Aletho News

ΑΛΗΘΩΣ

Government Minister Steps in to Defend Met Office as Fake Temperature Scandal Escalates

By Chris Morrison | The Daily Sceptic | December 19, 2025

In a couple of weeks’ time, the Met Office is likely to announce another ‘hottest year evah’ in the UK. The message will be broadcast faithfully by trusted messengers in mainstream media, keen to prop up the fading Net Zero fantasy, but greeted with howls of derision across social media. Eye-opening investigative research over the last two years has revealed a national temperature network mainly composed of ‘junk’ inappropriate sites and massive data inventions across over 100 non-existent stations. Now the British Government has stepped in with the suggestion that questioning the Met Office’s shoddy measuring systems “weakens trust in science”. Misinformation is said to have proliferated on “conspiracy networks”.

Step forward Lord Patrick Vallance, the former Government Chief Scientific Adviser at the heart of the Covid lockdown panic but now an unelected Science Minister in the Labour Administration. “There has been a growing online narrative in some online and social media spaces attempting to undermine Met Office observations and data,” he observes. Vallance’s conspiracy claims echo similar comments made earlier in the year by the Met Office. The investigative efforts of a small number of people were said by the state meteorologist to be an “attempt to undermine decades of robust science around the world ‘s changing climate”.

Only in the world inhabited by Vallance and the Met Office can a conspiracy be whipped up when rigorous examination and questioning is applied to scientific data. From Covid to climate, it seems the scientific process is a closed book to state scientists following the settled political narrative. One of the ‘conspirators’ is citizen sleuth Ray Sanders, who has undertaken a forensic examination of nearly 400 individual Met Office recording stations. Commenting on the official ministerial response, he observed that not one word constituted a scientific approach. “It is a political monologue of the lowest order,” he opined.

Regular co-conspiratorial readers will of course be aware of the reporting problems at the Met Office. Over the last 18 months, the percentage of sites in junk CIMO Classes 4 and 5 with ‘uncertainties’ due to nearby unnatural obstacles of 2°C and 5°C respectively has climbed from 77.9% to over 80%. In that period, the number of pristine Class 1 sites capable of measuring an uncorrupted ambient air temperature over a large surrounding area has fallen from 24 to just 19. Ray Sanders has catalogued most of the unsuitable sites producing measurements taken by airport runways, in walled gardens, near main roads and in the middle of solar farms. Daily high unnatural heat spikes, amplified by the recent introduction of more accurate electronic devices, are an obvious unaddressed problem, but they are often fed into the official statistics. One such 60-second spike in July 2022 pushed the temperature at RAF Coningsby up to 40.3°C, a declared national record that is widely publicised.

Meanwhile, temperature databases are awash with non-existent stations and invented data. Explanations that the ‘estimates’ are taken from ‘well-correlated neighbouring stations’ might be more convincing if those stations could be identified. Freedom of Information (FOI) efforts by Ray Sanders seeking such details have been dismissed as “vexatious” and “not in the public interest”. The picture has emerged of a very rough-and-ready network, suitable for specific local temperature reporting at places such as airports, but unconvincing in promoting widespread average temperatures down to one hundredth of a degree centigrade.

The Vallance explanations are contained in a letter written to the Conservative MP Sir Julian Lewis following concerns raised by Derek Tripp, a local councillor in his constituency. He notes that in September, the Met Office decided to remove estimated data from three non-existent stations on its historic temperature database. “They recognised that confusion could be caused when there appears to be a continued flow of data on this website from stations that have closed,” he said.

In fact the confusion was caused by the Daily Sceptic seeking FOI details in November of well-correlated neighbouring stations responsible for data at one of the stations, namely Lowestoft. The well-correlated explanation is often used by the Met Office and formed the basis of an earlier ‘fact check’ by Science Feedback that seems to have relied exclusively on text provided by the Met Office. Sanders had earlier determined that there were no such stations within a reasonable distance of Lowestoft. The Met Office admitted under FOI that it did not use such stations but rather made estimates using its HADUK-Grid. This was little more than passing the buck since HADUK-Grid inputs temperature information from nearby stations, none of which it seems can ever be identified.

Vallance went on to note that the historic dataset was for “general interest only and is not intended for climate monitoring purposes”. Curiously, Vallance failed to point out that this was a very recent explanation since it only appeared on the Met Office historic page after the Daily Sceptic submitted its FOI.

On the 80% junk nature of the Met Office’s temperature sites, Vallance rushes to the aid of the party. “It is misleading and inappropriate to interpret the CIMO classifications in isolation to question the quality of the Met Office’s observing network or the integrity of the UK’s climate record,” he states. What pompous piffle. In-house activists have been allowed to leverage the reputation of the Met Office to produce a flood of dubious measurements and statistics designed to create mass climate psychosis with the aim of promoting a hard-Left Net Zero agenda. The World Meteorological Organisation could not be clearer in stating that a CIMO Class 1 location can be considered as a “reference” site giving a true air temperature over a wide surrounding area. “A Class 5 site is a site where nearby obstacles create an inappropriate environment for a meteorological measurement that is intended to be representative of a wide area,” it notes. A site with a poor class number can still be valuable for a specified application, it adds.

In other words, a Class 5 is useful for giving jet pilots a vital runway temperature, but less so for telling us that the annual temperature in the UK was 0.06°C cooler in 2023 than the ‘record’ year of 2022.

Vallance also claims that the Met Office “follows a structured, requirements-driven process to identify and establish new land observing stations”. It is reasonable to ask what “requirements-driven” process is being used by the Met Office, given that a large majority of sites started over the last 30, 10 and five years are to be found in the junk 4 and 5 Classes. Even worse, the Daily Sceptic has disclosed using FOI information that 20 new sites have opened since April 2024, and of the 17 that have received CIMO classifications, a frankly incredible 64.7% started life in the Class 4 and 5 junk lane.

And they say we are the conspiracy nuts.

December 20, 2025 Posted by | Deception, Science and Pseudo-Science | , | Leave a comment

HHS to Prohibit Hospitals From Performing Sex-Change Surgery on Kids

By Suzanne Burdick, Ph.D. | The Defender | December 19, 2025

Federal health officials are taking action to prohibit hospitals from performing sex-rejecting procedures on children and support the families of children who underwent such procedures and now regret it, the U.S. Department of Health and Human Services (HHS) said Thursday at a live press conference.

Sex-rejecting procedures, or “gender-affirming care,” refers to the use of puberty blockers, cross-sex hormones and/or surgery as a treatment for gender dysphoria. The Mayo Clinic defines gender dysphoria as a “feeling of distress that can happen when a person’s gender identity differs from the sex assigned at birth.”

Children are falling prey to a “predatory multi-billion dollar industry,” said U.S. Health Secretary Robert F. Kennedy, Jr. Kennedy cited a study that reported profits from sex-rejecting drugs and surgeries surpassed $4.4 billion in 2023, and were on track to top $7.8 billion by 2031.

Kids’ and teens’ brains aren’t fully mature yet when they decide to undergo the procedures, said Centers for Medicare & Medicaid Services (CMS) Administrator Mehmet Oz.

Kennedy agreed, citing a comment by one doctor who “callously” described sex-rejecting procedures in kids as a “big money maker.”

Kennedy said:

“Hospitals rake in millions of dollars by convincing boys and girls that a lifetime of off-label prescriptions for estrogen and testosterone blockers, chest reconstruction surgeries and more are the only way to achieve true happiness and belonging in life.

“It’s wrong. The Trump administration will not stand by while ideology, misinformation and propaganda push young people into decisions they cannot fully understand and that they can never reverse.”

Kennedy told his audience — which included Congress members and several attorneys general — that he signed a declaration stating that healthcare practitioners who perform sex-rejecting procedures on minors would be deemed out of compliance with professionally recognized standards of healthcare.

The “overwhelming body of evidence” shows “these procedures hurt, not help children,” Kennedy said.

The declaration is based on an HHS peer-reviewed report published last month, “Treatment for Pediatric Gender Dysphoria: Review of Evidence and Best Practices,” which concluded sex-rejecting procedures have an unfavorable risk-benefit profile and fail to meet professionally recognized healthcare standards.

Hospitals that perform sex-rejecting procedures on minors will no longer be eligible for Medicaid or Medicare funding. And no Medicaid funding can be used to pay for the procedures, Oz said. “We’re not going to let taxpayer money go to hurt these children.”

CMS will release a notice of proposed rulemaking to bar hospitals from performing sex-rejecting procedures on kids as a condition of participation in Medicare and Medicaid. It will also release a notice of proposed rulemaking to prevent Medicaid dollars from going toward sex-rejecting procedures on kids.

CMS will issue its final rule after a 60-90 day period soliciting public comments.

HHS also announced it will work to reverse the Biden administration’s attempt to have gender dysphoria be considered a disability under federal law.

That’s important, so hospitals that no longer perform sex-rejecting procedures will not be charged with discriminating against those with a disability, according to an HHS press release.

Admiral Brian Christine, M.D., HHS assistant secretary and head of the U.S. Public Health Service Commissioned Corps, on Thursday signed a public health message telling medical providers, families and policymakers that sex-rejecting procedures are not safe or effective treatments for pediatric gender dysphoria.

“Evidence shows sex-rejecting puberty blockers, cross-sex hormones, and surgeries are dangerous,” Christine said in a statement. “Providers have an obligation to offer care grounded in evidence and to avoid interventions that expose young people to a lifetime of harm.”

Doctors should ‘start slowly’ when treating gender dysphoria

President Trump charged HHS to undertake actions against sex-rejecting procedures in his January executive order, “Protecting Children from Chemical and Surgical Mutilation.”

The MAHA Report also named the “overmedicalization” of U.S. youth as a key driver of the childhood chronic disease epidemic, Kennedy noted.

As the number of youth diagnosed with gender dysphoria has increased in recent years, thousands of children have been “fast-tracked” into sex-rejecting procedures, Oz said.

Doctors seeing kids who have gender dysphoria should “start slowly” with the least invasive treatments possible, such as psychotherapy and evaluating for other conditions like ADHD, autism, anxiety and depression.

Gender expression is complex, and scientists are still trying to find out all the factors that play a role.

For instance, research by Shanna Swan, an environmental and reproductive epidemiologist, suggests that prenatal exposure to endocrine-disrupting chemicals can blur physiological and behavioral sex differences in offspring.

However, she and other scientists conducting similar research acknowledged the issue’s political and ethical implications.

“We have to be very careful not to frame gender non-conforming as an adverse effect,” said Swan, an environmental and reproductive epidemiologist at the Icahn School of Medicine at Mount Sinai, in a report by Undark.

NIH to fund research supporting kids who want to ‘de-transition’

National Institutes of Health (NIH) Director Jay Bhattacharya announced his agency, which already stopped supporting research on gender transition, will do science aimed at helping kids who are “de-transitioning” — or wanting to “de-transition” back to their original sex — and their families.

Thousands of kids and their families have been harmed by these procedures, Bhattacharya said. “We are going to fund science to help them because what I don’t want is for the answers to those families to be based on basically no evidence or presumed knowledge that we don’t actually have.”

Chloe Cole, a 21-year-old, spoke at the press conference about detransitioning at age 16 after starting on puberty blockers at age 13 and undergoing an irreversible double mastectomy at 15.

“I, myself, and every other detransitioner I know have so many different medical concerns,” she said. “They’re not being addressed because our own doctors don’t have any standards of care to refer to. They don’t know what to do with us.”

‘Would you rather have a dead daughter or a living son?’

Cole, now an activist against sex-rejecting procedures, has a bill named in her honor.

The “Chloe Cole Act,” initially proposed under a different title by the U.S. Department of Justice, would ban hospitals, clinics and doctors from performing sex-rejecting procedures on kids.

It would also allow children who underwent such procedures and their parents to sue the healthcare provider for damages. On Sept. 18, the bill was referred to the Committee on Health, Education, Labor, and Pensions. The bill hasn’t yet come up for a vote.

On Dec. 17, a related bill championed by Rep. Marjorie Taylor Greene passed the House. The “Protect Children’s Innocence Act,” which has yet to be voted on in the Senate, would make it a federal crime to provide gender-affirming care to a minor.

“Every American needs to hear Chloe Cole’s story,” Greene wrote in a 2022 X post of a speech Cole gave about her experiences. “The gender clinic presented my parents with the classic false dichotomy: Would you rather have a dead daughter or a living son?” Cole said.

At yesterday’s press conference, U.S. Food and Drug Administration (FDA) Commissioner Marty Makary said that the notion that parents are putting their child at increased risk of suicide if they don’t consent to sex-rejecting procedures is a “baseless claim that has never been supported with good data.”

Bhattacharya agreed. He told the audience this true story:

“There was a researcher that the NIH funded that did a study to answer the question, was it more likely that a child who didn’t transition would commit suicide?

“That researcher found the answer was no, but because the researcher’s ideology was so enmeshed in this — because if the answer is no, that means she might get canceled  — she refused to release the study.”

The NIH obtained the researcher’s data and made it available for other researchers to work with, Bhattacharya said.

Makary also shared that the FDA will issue warning letters to 12 manufacturers and retailers that are illegally marketing breast binders to kids as a treatment for gender dysphoria.

Breast binders are a “class one medical device” usually used by women after breast cancer surgery, he said. Using them long-term can have negative effects, including pain, compromised lung function, lung collapse and difficulty breastfeeding.

“The warning letters will formally notify the companies of their significant regulatory violations and how they should take prompt corrective action,” Makary said.

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.

December 20, 2025 Posted by | Corruption, Science and Pseudo-Science | , | Leave a comment

Natural Solutions to Bladder Health

The Dr. Ardis Show | November 2025

In this week’s episode of The Dr. Ardis Show, Dr. Bryan Ardis explores natural solutions for common bladder problems – including UTIs, kidney or bladder stones, and interstitial cystitis.

You’ll learn what causes these painful conditions, why standard treatments like antibiotics can backfire, and how to restore urinary health naturally. Dr. Ardis dives into the immune, neurological, and detoxification factors that affect bladder function, and what you can do to address the root causes—not just the symptoms.

Sources and links

 

December 19, 2025 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | Leave a comment

Government Bodies Humiliated by Promoting Junk Climate Scares from Retracted Nature Paper

By Chris Morrison | The Daily Sceptic | December 12, 2025

The old academic putdown ‘it’s not even wrong’ comes to mind in considering the disgraced and now retracted science paper Kotz et al. The science writer Jo Nova has speculated on how the paper was even published in Nature, “given how awful it was”. With its unfalsifiable claims of $38 trillion of global damage each year by 2050 due to human-caused climate change, Kotz was patent nonsense. It was not even within touching distance of other extravagant claims of climate damage. Yet Kotz was avidly picked up by government agencies around the world seemingly desperate to use any old gobbledegook to push the Net Zero fantasy.

Being wrong assumes that something is within a ballpark of being right. The Kotz authors tried that and made some adjustments to the figures after initial criticism when the paper was published in April 2024. But in the end the task was hopeless and Nature retracted the work this month. But not before its conclusions on climate impacts have cascaded through numerous governmental operations tasked with determining and regulating public policy. A great deal of rewriting now looks to be in order.

Earlier this month, the Bank of England used “plausible” scenarios derived from Kotz to go into full climate catastrophising overdrive with suggestions that asset and bond markets could face stresses similar to the 2008 global crash. On Monday, the Daily Sceptic looked in detail at the Horlicks made by the UK’s Office for Budget Responsibility, which used Kotz to divest itself of the opinion that the country’s GDP would fall by nearly 8% unless humans stopped the weather changing. Annual state borrowing was forecast to rise by £50 billion by 2050 unless the Net Zero rain dance was successful. In a report to the British Parliament, the Climate Change Committee referenced Kotz in a section discussing economic damage arising from climate risk. Meanwhile, the Financial Conduct Authority (FCA) appears to have been a keen fan of Kotz and all its downstream impact works such as Network for Greening the Financial System (NGFS) Phase V. Over the last year there are many references with the FCA keen to emphasise non-linear economic losses and the need for conservative assumptions in financial stress testing.

What might be considered surprising is that all of this work closely connected to Kotz was produced at a time when serious doubts about the paper were raised in science circles. From the start of this year, concerns started to mount about data quality and extrapolation methods. It became apparent there were problems over an Uzbekistan economic database from 1995-1999 that led to model estimates of temperature impacts on growth inflating global projections by a factor of three. Attempts were made to revise the original paper but in the end the task was too great and Nature finally retracted it. It is hardly an exaggeration to observe that dodgy data from Uzbekistan cascaded through the paper out into the real world where it led the Bank of England just a few days ago to publish scares of climate-induced global crashes.

“This study was used to justify all kinds of economic decisions that otherwise make no sense. Ka-ching. Ka-ching,” notes Jo Nova. This is emblematic of the whole field of climate research, she observed, adding: “Monopsonistic research always finds what the one sole customer (the Blob) pays it to find. Thus the government-funded establishment loved it. Look how popular this junk research was.”

The Kotz paper arose from the Potsdam Institute for Climate Impact Research (PIK), a known nest of hard-line climate activists with substantial past climate catastrophising form. This is the number one place to go for disappearing sea ice, an overturning Gulf Stream and bazillion-dollar falls in global wealth. Needless to say it is backed by copious amounts of Government money from the European Union as well as private foundations. Considerable money appears to flow from individual project grants.

Interestingly, few US government bodies appear to have been caught out by the damage impacts model produced by Kotz that was later integrated into the NGFS catastrophising scenarios. The Trump Administration has been cleaning house of all the federal climate catastrophising BS this year. It didn’t take long for the Federal Reserve, the Federal Deposit Insurance Corporation and the Treasury Department to withdraw from the NGFS, an international body of regulators and banks set up at the height of the Green Mania in 2019.

Earlier this year, President Trump signed an executive order that said the results of federal scientists must be falsifiable, computer models must be explainable and negative results available. Not all activist-scientists were happy with this return to the ”gold standard”, with a group including Michael ‘Hockey Stick’ Mann writing in the Guardian – seemingly without irony – that it will “destroy American science as we know it”.

It certainly destroyed the ability of the American Central Bank to tout global financial collapse on the basis of a Government-funded science paper so bad even ideologically-captured Nature has been forced to retract it.

December 19, 2025 Posted by | Corruption, Science and Pseudo-Science | , | Leave a comment

The Five Big Lies of Vaccinology

By Clayton J. Baker, MD | Brownstne Institute | December 11, 2025

People will believe a big lie sooner than a little one, and if you repeat it frequently enough, people will sooner or later believe it. 

― Walter Langer

On November 19, 2025, the New England Journal of Medicine published an article entitled “Efficacy, Immunogenicity, and Safety of Modified mRNA Influenza Vaccine.” This article purportedly reviewed the results of Pfizer’s Phase 3 clinical trials testing its experimental, mRNA-based, gene therapy injections for Influenza, which Pfizer presents as an alternative to traditional Influenza vaccines.

Two weeks later, on December 5, 2025, the Centers for Disease Control’s Advisory Committee on Immunization Practices (ACIP) voted 8-3 to end the recommendation in the CDC’s pediatric vaccine schedule that all American children receive the Hepatitis B Virus (HBV) vaccine at birth. This recommendation would bring the CDC’s HBV vaccine recommendations closer to those in numerous other developed nations, countries that have both better overall pediatric health than the United States and no surplus pediatric HBV deaths.

To the casual observer, neither of these events may seem very noteworthy. However, in the post-Covid world of medicine, vaccinology, and politics, both fueled controversy that shows no sign of ending soon. Why?

The New England Journal of Medicine article of Pfizer’s self-conducted study of its own product has been extensively analyzed by independent reviewers. It has been identified as an object lesson in the scientific fraud that is endemic in vaccine research, development, and marketing. Detailed review of the study has revealed multiple systematic techniques of deceptive research methods, omission and concealment of unfavorable data, and outright misrepresentation of results.

The ACIP panel’s decision, which represents a minor change in the previously sacrosanct – if ever-expanding – CDC pediatric vaccine schedule, has been met with an onslaught of hair-on-fire, alarmist proclamations by the vaccine industry and its minions of impending disease and death in American children. These claims are unsupported by the existing scientific data and bear little relationship to objective reality as a whole.

The reasons these two events have sparked such controversy are:

  • The New England Journal of Medicine article – now thoroughly deconstructed – exposes the brazen, systematic dishonesty of both vaccine development and the clinical trial process as a whole.
  • Meanwhile, the results of the study, once fully uncovered and comprehensively reviewed, shatter the viability of the mRNA gene therapy platform as a substitute for conventional vaccines.
  • The unhinged response to the ACIP decision reveals the entire pediatric vaccine schedule to be a house of cards, built on falsehoods, that cannot withstand any criticism, reform, or revision whatsoever.

The awful truth (and it is both awful and the truth) is that vaccinology is overwhelmingly a façade, constructed on a shaky foundation of lies. In the wake of these two recent controversies, it is instructive to enumerate the five great lies propping up vaccinology (plus two Honorable Mentions). I shall outline them here, and provide a more detailed discussion of each in forthcoming essays.

The Five Big Lies of Vaccinology

Big Lie #1: Equating Antibody Production with Immunity to Disease

Big Lie #2: Using Fake Placebos

Big Lie #3: Insisting My Immunity is Dependent on Your Vaccination

Big Lie #4: Declaring Multiple Simultaneous Injections to be Safe

Big Lie #5: Declaring Vaccines Fundamentally “Safe and Effective” as a Class

Honorable Mention 1: Declaring mRNA Gene Therapies to be “Vaccines”

Honorable Mention 2: Allowing Criminal Corporations to Conduct their own Clinical Studies

In upcoming essays, we will analyze each of these Big Lies of Vaccinology. In the process, we shall see how each Big Lie is interdependent upon others, and how the entire vaccine narrative depends upon this web of falsehoods. We shall see why vaccine zealots such as Peter Hotez and Paul Offit would refuse to attend the ACIP meeting – which they were invited to do – and in fact why they refuse to debate these points.

The reckoning that is taking place regarding the vaccine industry is overdue, but it is hardly unique.

There was a time within living memory when pre-frontal lobotomy was considered cutting edge medicine (pun intended). Its founder won the Nobel Prize for Medicine.

There was a time within living memory when physicians accepted corporate payment to convince the public that cigarette smoking was safe.

There was a time – very recently – when mainstream medicine actively promoted OxyContin and other deadly narcotics as safe and minimally addictive. Hundreds of thousands died as a result.

The bloom is off the rose for the vaccine industry. It is long past time for its accounting. May we all open our minds, use our heads, and face the reality of this subject.


C.J. Baker, M.D., 2025 Brownstone Fellow, 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.

December 13, 2025 Posted by | Deception, Science and Pseudo-Science | , | Leave a comment

Flawed Study Downplays Children’s Risk of Myocarditis From COVID Vaccine

By Josh Mitteldorf, Ph.D. | The Defender | December 3, 2025

Readers of The Defender are familiar with the fact that the COVID-19 mRNA shots pose a risk of myocarditis, especially in children. But they may not know that myocarditis is usually permanently disabling, and in adults, it is often fatal within five years.

Tragically, we are now also learning what the trajectory of myocarditis in vaccinated children actually looks like.

This has been a public relations setback for industry and governments that have been advocating, and sometimes mandating, that children as young as 6 months get the vaccines — even though COVID-19 is almost always mild or symptom-free in young people.

This month, 22 British scientists from prestigious universities published a study intended to ease parents’ minds about risks of the vaccine, and simultaneously scare them about the dangers of getting COVID-19.

The message is that yes, there are rare cases — they always use the word “rare” — in which children get myocarditis after vaccination, but hey, no product can be perfect. And it’s better to risk the vaccine than risk getting COVID-19. Also, they claim, kids are more likely to get myocarditis if they get the virus than they are to get myocarditis from the vaccine.

That’s the message — and the authors and publisher have the clout to widely broadcast that message in a press release and in news headlines in Britain and America.

But what does the study actually say? In short, it asks the wrong question — and even so, the answer they get must be buried in the appendix, because it’s inconsistent with the message they want to promote.

Article summary omitted evidence of vaccine risk

The study design is deeply compromised because the 22 authors constructed a complicated model to avoid doing a straightforward comparison (vaccine only versus disease only).

And even after they cooked the books, even after they took data from almost 14 million children and teens under age 18 in England, they got a result that is barely statistically significant, with overlapping error bars for the risk from COVID-19 and the risk from vaccination.

It gets worse.

The results, which marginally favored the vaccination, were trumpeted in a summary at the top of the paper and announced to the press.

But buried in the appendix, published separately online, is a table that shows a more relevant version of the comparison.

The version in the summary is from an early time frame when the vaccine was not available. The appendix shows comparable data for the time frame in which the vaccine was available, limited to the ages for which the vaccine was offered.

In the appendix, the risk of myocarditis from the disease is half that of the risk from the vaccine. This blatantly contradicts the summary and the headlines generated by the article — and this was a response to the deceptive version of the question, not the more straightforward one that the researchers chose not to answer.

Study authors asked the wrong question

The most pertinent question is the simple one: Did vaccinated children have a higher incidence of myocarditis than unvaccinated children?

This is an easy question to answer, given the data that these authors (but not the public) had access to. In a few minutes, they could have calculated a rate of myocarditis among vaccinated and unvaccinated children.

However, if they did the calculation, they didn’t report the results. My guess is that they did the calculation, didn’t like what they saw, so they didn’t include it in the published article.

As I stated above, I believe the study authors “asked the wrong question.” What I mean is that the article compares the risk of myocarditis from COVID to the risk from vaccination.

But this is not the most relevant question. Why?

Because many people got the vaccine and then got COVID anyway, so they were unnecessarily exposed to both risks.

Conversely, many children who didn’t get the vaccine, didn’t get COVID. Or, they get such a mild case that they don’t even notice it. These children avoided both risks.

This is why comparing the risk of myocarditis from COVID to the risk from the COVID vaccine is not really the pertinent question. It’s not a question of “either or.”

Authors ‘muddied the waters’ by analyzing myocarditis in kids who got vaccine and the virus

The message the authors wanted to imply was that, even though the vaccine increased the risk of myocarditis, it decreased the risk of COVID — and since COVID itself can cause myocarditis, the total risk is actually lower with vaccination than without.

If that is their claim, it’s easy to determine if it is true. The simplest calculation they could have done with the data available to them was also the calculation most pertinent to what parents want to know: Is my child better off with or without the vaccine?

The authors chose not to offer us the simple answer to that straightforward question.

But — given that they asked the wrong question — they might have derived a clean answer just by comparing the subset of children who were vaccinated but never got COVID to the subset who got COVID but were never vaccinated.

Because the study included data spanning two years from all over the U.K., there were hundreds of thousands of children in these subcategories — more than enough to do a clean statistical comparison.

But again, the authors chose not to do this. Or, my guess, they did the comparison and didn’t like the result, so they didn’t include it in the publication.

Instead, the authors analyzed myocarditis in the large group of children who got both the vaccine and the disease. This muddied the waters because there is no clear way to determine whether it was the disease or the vaccine that damaged the child’s heart.

Hence, the complicated model, based on timing.

The possibility that seems likely is that children who got COVID after the vaccination had the highest heart risk of all. Of course, there is the logical possibility that children who got COVID after vaccination had a milder case, with a lower risk of myocarditis.

However, if that had been the result, I would think the authors would not only have included that result, but also headlined it.

One more thing — the study looked only at the Pfizer vaccine. Myocarditis risk from the Moderna vaccine is estimated to be three times higher than Pfizer. They had the Moderna data and chose not to look at it.

Or they looked at it, decided they didn’t like what they saw, and decided not to report it.

‘This is public relations masquerading as science’

So, to summarize:

  • The authors asked a complicated question when a simple one was more relevant.
  • Given this wrong question, they did not do the most straightforward analysis to answer it.
  • Even so, they found that the vaccine held almost twice the risk of myocarditis compared to the disease. This result was only in Table S16 of the Supplementary Appendix — but mentioned nowhere in the body of the paper, let alone in the summary at the top.
  • And still they made prominent announcements to the public, claiming that their study confirms that children are better off with the vaccine than without.

This is public relations masquerading as science. For an article like this to be peer reviewed and featured prominently in Britain’s most prestigious medical journal tells us just how deeply the ecosystem of medical research has been corrupted.

And this is the “science” that our U.S. Food and Drug Administration relies on when they approve dangerous vaccines for healthy children who are at almost no risk from the disease itself.

In most statistical articles, the raw data used for a study are published online and linked in an appendix to the article. However, in this case, the U.K. National Health Service (NHS) granted access to the data exclusively to this prestigious group of scientists.

Personally, I would like to see the raw data and perform the analysis that the 22 scientists should have done from the beginning. Children’s Health Defense is in the process of requesting access from the NHS. Stay tuned …

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.

December 13, 2025 Posted by | Deception, Fake News, Mainstream Media, Warmongering, Science and Pseudo-Science | , , | Leave a comment

Vaccine injury lawyer delivers scathing rebuke of childhood vaccine schedule — Offit, Hotez decline to debate

By Michael Nevradakis, Ph.D. | The Defender | December 5, 2025

The Centers for Disease Control and Prevention’s (CDC) vaccine advisory committee today heard from a vaccine injury lawyer who proposed the committee revisit the childhood vaccine schedule.

Attorney Aaron Siri told members of the Advisory Committee on Immunization Practices (ACIP) that the vaccines were recommended without sufficient data and that the expansion of the schedule coincided with a rise in chronic illness among U.S. children.

Siri, a vaccine critic and author of “Vaccines, Amen: The Religion of Vaccines,” called for a reexamination of the childhood immunization schedule based on “robust” safety data.

Siri challenged claims that the childhood vaccination schedule has been tested in its entirety, that the vaccines are safe and that routine childhood vaccines have been proven to prevent transmission.

He also questioned claims that scientists have conducted the testing necessary to assert definitively that there is no possible link between vaccines and autism.

Siri recommended ACIP revisit childhood vaccine recommendations based on “robust” clinical trial and post-licensure safety data and called on the committee to respect the “right of informed consent.”

“Mandates make vaccines political” and also “impact those who most need to avoid” certain vaccines, he said. When people report vaccine injuries, members of the medical community “pretend that they don’t exist.”

Siri represents plaintiffs in vaccine-related lawsuits against federal agencies and pharmaceutical companies.

Children’s Health Defense CEO Mary Holland said Siri “accurately compared the pre-1986 Act vaccine schedule with the post-1986 schedule, when doctors and vaccine manufacturers have been absolved from all real responsibility for the vast vaccine injuries they have caused,” Holland said.

The National Childhood Vaccine Injury Act of 1986 granted vaccine makers immunity from liability for most injuries caused by their products.

ACIP didn’t vote on any aspect of the childhood vaccine schedule today. In June, ACIP formed a committee to study the cumulative effect of all vaccines given during childhood.

Key vaccine advocates declined ACIP’s invitation to deliver presentations

Siri’s presentation came shortly after ACIP voted to end the recommendation that all infants born in the U.S. receive the hepatitis B (Hep B) vaccine within 12-24 hours of birth.

The committee also voted to recommend that families determine whether to give their child the Hep B shot at birth through individual decision-making and consultation with their physician.

Siri cited the licensing of Hep B vaccines as an example of flawed studies leading to the licensing of a vaccine. He called those studies “underpowered” and “industry-funded.”

Siri’s presentation stirred controversy even before it began. In a post on X yesterday, Sen. Bill Cassidy (R-La.), chairman of the U.S. Senate Health, Education, Labor & Pensions (HELP) Committee, dismissed Siri’s qualifications and said ACIP “is totally discredited.”

Siri responded that Cassidy’s post was “deeply ironic,” given that vaccine manufacturers are legally protected from lawsuits.

“Childhood vaccines are the only product in America where you cannot ever sue the company that killed or injured your child on the basis the company could’ve made the product safer. If vaccines are so safe, why do they need this protection?” Siri wrote on X.

ACIP member Dr. Cody Meissner called Siri’s presentation a “terrible distortion of all the facts” and said Siri shouldn’t have been invited. Earlier, Meissner voted against the proposal to end the universal Hep B vaccine recommendation for newborns.

ACIP also addressed controversy over Siri’s presentation and the lack of a pro-vaccine counterweight. Mina Zadeh, Ph.D., ACIP’s executive secretary, said the committee “invited several people to give us a broad perspective” on the childhood vaccination schedule.

Those invitees included two prominent and outspoken promoters of vaccines — Dr. Paul Offit and Peter Hotez, M.D., Ph.D. Both declined. Hotez told STAT that Siri “shouldn’t be there in the first place.”

Siri responded that the U.S. has “the worst health outcomes of all developed countries.”

Liability shield disincentivizes vaccine makers from performing proper safety testing

Siri used the opportunity today to criticize the National Childhood Vaccine Injury Act of 1986. He said the liability shield provided by that law disincentivized vaccine manufacturers from focusing on the safety of their products.

“Companies, including pharmaceutical companies, are driven by economic self-interest,” Siri said. “With drugs and non-routine vaccines, they … remain liable for the injuries caused by those products after they come to market and hence, they have an economic self-interest in doing robust clinical trials beforehand.”

“When it comes to routine childhood vaccines … they don’t have those same concerns,” Siri said.

He said the number of vaccines on the childhood schedule skyrocketed — from three to 72 — after Congress passed the 1986 act. Those initial three vaccines “were causing so much harm, all the manufacturers stopped making them or went out of business,” prompting the passage of the act.

“For every other product I’m aware of, the solution is to make a better, safer product. But when it came to these vaccines, Congress went a different way” by giving these companies “unprecedented broad immunity,” Siri said.

‘You can’t find what you’re not studying’

Siri also criticized the shortened clinical trial process for childhood vaccines, which results in recommendations being made on the basis of insufficient data and the inability to detect any long-term health impacts from the vaccines.

“Most recommendations for routine use by ACIP of a particular vaccine happened very shortly after its licensure, and hence the primary data often available for a specific vaccine would have been its clinical trial data,” Siri said.

He also criticized the lack of post-licensure safety monitoring.

“You can’t find what you’re not studying,” Siri said. “When you give a product to a baby or an infant in particular, you often won’t know what neurological, immunological or developmental issues that product can cause until you’ve tracked that child for at least a few years.”

Citing autism as the “injury claimed to be the most thoroughly studied,” Siri said the medical community has not conducted studies that would definitively eliminate a vaccine-autism link, even though the 1986 act listed autism as one of 11 conditions that warrant further study to determine a possible link with vaccination.

“It was a commonly claimed enough injury back in 1986 … to make it on this list of 11 conditions,” Siri said.

U.S. ‘an international outlier’ on childhood vaccination

Today’s meeting also included a presentation by Tracy Beth Høeg, M.D., Ph.D., who earlier this week was named the next leader of the FDA’s Center for Drug Evaluation and Research.

Høeg compared U.S. childhood vaccine requirements and health outcomes with those of her native Denmark. There are “eye-opening differences in the recommendations” between the two countries, she said.

While the U.S. requires 72 core childhood vaccine doses, Denmark requires 11 — in line with most other high-income countries. Høeg said this makes the U.S. “an international outlier” on childhood vaccination.

The higher vaccine load “results in an increased exposure to aluminum,” Høeg said, with U.S. children exposed to 5.9 milligrams (mg) of aluminum by age 2 and 8.0 mg by age 18. In Denmark, the corresponding figures are 1.4 and 2.9 mg, similar to other high-income countries.

While there isn’t “robust enough” data indicating “specific health concerns” resulting from this level of aluminum exposure, Høeg said there also is insufficient data to establish a safe level of exposure.

“We need to admit that we may not know what the side effects of doing this, especially all at once, could be,” she said.

Increased vaccination also hasn’t delivered better health outcomes for U.S. children, according to Høeg. She cited the examples of the Hep B and meningococcal vaccines, which Denmark does not recommend for children, unlike the U.S. Yet, levels of hepatitis B and meningitis among children in the two countries are similar.

Høeg said U.S. health agencies should “avoid overmedicalizing childhood” and owe American children recommendations that are “based on data and not politics.”

Potential risks of post-vaccine aluminum accumulation ‘a warranted concern’

Dr. Evelyn Griffin, an OB/GYN and member of three ACIP work groups called for more research into the safety of aluminum-based adjuvants used in vaccines.

Griffin said aluminum salts are the most widely used adjuvant. Yet, the mechanisms underlying the use of aluminum salts in vaccines “are not fully understood.” She said only one peer-reviewed study has examined the effects of aluminum in infants’ blood following vaccination — but that study used a small sample and didn’t collect long-term data.

According to Griffin, current FDA aluminum exposure limits are increasingly questioned, as “appropriate testing was not performed.” She said recent studies have suggested that aluminum accumulation is “a warranted concern” and called for studies on the long-term impact of aluminum exposure and who is most at risk.

Griffin called on ACIP to determine how it can assess the safety and effectiveness of adjuvants in currently recommended vaccines for all ages, including studies regarding whether multiple aluminum-containing vaccines should be administered on the same day during early infancy.

In October, ACIP announced the creation of a new work group that will study the safety of aluminum adjuvants. ACIP did not hold a vote relating to the aluminum content of vaccines at today’s meeting.

Watch the ACIP meeting here.

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.

December 6, 2025 Posted by | Science and Pseudo-Science | , , | Leave a comment

DR BOB SEARS DISCUSSES ‘VACCINES AND THE DISEASES THEY TARGET’

The HighWire with Del Bigtree | December 4, 2025

Pediatrician Dr. Bob Sears joins Del to unpack ACIP’s hepatitis B vaccine debate, the near-total absence of long-term safety data for newborn vaccination, and why the U.S. is an outlier in giving this shot on day one of life. He discusses the Physicians for Informed Consent’s new Silver Book “Vaccines and the Diseases They Target”, designed to give doctors and parents clear, side-by-side numbers on disease risk and vaccine risk so real informed consent can finally happen.

December 5, 2025 Posted by | Book Review, Science and Pseudo-Science, Video | | Leave a comment

No longer alive

Dr. John Campbell | November 29, 2025

Excess Deaths in the United Kingdom: Midazolam and Euthanasia in the COVID-19 Pandemic

https://www.researchgate.net/publicat…

Macro-data during the COVID-19 pandemic in the United Kingdom (UK) are shown to have significant data anomalies and inconsistencies with existing explanations.

This paper shows that the UK spike in deaths, wrongly attributed to COVID-19 in April 2020,

was not due to SARS-CoV-2 virus, which was largely absent,

but was due to the widespread use of Midazolam injections,

which were statistically very highly correlated (coefficient over 90%) with excess deaths in all regions of England during 2020.

Importantly, excess deaths remained elevated following mass vaccination in 2021,
but were statistically uncorrelated to COVID injections, while remaining significantly correlated to Midazolam injections.

The widespread and persistent use of Midazolam in UK suggests a possible policy of systemic euthanasia.

Unlike Australia, where assessing the statistical impact of COVID injections on excess deaths is relatively straightforward,

UK excess deaths were closely associated with the use of Midazolam and other medical intervention.

The iatrogenic pandemic in the UK was caused by euthanasia deaths from Midazolam and also,

likely caused by COVID injections,

but their relative impacts are difficult to measure from the data, due to causal proximity of euthanasia.

Global investigations of COVID-19 epidemiology, based only on the relative impacts of COVID disease and vaccination, may be inaccurate, due to the neglect of significant confounding factors in some countries.

Graphs

April 2020, 98.8% increase 43,796

January 2021, 29.2% increase 16,546

Therefore covid is very dangerous,

This interpretation, which is disputable, justified politically the declaration of emergency and all public health measures, including masking, lockdowns, etc.

Excess deaths and erroneous conclusions

2020, 76,000
2021, 54,000
2022, 45,000

This evidence of “vaccine effectiveness” was illusory, due to incorrect attribution of the 2020 death spike.

PS

Despite advances in modern information technology, the accuracy of data collection has not advanced in the United Kingdom for over 150 years,

because the same problems of erroneous data entry found then are still found now in the COVID pandemic,

not only in the UK but all over the world.

We have independently discovered the same UK data problem and solution for assessing COVID-19 vaccination as Alfred Russel Wallace had 150 years ago in investigating the consequences of Vaccination Acts starting in 1840 on smallpox:

The Alfred Russel Wallace as used by Wilson Sy

“Having thus cleared away the mass of doubtful or erroneous statistics,

depending on comparisons of the vaccinated and unvaccinated in limited areas or selected groups of patients,

we turn to the only really important evidence, those ‘masses of national experience’…”

https://archive.org/details/b21356336…

Alfred Russel Wallace, 1880s–1890s

1840 Vaccination Act

Provided free smallpox vaccination to the poor

Banned variolation

Vaccination compulsory in 1853, 1867

Why his interest?

C 1885

The Leicester Anti-Vaccination demonstrations (1885)

Growing public resistance to compulsory vaccination

Wallace’s increasing involvement in social reform and statistical arguments

Statistical critique of vaccination

Government data on:

Smallpox mortality trends before and after compulsory vaccination

Case mortality rates

Vaccination vs. sanitation effects

Mortality trends before and after each Act, 1853 and 1867

“Forty-Five Years of Registration Statistics, Proving Vaccination to Be Both Useless and Dangerous” (1885)

“Vaccination a Delusion; Its Penal Enforcement a Crime” (1898)

Contributions to the Royal Commission on Vaccination (1890–1896)

Wallace argued:

Declining smallpox mortality was due to improved sanitation, not vaccination

Official statistics were misinterpreted or biased

Compulsory vaccination was unjust

Re-vaccination did not reliably prevent outbreaks

These views were strongly disputed, then and now.

Wallace had a strong distrust of medical authority

He and believed in:

Statistical reasoning

Social reform

Opposition to coercive government measures

The primacy of environmental and sanitary conditions in health

December 1, 2025 Posted by | Science and Pseudo-Science, Timeless or most popular, Video, War Crimes | , | Leave a comment

How the Covid Inquiry Protected the Establishment

By Trish Dennis | Brownstone Institute | November 28, 2025

After four years, hundreds of witnesses, and nearly £200 million in costs, the UK Covid Inquiry has reached the one conclusion many expected: a carefully footnoted act of self-exoneration. It assiduously avoids asking the only question that truly matters: were lockdowns ever justified, did they even work, and at what overall cost to society?

The Inquiry outlines failure in the abstract but never in the human. It catalogues errors, weak decision-making structures, muddled communications, and damaged trust, but only permits examination of those failings that do not disturb the central orthodoxy.

It repeats the familiar refrain of “Too little, too late,” yet anyone paying attention knows the opposite was true. It was too much, too soon, and with no concern for the collateral damage. The government liked to speak of an “abundance of caution,” but no such caution was exercised to prevent catastrophic societal harm. There was no attempt to undertake even a basic assessment of proportionality or foreseeable impact.

Even those who approached the Inquiry with modest expectations have been startled by how far it fell below them. As former Leader of the UK House of Commons, Jacob Rees-Mogg recently observed, “I never had very high hopes for the Covid Inquiry… but I didn’t think it would be this bad.” Nearly £192 million has already been spent, largely enriching lawyers and consultants, to produce 17 recommendations that amount, in his words, to “statements of the obvious or utter banality.”

Two of those recommendations relate to Northern Ireland: one proposing the appointment of a Chief Medical Officer, the other an amendment to the ministerial code to “ensure confidentiality.” Neither insight required hundreds of witnesses or years of hearings. Another recommendation, that devolved administrations should have a seat at COBRA, reveals, he argues, “a naiveté of the judiciary that doesn’t understand how this country is governed.”

Rees-Mogg’s wider criticism goes to the heart of the Inquiry’s failures, as it confuses activity with accountability. Its hundreds of pages record bureaucratic process while ignoring substance. The same modeling errors that drove early panic are recycled without reflection; the Swedish experience is dismissed, and the Great Barrington Declaration receives a single passing mention, as if it were an eccentric sideshow. The report’s underlying message never wavers: lockdowns were right, dissent was wrong, and next time the government should act faster and with fewer restraints.

He also highlights its constitutional incoherence. It laments the lack of “democratic oversight,” yet condemns political hesitation as weakness. It complains that ministers acted too slowly, while elsewhere chastising them for bowing to public pressure. The result, he says, is “schizophrenic in its approach to accountability.” Behind the legal polish lies an authoritarian instinct, the belief that bureaucrats and scientists know best, and that ordinary citizens cannot be trusted with their own judgment.

The conclusions could have been drafted before the first witness entered the room:

  • Lockdowns were necessary.
  • Modelling was solid.
  • Critics misunderstood.
  • The establishment acted wisely.

It is the kind of verdict that only the British establishment could deliver about the British establishment.

The Inquiry treats the question of whether lockdowns worked as if the very question were indecent. It leans heavily on modeling to claim that thousands of deaths could have been avoided with earlier restrictions, modeling that is now widely recognised as inflated, brittle, and detached from real-world outcomes. It repeats that easing restrictions happened “despite high risk,” yet fails to note that infection curves were already bending before the first lockdown began.

Here Baroness Hallett makes her headline claim that “23,000 lives could have been saved” if lockdowns had been imposed earlier. That number does not come from a broad evidence base, but from a single modelling paper written by the same scientist who, days later, broke lockdown to visit his mistress because he did not believe his own advice or modeling figures. Treating Neil Ferguson’s paper as gospel truth is not fact-finding. It is narrative protection.

Even Dominic Cummings, Boris Johnson’s most influential adviser in early 2020, has accused the Inquiry of constructing what he calls a “fake history.” In a detailed post on X, he claimed it suppressed key evidence, ignored junior staff who were present at pivotal meetings, and omitted internal discussions about a proposed “chickenpox-party” infection strategy. He argued that the Inquiry avoided witnesses whose evidence would contradict its preferred story, and he dismissed the “23,000 lives” figure as politically spun rather than empirically credible. Whatever one thinks of Cummings, these are serious allegations from the heart of government, and the Inquiry shows little interest in addressing them.

It quietly concedes that surveillance was limited, urgency lacking, and spread poorly understood. These admissions undermine the very certainty with which it endorses lockdowns. Yet instead of re-examining its assumptions, the Inquiry sidesteps them. To avoid reconsidering lockdowns is to avoid the very heart of the matter, and that is exactly what it does.

During 2020 and 2021, fear was deployed and amplified to secure compliance. Masks were maintained “as a reminder.” Official documents advised that face coverings could serve not only as source control but as a “visible signal” and “reminder of COVID-19 risks,” a behavioural cue of constant danger.

The harms of lockdown are too numerous for a single list, but they include:

  • an explosion in mental health and anxiety disorders, especially in children and young adults
  • a surge in cancers, heart disease, and deaths of despair
  • developmental regressions in children
  • the collapse of small businesses and family livelihoods
  • profound social atomisation and damage to relationships
  • the erosion of trust in public institutions

The Inquiry brushes over these truths. Its recommendations focus on “impact assessments for vulnerable groups” and “clearer communication of rules,” bureaucratic language utterly inadequate to address the scale of the damage.

It also avoids the economic reckoning. Pandemic policy added 20 percent of GDP to the national debt in just two years, a cost already passed to children not yet old enough to read. That debt will impoverish their lives and shorten life expectancy, since wealth and longevity are closely linked.

Whenever Sweden is mentioned, a predictable chorus appears to explain away its success: better healthcare, smaller households, lower population density. Yet it is also true that Sweden resisted panic, trusted its citizens, kept schools open, and achieved outcomes better than or comparable to ours. The Inquiry refers vaguely to “international differences” but avoids the one comparison that most threatens its narrative. If Sweden shows that a lighter-touch approach could work, the entire moral architecture of Britain’s pandemic response collapses, and that is a question the Inquiry dares not ask.

The establishment will never conclude that the establishment failed, so the Inquiry performs a delicate dance:

  • Coordination was poor, but no one is responsible.
  • Communications were confusing, but the policies were sound.
  • Governance was weak, but the decisions were right.
  • Inequalities worsened, but that tells us nothing about strategy.

It acknowledges everything except the possibility that the strategy itself was wrong. Its logic is circular: lockdowns worked because the Inquiry says they worked; modeling was reliable because those who relied on it insist it was; fear was justified because it was used; Sweden must be dismissed because it challenges the story.

At times, reading the report feels like wandering into the Humpty Dumpty chapter of Through the Looking-Glass, where words mean whatever authority decides they mean. Evidence becomes “established” because the establishment declares it so.

A serious, intellectually honest Inquiry would have asked:

  • Did lockdowns save more lives than they harmed?
  • Why was worst-case modeling treated as fact?
  • Why were dissenting voices sidelined?
  • How did fear become a tool of governance?
  • Why did children bear so much of the cost?
  • Why was Sweden’s success dismissed?
  • How will future generations bear the debt?
  • How can trust in institutions be rebuilt?

Instead, the Inquiry offers administrative tweaks, clearer rules, broader committees, and better coordination that studiously avoid the moral and scientific questions. An Inquiry that evades its central task is not an inquiry at all, but an act of institutional self-preservation.

Perhaps we should not be surprised. Institutions rarely indict themselves. But the cost of this evasion will be paid for decades, not by those who designed the strategy, but by those who must live with its consequences: higher debt, diminished trust, educational loss, social fracture, and a political culture that has learned all the wrong lessons.

The Covid Inquiry calls itself a search for truth, but the British establishment will never allow something as inconvenient as truth to interfere with its instinct for self-preservation.

Trish Dennis is a lawyer, writer, and mother of five based in Northern Ireland. Her work explores how lockdowns, institutional failures, and social divides during Covid reshaped her worldview, faith, and understanding of freedom. On her Substack, Trish writes to record the real costs of pandemic policies, honour the courage of those who spoke out, and search for meaning in a changed world. You can find her at trishdennis.substack.com.

November 28, 2025 Posted by | Civil Liberties, Deception, Science and Pseudo-Science | , , | 1 Comment

3 Natural SUPPLEMENTS We LOVE Taking [As DOCTORS, we use THESE]

Dr. Suneel Dhand | November 21, 2025

Dr. Dhand’s Website: https://www.drsuneeldhand.com

Dr Dhand’s MetThrive Method Health Transformation Program: https://www.metthrive.com

Dr Dhand Free Newsletter Sign-Up: https://drsuneeldhand.com/free-newsle…

November 26, 2025 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | Leave a comment

BOMBSHELL: The CDC Has Updated Its “Autism and Vaccines” Page

This is a start to what honest science looks like

By Aaron Siri | Injecting Freedom | November 20, 2025

The new “Autism and Vaccines” page starts telling the truth, including:

“The claim ‘vaccines do not cause autism’ is not an evidence-based claim because studies have not ruled out the possibility that infant vaccines cause autism.”

“Studies supporting a link have been ignored by health authorities.”

“Scientific studies have not ruled out the possibility that infant vaccines contribute to the development of autism. However, this statement has historically been disseminated by the CDC and other federal health agencies within HHS to prevent vaccine hesitancy.”

Meaning, the CDC has simply been lying to you. The CDC’s website then continues its mea culpa stating:

“[M]ultiple reports from HHS and the National Academy of Sciences …. have consistently concluded that there are still no studies that support the specific claim that the infant vaccines, DTaP, HepB, Hib, IPV, and PCV, do not cause autism and hence the CDC was in violation of the DQA [Data Quality Act] when it claimed, ‘vaccines do not cause autism.’ CDC is now correcting the statement, and HHS is providing appropriate funding and support for studies related to infant vaccines and autism.”

“Of note, the 2014 AHRQ [Agency for Healthcare Research and Quality] review also addressed the HepB vaccine and autism. One cross-sectional study met criteria for reliability; it found a threefold risk of parental report of autism among newborns receiving a HepB vaccine in the first month of life compared to those who did not receive this vaccine or did so after the first month.”

“In fact, there are still no studies that support the claim that any of the 20 doses of the seven infant vaccines recommended for American children before the first year of life do not cause autism. These vaccines include DTaP, HepB, Hib, IPV, PCV, rotavirus, and influenza.”

As for the MMR vaccine, CDC’s website now says:

“[I]n 2012, the IOM reviewed the published MMR-autism studies and found that all but four of them had ‘serious methodological limitations,’ and the IOM gave them no weight. The remaining four studies and a few similar studies published since also have all been criticized for serious methodological flaws. Furthermore, they are all retrospective epidemiological studies which cannot prove causation, fail to account for potential vulnerable subgroups, and fail to account for mechanistic and other evidence linking vaccines with autism.”

November 22, 2025 Posted by | Science and Pseudo-Science | , | Leave a comment