Sandra Finley

Mar 202025
 

The changes in the last years are different.  . . .  The most recent development:

  • NDP – B.C. Premier  Eby’s  “free” dental plan for seniors is subject to conditions of MICROSOFT INC.  (Whaaat?! MICROSOFT?)
  • Un uh. Not to Microsoft, not me.   . . .  “enforcers” might back down today, BUT  they go at it again, and again.   In time they get their way.
  • “Mood changer” drugs are now used.  Fortunately, Kelly is strong in resisting drugs and in speaking up.  It is certainly not easy,  as you know.
  • IMHO,  Mark Carney (aspires to be Prime Ministership)  is more dangerous than Trudeau.  Like Trudeau, Carney is on the WEF Team, like Freeland.
  • RE  Independent Media.  Yesterday I watched a collection of Information re Carney.  From “Juno News”.  I would send you the link but it somehow slipped into Rebel News and I couldn’t find it again.  There appears to be a group of Independent Media working together and Juno News carried the ball on this presentation.   Well done.  Not Rebel content, except as part of a group, I believe.

 

From: Dan
Sent: March 14, 2025 10:00 AM
Subject: Re: FW: The limits of Immanent Critique

Bottom line for me is the line by Solzhenitsyn: “The simple step of the courageous individual is not to take part in the lie.”

 

As much as possible, I don’t take part, and it is damn inconvenient sometimes.

 

Balance – yes, thank god for nature. And now little Liska.

 

I remember a time before the internet. I read books. I had long engaging conversations with humans that were in my presence. Maybe I wasn’t as informed … but then again, how informed does a person need to be?

 

OK, enjoy your day, soak in some nature and engage in a way that gives you meaning!

A promising tool for social change may not be sufficient to contain medical fascism         ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏       ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­͏     ­

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The limits of Immanent Critique

A promising tool for social change may not be sufficient to contain medical fascism

Toby Rogers
Mar 14

 

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I. Introduction: What is Immanent Critique?

The first year of my Ph.D. program I had a supervisor who was a poststructuralist. I came out of every meeting with him more confused than when I went in. Eventually I organized a group with the four other doctoral students who shared this same supervisor and we met a few times for lunch to try to decode what he was saying to us.

At one of these meetings I said, “he keeps suggesting that I do an imminent critique and I have no idea what’s he’s talking about.” Yes, I should have asked for clarification when meeting with my supervisor but the Commonwealth postgrad educational system generally operates from the principle of ‘figure it out for yourself.’

A student in the group who was about to graduate graciously explained that it was not “imminent critique” (as in “happening soon”) but “IMMANENT critique” (“emerging from within”). Turns out Immanent Critique is a whole methodological approach with a rich history. Now after having studied and used it for years I think it’s a brilliant approach to social change.

The etymology of “immanent” is fascinating. From Grok:

The word “immanent” comes from the Latin term immanens, which is the present participle of the verb immanere.

·      Immanere is a compound of in- (“in, within”) and manere (“to remain, to stay”).

·      Thus, immanere means “to remain within” or “to dwell in.”

·      The participle immanens carries the sense of “remaining within” or “inherent.”

The explanation of immanent critique from Grok is so magnificent, I’m just going to quote it at length (even though it pains my soul to use this tool):

Immanent critique is a method of analysis where one evaluates a system, ideology, or set of ideas using its own internal standards, assumptions, or principles — rather than applying external criteria. The goal is to reveal contradictions, inconsistencies, or unfulfilled promises within the system itself, exposing its limitations or flaws from the inside out.

For example, if you were critiquing capitalism using immanent critique, you wouldn’t judge it based on, say, moral ideals from socialism, Christianity, or Stoic philosophy. Instead, you’d look at capitalism’s own stated goals — like efficiency, freedom, or prosperity — and show how it fails to meet those goals on its own terms (e.g., how free markets lead to monopolies that undermine free markets).

The term “immanent” comes from the idea of staying within the thing being examined, as opposed to “transcendent” critique, which brings in outside perspectives. It’s a way to challenge something by holding up a mirror to itself.

Immanent critique is similar to Rapoport’s Rules for how to compose a successful critical commentary:

1.  You should attempt to re-express your target’s position so clearly, vividly, and fairly that your target says, “Thanks, I wish I’d thought of putting it that way.”

2.  You should list any points of agreement (especially if they are not matters of general or widespread agreement).

3.  You should mention anything you have learned from your target.

4.  Only then are you permitted to say so much as a word of rebuttal or criticism.

The difference though is that with immanent critique, one should only offer criticism from within the logic and worldview of the other person rather than imposing it from the outside.

Immanent critique is the ultimate academic flex. It shows that you understand your opponent’s argument better than they understand it themselves. It disarms your opponent without a clash of swords (metaphorical or literal). In general it’s really difficult to change someone’s mind. But if one is to have any chance of changing someone’s mind, immanent critique is probably one of the best ways to do it.

A strong case can be made that the success of the abolition movement, the suffragette movement, Gandhi’s anti-colonial movement in India, and the civil rights movement, to name a few, stems at least in part from their skillful use of immanent critique (although one would have called it something different at the time and each of these movements used a blend of rhetorical and political organizing strategies).

The abolition movement and civil rights movement challenged oppressors in society to live up to the highest values of the Bible, the Declaration of Independence, and the Constitution.

Likewise the suffragettes in the U.S. critiqued the exclusion of women from voting using the internal logic of democracy and appealed to the sweeping emancipatory language of the Declaration of Independence and the Constitution (particularly the Equal Protection Clause of the 14th amendment).

Gandhi successfully challenged the British empire to live up to its stated values of justice, liberty, and the rule of law.

I suppose one could even argue that Luther’s 95 theses were an immanent critique of the Catholic Church in 1517 — particularly the claim in Thesis 21 that the sale of indulgences contradicted scripture and the Church’s own stated mission of salvation through faith and repentance.

II. The use of something akin to immanent critique by the medical freedom movement

When Robert Kennedy Jr. endorsed Donald Trump for president, he said it was to stop the epidemics of chronic disease in children.

Almost immediately the goalposts started to move.

As the medical freedom movement was rebranded as MAHA the focus on the harms of vaccines was broadened to include highly processed foods, seed oils, high fructose corn syrup, food dyes, regenerative agriculture, etc.

The medical freedom movement generally trusts Bobby and by November enough of his supporters shifted to Trump to provide the margin of victory in the election.

When RFK Jr. was nominated as HHS Secretary we were obviously elated and worked hard to get him confirmed (flooding Senator Cassidy’s phone lines with so many calls that his office ceased to function for several days). There was an assumption that RFK Jr. would get to pick his own team to lead NIH, FDA, CDC, and CMS and that he would pick the heroes in the movement including Aaron Siri, Pierre Kory, Joseph Ladapo, Paul Marik, James Neuenschwander, Larry Palevsky, Meryl Nass, Ryan Cole, etc. to lead those agencies.

But then the nomination process got bogged down in politics and we were left with modest institutional reformers (who think that they are radical reformers because that’s what their colleagues keep calling them but the fact that they were not fired during Covid suggests that they carefully stayed within the Overton window amidst the darkest days of the global fascist takeover of society).

Now the MAHA insiders appear to have settled on a strategy that sounds something like this, ‘We never promised that we would withdraw the shots on day 1. Our job is to release all the data and restore proper scientific practices to these agencies.’

I’m actually somewhat sympathetic to this approach (at least I was until Dave Weldon’s nomination to be CDC Director got torpedoed today). As I wrote in a Substack note back in January:

Robert Kennedy Jr.’s big bet is that he can turn institutionalists into paradigm shifting radicals (because modest reforms will not be enough to stave off collapse). It’s a crazy gamble. But I like the guy and hope it works. Quite literally the Republic itself and the future of humanity depend on Kennedy’s wager paying off.

RFK Jr., Del Bigtree, Calley Means, and other MAHA insiders are engaged in a sort of immanent critique. They believe that they can gather enough evidence and present it to the scientific and medical community and somehow move the entire industry to stop poisoning the people in their care.

Specifically, (using the language of immanent critique) the MAHA insiders seem to believe that they can inhabit the logic of allopathic medicine and public health and show that the vaccine program was never actually based on proper double blind randomized controlled trials (the gold standard of evidence for those professions) and that the vaccine program has produced more harm than good for society. (Or something like that — in the replies please post your own immanent critique of allopathic medicine if you wish.)

AND — the argument goes — IF they are successful at convincing the scientific mainstream to stop rigging studies and faking data, the change will be much more enduring and widespread than if we had attempted to overthrow the entire system all at once.

As I said above, changing hearts and minds is difficult. If one wants to change hearts and minds, immanent critique is probably one of the best ways to do it.

III. The limits of immanent critique

Thus far I’ve tried to make the best possible case for immanent critique. As the title of this essay suggests, however, I’m actually here to argue against the use of immanent critique for our purposes in the medical freedom movement.

It seems to me that there are at least two circumstances where immanent critique is the wrong approach to social change — 1.) when dealing with fascism; and 2.) when what you really need is a massive paradigm shift in science. And unfortunately we’re dealing with medical/scientific fascism, so we’re afflicted with both of these exceptions to the general rule.

Let’s take the fascism piece first. The White Rose movement in Germany in 1942, at least in their first leaflet, attempted to use immanent critique and nonviolent resistance to challenge the Nazi regime. They quoted German cultural icons including Goethe and Friedrich Schiller to argue that the regime was betraying core German values of honor and freedom. But the leaders of the White Rose movement were arrested and executed in 1943.

Regarding the sciences… German physicist Max Planck was one of the fathers of quantum theory in the early 20th century. In his autobiography he famously observed:

A new scientific truth does not triumph by convincing its opponents and making them see the light, but rather because its opponents eventually die, and a new generation grows up that is familiar with it.

That statement is often condensed in popular discourse to “science proceeds one funeral at a time.”

Planck knew the scientific process from the inside — he won the Nobel Prize in Physics in 1918. Yet in essence he argued that scientists don’t change their minds when presented with new evidence. For Planck, the process of change in science was more like a series of dynasties — one set of gatekeepers controls the discourse, then they eventually die and a new set of gatekeepers can control a new paradigm. The young guns never actually convince the old guard of anything.

Today the U.S. is characterized by medical and scientific fascism. As you know, vaccine makers were given liability protection in 1986 and over the next four decades they used that Get Out of Jail Free card to enslave society via iatrogenic injury.

I suppose, theoretically, immanent critique should work as well in dismantling fascism as it did with slavery. But fascism moves so quickly and comprehensively to shut down debate that immanent critique does not have time do its work (of changing hearts and minds). It’s notable that the expansion of the vaccine program was accompanied by the largest propaganda and censorship operation in American history.

Immanent critique seems to function best when the transcendent values of freedom, liberty, and/or love are already previously embedded in the system. With fascism I feel like order, hierarchy, and control are ends in themselves even if they were initially proposed as a means of reducing crime and chaos or increasing efficiency.

So too with the scientific community — theoretically, immanent critique should have a reasonable chance of success. In the scientific community internal consistency is a stated goal and it has accessible and explicit standards that one could harness to point out where actual practice falls short.

But the current culture of science and medicine is built to resist change:

·       The training follows a military hierarchy and is often abusive (long hours, lack of sleep) to the point of brainwashing.

·       New entrants in the profession are usually deeply indebted and financially dependent on those above them in the department.

·       Science and medicine are closed systems that do not accept critiques from outside their membership and certainly not from the public at large.

·       The actually existing scientific community is characterized by large egos, lack of self-awareness, rent-seeking behavior, and political fiefdoms even though many of these people believe that they are neutral observers following the data.

·       Whistleblowers cost their superiors money so feedback and reporting mechanisms are discouraged or blocked.

I also think that immanent critique fails in the scientific community because science as currently constituted is largely about economic class. The stated goal is to gather evidence and test hypotheses to better understand the material world. But that ideal gave way to economic self-interest a long time ago. The underlying goal, the end goal, appears to be giving a certain group of people wealth, power, and control over society by any means necessary. Science could be a tool of liberation but the actually existing scientific community is usually in league with its financial backers in the ruling class.

I would just add that Big Pharma started faking data and ignoring harms because they had quarterly profit targets to meet, actual innovation in medicine is really difficult, and regulatory capture is relatively inexpensive yet almost certain to increase revenue. None of those structural problems necessarily changed just because we had an election.

IV. Revolutionary critique

One alternative to immanent critique is revolutionary critique.

A revolutionary critique is an analysis or evaluation of a system, structure, or ideology that seeks to fundamentally challenge and overturn it, rather than merely reform or adjust it. It typically comes from a perspective that views the existing order — whether political, social, economic, or cultural — as deeply flawed, oppressive, or unsustainable, requiring radical transformation to address root causes of injustice or inefficiency.

I don’t want to save allopathic medicine from itself. The existing model of ‘vaccinate, cut, burn, and poison’ is never going to work because it’s based on a fundamental misunderstanding of how the body and the natural world work. At best allopathic medicine is stuck in an 18th century Newtonian understanding of the world that has since been surpassed in every scientific field except medicine and public health.

I want a revolution in how we think about health that will reveal the barbarity and savagery of our current era. I’m not here to restore trust in science and medicine — I want to smash the institutions that are engaged in iatrogenocide so that something new and better can take their place.

I think MAHA is making a tactical error by 1.) assuming that evidence will change minds and 2.) trying to bring along the existing gatekeepers into the new era. To my knowledge, MAHA has NOT solved the problem best described by Upton Sinclair — “It is difficult to get a man to understand something when his salary depends upon his not understanding it.”

If Planck is correct, the existing gatekeepers will never change their minds, the only political opening comes when they die. But in some ways Planck may have been too optimistic. It is entirely possible that the next generation, indoctrinated in the old ways, will just reproduce the same failed paradigms when they come to hold positions of power.

I think this is just a numbers game and we win through assembling the largest army of supporters and mobilizing them in every election from city council to the president and then engaging in grassroots lobbying during the year. I want Sherman’s March to the Sea, not inside baseball and compromise with people who don’t share our values.

One can make the case that these things are not mutually exclusive. An immanent critique can turn into a revolutionary critique. And one can argue that immanent critique is about methods and revolutionary critique is about aims. But in general, I think we need to push for much bigger and more wholesale changes across the board.

V. Conclusion

In the fight for medical freedom no one knows for sure what will work to change hearts and minds. We probably need to hedge our bets with a multitude of different strategies and may the best one win. MAHA is pursuing a strategy akin to immanent critique that seeks to shame/cajole/encourage the scientific and medical communities to live up to their highest standards. Immanent critique has a long track record of producing enduring change in society. But we might be making a category error. Given that immanent critique has not been shown to produce change in fascistic or scientistic systems, perhaps we would be better off pursuing revolutionary change to produce the profound paradigm shifts we seek.

Blessings to the warriors. 🙌

Prayers for everyone fighting to stop the iatrogenocide. 🙏

Huzzah for everyone building the parallel society our hearts know is possible. ✊

In the comments, please let share your thoughts on the way forward for the medical freedom movement.

As always, I welcome any corrections.

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© 2025 Toby Rogers
1600 Pennsylvania Avenue, Washington D.C. 20500
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Mar 202025
 

An Iowa House of Representatives subcommittee advanced a bill to bar the sale and administration of vaccines in the state unless manufacturers waive some of the liability protection granted under federal law for injuries caused by their vaccines.

iowa flag and vaccine bottle
Mar 202025
 

I thought that one day there would be no more reports of toddlers killed by vaccinations.

I wonder if people in Japan have discussions about whether they can afford to lose babies to vaccinations when their Fertility rate is  1.26 births per woman (2022)?    /S

—  – – – – – – – – – —

Citing the deaths of three Japanese children within 24 hours of receiving routine childhood immunizations, the authors of a peer-reviewed study called for a reevaluation of the “risks and benefits of currently approved vaccines” and a review of the childhood vaccination schedule.

vaccine bottle with words "childhood immunizations" and girl

Listen to this article    Download 00:00/09:51

Citing the deaths of three Japanese children within 24 hours of receiving routine childhood immunizations, the authors of a peer-reviewed study called for a reevaluation of the “risks and benefits of currently approved vaccines” and a review of the childhood vaccination schedule.

The study, published March 14 in Discover Medicine by Dr. Kenji Yamamoto, a cardiothoracic surgeon at Okamura Memorial Hospital in Japan, also addressed the increase in post-vaccination adverse events following the introduction of mRNA COVID-19 vaccines in Japan.

The study noted that Japan also has recorded an abnormal increase in excess deaths — or deaths above the amount expected under normal conditions — in the years since the COVID-19 vaccines were introduced.

The authors wrote:

“Globally, questioning vaccination has long been considered taboo, with strong social pressures to conform and be vaccinated. The aggressive promotion of the coronavirus vaccine through biased messaging remains vividly remembered. This atmosphere of conformity may partially explain the lack of significant progress in critically reviewing vaccination practices.

“Furthermore, consideration should be given to temporarily suspending the current vaccination program to determine the full extent of potential harm.”

According to TrialSite News, “These bold assertions — supported by troubling real-world data — pose a challenge to public health authorities, vaccine manufacturers, and media narratives that continue to frame questioning vaccination as ‘anti-science.’”

TrialSite News noted that the study received no external funding and was published in a prominent journal. Springer Nature, the publisher of Discovery Medicine, is the world’s largest academic publisher.

Daniel O’Connor, founder and publisher of TrialSite News, said the study’s publication in a prominent journal indicates “increasing concern post-COVID-19 about the need for validation of certain vaccines.

He said:

“In this case, a mainstream peer-reviewed journal is facilitating a critical examination of recent events, including the tragic deaths of three young children occurring just a day after receiving routine scheduled vaccines. Such incidents should not be happening, and a thorough investigation is necessary.”

Study raises questions about the safety of the childhood vaccination schedule

The study presented data from Japan’s Ministry of Health, Labour and Welfare on three post-vaccination child deaths that occurred within 24 hours of the administration of routine childhood vaccines. The deaths included:

  • A healthy 2-month-old boy who experienced sudden illness 30 minutes after receiving the Hib, rotavirus and pneumococcal vaccines. The boy died 59 minutes after vaccination.
  • A 6-month-old girl with “cold symptoms” who was found dead in her bedroom one day after receiving the hepatitis B, Hib, pneumococcal and four-in-one (pertussis, diphtheria, tetanus, polio) vaccines.
  • A 3-year-old boy with asthmatic bronchitis, allergic rhinitis and febrile convulsions who “appeared lethargic” and had a fever 8 hours after receiving the Japanese encephalitis vaccine and experienced cardiopulmonary arrest 10 hours after vaccination.

Detailed investigations, including autopsies, followed the children’s deaths, according to the study. However, “experts were unable to evaluate a causal link to vaccination.” Instead, the deaths were classified as “evaluation not possible.”

According to the study, such conclusions are “similar to assessments of deaths following coronavirus vaccinations” and raise concerns about “possible external pressures or vested interests influencing such determinations.”

Karl Jablonowski, Ph.D., senior research scientist for Children’s Health Defense, said that the time following vaccination “is one of the foundations” for determining causation when adverse events occur.

The study questioned the safety of the childhood vaccination schedule:

“In Japan, vaccines are administered starting at 2 months of age. By adulthood in 2024, a child will have received vaccines for almost 14 different diseases, with doses delivered either individually or simultaneously. The total number of inoculations increases significantly when booster doses are included.”

The study noted that newly developed vaccines, whose adverse event profiles may not be fully confirmed, are often administered simultaneously with existing vaccines. This raises concerns that promoting simultaneous vaccination could obscure causal links to adverse events from the outset.

A peer-reviewed study published in Cureus in 2023 examined childhood vaccination in highly developed countries, finding a positive correlation between the number of vaccine doses infants receive and infant mortality rates.

The findings of the Cureus study confirmed the outcome of a 2011 study that first identified a positive statistical correlation between infant mortality rates and the number of vaccine doses infants received.

Study links increase in adverse events, excess deaths to COVID vaccines

Yamamoto’s study also raised concerns regarding mRNA COVID-19 vaccines — and their connection to an increased prevalence of post-vaccination adverse events.

“There has been a rise in cases of shingles, monkeypox, syphilis, severe streptococcal infections, measles, sepsis, and post-operative infections in countries administering multiple vaccine doses,” the study stated.

According to the study, such adverse events usually occur in the first two weeks after vaccination, “particularly immunosuppression and lymphocyte reduction, which facilitate infections, especially by coronaviruses.”

Yet, patients experiencing such adverse events were often classified as “unvaccinated” by the Japanese Ministry of Health, Labor and Welfare. After this practice came under scrutiny, subsequent data showed a “low infection rate among unvaccinated individuals” — until the ministry “stopped releasing the statistics.”

The study was broadly critical of Japanese public health authorities, who have continued to promote widespread mRNA COVID-19 vaccination.

“The risk of immunodeficiency associated with frequent messenger ribonucleic acid (mRNA) vaccinations has become increasingly evident, leading to the widespread discontinuation of additional doses, except in Japan,” the study stated, noting that Japan regularly administers mRNA COVID-19 boosters to the elderly.

Japanese authorities have continued such practices despite an abnormally high level of excess deaths — over 600,000 — since the beginning of the COVID-19 vaccination campaign, the study stated.

Noting that the specific factors accounting for this increase remain “contentious,” the study suggested that the high number of excess deaths “cannot be explained solely by corona-related deaths or an aging population.”

Instead, the study suggests that “the increase in vaccine-related deaths may be a significant factor,” noting that “Similar trends are observed in other countries with intensive vaccination programs.”

The study cited the example of a 26-year-old healthcare worker in Japan, who “reportedly died of a brain hemorrhage 4 days after receiving a single dose of the mRNA vaccine early in the vaccination campaign.”

Though the worker’s death was found to be “potentially linked to vaccine-induced immune thrombotic thrombocytopenia,” Japan continued its COVID-19 vaccination campaign, which became “nearly mandatory.”

According to the study, over 99% of deaths occurring immediately after COVID-19 vaccination In Japan were classified as cases where “causality is difficult to determine” — even in instances where autopsies were performed.

The study noted that seven members of Japan’s Health Science Council, which investigates vaccine-related adverse events, “have received donations from pharmaceutical companies.”

“Japan is not alone in its struggles and afflictions,” Jablonowski said. “The U.S. legacy media is so entangled with Big Pharma that being critical of vaccines would be self-infliction. We also have a regulatory body with a high degree of conflicts of interest and have rampantly ignored adverse reactions to vaccines.”

This article was funded by critical thinkers like you.

The Defender is 100% reader-supported. No corporate sponsors. No paywalls. Our writers and editors rely on you to fund stories like this that mainstream media won’t write.

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Japanese public ‘now being inadvertently involved in clinical trials’

The study was also critical of the rapid timeline under which COVID-19 vaccines were developed and released to the public.

“While vaccine development typically requires 7-10 years, the coronavirus disease 2019 (COVID-19) pandemic accelerated the process, leading to the rapid development, approval, and distribution of vaccines without extensive animal or clinical trials,” the study stated.

However, Japan has gone a step further than other countries by becoming the first — and so far only — country to approve a self-amplifying mRNA vaccine, noting that these vaccines have also not been sufficiently tested for safety.

“Vaccination with this product has already commenced, sparking societal concern. It seems the Japanese public is now being inadvertently involved in clinical trials to gather data on vaccine safety and risks,” the study stated.

Japan is currently administering the self-amplifying vaccines to people 65 and over, and 60- to 64-year-olds with severe underlying conditions.

“A big problem with self-amplifying mRNA vaccines is that there’s no ‘off switch,’” Jablonowski said. “Once it’s injected, no one can control for how long or how much antigen your cells will be tricked into producing” potentially leading to immune dysfunction.

The study called for a review of vaccination campaigns “in order to respond to the current changing circumstances” and proposed pre-vaccination medical checks, including blood tests and a review of a patient’s mRNA vaccination history.

“A vaccine risk-aware pediatrician needs to consider this information to risk-benefit balance immunization,” Jablonowski said.

Related articles in The Defender

Mar 202025
 

2.   2025-03-20 Two doctors, with access to the Hospital’s medical records: the 6-year-old girl in Texas did NOT die from measles, as claimed.

2025-03-08 NCI Hearings. Coerced Pfizer Covid Vaccine, 24 year-old health-care worker, Red Deer AB. Cancer took 6 weeks to kill.

Links to the Previous 2 Selections:

2025-03-02    TOXIC COVID VACCINE LOTS IN CANADA  (B.C. info)

2025-02-25   For Your Selection, End of February The Ostriches riding herd on the CFIA!

 

– – – – – – – – – – – – – – –

2025-03-24 Kevin O’Leary:  Carney is Trudeau 2.0. Interview by Candice Malcolm

– – – – – – – – – – – – – – –

3.a.  Carney claims:  Video clips of Carney from news casts were challenged with ACTUAL history that Carney claimed to be his, but clearly wasn’t.   The truth is damaging to Carney.   Next day,  CBC News was a complete white-wash for Carney, as far as I could see.  It perturbed me.

– – – – – – – – – – – – – – –

3.b.      2025-02-17 Mark Carney, short video,  Kelowna.  Hopeful to be prime minister. All the Power he sees.  Sedition.

Carney addressing Liberal gathering.   I transcribed, Carney’s words:

Something that MY Government is going to do is use ALL the powers of the Federal Government, including the EMERGENCY POWERS of the Federal Government, to accelerate the major products that we need . . .

– – – – – – – – – – – – – – –

4.     2025-02-25      End of February The Ostriches riding herd on the CFIA! Includes THE LINKS FOR THE STRAIGHT LINE from about year 2000, for  the genetic engineering that brings us to genetically-engineered vaccinations:  2004, 2005, 2006, 2011, 2012,  2024.

– – – – – – – – – – – – – – –

5.     https://bcrising.ca/save-our-ostriches/           Keep  up-to- date on the fate of the 400 ostriches.   

– – – – – – – – – – – – – – –

7.    2004 We are TIPPED OFF! SUPERB documentary re-done in English, Bertram Verhaag, Life Running Out of Control. No, I think it’s human beings running out of control.

– – – – – – – – – – – – – – –

8.    2025-02-25 WHO DECIDES THE FUTURE? Dire consequences of secretive biotech regulation: Response to Asilomar. From CBAN. Related to Ostriches and Health Canada (CFIA).

– – – – – – – – – – – – – – –

9.     2025-02-24 Watch: How Pesticides Destroyed a Small Town (Ethanol production & neonicotinoid pesticide waste spread over land)

– – – – – – – – – – – – – – –

10.    2025-02-24 Utah Set to Become First State to End Water Fluoridation for All Residents, Brenda Baletti, CHD

– – – – – – – – – – – – – – –

11.    2025-02-19 Latest Measles Outbreaks a Result of Failed Vaccines — Not Failure to Vaccinate. By Sayer Ji, on CHD

– – – – – – – – – – – – – – –

12.    2025-02-18 USDA Has Spent $1.25 Billion on Mass Culling for H5N1 Bird Flu – With Disastrous Consequences

 

– – – – – – – – – – – – – – –

13.     2025-02-17 The Mother of All Frauds?

Mar 202025
 

Today’s interview CORRECTS the media reports that the child’s death (Texas)  was due to the measles virus.

unequivocally, “did NOT die of measles . . .

Tragic for everyone – – a medical mistake.  The parents of the girl provided the LEADERSHIP for the handling of this case.  It is  truly exemplary.

  • with great appreciation also to CHD, to Dr. Pierre Kory and
  • to  Dr. Ben Edwards for their examination and clear explanations.

 

 

https://live.childrenshealthdefense.org/chd-tv/shows/good-morning-chd/breaking-news-doctors-review-texas-measles-medical-records/?utm_source=luminate&utm_medium=email&utm_campaign=chdtv&utm_id=20250319

BREAKING: We, at Children’s Health Defense, have obtained access to the medical records of the girl in Texas with measles who died. After analyzing the documents, Pierre Kory, M.D. has come to the conclusion that this child, unequivocally, “did not die of measles.” His expert assessment on this death is that it resulted from a “grievous” medical error, not purely a breathing condition or viral illness like the media would like us to believe.

In this exclusive interview, Dr. Kory outlines the facts about this case. He explains how the hospital failed to treat with the proper antibiotics at the proper time and allowed for her to die “catastrophically” in a state of shock.

We also hear from Ben Edwards, M.D. — the doctor who has been treating this family and the other Mennonite families in the area. Dr. Edwards shares how the community has been responding to this outbreak and their perspective on the untimely loss, a “tragic mistake.”

 

The link to the earlier interview of the parents, should you wish:  – – –    https://live.childrenshealthdefense.org/chd-tv/shows/good-morning-chd/breaking-news-parents-of-child-in-texas-measles-outbreak-death/

Mar 192025
 

Mark Carney will likely call the Federal Election for  around Easter Time (April 28).

– – – – – – –

Mark Carney: I’m an “elitist and a globalist” but “that’s exactly what we need”

Liberal Leadership hopeful Mark Carney quoted by journalist

                                          Candice Malcolm

I (Sandra)  want to convince you:

Don’t vote for the (Liberals)  Mark Carney.  Carney is  about CONTROL.  A WEF-er, of Klaus Schwab’s ilk.   In a very short video,  in his own words:      (1)     2025-02-17 Mark Carney, hopeful to be prime minister. All the Power he sees.  Sedition.

 Please discuss with your friends.  Send them the 3 videos.   The way in which Carney was “anointed” to become PrimeMinister is disconcerting.

– – – – – – –

Liberal Leadership hopeful Mark Carney admitted to being a globalist and elitist on Saturday, but added that that is exactly what Canada needs.

He made the comments on Saturday February 15th, 2025 on The Rest is Politics podcast with hosts Alastair Campbell – a British journalist and former Labour strategist – and American financier and former Trump spokesman Anthony Scaramucci.

– – – – – – – – – – – – – –  – – – – – – – – – – – – – – – –  –

Video (2)     https://www.youtube.com/watch?v=yr9Vyp1Oepk   

Candyce   (Junonews.com)   and  Kris Sims (Canadian Tax-payers Federation)

 

(2)  https://www.youtube.com/watch?v=coq3oinnHQs

 

 

(3)

 

Mar 122025
 

Bless those who persist.

From today’s posting  “PLAINTIFFS WILL APPEAL . . . a North Carolina federal judge’s ruling, “

“Gardasil is one of Merck’s highest-grossing products. Global sales . . .  totaled $8.6 billion for the year (2024)”.

“(Judge)  Bell’s decision was made public the same day that Merck announced a new $1 billion facility — a 225,000-square-foot manufacturing plant in Durham, North Carolina — slated to produce the blockbuster Gardasil vaccine.”

The 4th posting below,  “Outrage of the father of a Gardasil- vaccinated boy . . .”.   WHY on Earth would a young boy get Gardasil shots?  . . .  As simple as revenue? totaled $8.6 billion for the year (2024).

The coverage I remember about Mothers organizing against the Gardasil vaccine were about injured GIRLS from other countries,  in large numbers.  Heart-breaking cases.  I listened to many of them.

Please share information.   It WORKS.    Canadians need to help out.

I am re-motivated because I reviewed what is known about Gardasil.  It almost makes me sick what these people do for making money.  HOWEVER!   there is GOOD NEWS.

Third link from the bottom of the list, EXCERPT:

A bill introduced late last week in the U.S. House of Representatives would end the liability protections Congress gave vaccine makers under the 1986 Childhood Vaccine Injury Act.

Thirty Republican lawmakers signed on as co-sponsors to House Bill 9828, End the Vaccine Carveout Act. The proposed legislation would end the broad protection from liability for injuries resulting from vaccines listed on the Centers for Disease Control and Prevention’s (CDC) Childhood Immunization Schedule.

“The … vaccine makers are criminal enterprises that have paid tens of billions in criminal penalties over the past decade,” Children’s Health Defense (CHD) founder and chairman on leave Robert F. Kennedy Jr. said in a statement on the bill.

Kennedy, who has long advocated for eliminating liability protection for vaccine manufacturers, added, “By freeing them from liability for negligence, the 1986 statute removed any incentive for these companies to make safe products. If we want safe and effective vaccines we need to end the liability shield.”

Today’s posting about THOSE WHO PERSIST   is below.

POSTINGS RELATED TO GARDASIL (HPV Vaccine).

2025-03-12 Plaintiffs Will Appeal Ruling in Merck Gardasil Vaccine Injury Case. Brenda Baletti, CHD        (below)

2019-05-15 RFK, Jr.: Gardasil “The Science” Video and Other Facts

2018-09-02 Vaccinations, Gardasil (HPV Vaccine), Update

2017-2018  Vaccines: outrage of the father of a boy vaccinated for HPV (Merck’s Gardasil) without parental consent. Wetaskwin, Alberta, Canada . Edmonton Journal “Opinion” is propaganda for Merck.   (Merck may have spent some of the $8.6 billion on advertising??)

2018-02-21 Vaccines, more on Gardasil (HPV): Letter to Alberta School Division. Using schools to cut parents out of Vaccination Decisions?

While it is not clear exactly what is causing so many adverse reactions, it is known that Gardasil contains genetically engineered virus-like protein particles as well as aluminum, which can affect immune function.    Further,  . . .   (go to the article if you’d like to read further)

That’s 26 reported deaths of young, previously healthy, girls after Gardasil vaccination in just one year  (INSERT, S:   in just one country, the U.S.)

While it is not clear exactly what is causing so many adverse reactions, it is known that Gardasil contains genetically engineered virus-like protein particles as well as aluminum, which can affect immune function.    Further,  . . .   (go to the article if you’d like to read further)

UPDATE:    It would have been nice if I had I received the

Maryland HPV letter, by Josh Mazer   before I sent my letter to the Alberta School Board!

2024-10-29 NIH (U.S.) EHR (Electronic Health Records). Spending $2.2 Million to ‘Nudge’ to Get More Vaccines. University “Nudge Units”. The “Nudge Ladder”. Baletti, CHD.

2024-09-30 Covid: 30 Lawmakers Sponsor Bill to End Liability Protection for Vaccine Makers

2022-01-20 Bill Gates, Indian Government Targeted in Lawsuit Alleging AstraZeneca Vaccine Killed 23-Year-Old

2017-11-28 High Aluminum Found in Autism Brain Tissue, Children’s Health Defense (Vaccinations)

= = = = = =  = = =

TODAY’S  NEWS:  APPEAL OF THE COURT DECISION

Plaintiffs in a bellwether lawsuit against Merck alleging the company concealed the risks of its Gardasil HPV vaccine today said they will appeal a North Carolina federal judge’s ruling, handed down Tuesday, in favor of the pharmaceutical giant.

merck building and gardasil box

Plaintiffs in a bellwether lawsuit against Merck alleging the company concealed the risks of its Gardasil HPV vaccine today said they will appeal a North Carolina federal judge’s ruling, handed down Tuesday, in favor of the pharmaceutical giant.

Michael Baum, lead attorney for the plaintiffs, told The Defender:

“We will be appealing the court’s order concluding that all of the Gardasil cases filed in federal court are preempted. In our view, none should have been.

“We believe the court failed to recognize that vaccine adverse event databases (VAERS and VigiBase), numerous case studies and Merck’s internal data clearly showed reasonable evidence of a causal association between Gardasil and autoimmune conditions like POTS [postural orthostatic tachycardia syndrome] and POI [primary ovarian insufficiency].”

The lawsuit against Merck was the first of the “bellwether cases,” 16 cases selected as exemplar cases from a larger pool of more than 200 lawsuits pending in federal court against Merck for injuries related to its Gardasil vaccine.

In August 2022, the cases were consolidated into multidistrict litigation in a single court. The consolidation allowed Gardasil lawsuits filed throughout the country to move into coordinated discovery and pretrial proceedings. It also means that the judge’s decision in this case can apply to all of the pending cases.

The plaintiffs in the first bellwether case alleged that Merck knew Gardasil carries multiple risks, including POTS and POI, more commonly known as ovarian failure, but violated the law by failing to warn the public.

However, U.S. District Judge Kenneth Bell ruled that Merck did not have authority under federal law to add warnings to the vaccine’s label without prior approval from the U.S. Food and Drug Administration (FDA).

Federal law preempts the plaintiffs’ claims that Merck violated state laws when it failed to warn the plaintiffs of potential side effects, Bell said.

Bell said his decision extends to all of the 200-plus cases pending against Merck in federal court.

Plaintiffs reject judge’s claim of insufficient evidence to justify label change

In his decision, Bell said Merck didn’t have enough evidence to justify a label change showing that Gardasil could cause POTS or POI by 2011 and 2013, respectively, when the plaintiffs’ expert witness said warnings should have first been given.

Bell said only a few cases of those conditions had been reported by then and that broader studies had not, at that time, established causal associations.

The plaintiffs, however, said that not only was there evidence of a link at that time — which the judge failed to consider — but also that considerable evidence has since accumulated demonstrating the link and that evidence should be considered.

The plaintiffs in the 16 bellwether cases all received multiple doses of the Gardasil vaccine between 2012 and 2021 — after the 2011 date cited by the court. They all developed either POTS or POI after vaccination and allege that Merck failed to add those conditions as possible vaccine side effects to the label.

Bell’s decision was made public the same day that Merck announced a new $1 billion facility — a 225,000-square-foot manufacturing plant in Durham, North Carolina — slated to produce the blockbuster Gardasil vaccine.

A Merck spokesperson told Fierce Pharma that the company is “extremely pleased” with the court’s decision.

‘The fight goes on’ for those injured by Gardasil

In his ruling, Bell said that, as per the regulation, a label change by Merck would be required if there was “reasonable evidence” of a causal association based on newly acquired information and “during the relevant timeframe.”

He cited testimony by plaintiffs’ expert, Stephen Amato, Ph.D., who argued warnings should have been added by 2011 for POTS and 2013 for POI.

That means, Bell said, his decision focused on whether Merck had convincing evidence that Gardasil could cause POTS and POI between 2006, when the drug was approved, and 2011, which he said was a relevant timeframe.

On that basis, Bell excluded all evidence that arose both before and after the 2005-2011 timeframe. That includes new analyses of pre-approval and post-marketing data and revelations of misreporting — including Merck’s failure to include data on the presence of DNA fragments in Gardasil vials.

In his expert testimony, Amato argued early warnings should have been added based on existing post-marketing data and also that over time — after 2011 and 2013 — substantially more evidence appeared through statistical analysis of adverse event reporting systems and case series published in the scientific literature.

Bell treated those dates as a date to limit his analysis instead of how Amato presented them, which was as a starting point for when sufficient evidence was first available.

“Limiting its analysis to pre-2011 data is, we believe, in error, especially in light of the significantly elevated reporting of POTS and POI since 2011,” Baum said.

“For example, in a Danish Health Authority analysis, POTS was reported in post-HPV vaccination over 100 times more than all other vaccines,” he said. “Our experts found similar significant elevated reporting of POTS.”

Baum added:

“The bottom line is that there was a large volume of evidence that we think was misapprehended by the court. We are optimistic that the Court of Appeals will recognize that this preemption decision should be reversed.”

Kim Mack Rosenberg, an attorney for the plaintiffs and general counsel for Children’s Health Defense, said, “While we are disappointed in the decision, we believe there is substantial evidence that shows that the court’s decision was an error and we’re hopeful that the U.S. Court of Appeals will reverse the decision.”

“The fight goes on for those who have been injured by the Gardasil vaccines,” said Mack Rosenberg, who is also co-author of “The HPV Vaccine on Trial: Seeking Justice for a Generation Betrayed.”

‘The fight goes on’ for those injured by Gardasil

In his ruling, Bell said that, as per the regulation, a label change by Merck would be required if there was “reasonable evidence” of a causal association based on newly acquired information and “during the relevant timeframe.”

He cited testimony by plaintiffs’ expert, Stephen Amato, Ph.D., who argued warnings should have been added by 2011 for POTS and 2013 for POI.

That means, Bell said, his decision focused on whether Merck had convincing evidence that Gardasil could cause POTS and POI between 2006, when the drug was approved, and 2011, which he said was a relevant timeframe.

On that basis, Bell excluded all evidence that arose both before and after the 2005-2011 timeframe. That includes new analyses of pre-approval and post-marketing data and revelations of misreporting — including Merck’s failure to include data on the presence of DNA fragments in Gardasil vials.

In his expert testimony, Amato argued early warnings should have been added based on existing post-marketing data and also that over time — after 2011 and 2013 — substantially more evidence appeared through statistical analysis of adverse event reporting systems and case series published in the scientific literature.

Bell treated those dates as a date to limit his analysis instead of how Amato presented them, which was as a starting point for when sufficient evidence was first available.

“Limiting its analysis to pre-2011 data is, we believe, in error, especially in light of the significantly elevated reporting of POTS and POI since 2011,” Baum said.

“For example, in a Danish Health Authority analysis, POTS was reported in post-HPV vaccination over 100 times more than all other vaccines,” he said. “Our experts found similar significant elevated reporting of POTS.”

Baum added:

“The bottom line is that there was a large volume of evidence that we think was misapprehended by the court. We are optimistic that the Court of Appeals will recognize that this preemption decision should be reversed.”

Kim Mack Rosenberg, an attorney for the plaintiffs and general counsel for Children’s Health Defense, said, “While we are disappointed in the decision, we believe there is substantial evidence that shows that the court’s decision was an error and we’re hopeful that the U.S. Court of Appeals will reverse the decision.”

“The fight goes on for those who have been injured by the Gardasil vaccines,” said Mack Rosenberg, who is also co-author of “The HPV Vaccine on Trial: Seeking Justice for a Generation Betrayed.”

2024 sales of Gardasil hit $8.6 billion

Gardasil is one of Merck’s highest-grossing products. Global sales for the drug dropped 3% in 2024 overall but still totaled $8.6 billion for the entire year.

Merck markets the vaccine as “safe and effective,” but the lawsuits allege the drugmaker fast-tracked Gardasil through the FDA approval process and deceptively conducted clinical trials to mask serious side effects and exaggerate the vaccine’s effectiveness.

Some of the signature reactions observed following HPV vaccination — which afflict a number of the plaintiffs — include permanently disabling autoimmune and neurological conditions, fibromyalgia and myalgic encephalomyelitis/chronic fatigue syndrome.

There have been thousands of reports of adverse events worldwide, peer-reviewed scientific literature from the U.S., Australia, Denmark, Sweden, France and Japan, and statistics published by public health agencies in each of these countries demonstrating associations between HPV vaccination and autoimmune conditions.

Recent documents made public in a similar case against Merck in California state court showed that Merck knew its Gardasil vaccine was contaminated with DNA, but covered it up.

Evidence from that trial also showed that Merck cherry-picked data to claim there was no link between its Gardasil vaccine and POTS.

Related articles in The Defender

Mar 082025
 

With thanks to Dianne for sending in:

“All three of my health agencies—NIH, CDC, and FDA—the acting heads of those agencies—have all recommended against the use of the bird flu vaccine.”

Nicolas Hulscher, MPH
Mar 7
 
READ IN APP
 

By Nicolas Hulscher, MPH

According to CBS News:

Federal health agencies oppose the use of bird flu vaccines in poultry right now, Health and Human Services Secretary Robert F. Kennedy Jr. said, weighing in publicly on it for the first time in his new role.

There’s no indication that those vaccines actually provide sterilizing immunity and all three of my health agencies, NIH, CDC, and FDA, the acting heads of those agencies have all recommended against the use of the bird flu vaccine,” Kennedy said in an interview on Fox News published this week.

Kennedy’s remarks mark a sharp turn from the Biden administration, multiple former officials said.

Kennedy said the new opposition from his health agencies was based on concerns that vaccinating poultry without being able to provide sterilizing immunity would amount to “turning those birds into mutant factories,” resulting in worrying genetic changes to the virus. “That could actually accelerate the jump to human beings,” Kennedy said.

We’ve in fact said, at the USDA, that they should consider maybe the possibility of letting it run through the flock so that we can identify the birds and preserve the birds that are immune to it,” Kennedy had said.

These comments provide a sigh of relief to the many who were deeply concerned about Medgene’s “protein-based prescription-platform vaccine,” which was on the verge of USDA approval for cattle vaccination:

BREAKING – USDA Approval Imminent for H5N1 Bird Flu Vaccine in Cattle

 

Nicolas Hulscher, MPH ·
Mar 1
By Nicolas Hulscher, MPH

 

Read full story

At last, America has public health leadership that uses common sense and the most up-to-date science. Mass animal depopulation for H5N1 bird flu prevents population immunity, while widespread vaccination would accelerate viral evolution—prolonging the crisis, destabilizing the food supply chain, and increasing the risk to humans.

A recent study by Li et al found that mass vaccination of animals against H5N1 with a non-sterilizing vaccine during a widespread animal pandemic can accelerate viral evolution, leading to more virulent strains and increasing the risk of a human pandemic:

Mass depopulated poultry farms remain non-operational for approximately four months following H5N1 pooled PCR detections. Under the “stamping out” protocol, entire flocks are culled within 24 to 48 hours of a positive pooled PCR test—where swabs from 11 birds are combined into a single test tube—even if most birds appear healthy. The lack of marking on swabbed birds makes it impossible to distinguish healthy birds from infected ones. As a result, farms remain non-operational for an average of 111 days, leading to a never-ending cycle of mass culling, human infections, and food supply chain disruptions. Current biosecurity protocols are not sustainable, as chickens will never obtain herd immunity and migratory birds continue to spread H5N1:

Nicolas Hulscher, MPH

Epidemiologist and Foundation Administrator, McCullough Foundation

www.mcculloughfnd.org

Please consider following both the McCullough Foundation and my personal account on X (formerly Twitter) for further content.

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Mar 052025
 

In January, after an appeals court ruled against Children’s Health Defense (CHD), CHD petitioned the Supreme Court to hear its case alleging Meta colluded with Biden administration officials to censor CHD. Meta waived its right to file a response to CHD’s petition. However, in a letter to the company’s attorneys, the court directed Meta to file a reply by March 31.

The U.S. Supreme Court last week asked Meta to respond to a petition filed by Children’s Health Defense (CHD) asking the court to hear its case against the social media giant over its collusion with government officials to censor CHD content on Facebook.

In January, CHD petitioned the Supreme Court to hear the case, which had been rejected in the 9th Circuit U.S. Court of Appeals. Meta waived its right to file a response to CHD’s petition, but in a letter to the company’s attorneys, the court directed Meta to file a reply by March 31.

Commenting on the news, CHD CEO Mary Holland told The Defender:

“We see this as a good sign. When we asked the Supreme Court to hear our case, Meta declined to file a reply, even though it had the right to do so. This latest move by the Supreme Court may delay the court’s final decision on whether it will hear our case, but it also suggests the court has questions that it believes Meta should address.”

CHD sued Facebook in November 2020, alleging Biden administration officials targeted the organization and its then-chairman Robert F. Kennedy Jr., and Facebook cooperated by censoring CHD’s speech — particularly speech related to vaccines and COVID-19 — that should have been protected under the First Amendment.

 

Mark Zuckerburg over fb and ig logos Notice of being unpublished fb and ig

Tell Mark Zuckerberg 
to Restore Our 
Facebook Account!
Sign the Petition

 

Facebook first took action against CHD in May 2019, removing or restricting CHD posts. Censored posts included data on the risks of COVID-19 vaccines, remdesivir, and ventilation, as well as having the temerity to raise the benefits of natural immunity and alternative treatment with ivermectin and other protocols.

In August 2022, Facebook, rebranded in 2021 as Meta, deplatformed CHD from Facebook and Instagram and has yet to reinstate the accounts.

On Aug. 9, 2024, the 9th Circuit ruled against CHD.

CHD General Counsel Kim Mack Rosenberg said, “Since this case was originally filed, and even since the 9th Circuit issued its decision, more and more information has come to light regarding Meta’s censorship activities, including some telling statements by Meta Chairman and CEO Mark Zuckerberg.”

She added:

“That the U.S. Supreme Court has now required Meta to respond seems a hopeful sign that the court is taking our petition seriously and that we also will get a chance to respond to Meta’s submission.”

Zuckerberg admitted caving to government censorship demands

CHD’s lawsuit against Meta also named “fact-checking” firms Science Feedback, and the Poynter Institute and its PolitiFact website.

On Jan. 27 — less than 24 hours after CHD asked the Supreme Court to hear its case — Zuckerberg announced the company was ending its third-party “fact-checking” program.

CHD launched a petition in January asking Zuckerberg to restore its Facebook and Instagram accounts. The petition has 20,804 signatures.

When Zuckerberg announced he was ending the company’s third-party fact-checking program, he admitted that during the pandemic, government officials pressured — as he told Joe Rogan, “would call up our team and, like, scream at them and curse” at them — Facebook to censor content that was factually accurate but didn’t align with the official government narrative.

Now, he says, his company is committed to “restoring free expression.”

After Zuckerberg made his public comments, CHD filed a letter with the Supreme Court, arguing that Zuckerberg’s public comments contradicted its statements to the lower courts that its decisions to censor CHD had been “internal decisions” and the White House’s actions hadn’t changed Meta’s behavior.

Attorney Roger Teich, who is representing CHD in its case against Meta, said he’s “grateful” the court has taken this latest step, given the importance of the issues CHD raised about Meta’s conflicting statements.

“Our state-action allegations cut across easy political characterizations,” Teich said. “Of course, Zuckerberg’s kowtowing to the new administration while continuing to censor CHD may also be a factor that gives us perhaps a fighting chance that the Court may want to review this issue.”

National healthcare and constitutional practice attorney Rick Jaffe, who is not involved in the case but represents CHD in other cases, said, “I view the order to the respondents to file a response despite their waiver as a positive indication. It seems that some members think enough of the petition that they want to hear the other side.”

“My speculation is that Zuckerberg’s recent admissions, adeptly pointed out by Roger Teich’s supplemental letter to the Court, made some members want a response from Meta,” he added.

In an op-ed published in January by RealClear Politics and the New York Post, Holland said the issues at stake in the case affect the entire American public.

She wrote:

“Ultimately, this debate is not about any one group or individual but all of us. How many people suffered or lost their lives because they didn’t have access to information that could have helped them make better-informed decisions about their health?

“The American public is better served with more information rather than less, especially when it is grounded on data-based scientific information. People are smart enough to make up their own minds.”

Related articles in The Defender