What’s “Living” in Your Body?

New Study from Japan: Covid Shots Installed Nanobots

A new Japanese study shows that Pfizer and Moderna vaccines contain unauthorized “animated worm-like” entities, invisible to the human eye, which swim, wiggle, and assemble themselves into complex structures, which cause clots inside the body. Researchers Dr. Young Mi Lee and Dr. Daniel Broudy isolated unused Pfizer and Moderna vaccine vials for 3 weeks, and then examined them under 400X magnification. They noticed that when the nano-technology was energized, it created “discs, chains, spirals, tubes, and right-angle structures.” The scientists believe these mysterious nanoparticles are responsible for the explosion of “turbo cancer” and autoimmune diseases around the globe. They also concluded that humans into controllable “Biohybrid Magnetic Robots.” The suggested that the smart microscopic components are part of the elite’s “long-planned well-funded Internet of Bodies,” which was described as a kind of “synthetic global central nervous system” turning humans into controllable “Biohybrid Magnetic Robots.” The researchers called for a ban on mRNA shots. They also demanded the labels “vaccine” and “safe and effective” be removed because the substances are not vaccines and they are dangerous..

Link for Study:   Real-Time Self-Assembly of Stereomicroscopically Visible Artificial Constructions in Incubated Specimens of mRNA Products Mainly from Pfizer and Moderna: A Comprehensive Longitudinal Study

From Seemorerocks:

Another Confirmation Of Self Assembly Nanotechnology In COVID Bioweapons: Remarkable Longitudinal Study And Culture Work Of COVID Shots For Up To 12 Months And Cellular Toxicity Studies

New Japanese study proves Pfizer and Moderna v*ccines contain unauthorized “animated worm-like” entities, invisible to the human eye, which swim, wiggle, and assemble themselves into complex structures, which cause clots inside the body. (What embalmer Richard Hirschman found and exposed in the film Died Suddenly).

Dr. Young Mi Lee and Dr. Daniel Broudy from Okinawa Christian University discovered these “undisclosed additional engineered components” by isolating unused vaxx vials for 3 weeks, and then examined them under 400X magnification.

Lee and Broudy saw that when the nanotechnology was energized it created “discs, chains, spirals, tubes, and right-angle structures.”

The researchers, who published their findings in the International Journal of Vaccine Theory Practice and Research, believe these mysterious nanoparticles are responsible for the explosion of “turbo cancer” and autoimmune diseases around the globe.

They also concluded in the study their suspicion that these smart microscopic components are part of the elite’s “long-planned well-funded Internet of Bodies,” which was described as a kind of “synthetic global central nervous system” turning humans into controllable “Biohybrid Magnetic Robots.”

The study ends by calling for a global ban on all mRNA shots, until these nanobots are studied long-term. They also demanded the labels “v*ccine” and “safe and effective” be removed because the concoction injected into billions is officially neither.

Another Confirmation Of Self Assembly Nanotechnology In COVID Bioweapons: Remarkable Longitudinal Study And Culture Work Of COVID Shots For Up To 12 Months And Cellular Toxicity Studies

In this important study, Dr Young Mi Lee with Dr Daniel Broudy describes her culture findings of Pfizer and Moderna Bioweapons. Many different studies were done, including incubation of the COVID injections, cellular effects upon blood and semen specimen. The tests showed direct toxicity to semen and death of all sperm within minutes up to 1.5 hours in the healthiest donor samples when put in contact with the “vaccine” solution. EMF exposure was also tested, in addition with different supplements and treatment solutions. For this substack, select images were taken from the article which is 66 pages long. Please refer to this link and download the paper – please share widely – this is one the most comprehensive and long term study of the COVID injections and their cellular effects to date. The findings are entirely consistent with all prior research findings of self assembly nanotechnology from the injectables.

Real-Time Self-Assembly of Stereomicroscopically Visible Artificial Constructions in Incubated Specimens of mRNA Products Mainly from Pfizer and Moderna: A Comprehensive Longitudinal Study

Abstract

Observable real-time injuries at the cellular level in recipients of the “safe and effective” COVID-19 injectables are documented here for the first time with the presentation of a comprehensive description and analysis of observed phenomena. The global administration of these often-mandated products from late 2020 triggered a plethora of independent research studies of the modified RNA injectable gene therapies, most notably those manufactured by Pfizer and Moderna. Analyses reported here consist of precise laboratory “bench science” aiming to understand why serious debilitating, prolonged injuries (and many deaths) occurred increasingly without any measurable protective effect from the aggressively, marketed products. The contents of COVID-19 injectables were examined under a stereomicroscope at up to 400X magnification. Carefully preserved specimens were cultured in a range of distinct media to observe immediate and long-term cause-and-effect relationships between the injectables and living cells under carefully controlled conditions. From such research, reasonable inferences can be drawn about observed injuries worldwide that have occurred since the injectables were pressed upon billions of individuals. In addition to cellular toxicity, our findings reveal numerous — on the order of 3~4 x 106 per milliliter of the injectable — visible artificial self-assembling entities ranging from about 1 to 100 µm, or greater, of many different shapes. There were animated worm-like entities, discs, chains, spirals, tubes, right-angle structures containing other artificial entities within them, and so forth. All these are exceedingly beyond any expected and acceptable levels of contamination of the COVID-19 injectables, and incubation studies revealed the progressive self-assembly of many artifactual structures. As time progressed during incubation, simple one- and two-dimensional structures over two or three weeks became more complex in shape and size developing into stereoscopically visible entities in three-dimensions. They resembled carbon nanotube filaments, ribbons, and tapes, some appearing as transparent, thin, flat membranes, and others as three-dimensional spirals, and beaded chains. Some of these seemed to appear and then disappear over time. Our observations suggest the presence of some kind of nanotechnology in the COVID-19 injectables.

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Figure 5. Direct microscopic findings observed in two dimensions magnified 400X: (a) Remnants and new Pfizer injectables, directly observed as well as after incubation for 1 -2 days. (b) Moderna and 4 dried COVID-19 injectables (Pfizer, Moderna, AstraZeneca, and Novavax).

Figure 6. Interactions observed for whole blood(a)/plasma(b) with Novavax at 400X magnification: (a) Within 1 hour, blood cells formed a prominent barrier against “vaccine” contents. (b) After 30 minutes, severe aggregates of red blood cells in rouleaux appeared in the plasma specimen.

Figure 7. Plasma reactions after two hours with four COVID-19 injectables — Pfizer, Moderna, Novavax, and AstraZeneca: (a) Pfizer showing cellular collapse (pyknosis) of white blood cells and damaged platelets; (b) Moderna with stacks of red blood cells (rouleaux); (c) Novavax with the nucleus of white blood cells disintegrating (karyorrhexis), abnormal platelet aggregations, and some rouleaux of red blood cells; and (d) AstraZeneca with prominent Rouleau of red blood cells.

Figure 8. Reaction of semen to COVID-19 injectables at 200X magnification: (a) semen with normal saline as a control added after two hours; (b) with flu vaccine added as a control after 1.5 hours showed sperm cells with intact morphology and with typical progressive natural reduction in sperm motility; (c) 30 minutes after Pfizer-1 injectable was added, sperm motility showed rapid reduction; (d) Pfizer-1 after one hour, all sperm motility ceased;

(e) 30 minutes after Moderna. injectable added; (f) one hour after Moderna was added sperm cells were completely immotile; (g) 30 minutes after Novavax was added; (h) one hour after Novavax, all motility ceased.

Figure 11. Findings for Pfizer incubation study for 372 days; (a) Day 22, this is what we describe as a beaded chain (at 400X magnification); (b) Day 24, 2- dimensional geometric self-assembly at the bottom (at 200X magnification) in normal saline; (c) Day 60, floating 3-dimensional detailed chip-like structures (at 400X magnification) in distilled water; (d) and (e) day 60, accumulated 3-dimensional chip-like structures within an oval shaped boundary (200X/400X) in distilled water; (f), (g), (h), (i) Floating filaments shedding bubbles inside and outside in normal solution at day 95 (100x/100x/200x/200x); (j), (k), (l), (m) Progressive degenerative changes in distilled water 200X (day 82/day 256/day 306/day 372).

 

Read full article from Seemorerocks at Substack

Warning:  Video contains graphic blood clot extraction.

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from:    https://needtoknow.news/2024/08/new-study-from-japan-covid-shots-installed-nanobots/

The Pfizer-Spider Web is Growing

Pfizer’s New Heart Pandemic

Is Accountability Coming?

___________________________________________________________________
Originally posted on The Tenpenny Report by Fed Up Texas Chick; Updated by Dr. Sherri Tenpenny

For years, we’ve been writing about how evil Pfizer is. Case in point: this article from 2017 where we featured Dr. Peter Rost, a former vice president of Pfizer and a pharmaceutical industry whistleblower. He is the author of The Whistleblower, Confessions of a Healthcare Hitman, and at the time was talking about how deadly the HPV vaccine was. Dr. Rost claimed that pharmaceutical companies intentionally design vaccines to keep the public in a state of illness for purposes of perpetual treatments.

That was seven years ago, and never has the evil of Pfizer been more apparent. In January 2024, the powers-that-be declared that the new coronavirus variant would likely cause a higher risk of heart problems.

This time, they presented research from RIKEN, Japan’s largest scientific institute, funded nearly entirely by the Japanese government. However, Riken also accepts “donations from individuals and corporations for the enhancement and development of research.” They even have a page where donors can send a direct credit card donation.

I’m sure that is all above board. In 2019, RIKEN had a budget of $900 million, yet they still needed credit card donations?

What types of corporations work with RIKEN? Corporations like Bayer work with RIKEN, like in the drug discovery collaboration they’ve been jointly working on for about five years.

In December 2021, Pfizer announced they would buy Arena Pharmaceuticals. Pfizer had its eye on etrasimod, Arena’s drug for ulcerative colitis. The drug was approved by the FDA in October 2023, and Pfizer now markets it as VELSIPITY™. Pfizer’s website says in the press release that “UC is a chronic and often debilitating condition that affects an estimated 1.25 million people in the United States.”

That’s a lot of people, but is it enough of a market to drive Pfizer to buy Arena at a 100% premium, a $6.7 billion cash deal? That doesn’t add up in my book. Pfizer sped the development of etrasimod because the drug is a potential therapy for all kinds of immuno-inflammatory diseases, including inflammation of the heart. Part of the deal was that Pfizer acquired all Arena assets in gastroenterology, dermatology, and cardiology.

The first links between the COVID-19 mRNA jabs and myocarditis began to be reported in July 2021. In December 2021, Pfizer entered into a formal agreement to purchase Arena, and by March 2022, it was a done deal.

Incredibly, myocarditis incidents began skyrocketing shortly thereafter. In one example from a May 2022 article, emergency cardiac arrest calls for young adults strongly correlated with the vaccine rollout of doses 1 and 2 in Israel, one of the most jabbed countries in the world.

An FDA-sponsored study looked at health records of children from December 2020 to June 2022 and found incidences of myocarditis and pericarditis to be high enough to trigger a safety signal in 12- to 17-year-olds. The timeframe from the jab to seeking cardiac care for myocarditis or pericarditis was 6.8 days. In a literature review from 2020 to 2022, males were approximately seven times more likely than females to present myocarditis/pericarditis. Another recent study concluded that a booster dose is associated with increased myocarditis risk in adolescents and young adults.

Cancer

In early 2023, Pfizer announced another huge deal with purchase of Seagen Pharmaceuticals.

Seagen is known for its pipeline of cancer drugs, and Pfizer really wanted that pipeline because they spent $43 billion on the deal. Pfizer Chairman and CEO Albert Bourla described it as “acquiring the goose that is laying the golden eggs.”

Once again, the purchase begs the question: Is this business prowess on the part of Pfizer, or is it all planned?

The concept of “turbo cancer” was introduced in January 2023 when fact-checkers across the internet began reporting that any connection between the mRNA jabs and turbo cancer was false. By summer, physicians started describing turbo cancers as the new pandemic, and scientists started to provide reasoning for the sudden and aggressive cancers that oncologists were witnessing.

They seemed to start after a COVID-19 booster shot in all cases. Soon, articles like this one were commonplace, with physicians professing they had never seen cancers with this form of aggression who were often dead within a few months, weeks, or sometimes, even days.

Bourla himself said that the world is experiencing a new type of cancer epidemic, which may explain the Seagen purchase. Seagen works with antibody-drug conjugate (ADC) technology, which uses monoclonal antibodies made to seek out cancer cells and deliver a drug to those cells while sparing the surrounding tissue. Bourla called the ADC technology “one of the greatest technologies to battle cancer” and said they were “very much like the mRNA for vaccines.”

Interestingly, Pfizer created the first ADC, Mylotarg, but had to remove it from the market in 2010 after studies showed the drug was more toxic than chemotherapy.

Bourla said the Seagen acquisition will “dramatically change the oncology presence of Pfizer, making it one of a kind. Seagen’s cancer therapy will bring cancer treatment to the world at a scale that has not been seen before.”

Problem. Reaction. Solution.

Unadulterated Greed

Pfizer was literally flooded with cash after 2021.

Pfizer’s revenues in 2021 were double their revenues from 2020 ($81.3 billion). In 2022, they bought Biohaven Pharmaceuticals for $11.6 billion to gain access to the company’s migraine drug. That same year, they also purchased Global Blood Therapeutics to gain access to the company’s sickle cell drug Oxbryta. But only approximately 100,000 Americans suffer from sickle cell; how can they make $3 billion off this drug? What does Pfizer know that the rest of us don’t? Will we see a blood cell disease epidemic as well?

Some analysts note that, ultimately, Pfizer may go bankrupt with all the lawsuits on the horizon. Will Pfizer go the way of Purdue Pharma, a company where greed and dishonesty allowed it to continue marketing harmful products to the public? Just as with Purdue, will Pfizer lose its legal protections when the millions of vaccine injury claims and charges of fraud land on Bourla’s desk?

The days of huge revenues from COVID-19 products have passed. The US government is returning $3.5 billion of unused Paxlovid treatments, and Pfizer is facing revenue losses from many patent expirations and unfulfilled government contracts worldwide.

Vigilant News noted that older, more experienced vaccine companies such as GSK did not enter the COVID-19 vaccine fray. That looks like it was a wise choice. However, they no doubt got paid well for sitting this one out.

Today, Pfizer’s stock is far less valuable than it was just a few years ago, despite the flashy acquisitions of companies like Arena and Seagen and the billions of dollars made from the COVID death jabs. In the last year, Pfizer has underperformed by 35% compared to the overall pharmaceuticals index.

We can only hope Pfizer – and all other players such as doctors, nurses, pharmacists, politicians, and governments will have soon pay dearly for their folly. That is the heart of the matter.

from:    https://drtenpenny.substack.com/p/pfizers-new-heart-pandemic?publication_id=931759&post_id=145808579&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email

Shedding a Light on Covid Vaccine Shedding

COVID Vaccine Shedding Is ‘Real’, FDA & Pfizer Documents Are Proof: Clinicians

BY TYLER DURDEN
MONDAY, FEB 19, 2024 – 10:05 AM

Authored by Marina Zhang via The Epoch Times (emphasis ours),

The topic of COVID-19 vaccine shedding has long been controversial, but now, some doctors say it is real.

(myboys.me, Naeblys/Shutterstock)

Shedding is unfortunately real,” said Dr. Pierre Kory at the Front Line COVID-19 Critical Care Alliance (FLCCC) conference in Phoenix, Arizona, in early February. “The FDA (U.S. Food and Drug Administration) knows that.”

Dr. Kory is a co-founder of the FLCCC, a non-profit advocacy group founded by physicians for the treatment of COVID-19, long COVID, and postvaccine syndromes. He is also the co-founder of the Leading Edge Clinic and has treated over a thousand long-COVID and postvaccine patients.

Fact-checkers have largely denied shedding on the basis of definition. The commonly cited definition comes from the U.S. Centers for Disease Control and Prevention (CDC) website, which defines shedding as the release of viruses, bacteria, and their components from live vaccines.

While mRNA and adenovirus vaccines are not live vaccines, they function similarly to gene therapy products.

All gene therapy products pose a risk of shedding, according to the FDA.

FDA Documents

In a 2015 document titled Design and Analysis of Shedding Studies for Virus or Bacteria-Based Gene Therapy and Oncolytic Products, the FDA defines shedding as “the release of [viral or bacterial gene therapy products] … from the patient through one or all of the following ways: excreta (feces); secreta (urine, saliva, nasopharyngeal fluids etc.); or through the skin (pustules, sores, wounds).”

In the same document, the FDA also explains what gene therapy products are: “All products that mediate their effects by transcription and/or translation of transferred genetic material.”

The COVID-19 mRNA and adenovirus vaccines fall into this category. They mediate their effects by inducing the body to translate mRNA genetic information into spike proteins.

Some gene therapy products known to shed include an eye treatment branded as Luxturna. Luxturna uses an adenovirus carrier to deliver eye protein DNA to retina cells in patients.

The Luxturna adenovirus and its DNA have been found in patients’ tears, according to the product’s package insert.

Similarly, mRNA and adenovirus COVID-19 vaccines may cause vaccinated patients to release spike proteins or other vaccine components, Dr. Kory explained.

For example, COVID-19 mRNA has been found in the breast milk of vaccinated mothers, indicating possible exposure of the vaccine to infants. Another study showed that spike protein, the product of COVID-19 vaccination, can last for at least half a year in the blood of vaccinated individuals, indicating prolonged spike protein persistence.

The FDA, however, denied that the 2015 document applies to COVID mRNA vaccines.

“COVID-19 vaccines are not regulated as gene therapy products by the FDA; therefore, the guidance document cited is not applicable to the COVID-19 vaccines,” an FDA spokeswoman told The Epoch Times.

Pfizer Investigators Told to Report ‘Environmental’ Vaccine Exposures

Another piece of evidence resides in Pfizer documents, Dr. Kory added.

In Pfizer’s COVID mRNA vaccine protocol, the company instructs investigators to report “environmental exposures” if trial participants expose people around them to the vaccine through inhalation or skin contact.

Examples of such environmental exposures are noted as follows:

  • A male participant who is receiving or has discontinued [vaccine] intervention exposes a female partner prior to or around the time of conception.”
  • “A female family member or healthcare provider reports that she is pregnant after having been exposed to the [vaccine] intervention through inhalation or skin contact.”

The protocol also goes into what Dr. Kory and his clinic co-founder, Scott Marsland, call “secondary shedding.” This occurs when a person who has had environmental exposure to the vaccine then exposes another person.

An example of environmental exposure during breastfeeding,” Pfizer writes, “is a female family member or healthcare provider who reports that she is breastfeeding after having been exposed to the study intervention (the vaccine) by inhalation or skin contact.”

Pfizer’s Documents Showing Indirect Exposures

Pfizer has documented hundreds of adverse events that occurred as a result of indirect exposures or exposure to babies during pregnancy or breastfeeding.

In its Periodic Safety Report submitted to the European Union, Pfizer listed several adverse events it deemed not attributable to the vaccine and that should be excluded from discussion.

The document listed 22 cases of adverse events in babies who had received “indirect exposure” to COVID mRNA boosters, suggesting exposure other than a direct vaccination.

The investigators also monitored several special adverse event cases. Two blood-related adverse events involved babies being exposed through breastfeeding. Ten cases of liver-related adverse events and one adverse event of the vasculature system were reported for the same reason.

Two cases of acute kidney or renal failure and eight respiratory cases also involved babies being exposed during pregnancy or breastfeeding.

Testimonies From Patients

Patients who may be affected by vaccine exposure tend to be those with a history of sensitivities and chronic diseases, said Dr. Kory and Mr. Marsland. They also tend to have bad experiences with pharmaceuticals and are more likely to be chronically debilitated by COVID-19 or the vaccine.

Dr. Kory said that after compiling over 800 anecdotal reports, they observed a clear pattern in symptoms that they determined to be shedding.

Typically, the manifestation of symptoms is repeatable and predictable, such as when a person repeatedly becomes symptomatic when going into supermarkets or crowded places.

Dr. Kory gave the example of a patient who noticed he could not handle going into grocery stores.

The patient told Dr. Kory that he just couldn’t “go into grocery stores anymore.” Within five minutes of entering a Trader Joe’s grocery store, he “feels so terrible” that he has to leave. He experienced the same aversion upon going to a crowded farmers market.

At the FLCCC event, Mr. Marsland also shared several cases where he believed shedding was involved.

One case involved a 54-year-old male, who previously suffered from symptoms after the COVID-19 vaccine, meeting up with a friend who received a COVID-19 booster.

They sat close to each other, talking and laughing. “Within hours of spending their time together, [the man] had a headache, myalgia, and joint pain, increased fatigue,” Mr. Marsland relayed.

When the patient went to a busy airport, he felt worse.

He returned home and had sexual contact with his spouse, exchanging bodily fluids. Within minutes, the spouse developed severe “nine out of 10” abdominal pain.

The two believed the pain was from shedding, so both took ivermectin, known to bind to and block spike proteins. Within about half an hour, the spouse’s abdominal pain receded.

“It’s the temporal association and the accumulation of symptoms,” Mr. Marsland reasoned.

Other doctors treating long COVID and postvaccine syndromes, such as Dr. Syed Haider and Dr. Ana Mihalcea, have also reported suspected cases of shedding.

Some Vaccinologists Disagree

Professors in vaccinology, however, do not acknowledge that mRNA vaccines may induce shedding.

“mRNA leads to the expression of proteins in cells, and this expression is different from shedding, as you would have if you are infected by certain viruses,” associate professor Paulo Verardi of the University of Connecticut told The Epoch Times.

While SARS-CoV-2 infection leads to virus shedding, and, therefore, transmission of the virus from person to person, shedding of the spike protein does not occur in individuals receiving the COVID-19 mRNA vaccine,” he continued.

While another definition of shedding refers to the release of live viruses in people infected or vaccinated with live vaccines, Dr. Kory reiterated that the shedding discussed in the case of COVID-19 vaccines is different from the shedding of live viruses.

Professor Florian Krammer at the Icahn School of Medicine at Mount Sinai also told The Epoch Times that shedding does not exist.

He did not reply when The Epoch Times presented him with information regarding the FDA’s documents on gene therapy and shedding.

from:    https://www.zerohedge.com/political/covid-vaccine-shedding-real-fda-and-pfizer-documents-are-proof-clinicians?utm_source=&utm_medium=email&utm_campaign=2287

Who is “THE SCIENCE”?

And The Truth of the Matter…

Researcher Naomi Wolf Says Babies Were Murdered by Pfizer Shots

The Department of Health and Human Services (HHS) was paying OB-GYN doctors millions of dollars to lie to mothers that COVID mRNA injections are safe. Naomi Wolf said that if the doctors tell the truth about the dangers of COVID injections, they will have to repay the money that they received. She said that they are criminals. She said that Pfizer is aware that babies died after their mothers received COVID jabs. She asserted that babies and unborn babies have been murdered.

CHECK IT OUT HERE:

Link for video:         https://www.bitchute.com/video/TyU52rcerJyi/

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Summary by JW WIlliams

Naomi Wolf, a researcher and the CEO of Daily Clout, said that the Department of Health and Human Services (HHS) was paying OB-GYN doctors millions of dollars to ‘stick to the script’ and to lie to mothers that COVID mRNA injections are safe. She said that if the doctors tell the truth about the dangers of COVID injections, they will have to repay the money that they received. Wolf called these doctors criminals.

She said that the American College of Obstetrics and Gynecology, a large lobbying group, had a portal where OB-GYN doctors could register to receive money directly fro HHS in 2020 if they attested that their patients had COVID as a primary diagnosis, or, if they were pregnant, COVID could be used as a secondary diagnosis. OB-GYN doctors were incentivized in 2020 to inflate COVID diagnosis numbers.

Wolf reported that maternal deaths are up 40% after COVID injections. She said that a doctor and midwives have told her that babies are being born prematurely, they are being born with fetal malformations, chromosomal malformations and breathing problems.

She said that babies and unborn have been murdered.

Wolf said that Pfizer documents reveal that they knew that two babies died in-utero and the vaccine manufacturer stated that the deaths were due to “trans-placental exposure” to the vaccine and then they sent that report to the CDC in April 10, 2021. Three days later, CDC head Rochelle Walensky gave a press conference from the White House stating that pregnant women should take the mRNA vaccines and that it was safe and effective at any time, before, during, or after pregnancy. Wolf said that Walensky knew that two babies had died from trans-placental exposure and another baby died from poisoned breast milk when she advised the women to take the COVID shots.

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Gateway Pundit:         https://www.thegatewaypundit.com/2023/08/must-see-video-naomi-wolf-we-know-pfizer/

from:    chttps://needtoknow.news/2023/08/researcher-naomi-wolf-says-babies-were-murdered-by-pfizer-shots/

Turing the Tide on mRNA Vaccine Administers

New Idaho Bill to Charge Those Who Administer mRNA Vaccines with Misdemeanor

A new bill has been introduced in Idaho that would make the administration of experimental mRNA COVID-19 vaccines illegal.

Representative Judy Boyle (R-Midvale) and Senator Tammy Nichols (R-Middleton) sponsored House Bill 154.

Sen. Nichols introduced the new bill on the 15th of February before the House Health and Welfare Committee, according to KTVB.

According to the bill text, “A person may not provide or administer a vaccine developed using messenger ribonucleic acid technology for use in an individual or any other mammal in this state.”

A person who violates the bill will be guilty of a misdemeanor.

The new legislation, if passed, would go into effect on July 1, 2023.

KTVB reported:

Nichols said during her presentation to the committee, “We have issues this was fast tracked.”

Nichols said there is no liability, informed consent or data on mRNA vaccines. She later clarified she was referring to the two COVID-19 vaccines, Pfizer and Moderna.

“I think there is a lot of information that comes out with concerns to blood clots and heart issues,” Nichols said.

Rep. Ilana Rubel, D-Boise, questioned Nichols’ statement that the vaccines were fast-tracked. She said her understanding was that the vaccines were approved and survived the testing, later approved by the FDA.

Nichols said she is finding it “may not have been done like we thought it should’ve been done.”

“There are other shots we could utilize that don’t have mRNA in it,” Nichols said.

More and more medical experts, scientists, and right group advocates all over the world are now demanding that the government should stop its COVID-19 vaccination campaign due to its devastating side effects among patients.

And yet governments still turn a blind eye to one of the most atrocious crimes against humanity.

from:    https://www.thegatewaypundit.com/2023/02/new-idaho-bill-charge-administer-mrna-vaccines-misdemeanor/

SO Here is Profitability Guarantee a la Pfizer

pfizer new thumb 2023

Pfizer Executive: ‘Mutate’ COVID via ‘Directed Evolution’ for Company to Continue Profiting Off of Vaccines … ‘COVID is Going to be a Cash Cow for Us’ … ‘That is Not What We Say to the Public’ … ‘People Won’t Like That’ … ‘Don’t Tell Anyone’

  • Jordon Trishton Walker, Pfizer Director of Research and Development, Strategic Operations – mRNA Scientific Planner: “One of the things we’re exploring is like, why don’t we just mutate it [COVID] ourselves so we could create — preemptively develop new vaccines, right? So, we have to do that. If we’re gonna do that though, there’s a risk of like, as you could imagine — no one wants to be having a pharma company mutating f**king viruses.”
  • Walker: “Don’t tell anyone. Promise you won’t tell anyone. The way it [the experiment] would work is that we put the virus in monkeys, and we successively cause them to keep infecting each other, and we collect serial samples from them.”
  • Walker: “You have to be very controlled to make sure that this virus [COVID] that you mutate doesn’t create something that just goes everywhere. Which, I suspect, is the way that the virus started in Wuhan, to be honest. It makes no sense that this virus popped out of nowhere. It’s bullsh*t.”
  • Walker: “From what I’ve heard is they [Pfizer scientists] are optimizing it [COVID mutation process], but they’re going slow because everyone is very cautious — obviously they don’t want to accelerate it too much. I think they are also just trying to do it as an exploratory thing because you obviously don’t want to advertise that you are figuring out future mutations.”

[NEW YORK – Jan. 25, 2023] Project Veritas released a new video today exposing a Pfizer executive, Jordon Trishton Walker, who claims that his company is exploring a way to “mutate” COVID via “Directed Evolution” to preempt the development of future vaccines.

Walker says that Directed Evolution is different than Gain-of-Function, which is defined as “a mutation that confers new or enhanced activity on a protein.” In other words, it means that a virus such as COVID can become more potent depending on the mutation / scientific experiment performed on it.

The Pfizer executive told a Veritas journalist about his company’s plan for COVID vaccines, while acknowledging that people would not like this information if it went public.

“One of the things we [Pfizer] are exploring is like, why don’t we just mutate it [COVID] ourselves so we could create — preemptively develop new vaccines, right? So, we have to do that. If we’re gonna do that though, there’s a risk of like, as you could imagine — no one wants to be having a pharma company mutating f**king viruses,” Walker said.

“From what I’ve heard is they [Pfizer scientists] are optimizing it [COVID mutation process], but they’re going slow because everyone is very cautious — obviously they don’t want to accelerate it too much. I think they are also just trying to do it as an exploratory thing because you obviously don’t want to advertise that you are figuring out future mutations,” he said.

“Don’t tell anyone. Promise you won’t tell anyone. The way it [the experiment] would work is that we put the virus in monkeys, and we successively cause them to keep infecting each other, and we collect serial samples from them.”

Walker drew parallels between this current Pfizer project and what may have happened at the Wuhan Institute of Virology in China.

“You have to be very controlled to make sure that this virus [COVID] that you mutate doesn’t create something that just goes everywhere. Which, I suspect, is the way that the virus started in Wuhan, to be honest. It makes no sense that this virus popped out of nowhere. It’s bullsh*t,” he said.

“You’re not supposed to do Gain-of-Function research with viruses. Regularly not. We can do these selected structure mutations to make them more potent. There is research ongoing about that. I don’t know how that is going to work. There better not be any more outbreaks because Jesus Christ,” he said.

Walker also told the Veritas journalist that COVID has been instrumental for Pfizer’s recent business success:

Walker:Part of what they [Pfizer scientists] want to do is, to some extent, to try to figure out, you know, how there are all these new strains and variants that just pop up. So, it’s like trying to catch them before they pop up and we can develop a vaccine prophylactically, like, for new variants. So, that’s why they like, do it controlled in a lab, where they say this is a new epitope, and so if it comes out later on in the public, we already have a vaccine working.

Veritas Journalist:Oh my God. That’s perfect. Isn’t that the best business model though? Just control nature before nature even happens itself? Right?

Walker:Yeah. If it works.

Veritas Journalist:What do you mean if it works?

Walker:Because some of the times there are mutations that pop up that we are not prepared for. Like with Delta and Omicron. And things like that. Who knows? Either way, it’s going to be a cash cow. COVID is going to be a cash cow for us for a while going forward. Like obviously.

Veritas Journalist:Well, I think the whole research of the viruses and mutating it, like, would be the ultimate cash cow.

Walker:Yeah, it’d be perfect.

Walker went on to explain how Big Pharma and government officials, such as at the Food & Drug Administration [FDA], have mutual interests, and how that is not in the best interest of the American people:

Walker:[Big Pharma] is a revolving door for all government officials.

Veritas Journalist:Wow.

Walker:In any industry though. So, in the pharma industry, all the people who review our drugs — eventually most of them will come work for pharma companies. And in the military, defense government officials eventually work for defense companies afterwards.

Veritas Journalist:How do you feel about that revolving door?

Walker:It’s pretty good for the industry to be honest. It’s bad for everybody else in America.

Veritas Journalist:Why is it bad for everybody else?

Walker:Because when the regulators reviewing our drugs know that once they stop regulating, they are going to work for the company, they are not going to be as hard towards the company that’s going to give them a job.

About Project Veritas

James O’Keefe established Project Veritas in 2010 as a non-profit journalism enterprise to continue his undercover reporting work. Today, Project Veritas investigates and exposes corruption, dishonesty, self-dealing, waste, fraud, and other misconduct in both public and private institutions to achieve a more ethical and transparent society and to engage in litigation to: protect, defend and expand human and civil rights secured by law, specifically First Amendment rights including promoting the free exchange of ideas in a digital world; combat and defeat censorship of any ideology; promote truthful reporting; and defend freedom of speech and association issues including the right to anonymity. O’Keefe serves as the CEO and Chairman of the Board so that he can continue to lead and teach his fellow journalists, as well as protect and nurture the Project Veritas culture.

Project Veritas is a registered 501(c)3 organization. Project Veritas does not advocate specific resolutions to the issues raised through its investigations.

from:    https://www.projectveritas.com/news/pfizer-executive-mutate-covid-via-directed-evolution-for-company-to-continue/

Pfizer Told 8 Months to Release “Vaccine” Data

Judge Rejects FDA’s 75 Year Delay On Vax Data, Cuts To Just 8 Months

by Tyler Durden
Friday, Jan 07, 2022 – 06:11 AM

A federal judge has rejected a request by the FDA to produce just 500 pages per month of the data submitted by Pfizer to license its Covid-19 vaccine – and has ordered them to produce 55,000 pages per month. Assuming there are roughly 450,000 pages, that means it will take just over eight months for the world to see what’s under the hood.

Attorney Aaron Siri, who represents the plaintiff in the case, has provided this stunning update via his blog, Injecting Freedom:

On behalf of a client, my firm requested that the FDA produce all the data submitted by Pfizer to license its Covid-19 vaccine.  The FDA asked the Court for permission to only be required to produce at a rate of 500 pages per month, which would have taken over 75 years to produce all the documents.

I am pleased to report that a federal judge soundly rejected the FDA’s request and ordered the FDA to produce all the data at a clip of 55,000 pages per month!

This is a great win for transparency and removes one of the strangleholds federal “health” authorities have had on the data needed for independent scientists to offer solutions and address serious issues with the current vaccine program – issues which include waning immunity, variants evading vaccine immunity, and, as the CDC has confirmed, that the vaccines do not prevent transmission.

No person should ever be coerced to engage in an unwanted medical procedure.  And while it is bad enough the government violated this basic liberty right by mandating the Covid-19 vaccine, the government also wanted to hide the data by waiting to fully produce what it relied upon to license this product until almost every American alive today is dead.  That form of governance is destructive to liberty and antithetical to the openness required in a democratic society.

In ordering the release of the documents in a timely manner, the Judge recognized that the release of this data is of paramount public importance and should be one of the FDA’s highest priorities.  He then aptly quoted James Madison as saying a “popular Government, without popular information, or the means of acquiring it, is but a Prologue to a Farce or a Tragedy” and John F. Kennedy as explaining that a “nation that is afraid to let its people judge the truth and falsehood in an open market is a nation that is afraid of its people.”

The following is the full text of the Judge’s order, a copy of which is also available here.

UNITED STATES DISTRICT COURT

PHMPT, Plaintiff v. FDA, Defendant, No. 4:21-cv-1058-P

ORDER

This case involves the Freedom of Information Act (“FOIA”). Specifically, at issue is Plaintiff’s FOIA request seeking “[a]ll data and information for the Pfizer Vaccine enumerated in 21 C.F.R. § 601.51(e) with the exception of publicly available reports on the Vaccine Adverse Events Reporting System” from the Food and Drug Administration (“FDA”). See ECF No. 1. As has become standard, the Parties failed to agree to a mutually acceptable production schedule; instead, they submitted dueling production schedules for this Court’s consideration. Accordingly, the Court held a conference with the Parties to determine an appropriate production schedule.[1] See ECF Nos. 21, 34.

“Open government is fundamentally an American issue” – it is neither a Republican nor a Democrat issue.[2] As James Madison wrote, “[a] popular Government, without popular information, or the means of acquiring it, is but a Prologue to a Farce or a Tragedy; or, perhaps, both. Knowledge will forever govern ignorance: And a people who mean to be their own Governors, must arm themselves with the power which knowledge gives.”[3] John F. Kennedy likewise recognized that “a nation that is afraid to let its people judge the truth and falsehood in an open market is a nation that is afraid of its people.”[4] And, particularly appropriate in this case, John McCain (correctly) noted that “[e]xcessive administrative secrecy . . . feeds conspiracy theories and reduces the public’s confidence in the government.”[5]

Echoing these sentiments, “[t]he basic purpose of FOIA is to ensure an informed citizenry, [which is] vital to the functioning of a democratic society.” NLRB v. Robbins Tire & Rubber Co., 437 U.S. 214, 242 (1977). “FOIA was [therefore] enacted to ‘pierce the veil of administrative secrecy and to open agency action to the light of public scrutiny.’” Batton v. Evers, 598 F.3d 169, 175 (5th Cir. 2010) (quoting Dep’t of the Air Force v. Rose, 425 U.S. 352, 361 (1976)). And “Congress has long recognized that ‘information is often useful only if it is timely’ and that, therefore ‘excessive delay by the agency in its response is often tantamount to denial.’” Open Soc’y Just. Initiative v. CIA, 399 F. Supp. 3d 161, 165 (S.D.N.Y. 2019) (quoting H.R. REP. NO. 93-876, at 6271 (1974)). When needed, a court “may use its equitable powers to require an agency to process documents according to a court-imposed timeline.” Clemente v. FBI, 71 F. Supp. 3d 262, 269 (D.D.C. 2014).

Here, the Court recognizes the “unduly burdensome” challenges that this FOIA request may present to the FDA. See generally ECF Nos. 23, 30, 34. But, as expressed at the scheduling conference, there may not be a “more important issue at the Food and Drug Administration . . . than the pandemic, the Pfizer vaccine, getting every American vaccinated, [and] making sure that the American public is assured that this was not [] rush[ed] on behalf of the United States . . . .” ECF No. 34 at 46. Accordingly, the Court concludes that this FOIA request is of paramount public importance.

“[S]tale information is of little value.” Payne Enters., Inc. v. United States, 837 F.2d 486, 494 (D.C. Cir. 1988). The Court, agreeing with this truism, therefore concludes that the expeditious completion of Plaintiff’s request is not only practicable, but necessary. See Bloomberg, L.P. v. FDA, 500 F. Supp. 2d 371, 378 (S.D.N.Y. Aug. 15, 2007) (“[I]t is the compelling need for such public understanding that drives the urgency of the request.”). To that end, the Court further concludes that the production rate, as detailed below, appropriately balances the need for unprecedented urgency in processing this request with the FDA’s concerns regarding the burdens of production. See Halpern v. FBI, 181 F.3d 279, 284–85 (2nd Cir. 1991) (“[FOIA] emphasizes a preference for the fullest possible agency disclosure of such information consistent with a responsible balancing of competing concerns . . . .”).

Accordingly, having considered the Parties’ arguments, filings in support, and the applicable law, the Court ORDERS that:

1. The FDA shall produce the “more than 12,000 pages” articulated in its own proposal, see ECF No. 29 at 24, on or before January 31, 2022.

2. The FDA shall produce the remaining documents at a rate of 55,000 pages every 30 days, with the first production being due on or before March 1, 2022, until production is complete.

3. To the extent the FDA asserts any privilege, exemption, or exclusion as to any responsive record or portion thereof, FDA shall, concurrent with each production required by this Order, produce a redacted version of the record, redacting only those portions as to which privilege, exemption, or exclusion is asserted.

4. The Parties shall submit a Joint Status Report detailing the progress of the rolling production by April 1, 2022, and every 90 days thereafter.[6]

SO ORDERED on this 6th day of January, 2022.


[1] Surprisingly, the FDA did not send an agency representative to the scheduling conference.

[2] 151 CONG. REC. S1521 (daily ed. Feb. 16, 2005) (statement of Sen. John Cornyn).

[3] Letter from James Madison to W.T. Barry (August 4, 1822), in 9 WRITINGS OF JAMES MADISON 103 (S. Hunt ed., 1910).

[4] John F. Kennedy, Remarks on the 20th Anniversary of the Voice of America (Feb. 26, 1962).

[5] America After 9/11: Freedom Preserved or Freedom Lost?: Hearing Before the S. Comm. on the Judiciary, 108th Cong. 302 (2003).

[6] Although the Court does not decide whether the FDA correctly denied Plaintiff’s request for expedited processing, the issue is not moot. Should the Parties seek to file motions for summary judgment, the Court will take up the issue then.

from:    https://www.zerohedge.com/covid-19/judge-rejects-fdas-75-year-delay-vax-data-cuts-8-months?utm_source=&utm_medium=email&utm_campaign=399

On Vaccine Shedding

Pfizer document describes vaccine “shedding” from person to person

by Jon Rappoport

August 6, 2021

(To join our email list, click here.)

Pop quiz: During their clinical trial…

If Pfizer insists that certain unvaccinated persons who come into contact with a vaccinated person creates a…

SAFETY SITUATION that must be reported to Pfizer within 24 hours…

Would you say that implies…

The transfer of vaccine components from person to person can occur?

If you answered YES, you win four tickets to Oobladee, a little-known island nation where vaccines are forbidden and the people naturally remain healthy and live to a ripe old age.

Here is a Pfizer document, admitting and warning of person-to-person transfer of dangerous vaccine components [1]: “A PHASE 1/2/3, PLACEBO-CONTROLLED, RANDOMIZED, OBSERVER-BLIND, DOSE-FINDING STUDY TO EVALUATE THE SAFETY, TOLERABILITY, IMMUNOGENICITY, AND EFFICACY OF SARS-COV-2RNA VACCINE CANDIDATES AGAINST COVID-19 IN HEALTHY INDIVIDUALS,” (see page 67).

I’m going to take this in small chunks, and translate the fake-speak clinical language as we go along.

“Exposure to the study intervention under study during pregnancy or breastfeeding and occupational exposure are reportable to Pfizer Safety within 24 hours of investigator awareness.”

The “study intervention” means the RNA COVID shot. That’s what the study is FOR—intervening with a jab. “Hi, I’m your intervener, you’re a volunteer in the clinical trial, and I’m going to hit you in the arm with this needle and inject you.”

“Exposure” to the shot doesn’t mean injection. It means somebody who hasn’t been injected gets physically close to somebody who has been injected. Or it could mean an un-injected person touches vaccine-liquid from a vial.

And that un-injected somebody would be a woman who is pregnant or breastfeeding. For example, she could be a lab worker, or a person who is giving the shots.

If THIS exposure event happens, it’s a safety situation, and it has to be reported within 24 hours.

A lab worker who is pregnant or breastfeeding gets physically close to a person who has received the vaccine and BANG, it’s serious, and it has to be reported.

Why? Because, obviously, there is a potential danger to the unborn baby. Or the mother, who is already breastfeeding her baby, could pass this danger to the baby through her breast milk.

The woman just came physically close to a person who already received the vaccine. That’s all. That’s all that happened. But it’s enough. It means THERE CAN BE A TRANSFER OF VACCINE COMPONENTS FROM PERSON TO PERSON, AND THIS IS NOT GOOD, THIS IS DANGEROUS TO PREGNANT AND BREASTFEEDING MOTHERS AND THEIR BABIES.

Here is the next piece of the Pfizer document. It’s crucial:

“An EDP [exposure to the vaccine during pregnancy] occurs if a male participant who is receiving or has discontinued study intervention exposes a female partner prior to or around the time of conception.”

This is a dangerous situation, too. A man who did get the shot then gets physically close to his female partner, who didn’t get the shot. This doesn’t necessarily mean sex. It means close physical contact. But the warning is obviously all about danger to the woman who is going to conceive a child or has just conceived, and the warning is also about a danger to that child. Some kind of severe injury. Or a miscarriage. Again, the document is obviously referring to the transfer of vaccine components from a vaccinated to unvaccinated person.

And then, in the Pfizer document, we find an example of this dangerous, immediately reportable situation: “A female family member or healthcare provider reports that she is pregnant after having been exposed to the study intervention by inhalation or skin contact….”

Here, as plain as day, we see two meanings of “come in close contact with.” Inhalation, and skin contact. Do not assume this has to mean physically rubbing up against or breathing in the liquid in the vaccine vial. Go back and read the other quotes I gave you from the Pfizer document. They are clearly talking about something much different. They’re talking about close contact between PEOPLE, one of whom has ALREADY had the shot, and one who hasn’t.

They’re talking about vaccine components passing from the inside of one person’s body to another person.

Call it shedding, call it transfer, call it transmission, call it whatever you want to. Pfizer was clearly worried about it, because they insisted that any such occurrence had to be reported to company safety personnel.

They were aware that damage could be the result. Damage to mothers conceiving, mothers pregnant, mothers who are breastfeeding, and damage to babies.

Through person to person passage of components in the vaccine.

A person might object, saying, “Well, maybe the pregnant woman had skin contact with someone who was just vaccinated, and the vaccinated person has a small amount of vaccine on his skin, because that tiny amount of liquid somehow escaped from the needle during injection.”

That’s highly doubtful. And if you go back and read the Pfizer statement about the man who received the vaccine and then had close contact with his female partner, there is no time line mentioned. A) He received the shot and then b) at some point later, he came into close contact with his female partner. It could be days later, weeks later. There would be no amount of vaccine left on his skin.

We ARE talking about the passage of vaccine components from the inside of one person’s body to another person.


SOURCES:

[1] https://cdn.pfizer.com/pfizercom/2020-11/C4591001_Clinical_Protocol_Nov2020.pdf

from:    https://blog.nomorefakenews.com/2021/08/06/pfizer-document-describes-vaccine-shedding-from-person-to-person/

Pay No Attention to he Facts

facebook

Facebook Labeling 100% Facts About Vaccine Company Corruption as ‘Misinformation’

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 2009, among other allegations of human rights abuses, Pfizer agreed to settle a lawsuit for $75 million after a lengthy court dispute in which it was charged with using Nigerian children as human guinea pigs.

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.

As we reported in 2016, the company was forced to pay out billions of dollars in several lawsuits for continuing the sale of products they knew were causing cancer.

J&J has also been found guilty of irresponsible marketing practices and penalized nearly 600 million dollars for their role in fueling the opiate epidemic. As well as having been caught hiding crucial laboratory data from safety inspectors — resulting in the deaths of hundreds of people.

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.

Facebook, as we have reported ad nauseam, works alongside government entities to facilitate their censorship. And more recently was even implicated in a lawsuit filed by Robert F Kennedy Jr as directly taking orders from the government to stifle concerns for vaccine safety on its platform.

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.

from:   https://thefreethoughtproject.com/facebook-labeling-100-facts-about-vaccine-company-corruption-as-misinformation/