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France: ANY Criticism Of The mRNA DEATHVAX™ Platform Punishable Up To 3 Years Imprisonment And 45,000 Euros

2nd Smartest Guy in the World | February 15, 2024

The WEF-captured government of France has pushed through a draconian new law entitled Article 4. This Orwellian and unconstitutional color of law power grab is a purposely poor attempt at obscuring the irrefutable slow kill bioweapon death and destruction data.

What makes Article 4 particularly incendiary is that the majority of the French population has been outright refusing all “vaccinations.” Throttling their free speech as it pertains to gene modifying poisons will only increase the already heightened tensions between the criminal Macron administration and the awakening French populace, by design.

Between WEF puppet Trudeau in Canada and WEF puppet Macron in France, there is now a race to create the most totalitarian technocommunist nation in the West, with France now taking a slight lead; to wit:

These policies and “laws” are nothing more than an extension of the ongoing democide, and the associated iatrocide.

Meanwhile, back in the USSA, the Center for Disease Crimes (CDC) is still at it with their “Trust the Science” mendacity and murder:

Readers of this Substack fully appreciate the myocarditis and turbo cancer epidemics currently underway — not to mention soaring excess non-PSYOP-19 mortality — since the rollout of the “vaccines:”

Removing all BigPharma legal liabilities and prosecuting the various “health” agencies like the FDA, CDC, NIH, et al. has never been more urgent.

France’s Article 4 is just a hint at what is to come, especially if the WHO’s Pandemic Treaty scam ever passes in the various nations that they are attempting to further hijack.

They want you dead.

Do NOT comply.

February 16, 2024 Posted by | Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science | , , , | Leave a comment

Freedom Convoy leaders sue Trudeau regime for targeting protesters with Emergencies Act

By Anthony Murdoch | Life Site News | February 15, 2024

OTTAWA, Ontario — On the second anniversary of Prime Minister Justin Trudeau’s government’s use of the Emergencies Act (EA) to quash the truckers’ Freedom Convoy in 2022, the heads of the protest, Tamara Lich and Chris Barber, and a host of others have filed a $2 million lawsuit against the Trudeau government.

The lawsuit, announced yesterday by Freedom Convoy lawyer Keith Wilson, includes Lich as well as other convoy leaders Chris Barber, Tom Marazzo, Danny Bulford, and a host of others.

“On the 2-year anniversary of the Federal Government illegally invoking war measures against its citizens and targeting key protestors in Ottawa by freezing their bank accounts, today Tamara Lich, Chris Barber, Tom Marazzo, Danny Bulford and other protestors who were targeted by @JustinTrudeau and @cafreeland have filed lawsuits against the Federal Government.”

Wilson said that Section 24 of Canada’s Charter of Rights and Freedoms “gives Canadians the right to sue their government for damages when Charter rights are violated.”

“Doing so affirms the seriousness of respecting Charter rights and is intended to deter future governments from breaching Canadians’ fundamental rights.”

Wilson noted that the lawsuits seek $2 million in damages.

Lich, on X (formerly Twitter) noted about the lawsuit on Wednesday that “Accountability is a thing. It’s go time!”

“Happy Emergencies Act Day! I hope you all look back and fondly remember how your government shot you with rubber bullets and tear gas for your own good!” she also wrote.

Tom Marazzo, who was also involved with the Freedom Convoy and is a 25-year Canadian army veteran, said about it that it was “2 years ago today, instead of celebrating Valentine’s Day, the most corrupt government in Canadian history, launched an all out illegal assault on the Rights and Freedoms of every Canadian citizen in Canada, with the help of the NDP, Bloc, MSM and the Banks.”

Further details about the lawsuit will be forthcoming in the next few days.

The lawsuit comes just after a Canadian federal court last month ruled that the Trudeau government’s use of the Emergencies Act to quash the truckers’ Freedom Convoy in 2022 was unconstitutional. The court ruled that the use of the EA was a direct violation of the Charter and thus “not justified.”

The EA controversially allowed the government to freeze the bank accounts of protesters, conscript tow truck drivers, and arrest people for participating in assemblies the government deemed illegal.

An investigation into the use of the EA, as per Canadian law, was launched by Trudeau. However, it was headed by Liberal-friendly Judge Paul Rouleau, who led the Public Order Emergency Commission. This commission was to investigate the Liberal government’s unprecedented use of the EA against the anti-mandate Freedom Convoy protest. Unsurprisingly, the commission exonerated Trudeau’s use of the EA.

Freedom Convoy leaders Lich and Barber have been involved in a lengthy trial after being charged and taken to court by the federal government for leading the protests. The trial has not yet concluded and has been put on hold, with its resumption date uncertain. It is also not yet clear how the recent court ruling will affect the trial.

In early 2022, the Freedom Convoy saw thousands of Canadians from coast to coast come to Ottawa to demand an end to COVID mandates in all forms. Despite the peaceful nature of the protest, Trudeau’s government enacted the EA on February 14, 2022. Trudeau revoked the EA on February 23.

During the clear-out of protesters after the EA was put in place, one protester, an elderly lady, was trampled by a police horse, and one conservative female reporter was beaten by police and shot with a tear gas canister. Rebel News reporter Alexa Lavoi, while covering the Freedom Convoy, was shot point blank in her leg with a rubber pellet, which police were using against protesters.

On February 14, 2022, the day the EA was invoked, Canadian Deputy Prime Minister and Minister of Finance Chrystia Freeland mandated certain bank accounts be frozen under the EA. In total, close to $8 million in funds from 267 people were locked. Additionally, 170 bitcoin wallets were frozen.

The freezing of bank accounts by Freeland without a court order was an unprecedented action in Canadian history and was only allowed through the Liberal government’s invocation of the never-before-used EA.

February 16, 2024 Posted by | Civil Liberties | , , | Leave a comment

New York’s Proposed Minor Consent Law ‘Dangerous’ and ‘Misleading,’ Critics Say

By Suzanne Burdick, Ph.D. | The Defender | February 12, 2024

New York state lawmakers are weighing legislation that would allow any child or teen under 18 to seek out and consent to medical treatment — including vaccines, dental procedures, hospitalization and even surgery — without parental consent, as long as the minor appears to have the mental capacity for making that decision.

Assembly Bill A6761, introduced by New York Assemblymember Karines Reyes (D-Bronx), also would allow Medicaid funds to pay for procedures and drugs administered to children.

Proponents of the legislation, such as the American Civil Liberties Union of New York, say the measure is about ensuring all youth have access to quality care.

But critics, including John Gilmore, founder and executive director of the nonprofit Autism Action Network, said the bill is dangerous.

“The bill’s biggest problem,” Gilmore told The Defender, “is that it allows any medical procedure to be done to children of any age without parental knowledge or consent. That’s the kicker.”

Gilmore said the bill has another problem, too: The “active summary” statement on the official New York Assembly website says it “allows homeless youth to give effective consent to certain medical, dental, health, and hospital services.”

But Gilmore said that statement is “deliberately misleading” because the bill’s text applies to more than just “homeless” youth seeking “certain” services.

The bill states:

“Any person, including a minor, who comprehends the need for, the nature of, and the reasonably foreseeable risks and benefits involved in any contemplated medical, dental, health, and/or hospital services, and any alternatives thereto, may give effective consent to such services for themself, and the consent of no other person shall be necessary.”

Albany is lying” about the bill, according to Autism Action Network.

Michael Kane, a New York resident and founder of Teachers For Choice, agreed. “It’s a complete lie to say the bill applies only to homeless children or runaways — and it’s a dangerous one,” Kane told The Defender. “It’s imperative that legislators understand what the bill really does,” Kane said.

With New York lawmakers considering close to 10,000 bills, legislators may rely on a bill’s one-sentence summary — rather than reading its full text — for deciding how they vote, according to Gilmore.

The bill has a companion in the Senate (S8352), introduced Jan. 19 by state Sen. Rachel May (D-Syracuse). The bills share identical text.

Unclear how practitioners would assess minor’s ‘capacity to comprehend’

According to the latest version of the bill, a minor could consent to:

  • General medical, dental, health and hospital services.
  • Mental health outpatient services.
  • Substance abuse treatment.
  • Immunizations.
  • Family planning services.
  • Sexually transmitted disease (STD) diagnosis and treatment.

The bill states that a practitioner may administer a vaccine if “they have reason to believe that a person in parental relation to the child … objects to the immunization.”

It also states, “A child who may give effective consent [to various medical interventions] … may give such consent to their own immunization, and the consent of no other person shall be necessary.”

The bill allows minors under 16, in certain circumstances, to access psychotropic drugs or psychotherapy without parental consent.

Psychotropic drugs include a host of pharmaceutical products, including medications for depressionanxiety, sleep disorders, schizophrenia, bipolar disorder and attention-deficit/hyperactivity disorder.

Current New York law allows minors 16 or older residing in a hospital to agree to psychotropic medications without parental consent if any of the following conditions are met:

  • A parent or guardian “is not reasonably available” and the physician determines “the minor has the capacity”; or
  • requiring parental consent “would have a detrimental effect on the minor”; or
  • the parent has refused consent, providing that two physicians (including a psychiatric doctor who does not work for the facility) agree the medications are in the minor’s best interests.

A6761/S8352 would allow minors under 16 in these circumstances to do the same, as long as the youth “comprehends the need for, the nature of, and the reasonably foreseeable risks and benefits involved.”

The bill does not include detailed information on how medical practitioners would assess a minor’s capacity to comprehend the potential risks of a potential treatment.

It does, however, define “capacity” as follows:

“The minor’s ability to understand and appreciate the nature and consequences of the proposed treatment, including the benefits and risks of, and alternatives to, such proposed treatment, and to reach an informed decision.”

Children’s Health Defense General Counsel Kim Mack Rosenberg told The Defender that informed consent is a “serious” thing, but this legislation devotes “little attention to how to determine if a child can truly exercise informed consent, how to obtain that consent and why true informed consent is critically important.”

Who is a ‘minor’?

The bill does not provide a clear definition of “minor” that applies across all amended laws. However, some sections of the law define or describe the age thresholds related to minor consent:

  • In the amendments to the mental hygiene law section 9.13(a), anyone under 16 would still need parental/guardian consent to be admitted as a voluntary patient to a hospital.
  • In amendments to mental hygiene law 33.21(a)(1), a “minor” is defined as a person under 18, excluding some special cases like emancipated minors or minors who are parents.
  • In amendments to section 2305 of public health law, treatment for STDs without parental consent is allowed for those under 21.

However, earlier sections of the bill do not specify any age range for minors, suggesting even young minors could consent as long as they demonstrate appropriate “capacity.”

Even infants?

It appears the bill’s sponsors may believe that even an infant can give consent. That’s because section 18 of public health law omits previous language stating that children older than 12 can determine who gets access to their medical records.

This deletion suggests that a child of any age no longer “may” but “shall be notified of any request by a qualified person to review their patient information” and deny access to it if they so desire.

The bill states that an infant can choose to withhold information from its parents, without explaining how that would be possible:

In summary, there isn’t one definition of “minor” in the bill, but it seems for most purposes “minor” refers to anyone under age 18.

Minor consent bills bulldoze’ over decades of laws honoring parental rights

The U.S. has a strong legal history going back many decades that honors parental rights and recognizes that the state should step in only where parents are unfit to care for their children, Rosenberg said.

“Minor consent bills bulldoze over those longstanding decisions,” she said. “They try to exclude parents from medical decision-making and take over the parenting role.”

Rosenberg said she’s seen more bills like this recently being introduced in other states, such as Vermont. “We [CHD] successfully stopped one in the District of Columbia and are fighting laws and regulations elsewhere,” she said.

Kane called the bill “just horrendous” because it “completely eradicates parental control over what happens medically to our children.”

Meanwhile, a staff member for Reyes’ office who chose to remain anonymous told The Defender she disagreed, saying the bill was primarily about ensuring all kids have “access to care” and that it included “guardrails” to ensure that not all parental consent was stripped away in all situations.

For instance, the bill explains that a minor must “knowingly and voluntarily” seek care, the staff member said.

But Rosenberg said she’s concerned about the legal ramifications of the bill’s broad language — which appears to erase parental consent for “any contemplated medical, dental, health, and/or hospital services, and any alternatives thereto.”

Rosenberg told The Defender the bill was “rife with problems too numerous to address in brief remarks.”

The bill makes clear, she said, that minors can consent to vaccinations without their parents’ knowledge or consent — and that medical staff and insurance companies must hide that vaccination information from the parents unless the child permits them to share it.

Children “literally may inadvertently take their lives into their own hands” if they make serious healthcare decisions without parental involvement, Rosenberg said.

For example, children frequently don’t know their own health history — let alone their family health history — which may put them at an increased risk for an adverse reaction to a medication or treatment, she explained.

Rosenberg said:

“The legislators supporting these bills need to ask themselves what they would do if a child or grandchild of theirs consented to a surgical procedure of whatever kind requiring anesthesia and the child suffered death or irreversible harm if they had a reaction to the anesthesia.

“Is that a phone call they’d like to receive?”

‘Not a chance’ bill’s sponsors unaware of misleading statement

New York already has a law on the books about homeless youth giving consent for certain services.

Passed in 2022, A09604/S08937 allows “runaways and homeless youth under the age of 18 who are receiving approved crisis or support services to consent to medical, dental, health and hospital services.”

Gilmore, who has done legislative analysis in New York for 23 years, said, “Both Rachel May and Karines Reyes voted for the bill that was passed in 2022.”

So why would they talk about homeless youth in the summary of the new measure they introduced?

A staff member for Reyes’ office told The Defender a bill’s summary statement is written by lawyers — not by the legislator who introduces the bill.

It’s plausible the lawyers chose that language since the bill amends the same section of public health law (2504) that was amended earlier in the law about homeless youth and runaways, the staff member said. However, the staff member confirmed that the present bill does pertain to all minors.

The Defender also reached out to May’s Legislative Director Eric van der Vort, but he did not respond by our publication deadline.

Gilmore said he contacted legislators, too, but didn’t get a straight answer. When he asked van der Vort about the summary language, “he simply refused to address it in any way,” Gilmore said.

Reyes’ Chief of Staff Justin Westbrook-Lowery confirmed for Gilmore that the bill applies to all minors in New York but didn’t explain why the summary statement talked about homeless youth.

Amy Paulin (D-Scarsdale), who chairs the Assembly Committee on Health and co-sponsored the bill, “has a large staff and they’re very good at what they do,” Gilmore said. “There’s not a chance that they aren’t quite aware” that the bill’s summary statement doesn’t match what the bill would do.

Kane said he’s heard from New York legislators and staffers that they believe the bill affects only homeless children.

“There’s a lot of people in the Assembly starting to co-sponsor the bill, which is scary,” he said. “We don’t want this thing passed so that we end up litigating against it for the next five years.”

The Defender asked May’s media relations staff what May would like to tell parents concerned about being excluded from medical decision-making regarding their child’s health, but did not receive a response by our publication deadline.


Suzanne Burdick, Ph.D., is a reporter and researcher for The Defender based in Fairfield, Iowa.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

February 13, 2024 Posted by | Civil Liberties, Full Spectrum Dominance | , | Leave a comment

“But those [Lipid] Nanoparticles can lead to dangerous side effects, especially if a patient has to take repeated doses”

Quote from a story following an interview in 2016 with Stéphane Bancel, CEO of Moderna

By Dr. Byram W. Bridle | COVID Chronicles | February 9, 2024

Please share this information with anyone considering taking another dose of a modified RNA shot.

Did you know that the lipid nanoparticles (LNPs) used to make Moderna’s and Pfizer’s COVID-19 shots were re-purposed to serve as vaccine platforms? They were originally intended to be a delivery mechanism for drugs and/or gene therapies. The problem is that the LNPs were toxic if administered multiple times. And treatment of cancers and other diseases with LNPs containing drugs or gene therapies required multi-dosing protocols.

For this reason, several companies abandoned the use of LNPs. Moderna decided to change course and use LNPs as a vaccine delivery system. Why? Because they understood that an ideal vaccine is one that requires a single dose and then the person is protected from getting the disease for the rest of their life. If you don’t believe me, please review Health Canada’s official definition of an ideal vaccine. This is the relevant quote…

“An ideal vaccine is: safe with minimal adverse effects; effective in providing lifelong protection against disease after a single dose that can be administered at birth; inexpensive; stable during shipment and storage; and easy to administer.“

So, problem solved. A good LNP-based vaccine would require only a single dose. No multi-dosing = none of the toxicities known to be associated with multiple administrations of LNPs.

But, don’t take my word for it. Instead, I defer to a journalist that interviewed Stéphane Bancel. He is the Chief Executive Officer of the American company Moderna, which makes one of the two available modified RNA COVID-19 shots. A story was published on September 13, 2016, after an interview with him. Please heed his serious concerns about the LNPs that his company is using. Here are quotes from the story about the interview; brace yourself…

“In nature, mRNA molecules function like recipe books, directing cellular machinery to make specific proteins. Moderna believes it can play that system to its advantage by using synthetic mRNA to compel cells to produce whichever proteins it chooses. In effect, the mRNA would turn cells into tiny drug factories. It’s highly risky. Big pharma companies had tried similar work and abandoned it because it’s exceedingly hard to get RNA into cells without triggering nasty side effects.

“Delivery – actually getting RNA into cells – has long bedeviled the whole field. On their own, RNA molecules have a hard time reaching their targets. They work better if they’re wrapped up in a delivery mechanism, such as nanoparticles made of lipidsBut those nanoparticles can lead to dangerous side effectsespecially if a patient has to take repeated doses over months or yearsNovartis abandoned the related realm of RNA interference over concerns about toxicity, as did Merck and Roche.

I encourage you to re-read the two quotes above a couple of times. Let them sink in. Then think about the billions of people around the world that have taken multiple doses. Isn’t it astonishing?

Why did Bancel not remind the world of these concerns in 2020 when he realized that his ‘vaccine’ was far from ideal and that multiple doses would be required.

I don’t know if it is relevant, but this is the second last sentence in Wikipedia’s description of Stéphane Bancel…

“In April 2020, with the Moderna share price rising on news of imminent phase 2 human trials for its potential COVID-19 vaccine, Bancel’s stake of about 9% became worth over $1 billion.“

Also, note that Moderna, which was a small start-up company not all that many years ago would have gone under had its attempt at a LNP-based vaccine not been successful. Moderna was ‘all in’ on this business move.

Remarkably, some people are still eager to get more doses. I have heard of some that have received at least nine doses. This is downright frightening in light of concerns identified after the interview with CEO Bancel, “especially if a patient has to take repeated doses over months or years.

I would love to know how many legitimate doses Stéphane Bancel has taken of his own COVID-19 shot.

And journalists should ask him to explain the information he relayed in 2016, as presented in the follow-up to his interview.

More doses anyone?

How about more LNP-based shots for other problems, like disease X, in the future?

February 12, 2024 Posted by | Deception, Timeless or most popular, War Crimes | , | Leave a comment

Audio recording leaked from AstraZeneca

Frank conversation comically revealing

BY JOHN LEAKE | COURAGEOUS DISCOURSE | FEBRUARY 7, 2024

Sasha Latypova recently published a leaked audio recording of an AstraZeneca internal executive meeting at the end of 2020.

I recommend reading her entire post about this recording. To me, two statements really stand out.

Speaker 2 [I believe that’s Mark Esser]: Excellent! So, thank you for the introduction, Mark, and it’s really a pleasure to share with all of you a little bit of the journey that the “long-acting antibody” team has taken in 2020, but actually our story begins back in 2017 in the basement of a Quality Inn in Tysons Corner VA at the Defense Department Industry Day [BARDA runs “industry days” on regular basis].  There, I met Col. Matt Hepburn, who is actually the architect of the Pandemic Prevention Program or P3, and the goal of P3 was going from the discovering a novel virus to producing drugs in less than 60 days – something that would normally take 6 years at best. To me that sounded more like science fiction than science, but we signed up in a small and committed team of virologists and molecular biologists and engineers and started working in 2018 on new technologies to discover and manufacture antibodies against viruses.

His statement reminds of something a mediocre prizefighter might say if a mafia boss tells him: “We’ve selected you to win the title from the reigning division champion?”

“Really, I can do that?” he would probably reply.

In this case, the capo (Col. Matt Hepburn) is a leading member of the DoD/HHS Countermeasure Racket that was erected following the passage of the PREP Act in 2005.

In fact, as Mark learned the hard way, his rapidly developed antibody product against SARS-CoV-2 did not work and was pulled from the market by the FDA in early 2023.

The second, highly notable statement was made by AstraZeneca’s CEO, Pascal Soriot:

Thank you, Mark, and congratulations again to you and the team. This long-acting antibodies are quite unique because this is the only combination that potentially will last more than 6 months, up to potentially 12 months and protect people for a long period of time.  And for those of you who may not be totally familiar with antibodies, you know, you have to know a number of people cannot be vaccinated, like if you have an immune disease, lupus or some other immune condition… or multiple sclerosis, you cannot be vaccinated. So, there are millions of people in the world that will need the protection that cannot be coming from a vaccine, so the long-acting antibody has the enormous potential.

Soriot clearly understood that the so-called COVID-19 vaccines would, best case scenario, only provide some protection for six months. He also understood that these injections were NOT appropriate for all of humanity, and would pose a serious health risk to people with or at risk of developing auto-immune syndromes.

February 9, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular | | Leave a comment

Who does ‘our’ NHS really serve?

Still relentlessly promoting covid ‘safe and effectives’

Health Advisory & Recovery Team | February 7, 2024

A concerned reader sent in this letter inviting him for more covid and flu injections, as he was considered a ‘priority’ case:

The fact that the NHS is wasting millions of taxpayer pounds continuing to promote and administer these ineffective and harmful products is symbolic of what the health service has become; another cog in the medical industrial machine, whirring to improve Pharma profits with little or no concern for end-user health. In a service allegedly crushed by lack of resources, why on earth are they still pushing these products on an unsuspecting public?

You will note in the full letter that:

  • There is no mention that the injections stop infection;
  • There is no mention that the injections stop transmission;
  • They make the dubious claim that injections lead to “less severe illness” without backing up this statement.
  • They use the misleading statement that ‘seasonal vaccines have proven safety records‘. This is certainly not the case for covid injections as they have not existed long enough and no-one has bothered to collect the data.

It seems that even the NHS has abandoned the mendacious claims originally attached to the ‘Safe and Effectives™’ probably because they know it would open them up to legal action. The propaganda job is complete. For those poor souls still unquestioningly worshipping at the alter of the quasi-religious NHS, a promise of real benefit is now surplus to requirements in the ad campaign. It has seamlessly transformed into an annual ritual to benefit drug companies whilst causing insidious harm to the collective health of the nation. What a clever spell they have cast to make entire populations believe that good health is only achievable by injecting unidentified substances into their body on a seasonal basis. And if they feel awful directly afterwards? It means its working!!

Evil genius.

If anyone can find the time and has received such a letter, the claim of “proven safety records” deserves a Freedom of Information request to “please supply all reports memos papers statistical analyses etc supporting the claim of “proven safety records”. We would love to see the response should one be forthcoming. We won’t hold our breath.

February 9, 2024 Posted by | Deception, Science and Pseudo-Science | , | Leave a comment

Professor Didier Raoult Calls for COVID-19 Vaccine Moratorium

BY JOHN LEAKE | COURAGEOUS DISCOURSE | FEBRUARY 4, 2024

Of the many remarkable characters we write about in our book The Courage to Face COVID-19: Preventing Hospitalization and Death While Battling the Bio-Pharmaceutical Complex, Professor Didier Raoult may be the most fascinating and colorful. A May 12, 2020 feature in the New York Times introduced him to American readers as follows:

Raoult … has made a great career assailing orthodoxy, in both word and practice. “There’s nothing I like more than blowing up a theory that’s been so nicely established,” he once said. He has a reputation for bluster but also for a certain creativity. He looks where no one else cares to, with methods no one else is using, and finds things.14

A tireless researcher, he has published 2,300 papers and is the most cited microbiologist in Europe. He and his team have discovered 468 species of bacteria—about 1/5 of all those named and described. The bacteria genus Raoultella was named in his honor. He is probably best known as the discoverer of the so-called giant virus, so large it had previously been mistaken for an intracellular bacterium. He has won 13 major awards and is a Commander of the National Order of Merit.

Like Dr. McCullough, Professor Raoult strongly advocated early treatment of COVID-19, and he conducted multiple studies demonstrating the efficacy of hydroxychloroquine combined with azithromycin, especially when administered early. In return for his efforts to save his patients, he has been relentlessly persecuted by France’s official medical establishment in Paris.

Now comes the news that Professor Raoult is calling for a moratorium on COVID-19 vaccines. The following is a translation from his recent, French language post on X:

Propaganda and knowledge. We’re the good guys, but we’re not ignorant! When vaccines were developed against Covid, 3 types of vaccines were proposed: – Traditional vaccines (as quickly available as the others) made in China with the entire inactivated virus. These vaccines have not been authorized in France for reasons that escape me. This type of vaccine, comparable to that against the flu, carries fewer unknown risks and does not fight against a single target of the virus: the Spike. I feared, and this happened, that the mutations of the virus and its respiratory specificity would not provide lasting immunity and that the vaccine would not have a very long duration of protection because I published the first known case of reinfection with covid. The disease being poorly immunizing, the vaccine would not do any better.

The second vaccine (the English one from Astra Zeneca, that from Johnson and Johnson, and the Russian Sputnik) is a vaccine based on a virus (Monkey Adenovirus for Astra Zeneca), transformed by integrating the Spike gene. It doesn’t integrate or replicate. I was the first in France to report an accident of cerebral venous thrombosis, this phenomenon is well described in particular in young women and England stopped its prescription for those under 50, followed by many countries and finally it is no longer used in France. There are millions of expired doses left.

The 3rd group of vaccine (Pfizer, Moderna) consists of the injection of RNA coding for the Spike whose elements have been modified so as not to be eliminated quickly. This vaccine is included in a lipid nanoparticle to be able to enter cells. This vaccine, in addition to the disadvantages common to the others, presented unforeseen side effects: extremely frequent menstrual disorders (now recognized by the CDC) of which no one can say whether they will be associated with consequences on fertility, myocarditis and sometimes fatal pericarditis in young people (mainly boys, now recognized by the CDC) and rare thromboses of the veins (recognized by all scientific authorities).

None of these vaccines had been evaluated for mild or asymptomatic forms and therefore for the prevention of contagion. They could not claim to eradicate a disease which, moreover, was circulating among animals. Vaccination was then only justified in those who were at risk of serious forms (subjects over 65 years of age and fragile subjects (obese, immunocompromised). Now we see that the quality controls on batches of Pfizer vaccines do not appear to meet required standards. There should be no DNA or minute doses due to the risk of introducing it into cells through nanoparticles, because DNA easily enters the nuclei and integrates into the chromosomes like a virus with consequences unknown because lymph node cancers can be the natural consequence (Epstein Barr virus, HTLV virus and Helicobacter pylori). The quantity of DNA in the vaccine doses is much higher than that announced in the samples tested. Each batch of Pfizer should be tested, it is easy in any laboratory to do a DNA PCR to check the quantity. Let those who don’t believe it do so!

Finally, we cannot inject a drug without knowing what it will produce in the body. A very unpleasant surprise published in Nature in December 2023 shows that modified RNAs can produce unknown proteins. This should be explored on a large scale because among the proteins that could be created in this way, one of them is an amyloid which would be released while it is in the natural Spike, coated in a protein and without danger. These free amyloids, which can be produced by vaccines through reading errors, can be the cause of amyloidosis plaques which cause various diseases, including neurological ones. All this is knowledge for the knowers, not opinions for scavengers. Given the demonstration of this phenomenon, the consequence of vaccination must be studied in humans, which has not been done.

At this stage of knowledge, it is reasonable to follow Denmark into a moratorium on Covid vaccination. Indeed, the effectiveness is doubtful because new variants appear which make current vaccines ineffective (millions of doses have been thrown away) and the manufacturing of new vaccines based on current variants will be outdated when they are available because new variants will circulate. Other countries are reaching these conclusions, the “surgeon general” of Florida has called for a total stoppage of the Pfizer vaccine, the attorney general of Texas (Mr. Paxton) has just attacked Pfizer for disinformation and censorship (what a reversal!). American and English parliamentarians question administrative and political leaders about their decisions, where we are surprised to see Fauci, the head of covid management in the USA, saying that social measures (masks, confinement, curfew) do not serve to nothing and B. Johnson apologize for his management in England! Humans are not stupid, covid vaccination rates and Pfizer shares are plummeting. It is time to take up the problem, de-dramatize it and treat the patients, re-evaluating it by competent people. At least ten molecules have shown effectiveness on the disease and do not cost much. This must stop being an opportunity for the industry and become a problem for doctors again!

February 5, 2024 Posted by | Science and Pseudo-Science | , | Leave a comment

The covid booster cancer time bomb

By Professor Angus Dalgleish | TCW Defending Freedom | January 30, 2024

I have previously reported on my concern about the rise in stable cancer relapses that I have witnessed in my melanoma clinic.

None of these patients of mine presented with the classic prodrome of relapse that I had always noticed previously, such as severe depression due to bereavement, divorce or bankruptcy. Indeed the only thing I found they had in common was to have had a recent booster mRNA covid vaccine. I phoned around my colleagues not only in the UK but also in Australia to check their experience. In no case did they deny such a link. Indeed, they were equally alarmed at the association between booster vaccines and relapse that they too were witnessing, as well an increase in new cancers, particularly in those below 50 years old. In addition to melanoma these colleagues were also very concerned about a sudden big increase in young patients with colorectal cancer.

Rather than instigating a proper inquiry to investigate this when we raised these concerns, the medical authorities told us all that what we were witnessing was a coincidence, that we had to prove it and above all, not to upset our patients.

Recently the American Cancer Society (ACS) has warned of a surge in new cancer cases in the US this lastyear of over 2million, with many of these cases occurring in younger patients. Indeed, the chief scientific officer of the ACS, William Dahat, announced in addition that cancers were presenting with more aggressive disease and larger tumours at the time of diagnosis, especially in younger patients. Of further interest it noted a difference in the microbiome (the community of micro-organisms such as fungi, bacteria and viruses that exist in a different environment) between patients under 50 compared with those over 50.

This surge mirrors a report from Phinance Technologies of late last year which analysed in detail data from the UK Office for National Statistics (ONS) which showed that disability and deaths in 2021 and 2022 had increased dramatically in all age groups, but especially in the 15-44 age group.

The Lancet also published an article before Christmas reporting excess deaths post covid pandemic to be up by 11-15 per cent over than expected for under-25s and for between 25-49 year olds. This is in fact the pattern found in many countries that have looked at the data. Germany for example has reported excess deaths rising from 7 per cent in 2020 to 24 per cent in 2023. 

What makes this all the more surprising is that negative deaths should be the norm after a pandemic as you cannot die twice!

The link between covid vaccines and myocarditis and early death particularly in the young, highlighted by Peter McCullough and colleagues as well as by Aseem Malhotra here in the UK, is incontestable. Now we have a confirmatory report from the CDC in the US, data that the authorities here have refused to act on so as not to alarm vaccinated patients!

Although it is obvious that these excess deaths are real and are continuing to rise, all we get from our Chief Medical Officer, Sir Chris Whitty, are risible attempts to explain away the increase, such as that it is a result of patients not getting their statins in lockdown (hey, patients under 55 do not get statins routinely!) The situation is no better in the US where Harvard researchers have put the blame on sleep disturbance!

The first obvious candidate is lockdown itself when the National Health Service became the National Covid Service and all screening was cancelled or delayed, resulting in an increase in cancer detection and late presentation. Many negative lifestyle factors almost certainly increased as a result of lockdown, such as a lack of exercise and too much food, especially takeaways.

What very few of these reviews consider is that this rise in excess deaths could be a result of the booster vaccine programme, even it clearly follows the vaccine rollout programme starting in 2021 and increasing in 2022 and 2023.

With regards to the link to cancer, there are numerous reports in the literature of cancers arising within days of the vaccines being administered, especially in the case of lymphomas and leukaemias. There are several reports of PET scan mapped tumours exploding at the site and draining area of covid injections with the advice to inject covid vaccines away from known cancers! Outside my clinical observations, several friends have developed cancer after a totally unnecessary covid booster taken only to facilitate travel.

For a possible association between a booster vaccine and the appearance of cancer we need a plausible scientific causal explanation. Unfortunately for those who still insist that these cases are mere coincidences, there are several compelling ones to choose from:

Firstly, it has been reported that T cell responses are suppressed after the boosters (not the first two injections) and that this is especially marked in some cancer patients.

Secondly, the antibody repertoire switches after the first booster from a protective IgG1 and IgG3 dominant B cell response to a tolerising IgG4 one, made worse by further boosters, as reported in a recent Science Immunology paper. As many cancers are controlled by effective T cell led immunity, the sudden perturbation of this control would clearly explain the development of B cell leukaemia and lymphomas, melanoma renal cell cancers and colorectal ones, all tumours which can respond to immunotherapy.

Another report by Loacker et al in Clin Chem Lab Med shows that mRNA vaccines increase PD-L1 on granulocytes and monocytes, which means they effect the very opposite of what the immunotherapy agents do against these tumours, and whichin turn explains why many of these tumours appear to be resistant to this otherwise effective therapy. Taken together, the effect on the immune response of these boosters can easily explain the relapses and so-called turbo-charged cancers appearing.

Other reports document the presence of DNA plasmids and SV 40 (a known cancer-inducing gene) sequences, as well as the ability of mRNA to bind to important suppressor genes. Although this is controversial and has been challenged, it has led to the realisation of significant batch-to-batch variation that could enhance the cancer process yet probably not manifest itself for a few years. The very possibility that we could be sitting on a vaccine-inducing cancer time bomb means that we must never again get involved into a mass vaccine programme for another possible Disease X.

But unless the government wakes up to this now, we will be at the mercy of the World Health Organization doing the very same thing when they decide to release the Disease X virus in order to take back control and destroy our lives all over again.

February 3, 2024 Posted by | Science and Pseudo-Science | , | Leave a comment

The “NO LIABILITY” aspect of the unlicensed, novel vaccine developed in 100 days is in-your-face in the WHO’s proposed treaty

BY MERYL NASS | FEBRUARY 2, 2024

The globalist lawyers who drafted the pandemic treaty definitely anticipated injuries from the 100 day vaccines. So what did they do? They made sure that all the nations signing up to the Treaty “shall shall shall” i.e., MUST give the WHO, its lawyers, the nations, the manufacturers, the doctors and anyone else involved a bullet-proof liability shield.

Just in case someone did not understand, they said it 3 times3 different ways, in 3 paragraphs. I screenshot what they said so there would be no confusion.

If you don’t want the mandated experimental vaccines for which nobody is liable, join us to fight against this nonsense. DoorToFreedom.org

https://apps.who.int/gb/inb/pdf_files/inb7/A_INB7_3-en.pdf

February 3, 2024 Posted by | Aletho News | , | Leave a comment

CDC IN HOT SEAT OVER SKEWED COVID DATA

The Highwire with Del Bigtree | February 1, 2024

During COVID, the public was fed fearful numbers showing exaggerated death rates in unvaccinated populations. Where did they get this data and how accurate was it?

February 2, 2024 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, Video, War Crimes | , | Leave a comment

Medicine Has Been Fully Militarized

By Clayton J. Baker, MD | Brownstone Institute | January 30, 2024

I am thinking of a certain industry. See if you can guess what it is.

This industry is huge, constituting a large portion of the nation’s GDP. Millions of people earn their living through it, directly or indirectly. The people at the top of this industry (who operate mostly behind the scenes, of course) are among the super-rich. This industry’s corporations lobby the nation’s government relentlessly, to the tune of billions of dollars per year, both to secure lucrative contracts and to influence national policy in their favor. This investment pays off richly, sometimes reaching trillions of dollars.

The corporations supplying this industry with its materiel conduct advanced, highly technical research that is far beyond the understanding of the average citizen. The citizens fund this research, however, through tax dollars. Unbeknownst to them, many of the profits gained from the products developed using tax dollars are kept by the corporations’ executives and investors.

This industry addresses fundamental, life-or-death issues facing the nation. As such, it relentlessly promotes itself as a global force for good, claiming to protect and save countless lives. However, it kills a lot of people too, and the balance is not always a favorable one.

The operational side of this industry is emphatically top-down in its structure and function. Those who work at the ground level must undergo rigorous training that standardizes their attitudes and behavior. They must follow strict codes of practice, and they are subject to harsh professional discipline if they deviate from accepted policies and procedures, or even if they publicly question them.

Finally, these ground-level personnel are handled in a peculiar manner. Publicly, they are frequently lauded as heroes, particularly under declared periods of crisis. Privately, they are kept completely in the dark regarding high-level industry decisions, and they are often lied to outright by those at higher levels of command. The “grunts” even significantly forfeit some fundamental civil liberties for the privilege of working in the industry.

What industry am I describing?

If you answered, “the military,” of course you would be correct. However, if you answered “the medical industry,” you would be every bit as right.

In President Eisenhower’s farewell speech of January 17, 1961, he stated that “…in the councils of government, we must guard against the acquisition of unwarranted influence, whether sought or unsought, by the military-industrial complex.” Sixty-three years on, many Americans understand what he was referring to.

They see the endless cycle of undeclared wars and decades-long foreign occupations that are undertaken on nebulous or even outright false pretenses. They see the ever-hungry mega-industry that produces super-expensive, high-tech killing devices of every imaginable form, as well as the steady stream of traumatized soldiers that it spits out. War (or, if you prefer its Orwellian nickname, “defense”) is big business. And as Eisenhower warned, as long as those profiting from it drive the policy and the money stream, it will not only continue, it will continue to grow.

Other mega-industries – the medical industry in particular – have generally fared better in public perception than the military-industrial complex. Then came Covid.

Among its many harsh lessons, Covid has taught us this: if you substitute Pfizer and Moderna for Raytheon and Lockheed Martin, and swap the NIH and CDC for the Pentagon, you get the same result. The “medical-industrial complex” is every bit as real as its military-industrial counterpart, and it is every bit as real a problem.

As a physician, I am embarrassed to admit that until Covid, I possessed only an inkling that this was so – or more accurately, I knew it, but didn’t realize how bad it was, and I didn’t worry about it too much. Sure (I thought), Pharma engaged in dishonest practices, but we’d known that for decades, and after all, they do make some effective drugs. Yes, physicians were increasingly becoming employees, and protocols were dictating care more and more, but the profession still seemed manageable. True, healthcare was far too expensive (gobbling up a reported 18.3 percent of the US GDP in 2021), but healthcare is inherently expensive. And after all, we’re saving lives.

Until we weren’t.

By early-to-mid 2020, it became obvious to those paying attention that the Covid “response,” while promoted as a medical initiative, was in fact a military operation. Martial law had effectively been declared approximately on the Ides of March 2020, after President Trump was mysteriously convinced to cede the Covid response (and practically speaking, control of the nation) to the National Security Council. Civil liberties – freedom of assembly, worship, the right to travel, to earn one’s living, to pursue one’s education, to obtain legal relief – were rendered null and void.

Top-down diktats on how to manage Covid patients were handed down to physicians from high above, and these were enforced with a militaristic rigidity unseen in doctors’ professional lifetimes. The mandated protocols made no sense. They ignored fundamental tenets of both sound medical practice and medical ethics. They shamelessly lied about well-known, tried-and-true medicines that were known to be safe and appeared to work. The protocols killed people.

Those physicians and other professionals who spoke out were effectively court-martialed. State medical boards, specialty certification boards, and large healthcare system employers virtually tripped over each other in the rush to delicense, decertify, and fire dissenters. Genuine, courageous physicians who actually treat patients, such as Peter McCullough, Mary Talley Bowden, Scott Jensen, Simone Gold, and others, were persecuted, while non-practicing bureaucrats like Anthony Fauci were hailed with false titles like “America’s Top Doctor.” The propaganda was as nauseating as it was blatant. And then came the jabs.

How did this happen to medicine?

It all seemed so sudden, but in fact it has been in the works for years.

Covid taught us (by the way, Covid has been such a harsh tutor, but haven’t we learned so much from her!) that the medical-industrial complex and military-industrial complex are deeply connected. They are not just twins, or even identical twins. They are conjoined twins, and so-called “Public Health” is the tissue shared between them.

The SARS CoV-2 virus, after all, is a bioweapon, developed over a period of years, funded by US tax dollars in a joint effort between Fauci’s NIH and the Department of Defense to genetically manipulate the transmissibility and virulence of coronaviruses (all done in the name of “Public Health,” of course).

Once the bioweapon was out of the lab and into the population, the race was on within the medical-industrial complex to develop and market the supremely profitable antidote to the bioweapon. Cue the full-on military takeover of medicine: the martial law lockdowns, the suppression of cheap and effective treatments, the persecution of dissidents, the ceaseless propaganda and anti-science, and the unabashed whoring of most hospital systems for CARES Act money.

We know the rest. The ill-conceived, toxic, gene-therapy antidote, falsely billed as a “vaccine,” was foisted upon the population by blackmail (“the vaccine is how we end the pandemic”), the effective bribery of medical authorities and politicians, as well as other Deep-State directed psyops designed to divide the population and scapegoat dissenters (“pandemic of the unvaccinated”).

The end result even sounds like the aftermath of a gigantic military operation. Millions are dead, many millions more are psychologically traumatized, economies are in tatters, and a few warmongers are fantastically rich. Moderna CEO Stephane Bancel (who, incidentally, oversaw the construction of the Wuhan Institute of Virology years ago) is a freshly minted billionaire. And not one of those who caused all the mischief are in prison.

At this writing, virtually all the major healthcare systems, specialty regulatory boards, specialty associations, and medical schools are standing at attention, still in lockstep with the received – and by now, clearly false – narrative. Their funding, after all, be it from Pharma or the Government, depends upon their obedience. Barring dramatic change, they will respond in the same fashion when orders come down from above in the future. Medicine has been fully militarized.

In his farewell address, Eisenhower said something else that I believe is most prescient here. He described that a military-industrial complex fostered “a recurring temptation to feel that some spectacular and costly action could become the miraculous solution to all current difficulties.”

Enter Disease X.

C.J. Baker, M.D. is an internal medicine physician with a quarter century in clinical practice. He has held numerous academic medical appointments, and his work has appeared in many journals, including the Journal of the American Medical Association and the New England Journal of Medicine. From 2012 to 2018 he was Clinical Associate Professor of Medical Humanities and Bioethics at the University of Rochester.

January 31, 2024 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | , , | Leave a comment

Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule

By Brenda Baletti, Ph.D. | The Defender | January 29, 2024

Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science.

Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review.

The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule.

After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail.

Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs).

Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials.

They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.”

They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters.

“It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote.

Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies.

It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender.

“Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added.

According to McCollough, “mRNA should never have been authorized for human use.”

Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.”

Here are six takeaways from the review:

1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner

Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years.

To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote.

The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease.

However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines.

There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction.

The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself.

The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.”

The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added.

2. Steps were taken in trials to overestimate vaccine efficacy 

Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do.

“No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote.

Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.”

Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19.

There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%.

The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety.

Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote.

Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine.

The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate.

One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large.

According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility.

While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively.

“A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote.

As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death.

However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote.

And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.”

They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19.

One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19.

A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues.

3. The trials underestimated the adverse events, including death, despite evidence in the data. 

Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here.

First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group.

“Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked.

Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population.

None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote.

Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended.

During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data.

And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports.

Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.”

In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.”

This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.”

4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary.

Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population.

The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants.

Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.”

After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke.

And millions of AEs have been reported to those systems.

Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system.

In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervousimmune, reproductive and other systems.

The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious.

In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal.

“The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.”

5. The failure to appropriately test for safety and toxicity poses serious problems. 

Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs.

Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues.

That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids.

Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown.

McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns.

Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time

This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown.

6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness.

The review points readers to a series of papyrus that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines.

“The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection.

They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself.

They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants.


Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

January 30, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular | | Leave a comment