Tag: vaccines

New study may have identified an “off switch” for spike proteins produced in the body caused by mRNA injections

Covid-19 mRNA “vaccines” have shown wider distribution in the body than initially claimed, raising concerns about unintended effects and the need for an “off switch” to stop ongoing spike protein production. A recent study identifies a treatment that may act as an “off switch.”

A preprint study led by Dr. Peter McCullough suggests using siRNA and RIBOTACs to target and degrade residual mRNA from covid-19 vaccines, potentially mitigating long-term health risks associated with persistent spike protein production.

The study proposes using siRNA and RIBOTACs as potential methods to bind to and degrade vaccine mRNA in cells, offering a targeted approach to prevent adverse events from mRNA-based therapies.

“Long vax” symptoms, similar to long covid, have been reported following vaccination, including fatigue, brain fog, numbness and cardiovascular issues, highlighting the need for effective treatments for those affected.

Another study led by McCullough found a significant increase in cerebral thromboembolism risk associated with covid-19 vaccines compared to other vaccines, leading to calls for a moratorium on their use.

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NewsGuard fact-checked me today, providing the opportunity to clarify questions about the Audenz vaccine and the extremely high mortality rate in its small trial.

The big guns, the Health Editor, approached me this afternoon. Happy to learn the presentation is getting attention.

Below is the email I received and below that is my detailed reply.

On Jul 3, 2024, at 1:26 PM, John Gregory <john.gregory@newsguardtech.com> wrote:

Dr. Nass, 

My name is John Gregory, health editor at NewsGuard. We’re a news organization that reports on and tracks online misinformation. 

I’m emailing in regards to your April 20, 2024, CHD video in which you cited the FDA package insert for the H5N1 vaccine Audenz, and said, “One in 200 people who got this vaccine in a clinical trial died,” and later added, “This is a dangerous vaccine for a nothing disease.”

Video of your remarks has begun circulating widely on social media platforms in the past two weeks, used as evidence for claims like “Dr. Meryl Nass: One of the approved Bird Flu quackccines, Audenz… had a death rate of 1 in 200 during clinical trials.” 

I noticed the screenshot included in your original video highlighted the sentence, ““Fatal SAEs [Serious Adverse Events] included 11 (0.5%) Audenz recipients and 1 (0.1%) placebo recipients,” even though the very next sentence said, ““No SAEs were assessed as being related to Audenz,” meaning that none of the reported serious adverse events – including deaths – that occurred among trial participants were caused by the vaccine.

You also did not mention that the FDA’s own statistical review of Audenz stated that, “No deaths occurred that were considered related to the vaccine,” and concluded, “No major statistical or safety issues have been identified” with the vaccine, or that the published results of the Audenz trial said:

None of the serious AEs or AEs of special interest reported by subjects who received aH5N1c were considered vaccine related. Two subjects in the placebo group reported a related AE of special interest (immune thrombocytopenic purpura and polymyalgia rheumatic); these events were also considered serious AEs. During the study, 12 (0.4%) subjects had serious AEs with a fatal outcome, none of which were attributed to the study treatment, and most (n = 11) occurred after Day 43 during the follow-up period in subjects ≥65 years with underlying severe comorbidities and multiple concomitant medications.

Is there any reason why you did not mention any of this countervailing information?

My deadline is 5pm eastern today, July 3. Thank you. 

— 

Best regards, 
John Gregory

john.gregory@newsguardtech.com

Office: ‪(312) 489-8676

More about NewsGuard criteria here.

Dear Mr. Gregory,

Since I provided a screenshot of the package insert of the Audenz licensed vaccine and repeated what it said, this can hardly be characterized as misinformation, which you claim to be investigating.  Since I included the next sentence in the presentation, it cannot even be construed as incomplete.

Had you been working on issues of vaccines for over 25 years as I have, you would have been aware that the sponsor (mfr) and FDA, who together craft the vaccine labels aka package inserts, ALWAYS assert that most or all of the deaths and serious adverse events occurring during a clinical trial were adjudged to be not due to the vaccine.  Had they judged otherwise, a license would probably not have been issued.  A license was issued for Audenz.

Later, when a vaccine is given to millions of people, not just a few hundred as in this case, one learns which side effects are IN FACT attributable to the vaccine.

For example, at least a hundred million Americans had received an mRNA COVID vaccine before it was determined to cause myocarditis, in late May of 2021 by FDA.

That is the reason why the raw data, which I presented, are important.  So that people have the information to judge for themselves what risks they may face when choosing vaccination.  In fact, clinical trials often exclude sick subjects, and drugs and vaccines almost invariably appear more safe and effective in clinical trial data than they do later, in the real world—a fact known to all medical researchers.

Why did I not mention material from an article?  Because I was referring to the Audenz label, which is the legal document that FDA attests is true, unlike published articles which are generally written by the vaccine sponsor and have a lesser degree of reliability.  In fact, the numbers in the article versus those in the label are not exactly the same.

Furthermore, if the US government was comfortable with the H5N1 Audenz vaccine, why did DHHS’ BARDA just place an order with Moderna for H5N8 mRNA vaccines, even though the avian flu circulating in the US is H5N1?  Even though it makes much more sense to match the neuraminidase portion of the vaccine to the circulating strain…  which is done every year when seasonal influenza vaccines are produced?

Finally, I invite you to take a look at the WHO data on deaths in humans worldwide from the H5N1 bird flu, which confirms it is a nothing disease in humans, having mutated to a different form than it once had.  The federal health agencies have monitored 9,000 farm workers and all they found were 4 mild cases of disease, no hospitalizations and no deaths in the US over the past several years.

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Biden’s FDA rushed COVID-19 vaccine approval for children despite experts’ appeals for more time to study negative effects

The Biden administration pressured medical professionals to rush approval of the COVID-19 vaccine for children before there was sufficient testing to ascertain its safety, experts have testified, and when top FDA vaccine experts asked for more time to study the side effects of the jabs in young adults and children, they were fired.

This is according to testimony before the House Judiciary Subcommittee on the Administrative State, Regulatory Reform, and Antitrust this week looking into the politicization of the FDA during the pandemic.

The subcommittee also released an interim staff report about the topic, “Politics, Private Interests, and the Biden Administration’s Deviation from Agency Regulations in the COVID-19 Pandemic,” which explained how the Biden administration pressured the FDA to work outside of its regulatory authority to cut corners and change procedures to push through authorization of the Pfizer jab and booster shots, which effectively enabled them to issue vaccine mandates even as concerns persisted about vaccine injury.

During the hearing, Chairman Thomas Massie (R-Kentucky) read testimony from the former director of the FDA’s vaccine office, Dr. Marion Gruber. She told the FDA’s top vaccine regulator, Dr. Peter Marks, that the vaccine needed to undergo more testing in younger people, especially males aged 12 to 17. However, Dr. Marks reportedly brushed off her concerns.

Massie recounted: “Right when they were getting the warnings that myocarditis and pericarditis are real and serious side effects to the vaccine, the top scientists at FDA had already agreed to compress the schedule as much as possible, right when they got the message that there were serious side effects.”

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Vaccine-induced sicknesses increase exponentially in infants with each additional vaccine

In the research article, “Adverse Outcomes Are Increased with Exposure to Added Combinations of Infant Vaccines,” published in the International Journal of Vaccine Theory, Practice, and Research, Children’s Health Defense (CHD) scientists reveal the sheer number of vaccine-induced diseases in infants and children increases exponentially– more than doubling– with every vaccine added.

The CDC has never performed safety studies on any of the combinations of vaccines it recommends on its CDC Child and Adolescent Immunization Schedule.

In practice, except for the hepatitis B vaccine recommended in the first 24 hours of life, infants rarely receive a single vaccine. Most are administered in combination with other vaccines.

A two-month-old infant adhering to the CDC’s childhood immunization schedule will receive eight recommended vaccines at one time, in combination. The infant will receive an additional seven doses when four months old, and could receive eight vaccine doses again when six months old.

“Each additional vaccine more than doubles the number of diseases detected in the study,” said CHD Chief Scientific Officer Brian Hooker. “The article presents evidence of the risks that should be considered in personal and medical decision-making.”

The study looked at over 1.5 million infant vaccine combinations. The authors revealed that a total of 45 different diseases were diagnosed within the first 30 days after vaccination, including infection and developmental delays.

Respiratory disease was the most recurring condition, with acute and chronic bronchitis presenting as an elevated risk in five different vaccine combinations.

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Covid Vaccine Injuries Go Mainstream in Australia

Propaganda narratives shift slowly over time to absorb aspects of undeniable reality, whilst minimising damage to the interests of those benefiting from the big lie.

First, the Covid vaccines were safe and effective, and we were set to experience a pandemic of the unvaccinated. Get vaccinated to protect your community!

Next, the shots were safe and effective, but with rare side-effects, mostly mild. Still, the benefits outweighed the risks. Get vaccinated to protect your healthcare system!

In the latest narrative update, experts say all the shots except AstraZeneca’s are safe and effective, and they admit that vaccine injuries can be life-ruining, though still very rare. But Covid is worse. Get vaccinated to protect against Long Covid!

In an ‘After Covid’ Spotlight special on commercial media channel 7NEWS over the weekend, a panel of experts reflected on Australia’s Covid response. Tellingly, vaccine safety (or rather, lack thereof) occupied 17 out of a total 53 minutes, more than a quarter of the airtime.

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U.S. Will Pay Moderna $176 Million to Develop mRNA Bird Flu Vaccine

The United States government will pay vaccine manufacturer Moderna $176 million to develop a new mRNA vaccine to treat bird flu.

The U.S. Department of Health and Human Services will pay Moderna $176 million for a vaccine containing the same mRNA technology as the company’s COVID-19 vaccine.

Bird flu, or H5N1, has been reported in dairy cows and has infected three people in the United States.

In total, 135 dairy herds have been infected with bird flu in 12 states.

Per AP:

The U.S. government will pay the vaccine maker Moderna $176 million to develop a pandemic vaccine that could be used to treat bird flu in people as cases in dairy cows continue to mount across the country, federal officials announced Tuesday.

The funds are targeted for release through the U.S. Department of Health and Human Services and will pay for continued development of a vaccine that uses the same mRNA technology that allowed rapid development and rollout of vaccines to protect against COVID-19. The award was made through the Biomedical Advanced Research and Development Authority, or BARDA, a program focusing on medical treatments for potential pandemics.

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Pandemic Preparedness: Arsonists Run the Fire Department

Imagine if you will, an exceptionally ambitious city Fire Department, located in a city with very few naturally occurring fires.

These ambitious firemen don’t have nearly enough work, prestige, or pay for their liking. Uninterested in simply polishing their trucks, lifting weights, and cooking chili, these firemen want more. A lot more.

They construct a plan. They will start a research program, funded by taxpayers, whereby they will develop an arsenal of the biggest, scariest, most flammable products on earth. They will justify this program under the pretense that these destructive creations are absolutely necessary for the development of bigger and better fire extinguishers. Incidentally, they will also develop, market, and sell these fire extinguishers themselves.

These proprietary fire extinguishers will net the ambitious firemen an incredible fortune – if they can just get every man, woman, and child in the city to buy one.

The Fire Department, working with the corporations that would manufacture their miracle extinguishers, actively publicizes the supposedly tremendous, ever-increasing risk of fires that they claim threaten the population. According to the ambitious firemen, risk factors for worsened fires are everywhere and are ever-increasing – global warming, population growth, take your pick – and the next “big one” is just around the corner. 

Credulous, fearful citizens and heavily lobbied politicians fall for their story, pumping ever more tax dollars into the Fire Department’s research and development program.

The Fire Department develops and grows its stockpile of manufactured fire super-hazards, until one day…

OOPS! 

Somehow, one of the flammable products is released, and a raging conflagration ensues. No one knows exactly how it started – in fact, the chief firemen gather together and publicly deny that any of their products could be responsible. 

But by terrifying the public and confusing the politicians, the firemen coerce the population to shelter in place and follow their strict instructions, lest they perish in the holocaust. After all, the firemen are the experts. 

They heavily promote their special fire extinguishers as the only solution, even managing to get water outlawed for firefighting purposes! (Water wouldn’t work on this kind of fire, they insist. Only the Fire Department’s special extinguishers will suffice.)

Using a huge injection of taxpayer funds, the Fire Department gets their fire extinguishers built in record time, and they hard-sell them to everyone they possibly can. In the meantime, large swaths of the city burn to the ground. And due to the fire extinguishers’ poor design and hasty construction, these devices turn out to be every bit as deadly as the fire, if not worse, for their damaging effects linger long after the fire has burned itself out.

But the firemen and their corporate cronies have secured their fortunes.

The bewildered, traumatized population can’t figure out what happened, any more than the feckless politicians. The Fire Department emerges as the most powerful entity in the city. They resume their “research,” fortified by their growing wealth and power. 

After all, the next big conflagration is just around the corner.

Sound implausible? Think again. Because in the realm of “pandemic preparedness,” the arsonists are running the Fire Department.

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Japanese oncologist: I didn’t have a covid vaccine because I thought the genetic vaccines were foolish from the beginning

On 19 April 2024, Commissione Medico Scientifica Indipendente (“CMSi”) held an online conference titled ‘Perspectives of the World Health Organisation: from advisory body to world government?’.  One of the experts giving a presentation was Prof. Masanori Fukushima. 

Prof. Fukushima is a Professor Emeritus of Kyoto University, Director of the Translational Research Centre for Medical Innovation and the Foundation for Biomedical Research and Innovation, President of the Foundation of Learning Health Society Institute and former Director of the Outpatient Oncology Unit of Kyoto University Hospital. He is the author of more than 290 scientific publications.

During his presentation, hosted by Italian biologist Dr. Panagis Polykretis, Prof. Fukushima said:

 “Genetic vaccines are totally unacceptable. The introduction of transgenes into the human body is gene therapy.   How can this be considered acceptable for creating vaccines?

“If you encapsulate mRNA in nanoparticles and administer it you only get off-target effects starting from the ovaries, to the brain, liver, spleen and bone marrow. The biggest problem is going to the bone marrow, the reproductive organs like the ovaries and then every possible organ.

“The fact that spike proteins are still detected in the rash after more than a year makes it obvious that mRNA is producing spike proteins. There is no way for a year-old spike protein to remain in the rash and be detected.

“I didn’t choose to get vaccinated because I think it was a foolish decision from the beginning.  I haven’t even opted for the flu shot because I consider it an unwise choice.”

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Lancet Autopsy Paper Finally Published After Being Censored

In 2023, The LANCET censored & CANCELLED a ground-breaking COVID-19 Vaccine Injury & Autopsy paper within 24 hours following over 100,000 downloads. It has just passed peer review & is now published

The rapid development of COVID-19 ‘vaccines’, combined with a high number of adverse event reports, has led to concerns over possible mechanisms of injury, including systemic lipid nanoparticle (LNP) and mRNA distribution, Spike protein-associated tissue damage, thrombogenicity, immune system dysfunction, and carcinogenicity.

This systematic review aims to investigate possible causal links between COVID-19 vaccine administration and death using autopsies and post-mortem analysis.

“We found that 73.9 percent of deaths were directly due to or significantly contributed to by COVID-19 vaccination,” said Dr. Wiliam Makis, a radiologist, oncologist, cancer researcher, and author of 100+ publications. The study examined 325 autopsy cases.

“Our data suggest a high likelihood of a causal link between COVID-19 vaccination and death,”

This is a victory of SCIENCE over CENSORSHIP!!

As Makis outlines, Author Nicolas Hulscher’s Incredible perseverance first. They didn’t give up after LANCET pulled our paper within 24 hours after 100,000 downloads for no legitimate reason.

Big pharma put the squeeze on @TheLancet but surprisingly failed to stop us.

The paper was delayed by one year, and many deaths could have been prevented. This paper SHOULD be a game changer. Dr. Makis says that this is the most comprehensive medical report linking autopsies & sudden deaths to the COVID Vaccines.

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Pfizer purchased companies that produce drugs to treat the same conditions caused by covid vaccines

In 2017 a former vice president of Pfizer blew the whistle and said that pharmaceutical companies intentionally design vaccines to keep the public in a state of illness to profit from the treatments of vaccine-induced illnesses. 

Pfizer’s acquisitions of other pharmaceutical companies since the rollout of its covid vaccine seem to indicate this is indeed the case.

In 2021, Pfizer’s acquisition of Arena Pharmaceuticals raised eyebrows. The purchase price seemed disproportionate to the market size of the drug they acquired – a drug that is a potential therapy for all kinds of immuno-inflammatory diseases, including inflammation of the heart.  As we know, myocarditis began to skyrocket after the rollout of Pfizer’s mRNA vaccines.

In 2023, Pfizer purchased Seagen Pharmaceuticals, known for its cancer drugs.  Was this because of the connection between the mRNA injections and “turbo cancers”?

In 2022, Pfizer purchased Global Blood Therapeutics for its drug to treat sickle cell disease, again for an amount that seemed disproportionate to the profit the company could make off the drug considering how many people have the disease.  Does Pfizer know something we don’t? Will we see a blood cell disease epidemic as well?

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