenes or chemical exposures capable of mutating normal primary cells into immortal tumor cells.
According to FDA’s “The Pink Sheet” dated Nov. 29, 1999, for two decades the agency has been acutely aware of the inherent risks of using immortalized cell lines for vaccine development. The FDA CBER Director Dr. Peter Patriarca, M.D. explained that continuous cell lines are used for their ability to self-propagate, making them an ideal substrate on which to grow viruses, “the worst thing we are concerned about is … malignancy, because some of these continuous cells have the potential for growing tumors in laboratory animals.”
Patriarca further conceded that “the technology to make these vaccines actually exceeds the science and technology to understand how these vaccines work and to predict how they will work.” …
We call vaccines “biologics” because vaccinologists have traditionally grown their antigens on biological substrates — usually animal tissue. Competing companies culture COVID vaccines on a variety of animal strata. The Merck and IAVA COVID vaccines are manufactured in vero monkey cells, and thus contain cellular debris and DNA fragments from vero monkeys in the final product. The Sanofi, GSK, and Novavax COVID jabs are manufactured in insect cells and thus contain insect cellular debris and DNA fragments in the final products.
Public health advocates criticize the use of animal tissues in vaccines due to risks that they carry endogenous viruses, microbes, parasites and lack safety testing. (Plague of Corruption, Mikovits 2020). …
Researchers and regulatory agencies have worried for more than 50 years about the potential for injected DNA to cause cancer. …
Regulators have in the past predicted that the odds of that happening were less than 1 in a trillion. However, in early gene therapy trials this event did indeed occur in 4 of 9 boys, 1 of whom died from the leukemia the insertions caused.
But as corrupt as FDA is, the internal panels — VRBAC — that approve new vaccines make the rest of the agency look like a Sunday church picnic.
When Dr. Fauci, Paul Offit, Peter Hotez and Bill Gates tell you that you needn’t worry because FDA is the “gold standard” for vaccine safety and that the ultimate licensing decision will be made by an “independent panel of experts,” they are talking about VRBPAC. But VRBPAC is far from “independent.” It is not even comprised exclusively of public officials. Instead, it is populated by outside “experts” who are almost all pharmaceutical industry insiders.
In 2003, following a 3-year investigation, the United States Congress’s House Oversight Committee found VRBAC was completely dominated by the vaccine industry.
“Examples of Conflicts of Interest:
“For instance, 3 out of 5 FDA advisory committee (VRBPAC) members who voted to approve the rotavirus vaccine in December 1997 had financial ties to pharmaceutical companies that were developing different versions of the vaccine.
“One out of five voting members’ employer had a $9,586,000 contract for a rotavirus vaccine.
“One out of five voting members was the principal investigator for a Merck grant to develop a rotavirus vaccine.
“One out of five voting members received approximately $1 million from vaccine manufacturers toward vaccine development.”
Congressional investigators concluded that, “Altogether, four out of the five committee members had conflicts of interest that required waivers, and their recommendation for approval of the vaccine was unanimous.”
Here’s what happened at the 2012 FDA meeting on fetal cells
HHS acknowledges that the FDA and Centers for Disease Control committees that contract and review new vaccines have historically not used “evidence-based medicine.” To illustrate what this means, one only need read (below) the astonishing transcript of the 2012 panel that first approved the use of adult cancer tumor cells in vaccines.
This transcript shows what the public is never supposed to see: the behind-the-scenes sausage-making of federal vaccine approvals. Here, you will read for yourself how the “independent,” “gold standard” panelists entrusted with protecting your children made monumentally consequential decisions, not on evidence-based science, but by rolling the dice and taking what they knew was a horrendously risky bet on public health
In any other realm, this transcript would be proof of negligent homicide. … We are all lab rats in their high-risk population-wide experiment. At FDA’s vaccine division, that sort of reckless decision-making is routine.
In 2012, most live virus vaccines were from animal tissue and the idea of putting potentially cancerous tumor cells from adult “donors” in vaccines was still a daring and audacious gamble. That September, the FDA VRBPAC committee met to discuss this risky innovation. The transcript of that meeting — showing captive FDA officials considering a proposal by the pharma cabal to allow the use of human cancer cells (HeLa) to replace animal tissue in the manufacture of vaccines — is proof of reckless criminal conduct.
Unbelievably, FDA voted to allow pharmaceutical companies to produce vaccines using human cells without reviewing a single scientific study to determine if the outcome would be safe.
Before, I quoted some of the criminally reckless statements from the meeting directly. A more detailed account appears in this article.
This was a full meeting of FDA’s VRBPAC in 2012 to decide on the use of human tumor cell lines for the production of vaccines. I list these speakers and their titles at that time:
Dr. Philip Krause, Acting Deputy Director of OVRR (Office of Vaccine Research and Review) and FDA’s CBER (Center for Biologics Evaluation and Research). Also, Principal Investigator for Vaccine Safety: Virus Detection and Latency.
Dr. Doug Lowy, Director of the National Cancer Institute of the NIH.
Dr. Robert Daum, Chair of the VRBPAC.
Donald W. Jehn M.S., Designated Federal Officer for VRBPAC.
Keith Peden, PhD, Chief of LDNAV, DVP/OVRR/CBER.
Dr. Marion Gruber, Director of the FDA’s Office of Vaccines.
Dr. Nathanial Brady, a self-described clinician.
Dr. Pamela McInnes, a vaccine development expert and the Director of the Division of Extramural Research at the NIH’s National Institute of Dental and Craniofacial Research, and previously a Deputy Director under Anthony Fauci at the National Institute of Allergy and Infectious Diseases.
Pharma knew that their tumorigenic vaccines might cause tumors in recipients.
FDA officials knew that tumors might occur decades after vaccination.
FDA openly acknowledged that its primary objective was not to assure public safety but to help vaccine manufacturers.
FDA officials knew that they could not prove vaccine safety using test animals to assess oncogenicity.
FDA officials deliberately terminated animal safety tests too early in order to conceal consequences.
FDA decided to keep the tumor cell lines secret, because doctors and the public may be alarmed and say “Oh, my God!” if they knew the truth.
FDA decided to use deceptive language to convince doctors and the public that the vaccines were safe even when they, themselves, were unconvinced of safety.
FDA decided to hide information about their use of tumor cells and omit it from package inserts.
Health authorities were skeptical about safety of the tumor lines, but they decided to subject the public to the risk, so that they could perform a global population-wide live human experiment.
FDA officials opted to toss the dice, perform the population-wide human experiment, and learn about the risks as time goes by.
The committee formally approves the method of making vaccines from human cancer tumors.
Prior to voting to go forward, the committee made the following conclusions:
Making vaccines with cells that are directly derived from human cancer tumors is faster and cheaper than breeding animals for the culture media.
Millions of potentially cancer-causing vaccines will be produced.
The vaccines may possibly cause genetic mutations.
Millions of dollars will be made by vaccine promoters.
The health of millions of consumers may be jeopardized.
Information about how vaccines are made will be hidden from doctors and
The most significant scientific discovery since gravity has been hiding in plain sight for nearly a decade and its destructive potential to humanity is so enormous that the biggest war machine on the planet immediately deployed its vast resources to possess and control it, financing its research and development through agencies like the National Institutes of Health (NIH), the Defense Advanced Research Projects Agency (DARPA) and HHS’ BARDA.
The revolutionary breakthrough came to a Canadian scientist named Derek Rossi in 2010 purely by accident. The now-retired Harvard professor claimed in an interview with the National Post that he found a way to “reprogram” the molecules that carry the genetic instructions for cell development in the human body, not to mention all biological lifeforms.
These molecules are called ‘messenger ribonucleic acid’ or mRNA and the newfound ability to rewrite those instructions to produce any kind of cell within a biological organism has radically changed the course of Western medicine and science, even if no one has really noticed yet. As Rossi, himself, puts it: “The real important discovery here was you could now use mRNA, and if you got it into the cells, then you could get the mRNA to express any protein in the cells, and this was the big thing.”
It was so big that by 2014, Rossi was able to retire after the company he co-founded with Flagship Pioneering private equity firm to exploit his innovation, – Moderna Inc., attracted almost a half billion dollars in federal award monies to begin developing vaccines using the technology. No longer affiliated with Moderna beyond his stock holdings, Rossi is just “watching for what happens next” and if he’s anything like the doting “hockey dad” he is portrayed to be, he must be horrified.
Remote Control biology
As early as 2006, DARPA was already researching how to identify viral, upper respiratory pathogens through its Predicting Health and Disease (PHD) program, which led to the creation of the agency’s Biological Technologies Office (BTO), as reported by Whitney Webb in a May article for The Last American Vagabond. In 2014, DARPA’s BTO launched its “In Vivo Nanoplatforms” (IVN) program, which researches implantable nanotechnologies, leading to the development of ‘hydrogel’.
Hydrogel is a nanotechnology whose inventor early on boasted that “If [it] pans out, with approval from FDA, then consumers could get the sensors implanted in their core to measure their levels of glucose, oxygen, and lactate.” This contact lens-like material requires a special injector to be introduced under the skin where it can transmit light-based digital signals through a wireless network like 5G.
Once firmly implanted inside the body, human cells are at the mercy of any mRNA program delivered via this substrate, unleashing a nightmare of possibilities. It is, perhaps, the first true step towards full-on transhumanism; a “philosophy” that is in vogue with many powerful and influential people, such as Google’s Ray Kurzweil and Eric Schmidt and whose proponents see the fusion of technology and biology as an inevitable consequence of human progress.
The private company created to market this technology, that allows for biological processes to be controlled remotely and opens the door to the potential manipulation of our biological responses and, ultimately, our entire existence, is called Profusa Inc and its operations are funded with millions from NIH and DARPA. In March, the company was quietly inserted into the crowded COVID-19 bazaar in March 2020, when it announced an injectable biochip for the detection of viral respiratory diseases, including COVID-19.
A wholly-owned subsidiary
In July, a preliminary report funded by Fauci’s NIAID and the NIH on an mRNA Vaccine against SARS-CoV-2 was published in The New England Journal of Medicine, concluding that mRNA-1273 vaccine. provided by Moderna for the study, “induced anti–SARS-CoV-2 immune responses in all participants, and no trial-limiting safety concerns were identified,” and supported “further development of this vaccine.”
A month earlier, the NIH had claimed a joint stake in Moderna’s mRNA COVID-19 vaccine, citing a contract signed in December, 2019, stipulating that the “mRNA coronavirus vaccine candidates [are] developed and jointly owned” by both parties. Moderna disputes the federal government’s position, stating that the company “has a broad owned and licensed IP estate” and is “not aware of any IP that would prevent us from commercializing our product candidates, including mRNA-1273.”
The only obstacle is a delivery system, which though Moderna claims to be developing separately, is unlikely to get FDA approval before the federal government’s own DARPA-developed hydrogel technology, in tandem with Profusa’s DARPA-funded light sensor technology, which is expected to receive fast track authorization from the Food and Drug Administration by early 2021 and, more than likely, used to deploy a coronavirus vaccine with the capacity to literally change our DNA.
In addition, the Department of Health and Human Services (HHS), is currently investigating Moderna’s patent filings, claiming it failed to disclose “federal government support” in its COVID vaccine candidate patent applications, as required by law. The technicality could result in the federal government owning a 100 percent stake in mRNA-1273.
About the Author
Raul Diego is a MintPress News Staff Writer, independent photojournalist, researcher, writer and documentary filmmaker.
Memo to Dr. Scott Atlas, new White House coronavirus advisor
He’s already made two forward-looking points: positive PCR tests in asymptomatic people mean nothing; and the only way to establish mass immunity is through mass exposure out in the open, not lockdowns.
by Jon Rappoport. September 8, 2020
Where to begin? No new virus was ever shown to exist via proper proof. Worthless diagnostic test. Sixteen ways case and death numbers are being faked. If there were a virus, the only way to stop it would be through open massive public exposure and the gaining of natural immunity. Therefore, no lockdowns, no masks, no distancing, no vast economic destruction under the watch of a president whose whole program was based on expanding the economy. Is that enough for starters?
I’d really like to know what went on the room, back in March, when Fauci walked in with Neil Ferguson’s preposterous computer predictions of COVID deaths in the US and spoke with Trump.
Did no one bring up the fact that Ferguson’s whole career has been a string of failed predictions? Was there zero due diligence? Did some economic advisor open his mouth and tell the president what a long-term lockdown would do to the economy? Fifty million people unemployed? Well over a million businesses destroyed?
I hope you understand that Moderna is Fauci’s favorite vaccine company, and his agency, NIAID, stands to rake in cash if Moderna’s shot turns out to be the choice for COVID—when, in fact, no vaccine is necessary.
I hope you know Moderna is a little punk firm that has never brought a product of any kind to market, and yet garnered $500 million in fed funds to research a vaccine.
On top of that, Moderna is deploying RNA technology, which has never been approved for any pharmaceutical product, and has caused, in trials, serious adverse effects.
Are you aware the NY Times recently reported on a large study showing up to 90 percent of all US COVID cases have been false positives, owing to the extreme sensitivity of the PCR test? Not enough virus present in humans to harm a flea. No likelihood of contagion, either.
Have you read the results of a New York study revealing patients over the age of 65 who are put on ventilators die at the staggering rate of 97.2 percent? Yet, Cuomo and Trump keep pushing ventilators.
COVID is old people. Period. No virus necessary. They’re all suffering from long-term, multiple, serious health conditions. They’ve all been treated, for years, with toxic medical drugs. They’re terrified at the possibility of a COVID diagnosis. Then they are diagnosed with COVID. Then they’re isolated and cut off from family and friends. And they die. NO VIRUS NECESSARY.
And THAT makes the recent CDC revelation about death numbers more relevant than most people can fathom. The CDC states that only 6 percent of all US COVID deaths have been unambiguously caused by a virus alone. The other 94 percent are overwhelmingly the old people I just described. Get it?
And now comes a new group of lunatics—computer modelers from the University of Washington, who are predicting the US death toll from COVID will rise above 600,000 this winter. Pressed into their amateur thickly sliced baloney—they ignore the CDC “correction” of death numbers I just mentioned.
Do not let the White House buy this latest death-number projection. Tell Trump one unimaginable screw-up (accepting Ferguson’s criminal projection) is quite enough.
Gather up your forces, Scott. Talk to Dr. John Ioannidis and his merry band of colleagues who tried to get through to Trump and failed, just before you were appointed coronavirus advisor.
Bring the house. You know Fauci and Gates and their sub-honchos are angling for another serious lockdown this winter, when they’re going to make every possible case of flu-like illness over into COVID.
You accepted the White House invite. You bought the ticket, now take the ride. The full ride. Don’t stint.
In case you haven’t figured it out yet, this is an operation to wreck economies worldwide. The preposterous virus narrative is the cover story, concealing the objective of the actual war.
Don’t let the DC attack dogs back you into a corner and shut you up.
You have nothing to lose but your reputation in the eyes of people who don’t matter. They’ve already taken you off their dance card.
The country could lose itself.
In this situation, there is no defense. There is only offense.
If they kick you to the curb, you can come and work with us. You don’t get paid, but the one perk is enormous. You get to define the terms of the battle. And oh yes, you don’t have to speak with numbskulls, hustlers, shysters, and sociopaths.
As I promised earlier this week, most(but not all) of this week’s honorable mentions concern the planscamdemic. I’ve tried to gather the most informative, and in some cases most helpful, articles on how to fight the medical technocratic tyranny. My thanks to all the following: