The COVID shots are known to increase in lethality after repeated doses. The ‘vaccines’ are linked to turbocancers, reproductive destruction, miscarriages in pregnant women, paralyzation, tinnitus, increased excess death rates, autoimmune disorders in the thyroid, headaches, seizures, heart inflammation and more. Children who received mRNA ‘vaccines’ have also been affected. The mRNA jabs contain hundreds of times the allowable levels of DNA contamination leading to mutagenic effects that change genetic material and increase mutations, contaminating the blood supply, and permanently altering the DNA of the vaccinated and their offspring. Dr. Peter McCullough estimated that over 600,000 Americans have died from COVID ‘vaccines’. The jabs are expected to kill people for a very long time into the future.
The McCullough Foundation published a new study that proposes an intervention to turn off the mutagenic effects of COVID mRNA injections by using small interfering RNA (siRNA) to bind to COVID vaccine mRNA so that the body may eliminate it, and ribonuclease targeting chimeras (RIBOTAC) that can sandwich the mRNA. The introduction of siRNA and RIBOTAC may potentially prevent uncontrolled Spike protein production and reduce toxicity. The targeted nature of siRNA and RIBOTACs allows for precise intervention to inactivate and degrade residual vaccine mRNA, offering a path to prevent and mitigate adverse events of mRNA-based therapies. Dr. McCullough said that some siRNAs [pitirosan and incleanseran] are already used in practice and that he hopes that a biological technology company will produce RIBOTAC.
Dr. McCullough recommends his Base Spike Protein Detoxification protocol that includes nattokinase, bromelin, and curcumin that are available at the Wellness Company He said that nattokinase dissolves blood clots and gave dosages in the video.
mRNA from the jabs has been shown to circulate in the blood for at least 28 days and can be stuck in lymph nodes for at least two months. Spike proteins are said to be circulating at high levels, based on antibodies against the spike protein.
Moderna has had several more mRNA ‘vaccines’, including one for the flu, approved. More mRNA injections will make people more progressively sick because it is synthetic and resistant to the body breaking it down naturally.
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A preprint study coauthored by Dr. Peter McCullough, published in May, described a novel method of deactivating the genetic alteration effects of the mRNA Covid vaccinations, providing hope to the billions of people who’ve been genetically mutated.
“The Pfizer-BioNTech and Moderna biodistribution studies refute the assertion that nanolipid-bound nms-mRNA remains in the deltoid muscle or axillary lymph nodes. Detectable vaccine mRNA levels remaining in various tissues raises potential safety concerns,” the study said in the ‘Conclusions’ section. “The possibility of vaccine mRNA integration into the host genome and the prospect of unintended protein production due to read through advocate for a mechanism to eliminate lingering synthetic mRNA and halt damaging Spike protein production. The use of siRNA and RIBOTACs to target and degrade vaccine mRNA are promising approaches to mitigate deleterious health effects. The ability to readily tailor the siRNA and RIBOTACs to target an mRNA of interest makes these techniques particularly appealing, although further investigation is warranted to address challenges which include possible off-target effects and immune system activation.”
Messenger RNA (mRNA) technology, referred to in Moderna’s patents as modified mRNA or mmRNA for modified messenger RNA, is an exotic technology that encapsulates an altered RNA sequence within a lipid nanoparticle so as to introduce it into the cells of the vaccinated individual. The foreign man-made sequence is then incorporated into the cells of the vaccinated individual, thus acting more as a gene therapy than a traditional vaccine.
While the exotic injection makes the individual begin to produce the dangerous Covid spike protein, currently there is no way to stop the individual from producing that spike protein forever. There is no ‘off’ switch, at least until now.
The study described a method of turning off the production of the spike protein.
“…the longevity of the encapsulated mRNA along with unlimited production of the damaging and potentially lethal Spike (S) protein call for strategies to mitigate potential adverse effects,” the study said in the ‘Abstract’ section. “Here, we explore the potential of small interfering RNA (siRNA) and ribonuclease targeting chimeras (RIBOTACs) as promising solutions to target, inactivate, and degrade residual and persistent vaccine mRNA, thereby potentially preventing uncontrolled Spike protein production and reducing toxicity. The targeted nature of siRNA and RIBOTACs allows for precise intervention, offering a path to prevent and mitigate adverse events of mRNA-based therapies.”
Even though the mRNA COVID jabs are the most dangerous medical products ever to hit the market, vaccine makers and U.S. health agencies are steamrolling right ahead with a long list of mRNA-based shots, including combination shots to cover multiple viral infections
If the COVID shots are the most dangerous injections we’ve ever seen, what makes them think mRNA shots for cancer, heart disease, influenza, respiratory syncytial virus (RSV), HIV or any other condition will be any safer?
Moderna is planning to offer a personalized cancer shot by the end of 2028. The U.S. Food and Drug Administration has already designated it as a “breakthrough therapy,” which means the regulatory review will be expedited. The European Medicines Agency (EMA) is also fast-tracking it under the European “priority medicines” (PRIME) scheme
mRNA-based influenza shots are also in the works. Pfizer and Moderna both launched mRNA flu jab trials in the fall of 2022
Moderna is also developing mRNA shots for shingles and genital herpes based on the same platform used for its COVID jab — a technology that doesn’t stop infection and can depress your immune function such that you become more prone to infections and chronic diseases of all kinds
Even though the mRNA COVID jabs are the most dangerous medical products ever to hit the market, vaccine makers and U.S. health agencies are steamrolling ahead with a long list of mRNA-based shots, including combination shots to cover multiple viral infections at the same time.
If the COVID shots are the most dangerous injections we’ve ever seen, what makes them think mRNA shots for cancer, heart disease, influenza, respiratory syncytial virus (RSV), HIV or any other condition will be any safer?
It’s a science experiment gone completely off the rails. No one is safeguarding public health anymore. You could say our health agencies have sold out the public to the drug industry, allowing them to conduct wild population-wide genetic experimentation aimed at furthering the transhumanist agenda at breakneck speed.
Personalized Cancer Shot Is Being Fast-Tracked
As reported by The Guardian in early April 2023,1 Moderna, for example, is planning to offer a personalized cancer shot by the end of 2028. The U.S. Food and Drug Administration has already designated it as a “breakthrough therapy,” which means the regulatory review will be expedited.
The European Medicines Agency (EMA) is also fast-tracking it under the European “priority medicines” (PRIME) scheme.2 Here’s how Moderna’s personalized cancer gene therapy is said to work:3
A biopsy of your cancerous tumor is collected
Mutations in the genetic sequence of the tumor are identified
A machine learning algorithm determines which of the identified mutations might be driving the cancer’s growth. Abnormal proteins produced by those mutations are also identified
A synthetic mRNA molecule is created, containing instructions for your cells to make an antigen that your immune system will respond to
Once injected, the mRNA is translated into proteins that are, supposedly, “identical” to those found in your tumor. When immune cells encounter cancer cells that carry these proteins, they destroy them
It sounds good in theory, but as we’ve seen with the COVID shots, any number of things can go wrong once your cells are turned into toxic protein factories. Contrary to transhumanist belief, your body is not a “hardware platform” and your immune system is not like a piece of software that can simply be “updated” with a new set of genetic instructions.
Not even close. It’s more like a spider’s web of interconnected systems and pathways. Pull on one string and the whole network responds with cascades of activity, much of which we still do not understand. It’s beyond foolish to think you can just insert a new genetic instruction on one of the strings and not disturb or impact the rest of the web.
mRNA Flu Jabs Coming Soon
mRNA-based influenza shots are also in the works. Pfizer and Moderna both launched mRNA flu jab trials in the fall of 2022.4 We now know the COVID shot doesn’t protect you against SARS-CoV-2 infection or transmission, so will the flu shot be any different? Are they tweaking it somehow to block infection? Or will it be a repeat of COVID — all risk and no benefit?
In my view, there’s cause for additional concern when it comes to mRNA flu shots, because they’ve already admitted that the viral strains targeted can and will be updated on the fly in the middle of the flu season, should it turn out that the flu strains selected in February are a mismatch to the circulating strains that following winter.5
The industry wants you to believe that changing the antigen has no bearing on the potential side effects, but they have no evidence to support that assertion. Whenever you change the antigen, you run the risk of new side effects, because not all antigens affect your immune system the same way.
For example, the reason why no coronavirus vaccine was ever brought to market despite 20 years of research and experimentation was because they kept causing worse infection. Many vaccines against other viruses don’t have this effect.
And, even though the mRNA platform is completely different from conventional vaccine manufacturing that uses live or attenuated coronaviruses, the effect on the immune system is still clearly an adverse one. So, changing the method didn’t eliminate the problem.
Since the mRNA platform allows for endless customization without additional safety testing to make sure the antigen chosen won’t cause unsuspected problems, it poses a unique threat to public health. Millions will likely be injected before a problem is identified.
Gene Therapies Don’t Work Like Vaccines Do
It’s important to remember that mRNA-based “vaccines” aren’t vaccines. They’re gene therapies. The only reason drug companies and health agencies now insist on calling them vaccines is because they changed the definition of the word so that a vaccine no longer has to protect you from the infection in question. All it must do is stimulate your body’s immune response against the disease.
But if a vaccine doesn’t prevent you from infection, what is the point of it? Natural infection also stimulates your immune response, but you develop immunity. So, all the shot is doing is stimulating — and possibly overstimulating and contributing to autoimmune diseases — your immune system without providing immunity.
mRNA Dosing Conundrum Has yet To Be Solved
Originally, modified mRNA was thought to hold the key to a new source of embryonic stem cells that researchers planned to use to treat anything from Parkinson’s disease to spinal cord injuries. Using modified synthetic mRNA, they hoped to sidestep the controversy of using stem cells from aborted fetuses.
The promise hinged on safe dosing, but in animal studies scientists ran into a now-familiar problem with the mRNA doses. The therapy triggered dangerous immune reactions, yet the lower doses were too weak to show benefit.
There’s no compelling evidence that this dosing problem was ever solved. In fact, it appears sloppy COVID jab manufacturing has resulted in varying strengths of the shots, with some batches being associated with vastly higher rates of injury and death, as detailed on HowBadIsMyBatch.com.6
Also, let’s not forget that the COVID shots appear to be massively accelerating cancer development, as “turbo-charged cancers” are now becoming more common. So, what can we expect from an improperly dosed mRNA cancer jab?
Will mRNA Shots for Herpes and Shingles Prevent Infection?
Moderna is also developing mRNA shots for shingles and genital herpes7 based on the same platform used for its COVID jab — a technology that doesn’t stop infection and can depress your immune function such that you become more prone to infections and chronic diseases of all kinds.
The mRNA COVID shots are also suspected of causing autoimmune conditions by way of molecular mimicry.8 This occurs when similarities between different antigens confuse your immune system.
So, will mRNA shots against herpes and shingles prevent infection? Or will they increase your risk, just like the COVID shots have done? We’ll have to wait and see, but I wouldn’t recommend lining up to test them.
mRNA Integrity Is Another Technical Difficulty
Another technical difficulty that is unlikely to have been solved is the mRNA integrity. As detailed in “Data Leaks Reveal Disturbing Facts About mRNA Instability,” hacked Pfizer COVID jab data show European regulators had significant concerns over the lack of intact mRNA in the commercial batches sampled.
Compared to the clinical batches, i.e., the shots used in the clinical trial, 55% to 78% of the commercial shots had “a significant difference in % RNA integrity/truncated species.”
This is important because intact mRNA is essential for efficacy. According to Daan Crommelin, a professor of biopharmaceutics, “Even a minor degradation reaction, anywhere along a mRNA strand, can severely slow or stop proper translation performance of that strand and thus result in the incomplete expression of the target antigen.”
For an effective product, mRNA integrity needs to be 100%. Considering how ineffective the jabs are, it seems fair to question whether lack of mRNA integrity might be to blame. We also do not know whether fragmented mRNA might be harmful, and to what degree.
While public health agencies claim fragmented RNA poses no health risk, just how do they know that? The leaked documents revealed they did not have an answer to that question. There’s also no evidence that manufacturing processes have been perfected to prevent the fragmentation of mRNA. Like so many other things, the ins and outs of the manufacturing process of mRNA injections are not disclosed or discussed.
The Transhumanist Race Toward Human 2.0
It’s hard to assess the recklessness with which drug companies and health agencies approach mRNA therapy as anything other than an attempt to fulfill a transhumanist dream in the quickest way possible. To perfect the genetic manipulation of human beings would under normal circumstances take many decades, perhaps close to a century, or more.
It would seem the globalist cabal driving the transhumanist agenda decided instead to launch population-wide experimentation to speed up the process. Large-scale studies are always required when you want to prove safety and effectiveness, and the global population has basically been turned into guinea pigs. They don’t care how many are injured or killed in the process. They’ve proven this much by ignoring the mounting death toll.
To the cabal, it’s probably a numbers game. Inject billions of people with gene therapies of various kinds in varying dosages, see what happens and tweak from there. Ultimately, the general population are not the intended beneficiaries of this large-scale experimentation. The globalists are. The guinea pigs are expendable.
National vaccine policy recommendations in the U.S. are made at the federal level but vaccine laws are made at the state level. It is at the state level where your action to protect your vaccine choice rights can have the greatest impact.
It is critical for EVERYONE to get involved now in standing up for the legal right to make voluntary vaccine choices in America because those choices are being seriously threatened.
Not only are lobbyists representing drug companies, medical trade associations and public health officials trying to persuade legislators to strip all vaccine exemptions from public health laws, but global political operatives lobbying the United Nations and World Health Organization are determined to take away the human right to autonomy and protection of bodily integrity.
We must take action to defend our constitutional republic and civil liberties, including the right to autonomy, in America. That includes reforming oppressive mandatory vaccination laws and stopping the digital health ID that will make vaccine passports a reality for us, our children and grandchildren if we don’t take action today.
Signing up to use the free online Advocacy Portal sponsored by the National Vaccine Information Center at www.NVICAdvocacy.org gives you immediate, easy access to your own state and federal legislators on your smartphone or computer so you can make your voice heard.
NVIC will keep you up to date on the latest bills threatening to eliminate — or expand — your legal right to make vaccine choices and give you guidance about what you can do to support or oppose those bills. So, please, as your first step, sign up for the NVIC Advocacy Portal.
Share Your Story With Your Legislators and People You Know
If you or a family member has suffered a serious vaccine reaction, injury or death, please talk about it. If we don’t share information and experiences with one another, everybody feels alone and afraid to speak up.
If you want to protect your legal right to say “no” to vaccines you do not believe are safe or effective, make an appointment to personally talk with someone you have elected to office at the local, state and federal level or write a letter in your own words stating your concerns.
Attend school board and city council and town hall meetings in your community that will impact your right to know and freedom to make decisions about how you or your children will live and stay healthy. If you have a different perspective on a story about vaccination that appears in your local newspaper, write a letter to the editor.
I must be frank with you: You have to be brave because there is a lot of censorship of conversations that challenge “official” narratives about vaccination. You likely will be strongly criticized for daring to talk about the “other side” of the vaccine story and for defending your informed consent rights. Be prepared for it and have the courage to stand your ground.
Only by sharing our perspective and what we know to be true will the public conversation about vaccination open up so people are not afraid to talk about it.
While our rights are being threatened, the vaccine injured are being swept under the carpet and treated like nothing more than statistically acceptable “collateral damage” of one-size-fits-all mandatory vaccination laws. Way too many people are being put at risk for injury and death and there is nothing scientific or moral about that. We should not be treating human beings like guinea pigs.
Internet Resources Where You Can Learn More
I encourage you to visit the four websites of the National Vaccine Information Center (NVIC), at www.NVIC.org, a nonprofit charity that has been educating the public about the need to prevent vaccine injuries and deaths since 1982. The information you get on their websites is fully referenced and will help you become an effective vaccine choice advocate in your community:
NVIC.org — This website was established in 1995 and is the oldest and largest consumer operated website publishing information on diseases and vaccines on the internet. Learn about vaccine reactions, injuries and deaths and the history and current status of vaccine science, policy, law and ethics in the U.S. on more than 2,000 web pages.
NVICAdvocacy.org — This communications and advocacy network, established in 2010, is your gateway to taking action to protect your right to make vaccine choices where you live.
TheVaccineReaction.org — This weekly journal newspaper published by NVIC since 2015 is dedicated to encouraging an “enlightened conversation about vaccination, health and autonomy.”
MedAlerts.org — This is a user-friendly search engine for the federal Vaccine Adverse Event Reporting System (VAERS) established under the 1986 National Childhood Vaccine Injury Act and sponsored by NVIC since 2006. Search for descriptions of vaccine injuries and deaths reported to VAERS on this popular website.
Find a Doctor Who Will Listen and Care
If your doctor or pediatrician refuses to provide medical care to you or your child unless you agree to get vaccines you don’t want, I strongly encourage you to have the courage to find another doctor. Harassment, coercion and refusal to provide medical care to someone declining one or more doses of government recommended vaccines is a violation of the informed consent ethic.
Unfortunately, it is becoming routine among members of the medical establishment to be reluctant to share vaccine decision-making power with patients and parents of minor children, especially during the aggressive push for all Americans to get COVID shots.
There are doctors out there who respect the precautionary and informed consent principles, so take the time to locate a doctor who treats you with compassion and is willing to listen and respect the health care choices you make for yourself or your child.
The censors at Facebook’s ministry of truth have sunk to a new low. Yesterday at 1:35 p.m. EST, TFTP journalist Don Via Jr received a 24-hour ban on the platform for posting a completely factually accurate meme acknowledging big pharma’s history of rampant corruption.
Unlike other instances of individuals being censored on the platform however, in which the social media company attempts to thinly veil their censorship behind openly biased fact-checkers. This time there was none. No “fact check” for “false information”. Simply a notification of the post being removed from Mr. Via’s Break The Matrix Facebook page, and a notice that all of his accounts were restricted for 24 hours.
Below is the meme in question.
What makes this act of censorship particularly egregious is the blatant nature with which Facebook is now suppressing 100% verifiable facts.
After disputing the decision, Facebook replied with an automated message stating “We don’t allow false information that could cause physical harm. In some cases this includes information that recognized health organizations say could mislead people about how to cure or prevent a disease or that could discourage people from seeking medical treatment.”
In this case though, none of the information stated was false.
For instance, the first tier of the graphic claims that since inception in 1848, Pfizer has racked up nearly 5 billion dollars in criminal charges. While the exact total may vary a bit, the facts regarding their history of rampant corruption and medical malfeasance is.
In 1991, the FDA charged Pfizer subsidiary Shiley with withholding information from safety regulators and deliberately falsifying manufacturing records with regards to faulty heart valves. Nearly 300 people died from Pfizer’s faulty products and ultimately the company spent 205 million dollars settling the tens of thousands of lawsuits filed against them.
Despite this, Pfizer resisted to comply with FDA orders to notify patients and ultimately paid an additional $10 million when the Department of Justice charged them with lying to regulators.
In 2012 the company was forced to pay 60 million dollars after it was exposed for bribing foreign doctors to sell their products.
These are only a select few examples of the company’s history rife with criminal activity. More can be seen under Pfizer’s corporate rap sheet via the Corporate Research Project.
The second tier of the meme asserts that Moderna has not successfully completed the production of a viable vaccine in the company’s history. This can be confirmed via a simple internet search. In May of 2020, it was reported by The Daily Mail and CNN that Moderna has a track record of never bringing a successful vaccine to market since the company’s founding in 2010.
Furthermore, despite the company’s dubious past it was reported that Moderna was first tapped to lead U.S. vaccine development in what equated to a gamble. Simply because the company’s slick talking CEO was able to get the attention of former President Trump with bold promises during a meeting with biotech executives.
The third tier of the meme acknowledges the well-documented history of heinous crimes committed by Johnson & Johnson. Of which TFTP has also extensively covered in recent years.
But these only scratch the surface of the company’s flagrant human rights abuses. Among them, being one of the main financiers alongside, Dow Chemical and the United States Army, funding 20 years of unethical human experiments by Dr. Albert Kligman in Pennsylvania’s Holmesburg prison. Experiments which entailed prisoners being financially coerced to “volunteer” as research subjects to study mind-altering drugs, painful medical procedures, radiation, and chemical weapons such as Agent Orange.
As a matter of fact, in addition to Pfizer and Johnson & Johnson — It is thoroughly documented by the Corporate Research Project that nearly every major company involved in the development of Covid-19 vaccines has an abhorrent history of medical malfeasance, and criminal charges.
Finally, the last section of the meme asserts that AstraZeneca’s covid-19 vaccine has itself already been suspended in 24 countries due to health concerns. Yet again, a simple query in your preferred search engine can corroborate this as a fact.
As a March 16th report from Al Jazeera explains; the countries of Sweden, Latvia, France, Germany, Italy, Spain, Luxembourg, Cyprus, Portugal, Slovenia, Indonesia, the Netherlands, Ireland, Bulgaria, the Democratic Republic of Congo, Thailand, Romania, Iceland, Denmark, Norway, and Austria have all suspended the Oxford / AstraZeneca jab in some capacity.
Since that report the Philippines and Australia have also suspended the shot for individuals under 60 years of age. Venezuela has also refused to authorize it.
What Facebook is doing by deleting this content, which by all accounts is completely accurate, is suppressing vital information that the people have a right to know. Informed consent matters, and it’s not something that can be so freely thrown to the wayside — certainly not as adverse events reported to the CDC are at an all-time high.
The company is now essentially working as a cover-up crew to protect those with which they have a vested financial or political interest. While their counterparts in the mainstream media ingloriously propagate the notion that those concerned with vaccine safety are domestic terrorists.
Bodily autonomy is paramount, and individuals have an inherent right to be given all the facts so that they are adequately informed to make proper decisions with regard to their health.
Just because the truth is unpleasant, does not make it misinformation. As a matter of fact, censoring unpleasant truths in favor of biased one-sided narratives is the greatest danger of all.
‘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.
As The Defender reported, in the U.S., 66 deaths have been reported to the Vaccine Adverse Event Reporting System (VAERS). These haven’t been fully investigated yet, but clearly many people, mostly the frail elderly but also some younger (as in the 56-year-old Florida doctor) are reporting serious injuries, even death. “People are dying from these vaccines. That can’t be swept under the rug by mainstream media.”
Adverse reactions to COVID vaccines that are being reported “are similar to those we’ve seen from HPV vaccines, only worse.”
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.
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FDA officials knew that tumors might occur decades after vaccination.
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FDA openly acknowledged that its primary objective was not to assure public safety but to help vaccine manufacturers.
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FDA officials knew that they could not prove vaccine safety using test animals to assess oncogenicity.
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FDA officials deliberately terminated animal safety tests too early in order to conceal consequences.
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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.
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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.
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FDA decided to hide information about their use of tumor cells and omit it from package inserts.
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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.
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FDA officials opted to toss the dice, perform the population-wide human experiment, and learn about the risks as time goes by.
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The committee formally approves the method of making vaccines from human cancer tumors.
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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
Finally, it’s worth considering that cancer treatment drugs like Keytruda are among pharmaceutical companies’ largest profit makers. Precipitating a cancer epidemic in human populations only benefits vaccine makers’ bottom line.
Remember, these are the same companies and the same FDA regulators that brought us the opioid epidemic.
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
Scott,
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:
