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CHD Scientist: CDC, FDA COVID Vaccine Safety Monitoring ‘Insulting, and Many People Are Injured’

By Suzanne Burdick, Ph.D. | The Defender | April 29, 2026

Federal health officials under the Biden administration failed abysmally to look for COVID-19 vaccine safety signals, according to congressional testimony delivered today by Children’s Health Defense (CHD) Senior Research Scientist Karl Jablonowski.

The government’s vaccine safety monitoring “over the past several years has been insulting, and many people are injured,” Jablonowski wrote in his written testimony.

History repeats itself if we don’t learn our lessons, Jablonowski warned.

“The COVID-19 pandemic created over 100 billionaires in the United States and over 1,000 billionaires around the world,” Jablonowski wrote. “Anything that profitable is going to repeat.”

Jablonowski, who holds a doctorate in biomedical and health informatics from the University of Washington’s School of Medicine, spoke as a witness at the U.S. Senate Permanent Subcommittee on Investigations hearing, “Unmasked: How Biden Health Officials Purposely Turned a Blind Eye Toward COVID-19 Vaccine Safety Signals.”

Hours before the hearing, Sen. Ron Johnson (R-Wis.), subcommittee chair, released a report detailing how Biden-era federal health officials refused to use a state-of-the-art statistical tool for detecting COVID-19 vaccination signals in VAERS — even though they knew the tool they were using was too broken to pick up on safety signals, including sudden cardiac death.

Johnson’s report, which cited roughly 600 pages of emails, revealed that in 2021, officials with the U.S. Food and Drug Administration (FDA) told an FDA researcher to “cease and desist” using the state-of-the-art tool to analyze COVID-19 vaccine injury reports in the Vaccine Adverse Event Reporting System (VAERS).

Johnson obtained the emails after he subpoenaed the U.S. Department of Health and Human Services in January 2025 for COVID-19 vaccine safety records and pandemic-related communications.

FDA was ‘blind’ to COVID vaccine injury reports in VAERS

In his testimony, Jablonowski detailed how each of the federal government’s three vaccine safety monitoring systems — VAERS, V-safe and Vaccine Safety Datalink (VSD) — had “pitfalls” and “failed” to adequately assess safety issues with the COVID-19 vaccine and other vaccines.

The failures of vaccine safety monitoring “can be, and were, catastrophic,” he said.

For instance, the FDA insisted on monitoring COVID-19 vaccine reports using a method that it knew didn’t work. The FDA knew the method was likely to give inaccurate results if similar vaccines — such as the Pfizer and Moderna COVID-19 vaccines — were included in the dataset. This is called masking.

“The FDA was completely blind to COVID-19 vaccine adverse events,” Jablonowski wrote. He said the FDA could have used an improved statistical method accounting for masking.

A 2022 peer-reviewed paper in Drug Safety showed that the improved method detected roughly 25 statistically significant COVID-19 vaccine safety signals — including sudden cardiac death, Bell’s palsy and pulmonary infarction — that the FDA’s older method missed.

In an earlier interview with The Defender, Jablonowski explained why it was so harmful for the FDA to continue using the older method:

“Imagine a night watchman has to find something on the ground. But instead of holding a flashlight, he is wearing sunglasses. In the morning, he says he didn’t find anything. That’s true, but it’s because he was using a tool that impeded his ability to see.”

As of March 27, 1,675,590 adverse events were reported to VAERS following COVID-19 vaccination, according to OpenVAERS. That number includes over 39,077 reports of death, 29,200 reports of myocarditis or pericarditis, and 18,009 reports of Bell’s palsy.

A national survey conducted in November 2025 found that roughly 1 in 10 U.S. adults who received the COVID-19 vaccine experienced “major” side effects.

V-safe was designed to collect ‘inconsequential’ data

Jablonowski told lawmakers that the Centers for Disease Control and Prevention’s (CDC) COVID-19 vaccine safety monitoring tool, V-safe, was designed to collect only “inconsequential” information that no one really cares about.

The V-safe app invited COVID-19 vaccine recipients to check off boxes to indicate what, if any, side effects they experienced after getting the shot.

However, the box options were for common short-term vaccine side effects that most people would consider “inconsequential,” such as chills, headache, joint pain, muscle or body aches, fatigue or tiredness, nausea, vomiting, diarrhea, abdominal pain or rash.

If a person experienced a more serious problem, they had to manually type it into the “other” text field, Jablonowski noted. He said:

“It is with horror that we find 366 individuals typed ‘myocarditis’ in the ‘other’ free-text field, a condition requiring a medical diagnosis. The horror is amplified by the nearly 50,000 registrants who typed ‘chest pain’ into the ‘other’ free-text field.”

Vaccine Safety Datalink is off-limits to independent researchers

Jablonowski also detailed how VSD, a collaborative database of patient information from 13 integrated healthcare organizations covering over 15.5 million people, also fails the public.

VSD data can ostensibly be used to detect vaccine safety issues in near-real time, Jablonowski said.

The problem is that only a small handful of scientists are ever allowed to look at the data. Jablonowski said:

“This many million-dollar taxpayer funded resource is not available to any scientist outside of the 13 Managed Care Organizations (MCO) or the federal government without independent IRB [independent review board] applications approved by all 13 MCOs, an estimated $250,000 per project.”

In other words, independent researchers are realistically barred from analyzing the data. “Transparency is simply unattainable,” Jablonowski said.

Watch Jablonowski’s opening statement 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.

May 2, 2026 Posted by | Deception, Science and Pseudo-Science | , , , | Comments Off on CHD Scientist: CDC, FDA COVID Vaccine Safety Monitoring ‘Insulting, and Many People Are Injured’

COVID Conniving Receives First Federal Indictment

By Jim Bovard | The Libertarian Institute | May 1, 2026

David Morens, a former top advisor to COVID Czar Tony Fauci was indicted this week and “charged with conspiracy against the United States; destruction, alteration, or falsification of records in federal investigations; concealment, removal, or mutilation of records; and aiding and abetting,” according to the Justice Department press release.

Morens allegedly helped top federal health officials cover up the potential role of federal grants in spurring the COVID pandemic. The Freedom of Information Act (FOIA) requires federal agencies to preserve and disclose federal records with some narrow exceptions. In early 2021, Morens emailed a colleague, “I learned from our foia lady here how to make emails disappear after i am foia’d but before the search starts, so i think we are all safe.”

Morens added, “Plus i deleted most of those earlier emails after sending them to gmail.” In a previous email, he assured his collaborators, “I have spoken to our FOIA folks” and “I should be safe from future FOIAs. Don’t ask how…”

Fauci doesn’t need to worry about getting indicted since President Joe Biden, on his last morning in office, pardoned any crimes that Fauci might have committed in the previous decade. Fauci justified COVID mandates because average citizens “don’t have the ability” to determine what is best for them. Congressional investigations revealed that Fauci was at the center of string-pulling to shirk responsibility on COVID.

Top federal officials scrambled to erase the federal role in bankrolling reckless gain of function research at the Wuhan Institute of Virology in China, the most likely source of the COVID virus that killed more than seven million people around the world. That type of research seeks to genetically alter organisms to enable the spread of viruses into new species. As MIT professor Kevin Esvelt asked in 2021, “Why is anyone trying to teach the world how to make viruses that could kill millions of people?” The risks were compounded because the Wuhan Institute had a very poor safety rating. Two years earlier, the State Department confidentially “warned other federal agencies about safety issues at Wuhan labs studying bat COVID,” but the public disclosure of that alert was delayed until 2022—long after President Biden illegally mandated COVID vaccines for a hundred million American adults.

If COVID-19 had been initially recognized as the result of one of the biggest government boondoggles in history, it would have been far more difficult for American politicians and government scientists to pirouette as saviors as they seized sway over daily life. Instead, politicians, bureaucrats, and the media stampeded most of the American public with the notion that total submission to boneheaded decrees was their only hope to survive.

Attorney General Todd Blanche issued a statement on the indictment of Morens:

“These allegations represent a profound abuse of trust at a time when the American people needed it most—during the height of a global pandemic.”

Luckily, there haven’t been any “profound abuses of trust” since Trump took office again—at least according to his Justice Department. Blanche added, “Government officials have a solemn duty to provide honest, well-grounded facts and advice in service of the public interest — not to advance their own personal or ideological agendas.”

Be still my beating heart. Is this a subtle signal that the Trump team will disclose the other three million documents on the Epstein scandal?

FBI chief Kash Patel announced at the indictment press conference, “Circumventing records protocols with the intention of avoiding transparency is something that will not be tolerated by this FBI.”

Has the FBI turned over a new leaf or what? The FBI is one of the most notorious FOIA violators in Washington. When FOIA was first passed in 1966, FBI chief J. Edgar Hoover ordered his agency to totally refuse compliance with the law. A federal judge slammed the FBI in 2017 for claiming it needed seventeen years to fulfill a FOIA request on surveillance of antiwar activists in the 1960s. The FBI deleted the names of Clark Kent and Lois Lane from a letter that made reference to the famous Superman characters—because disclosing them in a FOIA response would “constitute a clearly unwarranted invasion of personal privacy.” Louis Freeh, director of the FBI from 1993-2001, repeatedly denounced my articles on Ruby Ridge; but when I filed a FOIA, the FBI claimed to have no records of those published letters to the editor. They sent their response to “Mr. Brovard” so maybe that helped them not find anything.

FBI FOIA trampling is par for the Bureau covering up its destruction of freedom of speech and freedom of the press. As federal judge Terry Doughty declared in a 2023 decision, “The FBI [acted] as doorman to a vast program of social media surveillance and censorship, encompassing agencies across the federal government—from the State Department to the Pentagon to the CIA.”

Morens may be the first federal official to ever be charged with a crime for actions to evade FOIA requests. Certainly, in more than fifty years, no federal FOIA official has ever been jailed for violating the law by refusing to disclose information. I’ve received so many BS responses from FOIA officers over the decades that I have lost count. When I filed a FOIA with the Office of the U.S. Trade Representative to see what information they had on me in their files, they replied in 2010, “We have no records on Kevin Bovard.” But I wasn’t asking about my cousin.

In 2015, I heard scuttlebutt that the Justice Department pressured USA Today to cease publishing my articles bashing Attorney General Eric Holder. I filed a FOIA to get the department’s official emails to my editors, but DOJ FOIA claimed it had nothing. I only got the damning emails after I filed a follow-up FOIA request and made a lucky guess on the exact day, hour and minute the emails were sent.

For too long, deceiving the American people has been treated like a victimless crime in Washington. If the Morens indictment can set a precedent leading to more such criminal investigations of bureaucratic cover-ups, that will be a booster shot for American democracy.

May 2, 2026 Posted by | Civil Liberties, Deception, Full Spectrum Dominance | , , , | Comments Off on COVID Conniving Receives First Federal Indictment

REPORT: United States Now Global Outlier Ignoring Vaccine Injured as UK Inquiry Acknowledges Harms

By Jefferey Jaxen | April 17, 2026

Baroness Hallett is the Chair of the UK’s COVID-19 Inquiry – an independent public investigation established to examine the country’s response to and impact of the Covid-19 pandemic.

‘Module 4’ was just released today and it dealt primarily with those harmed by the rushed rollout of an experimental mRNA jab.

THE NEW INQUIRY ACKNOWLEDGED THE FOLLOWING:

“The current system of payment for those injured as a result of having a Covid-19 vaccine requires reform.”

“The Inquiry acknowledges the suffering of those for whom vaccines led to serious injury and death. It is imperative that a sufficiently supportive government scheme is in place to help the minority of people (and their loved ones) who suffer serious injury following vaccination.”

“The Inquiry recognises that some of the vaccine injured and bereaved sharing their experiences online felt stigmatised and ignored when their content was labelled as misinformation“

“The Inquiry was also told that, when the Covid-19 vaccines were rolled out, little was done to publicise the scheme and a significant number of those who had been injured or bereaved as a result of the vaccine were unaware of it.“

The inquiry’s overarching recommendation was the following:

“… reforming the Vaccine Damage Payment Scheme as soon as possible, with an increase in the minimum payment awarded to those injured by a vaccine and a fairer system for determining payment.“

For many, these admissions are a welcomed surprise from slow-acting governments who have dragged their feet to recognize citizens harmed by products they mandated.

What wasn’t included in the UK inquiry was any mention of the violations of informed consent that occurred during the failed pandemic response. A particularly telling point especially in the UK where, in addition to the garden variety slights of lockdowns, forced vaccinations, blanket ‘do not resuscitate orders in care homes, the media openly boasted about the Army’s psychological warfare unit being deployed domestically on citizens.

The UK announcement now shamefully places the United States as the global outlier in recognizing and beginning the plan to develop better care and ultimate justice for the COVID-vaccine injured.

Most U.S. government officials and compliant corporate media outlets are still satisfied with calling the injured who question vaccines ‘anti-vaxxers’ and other divisive names to neutralize them and their rightful quest for help, the world is changing and America is beginning to look not as great on this vitally important subject.

The legal cancellation of the recent Advisory Committee on Immunization Practices (ACIP) by a lawfare Massachusetts judge took away the opportunity for American COVID vaccine injured who were scheduled to testify at the federal meeting. Recognition was denied and shockingly, few politicians and media pundits cared.

For the first time in U.S. history, a dedicated ICD-10 diagnostic code specific to adverse effects of COVID-19 vaccines is moving forward. React19 advanced the proposal at the March 17–18, 2026 ICD-10 Coordination and Maintenance Committee Meeting, and it has now entered a 60-day public comment period ending May 15, 2026.

CLICK HERE TO SUBMIT PUBLIC COMMENT HERE

Why An ICD-10 Code Matters

The ICD-10 code proposal aims to address a critical gap: currently, no specific ICD-10-CM code exists for adverse effects following COVID-19 vaccination. This has led to widespread miscoding, under-recognition, and difficulty in tracking, researching, and treating these conditions. The proposed code would give clinicians, researchers, and public health officials a clear way to document these cases.

In a separate effort to petition the appropriate U.S. agencies seeking proper care, React19 petitioned the Social Security Administration’s Compassionate Allowances program only to be greeted with the following writes The Defender :

Last year, React19 and Florida Surgeon General Joseph A. Ladapo asked the CAL program to include the 10 conditions. The CAL program is designed to fast-track disability benefits for people with severe illnesses that clearly meet SSA criteria.

The program rejected all 10 requests within 48 hours.

In response, React19 filed a FOIA request seeking documents and data that could shed light on the decision-making process behind the rejections.

The ‘help’ the U.S. government does offer the COVID-vaccine injured is in the form of the Countermeasures Injury Compensation Program (CICP).

The latest numbers from that program have just been released. Shamefully, less than 1% of injury claims have been compensated.

Full article

April 19, 2026 Posted by | Civil Liberties, Full Spectrum Dominance | , , | Comments Off on REPORT: United States Now Global Outlier Ignoring Vaccine Injured as UK Inquiry Acknowledges Harms

The Gratitude of the Captured

An Essay on the Four Walls That Make the Injured Defend the Injury

Lies are Unbekoming | April 12, 2026

1. The Testimony That Should Not Exist

A woman films herself from a hospital bed. Her left side will not move. Her speech is slurred. She took the COVID vaccine three weeks earlier and had a stroke within days. The camera shakes because she is holding it with the hand that still works. And she says, into the lens, that she is glad she took it. Because it could have been worse.

By every ordinary standard of how people respond to injury, the woman in the bed should be angry. She should want to know what happened to her body, who gave her the injection, what was in it, why she was not warned. Instead she is defending the thing that harmed her, and she is doing it sincerely, from a bed she may never leave.

The pattern repeated at scale throughout 2021 and 2022. Myocarditis in young men, received with gratitude. Sudden hearing loss, received with gratitude. Menstrual disruption, miscarriage, Bell’s palsy, shingles, tinnitus, cognitive fog — received with gratitude. The injured gave television interviews thanking the health authorities. They wrote newspaper columns urging others to take the product that had injured them. They volunteered at vaccination centres. The more severe the injury, the more fervent the testimony.

The COVID case is the clearest and most recent instance of something older. Chemotherapy patients credit the treatment with saving them while enduring a devastation that is the treatment.¹ Flu shot recipients who get the flu report that the shot made it milder — a claim no one can check. Statin patients who develop muscle weakness, diabetes and cognitive decline continue taking the drug in gratitude for a heart attack that may never have been coming.² SSRI patients who cannot feel, cannot sleep without the pill, cannot leave the house without the prescription, describe the drug as having saved their lives.³ Parents whose children regress after vaccination defend the schedule that preceded the regression.

The gratitude is real. That is what makes it devastating. These patients are not lying or performing. They feel what they say they feel. They are captured, and the gratitude is what their captivity looks like when it speaks.

What follows rests on one claim. The phenomenon is an engineered room, not a cognitive error or a cultural drift. Four walls stand around the captured person, each sealing a different exit, built by identifiable actors serving documented interests. The same four walls stand around every major medical intervention of our time.

The essay names the walls, shows them at work across several medical domains, names their architects, and ends where it must — with the one act that brings them down.


2. The Sealed Room

Four walls hold the captured person in place. Each seals a different kind of escape. Together they form a room from which the individual patient, acting alone, cannot exit. The walls fail only at population scale, and only when enough of the captured begin to speak at once — a condition the later sections will examine.

Wall One — The Counterfactual Shield. The intervention is defended by an imagined alternative that never happened. It would have been so much worse without it. The worse outcome is unfalsifiable. It did not occur and cannot be examined. It exists only as a claim, and a claim that cannot lose.

Wall Two — Injury as Vindication. Actual harm from the intervention is converted, at the moment of appearance, into evidence the intervention was necessary. Side effects become signs the drug is working. Adverse events become imagine how bad it would have been otherwise. The harm is recruited to defend the thing that caused it.

Wall Three — The Sunk Cost Bind. The patient has submitted their body to risk, cost, violation. The psychological price of admitting the submission was unnecessary — or worse, actively harmful — is unbearable. Every subsequent piece of evidence gets reorganised to vindicate the original decision, and the reorganisation strengthens with time.

Wall Four — The Tribal Seal. The intervention is tribal. Taking it is membership. Refusing it is defection. Honest testimony about injury breaks ranks with the tribe that formed around the intervention. The social cost of speaking is exile, so the injured stay silent, or perform gratitude to remain inside.

The walls appear here in the order the captured person meets them psychologically. Wall One is intellectual — it is installed before anything happens, as the framing of the intervention. Wall Two is empirical — it activates when harm arrives, renaming it before the patient can. Wall Three is interior — it operates in the self, on the self. Wall Four is social, and it closes the last door, the one that opens onto another person.

The sections that follow examine the walls one by one, and then name the people who built them.


3. Wall One: The Counterfactual Shield

A man takes the COVID vaccine in March 2021 and does not get COVID for the next year. He reports that the vaccine worked.

A woman takes the same vaccine and gets COVID in September. She reports that the vaccine worked, because it would have been worse without it.

A second woman ends up in hospital with COVID in October. She reports that the vaccine worked, because without it she would have died.

A third ends up on a ventilator, survives, and reports that the vaccine saved her life.

Every possible outcome confirmed the intervention. The counterfactual shield is the mechanism that made this possible. For each real outcome, an imagined worse outcome was available for comparison, supplied by the same system that administered the injection. The patient did not compare their actual experience to another actual experience. They compared it to a hypothetical that could never be tested.

This is the structure of every statin prescription. The patient cannot feel cholesterol. They cannot feel the heart attack that did not occur. What they can feel is the muscle pain, the fatigue, the cognitive changes, the new diabetes — and they are told this is the acceptable cost of preventing something invisible. Prevention is the absence of an event, which means the benefit can never be observed, only claimed. Every year without a heart attack is credited to the drug. When a heart attack arrives anyway, the cardiologist explains how much worse it would have been.

The shield needs a particular statistical apparatus to stand. The patient does not invent the imagined alternative from nothing; it is delivered to them, precisely calibrated, by the medical literature. Relative risk reduction is the instrument. A drug that cuts heart attacks from two per hundred to one per hundred is described as producing a fifty percent reduction. The absolute change — one person in a hundred — is rarely spoken. The patient hears fifty percent and pictures a world in which they were twice as likely to die. The shield, built from numbers the patient cannot audit, is in place before the first dose.

Notice what the wall does with time. It is installed before the intervention. The patient arrives already committed to the counterfactual, and every subsequent event gets filtered through it. The shield is not a defence the patient raises under challenge. It is the prior condition of the encounter.

COVID delivered this with unprecedented coordination. The vaccine reduced severe illness by ninety-five percent.⁴ The number appeared in advertising, press conferences, pharmacy windows, social media posts. It was a relative risk reduction calculated from a trial of approximately forty thousand people in which one hundred and seventy total COVID cases occurred.⁴ The absolute reduction was roughly zero point eight percent. The ninety-five percent was mathematically real and useless to any individual patient, but it did the only thing it needed to do — it installed the counterfactual. By the time a person rolled up their sleeve, the severe illness they had been rescued from was already in their head. Every later event could only confirm it.

A patient who wants to question the shield has no tools. They cannot run the experiment on themselves. They have no access to an un-treated version of their own body. They can only trust the number, and the number was given to them by the people who sold the intervention.


4. Wall Two: Injury as Vindication

The second wall turns on when the intervention produces harm. It renames the harm, before the patient can examine it, as evidence the intervention was needed.

Chemotherapy is where this wall stands most nakedly. The treatment produces hair loss, nausea, vomiting, bone marrow suppression, secondary cancers, organ damage, cognitive decline, and in a significant fraction of patients death directly attributable to the treatment itself rather than the disease.¹ Every one of these effects is explained to the patient in advance as a sign the treatment is working. Worse side effects mean the cancer is being fought harder. The patient who is destroyed by the treatment is told, and comes to believe, that the destruction is evidence of the drug doing its job.

In any other domain, a substance that caused hair loss, marrow suppression, neuropathy and death would be called poison. In oncology, it is called treatment, and the symptoms of poisoning are called response. A patient loses her hair and is congratulated. A patient vomits for six hours and the oncologist nods with satisfaction. A patient’s white cell count collapses and the number is entered into a chart labelled progress.

The vindication continues after the treatment ends. Survivors describe the treatment as having saved them, even though the untreated survival rate for many cancers — particularly low-grade and early-stage — is substantial and, in some studies, superior.¹ Patients who do not survive are said to have succumbed to the disease. The treatment itself, in the grammar of the explanation, cannot lose. Recovery means the treatment worked. Decline means the cancer was too aggressive. Death from treatment-induced organ failure becomes death from cancer. The death certificate rarely names the chemotherapy.

The same inversion ran through the COVID rollout with identical logic. Myocarditis in a young man after the second dose was classified as mild and self-limiting, and official guidance explicitly declined to treat it as a reason to halt the programme.⁵ The injury was converted, in real time, from a reason to stop into what officials called a sign the body was responding as intended. A teenage boy who developed pericarditis was described as fortunate to have been vaccinated, because imagine how bad it would have been otherwise. The inversion operated not only in the patient but in the cardiologist giving the diagnosis, in the journalist writing the story, in the regulator reviewing the report. The injury was never an injury. It was always a sign.

Pfizer’s own documents, obtained by court order after the FDA requested seventy-five years to release them, list over one thousand two hundred distinct adverse events in the first twelve weeks of the rollout.⁶ The company had to hire more than two thousand additional staff to manage the caseload. Of two hundred and seventy pregnant women who reported injury, only thirty-two were followed up, and twenty-eight of their babies died — an eighty-seven point five percent fetal death rate in the followed cohort.⁶ These numbers were not volunteered by Pfizer. They were extracted through litigation. In the public conversation of 2021 and 2022, the events they describe were either denied or converted into evidence the programme was working.

The wall holds because the patient has no independent framework from which to resist it. When the oncologist says hair loss is good, the patient has no counter-language. When the cardiologist says myocarditis is mild, the young man has no access to population data. When the physician calls the side effects signs of the body responding properly, the patient accepts it because no other account is available in the room. The injury is named by the apparatus that produced it, and the name replaces the thing.

By the time the patient might think to examine the injury on their own terms, the third wall has already closed behind them.


5. Wall Three: The Sunk Cost Bind

The third wall stands inside the patient rather than outside, which is why it is the hardest to see. From inside, it feels like the patient’s own mind.

Consider a woman who has taken a selective serotonin reuptake inhibitor for fifteen years. She began after a divorce. The initial diagnosis was depression. She was told her brain had a chemical imbalance that the medication would correct.³ Within weeks she felt a kind of emotional flattening that her doctor called the medication working. She stayed on it. Over years she noticed she could not cry at funerals, could not feel desire, could not grieve her mother’s death when it arrived. She tried twice to come off the drug. Both times the withdrawal was catastrophic — electric shocks in her head, intrusions of suicidal thought, panic that kept her awake for days — and both times she went back on, convinced by the severity of the symptoms that she needed it.

Ask this woman whether the medication saved her and she will say yes. She will say it without hesitation and without calculation. She will also say she does not know who she was before it, because the person who took the first pill is no longer available for comparison. Fifteen years of her life have been built around the diagnosis and the drug. Her identity contains the diagnosis. Her marriage, her friendships, her children’s memories of their mother all include the medication as a feature of her personality.

To admit the medication was not needed — that her grief had been grief, that the withdrawal was the drug rather than the return of her underlying condition, that the emotional flattening was damage rather than improvement — would require her to accept that fifteen years of her life were spent inside a false frame. She would have to grieve what the medication took from her. She would have to face her absence from her children, her distance in her marriage, her unfelt goodbye to her mother. The cost of that reckoning is more than most people can pay. So she stays on the drug and says it saved her life. The gratitude is real because the cost of it being otherwise is unbearable.

Wall Three most resembles ordinary human psychology, which is why it reads as personal rather than architectural. Everyone has known some version of it — the defence of a choice after it has gone wrong, memory quietly rewriting itself to fit where money and years have already been spent. What makes the medical version structural is the scale of what has been paid in and the absence of any exit that does not require grieving it.

A man who has taken statins for twenty years, and who has watched his strength fade, his memory slip and his diabetes arrive — the exact trio the drug is known to cause² — is asked whether the statins helped. He says yes. He has to say yes. Saying no would mean accepting that two decades of growing weakness were caused by the drug he took to protect himself. It would mean admitting the heart attack he was preventing may never have been coming, that the cholesterol number he was taught to fear was a fabricated risk marker, that the man he became — slower, forgetful, diabetic — is a product of a prescription rather than of ageing. The alternative is gratitude, and he is grateful.

A mother whose child regressed after the MMR vaccination is asked whether she regrets it. Most of the time she says no. She says the vaccine was necessary. She says the autism was coming anyway. Admitting otherwise would mean accepting that she brought her child to be injured, held him down while the injection was delivered, paid for it and thanked the paediatrician afterwards. The grief on the other side of that admission is more than most parents can carry, and the wall is shaped precisely so she does not have to carry it. She can stay grateful. Her paediatrician will reinforce the gratitude. Her friends will reinforce it. The media will reinforce it. Wall Four will hold her there.

Wall Three has a property worth naming directly. It thickens with time. The longer the patient has been inside the frame, the higher the cost of leaving it becomes, and so the more fervent the defence. This is why the elderly chemotherapy survivor speaks with more heat about the drug that saved her than the recent survivor does. This is why the twenty-year statin patient is more certain of the drug’s necessity than the one-year patient. The wall grows. At some point it becomes unbreachable by any means available to the patient alone.

What completes the bind is that the captured person becomes a recruiter. The grateful SSRI patient urges her grieving friend to see a psychiatrist. The grateful chemotherapy survivor tells the newly diagnosed to accept the protocol. The grateful vaccinated parent shames the unvaccinated one at the school gate. Each captured person, defending their own wall, helps build walls around others — because their own wall depends on the walls around others holding. If the friend refuses medication and flourishes, fifteen years come into question. So the friend must be pressured, shamed, or cut off. The sunk cost in one person becomes the tribal pressure on the next, which brings the architecture to its final closure.


6. Wall Four: The Tribal Seal

The fourth wall operates outside the patient, in the community. It is the social enforcement of the narrative the patient has begun to perform, and it closes the last available exit.

Throughout 2021 this wall stood in open view. Taking the COVID vaccine was an act of public membership — selfies from vaccination centres, profile frame overlays, stickers worn on lapels, doses announced on social media. Refusing was public defection. The refusers lost jobs. They were barred from restaurants, gyms, concert venues, churches, universities, sometimes from hospitals even as visitors. They were removed from family gatherings. They were called murderers on national television by the president of France, by the prime minister of Canada, by physicians on major networks. Official communications described them as a selfish minority whose refusal was costing the compliant their freedom.

Inside that environment, an injured person who testified honestly about their injury was not merely raising a medical concern. They were defecting. Their testimony confirmed what the refusers had been saying. Their testimony was a gift to the outgroup. The tribe could not absorb it, because tribal cohesion depended on the intervention being unquestionable. So the injured were managed. Sometimes through silence — their accounts went unpublished, their videos removed, their doctors declining to code the injury as vaccine-related. Sometimes through reframing — the injury classified as COVID, as long COVID, as coincidence, as pre-existing. Sometimes through direct punishment — the injured person who insisted on naming the cause was accused of spreading misinformation, of harming public health, of serving the outgroup.

Every injured person watched this happen to others before it happened to them, and the lesson was not subtle. Most adjusted. They stopped describing their injury as an injury. They began describing it as unfortunate but acceptable. They began saying the words that returned their membership: I’m glad I took it. It could have been worse. The gratitude was not only psychologically needed. It was socially required.

Wall Four is not specific to COVID. It has stood around childhood vaccination for decades.⁷ A parent who questions the schedule loses access to paediatric practices that refuse unvaccinated patients. She is asked to leave mothers’ groups. Family members cut her off on the grounds that her choice endangers their vaccinated grandchildren. Her children are barred from schools. Any paediatrician willing to accommodate her operates under constant professional threat. Entire parenting communities organise around the vaccination question, and the penalty for dissent is exile. Parents whose children regress after vaccination, and who begin to suspect a causal link, face a choice between silence and exile. Most choose silence. Many perform gratitude instead, because gratitude reopens the community. The mother who says I’m so glad we vaccinated; his regression was just coincidence keeps her paediatrician, her friends, her family. The mother who says I believe the vaccine injured my child loses all of them.

The same seal stands around psychiatric medication, around cancer treatment, around mainstream obstetric care. In each, the patient who voices doubt is pressured first by the clinician, then by the family, then by the wider community that has already accepted the intervention as standard. Doubt is not only intellectually costly. It is socially costly, and the social cost arrives first. By the time the patient has finished working through their own doubts, the tribal apparatus is already at work on them, and the route back into membership requires the precise language of the first two walls. I’m so glad I took it.

What makes Wall Four the final seal is that it closes the one exit the other walls do not reach — the exit through honest testimony to another person. An intellectually awakened patient, who has seen through the counterfactual shield, recognised the injury as injury and refused to let sunk cost rewrite their history, still cannot speak, because speaking costs their community. The wall holds them silent. And in silence, the other three walls rebuild. The shield recloses. The injury reverts to vindication. The sunk cost reasserts its grip. The captive, left alone with the structure, returns to gratitude — because gratitude is the one posture that lets them remain intact on every side at once.


7. The Architects

The walls do not grow. They are built, funded, and maintained by identifiable actors working in documented financial arrangements. Nothing here is hidden. Everything is filed, recorded, disclosed in annual reports, visible in congressional testimony, available by Freedom of Information request. The architects have names and budgets.

Wall One — Who Builds the Counterfactual Shield

The shield is built from clinical trials and the statistical practices that translate trial results into claims patients can repeat to themselves. Most clinical trials are now run by for-profit Contract Research Organisations in jurisdictions with minimal oversight.⁸ Forty percent of medical journal articles are ghostwritten by the pharmaceutical industry.⁸ Authors with industry conflicts of interest are twenty times less likely to publish negative findings.⁸ Richard Horton, editor of The Lancet, has written that perhaps half the scientific literature is simply untrue.⁸ Marcia Angell, former editor of the New England Journal of Medicine, has written that the profession has been bought.⁸

The statistical habit that builds the counterfactual — relative risk reduction as the default metric — is a choice, not a necessity. Absolute risk reduction tells the patient what actually changes for them. Relative risk reduction amplifies the apparent effect. Every major drug marketing campaign of the last forty years has preferred the relative figure. The FDA permits it. Journals publish it. Physicians pass it along to patients who cannot tell the two apart.

For COVID, the ninety-five percent figure came from a trial of roughly forty thousand participants that recorded a total of one hundred and seventy COVID cases — one hundred and sixty-two in the placebo arm, eight in the vaccinated arm.⁴ The trial was not designed to measure transmission, hospitalisation, or death.⁴ Pfizer’s own documents show the company knew the lipid nanoparticles crossed the blood-brain and blood-testicular barriers, accumulated in ovaries and testes, and had caused reproductive harm in earlier nanoparticle studies — and proceeded without reproductive toxicity studies, citing urgency.⁶ The shield that reached hundreds of millions of minds was built from this data, presented in relative terms, and installed before the first injection.

Wall Two — Who Converts Injury Into Vindication

The apparatus that turns harm into proof operates across three layers: pharmacovigilance, physician training, and media framing.

Pharmacovigilance is structurally designed to undercount. The U.S. Vaccine Adverse Event Reporting System is passive; physicians are not required to file, and most do not. A Harvard Pilgrim Health Care study, funded by the federal government, concluded that fewer than one percent of vaccine adverse events are reported.⁹ If that figure is correct, official vaccine injury numbers understate real injury by a factor of one hundred. The study was delivered to the CDC, which declined to act on it and declined to implement active surveillance. The undercount is the default.

Physician training teaches doctors to name injuries in ways that protect the intervention. Hair loss is treatment response. Myocarditis is mild and self-limiting. Autism is coincidental regression that would have happened anyway. Death during treatment is disease progression. Medical school curricula are funded, in part, by the pharmaceutical industry.¹⁰ Two-thirds of medical school department chairs have financial ties to pharmaceutical companies.⁸ Continuing medical education — the system through which practising doctors update their knowledge — is dominated by industry-funded programmes. The doctors performing the reframing are not reading from a cynical script. They have been trained to see what they say they see.

Media framing completes the conversion. Pharmaceutical companies are the largest advertiser on American evening news.¹⁰ Twenty-seven billion dollars flows annually into pharmaceutical marketing — more than the entire NIH budget.⁸ The major news divisions are owned by investment firms — BlackRock, Vanguard — that also hold substantial stakes in pharmaceutical companies. When a young man develops myocarditis after a COVID shot and his story reaches the local news, the frame — rare, mild, unrelated to vaccination, which remains safe and effective — is not written in the newsroom. It arrives through press releases, expert contacts, and editorial relationships supplied by the same apparatus that sold the intervention.

Wall Three — Who Reinforces the Sunk Cost

The sunk cost bind is thickened by patient advocacy groups and chronic disease management organisations, most of which are funded, directly or indirectly, by the pharmaceutical industry. Depression advocacy organisations receive substantial funding from SSRI manufacturers. Cancer advocacy organisations receive funding from chemotherapy manufacturers. The official vaccine safety organisations — not the dissident ones — receive funding from vaccine manufacturers, or from the CDC, which is itself funded in part by industry through its foundation.⁸

These organisations produce the narratives that keep the bind in place. The chemotherapy survivor community is built around the claim that the treatment saved them; dissenting voices are marginalised. The depression survivor community is built around the claim that medication saved them; those who question the diagnosis or the drug are accused of encouraging suicide. The vaccinated parent community is built around the claim that vaccines are necessary; parents who describe injury are labelled anti-vaccine and removed. In each case, the community functions as a structure that reinforces the patient’s need to stay grateful.

Chronic disease management delivers the reinforcement annually. The decade-long statin patient is told, at every physical, that her cholesterol is still elevated and she should continue the drug. The SSRI patient who describes emotional flatness is told the dose may need adjusting. A patient reporting withdrawal symptoms is told she is experiencing the return of her underlying condition. The clinical encounter reinforces the sunk cost every time she walks in. Her doubts, if she has any, are resolved by the clinician in favour of continued treatment.

Wall Four — Who Builds the Tribal Seal

The seal is built through public health communication, employer mandates, regulatory policy, media coordination, and the enforcement infrastructure of digital platforms.

COVID-era public health communication was produced and coordinated across federal agencies, corporate media, social media companies, and advertising campaigns. The specific framing — that the unvaccinated endangered the vaccinated, that refusal was antisocial, that vaccination was a civic duty — was not organic. It was produced. The Biden administration funded a multi-hundred-million-dollar campaign to promote vaccination.¹¹ Equivalent campaigns ran in every Western country. The narrative was coordinated enough that the same talking points surfaced nearly simultaneously across English-language media in multiple nations.

Employer mandates provided the enforcement. Workers were required to accept the injection as a condition of employment. Refusers were dismissed, often for cause, stripped of unemployment benefits and professional licences. Healthcare workers, teachers, service members, and federal contractors faced mandates that ended careers built over decades. The mandates did not issue from a vacuum. They were produced by regulatory decisions, legal memoranda, and executive orders that made refusal economically catastrophic.

Platform moderation finished the seal. Social media companies, under pressure from federal officials, removed accounts, posts and videos describing vaccine injury.¹¹ The label misinformation was applied to accurate first-person accounts. Fact-checking systems, funded in part by industry-adjacent foundations, rated injury reports false. The injured could not speak publicly about their own injury without suppression. In the digital age, the fourth wall was algorithmic.

Opioids: The Paradigm Run to Completion

The four walls can be seen at their fullest — and their eventual failure — in the OxyContin case, because that one ran all the way to the end.

Purdue Pharma received FDA approval for OxyContin in 1995. The approval process included language, permitted by the FDA, describing the drug as less addictive than other opioids because of its delayed-release formulation. The language was not supported by evidence. It was promotional text permitted into the regulatory record.¹² The company built a sales force that trained physicians to prescribe OxyContin for chronic pain, funded pseudo-science suggesting that patients seeking more of the drug were suffering from pseudo-addiction to be treated with higher doses, and paid consultants and patient advocacy groups to reinforce the claim that OxyContin was safe.¹²

The counterfactual shield was installed: patients were taught that without adequate pain management they would suffer unnecessarily. Wall Two took over when harm arrived: patients who developed tolerance and needed higher doses were told they had pseudo-addiction and required more of the drug, not less. Wall Three tightened as the months passed: patients who had been on OxyContin for years had organised their lives around it and could not stop without devastating withdrawal, and the withdrawal was interpreted as proof they had needed the drug all along. Wall Four held: patients who became dependent were categorised as addicts — a moral failing, a personal weakness — a category that separated them from each other and from the community that might otherwise have listened to them.

Patients thanked the physicians who prescribed it. They gave interviews thanking Purdue. Many became dependent and many of them died, and among those who died some were still grateful at the end. Then the bodies became too many to hide. Hundreds of thousands of deaths, families documenting the progression from legitimate prescription to heroin to fentanyl, internal Purdue documents forced into the open through litigation, Sackler family settlements, DEA investigations and congressional hearings. The walls came down twenty years late, with bodies stacked against them.

The lesson of OxyContin is not that the system corrects itself. The system corrects only when the damage becomes too visible to contain, and by then most of the damage is already done. Everything known at the end was knowable at the beginning. The FDA had the data. Purdue had its internal memoranda. The paid consultants had the complaints. The patients did not know, because the four walls stood around them, and most of them died grateful.


8. What the Captured Person Is Owed

If the architecture is engineered, the captured person is not a fool. They were not gullible or poorly educated. They were inside a structure built by specific actors for specific reasons, and its purpose was to produce exactly the response they gave — gratitude from the injured, defence from the captured, compliance from the well.

This is the first thing they are owed: the return of their dignity. The woman in the hospital bed who thanked the vaccine that stroked her is not a fool. She is inside the room, and her gratitude is the designed output of a designed apparatus. The same goes for the chemotherapy survivor who credits the poisoning, the parent who defends the schedule, the grandfather on his twentieth year of statins, the widow who still has OxyContin in the cupboard. None of them failed. A structure was built around them. The structure is what failed, because it was never designed to succeed at healing. It was designed to succeed at extraction, and at that it succeeded brilliantly.

The second thing they are owed is clarity about what their gratitude costs. When the injured cannot testify honestly about their injury, the injury does not appear in the record. It never becomes a safety signal, never gets studied, never reaches the next person considering the same intervention. The apparatus that produced the injury continues to produce it. The signals that might have shut down OxyContin in 1997 rather than 2017 were there in 1997, in the voices of the first dependent patients. Those voices were absorbed into the gratitude of the captured and converted into testimonials. The delay cost hundreds of thousands of lives.

The captured person’s dissenting voice is the most valuable instrument in medicine. Grateful testimony has been manufactured at scale for a century — that is what the previous sections have shown. What cannot be manufactured is the captured person turning, after years of defending the injury, and naming it. Once one captured person speaks that way, others recognise themselves in the testimony, and the walls begin to fail at the only point where they can fail — in the social layer, from inside the community. The injured testifying to the injured breaks the tribal seal. The tribal seal failing exposes the sunk cost. The sunk cost examined reveals the injury as injury rather than as vindication. The injury named dissolves the shield. The walls depend on each other, and the one that gives first is the fourth, because the fourth is the only one where another person’s voice can reach.

This is why the essay closes here, and not with a call to action. There is nothing general to be done. There is only the specific, costly, socially expensive act of breaking the silence — by the captured person who survives long enough to recant their gratitude, or, where the captured cannot speak, by those close enough to them to testify on their behalf. That single act, repeated, is the entire dismantling. It is what the apparatus was never designed to process, and it is the only thing that has ever worked against it. The OxyContin walls came down because the families of the dead spoke for those who could no longer speak. The Vioxx walls came down because injured patients outlived the cover-up long enough to name it. The DES walls came down because the daughters, injured in utero by what their mothers had been given, lived to testify to the inheritance. The machine ran, in each case, until the testimony arrived from someone it could not silence. Then it stopped.

The captured person speaking honestly is not an act of politics or rebellion. It is accurate description. What was done to the body was real, the captivity that followed was real, and the people who built it can be named. Under the gratitude is a person who has the right to say, at last, what actually happened.

That voice is what the room was built to prevent. It is also the only thing that has ever brought a room like this down.


References

  1. Thomas Cowan, discussed in When Your Body Whispers, Listen: The Intelligence of SymptomsNew England Journal of Medicine finding on breast cancer overdiagnosis: approximately 1.3 million American women overdiagnosed over thirty years. On lead-time bias and survival statistic manipulation in early-stage cancer screening, see H. Gilbert Welch and colleagues’ work on overdiagnosis.
  2. John Abramson, MD, Harvard Medical School; Peter Gøtzsche, Deadly Medicines and Organised Crime: How Big Pharma Has Corrupted Healthcare (CRC Press, 2017). On the chronic disease cascade around statins — muscle pain, memory effects, diabetes — see Extraction: The Middle Class as Colony.
  3. Andrew Kaufman, MD, on SSRI mortality and pediatric prescribing pressures; Peter Breggin’s work on the suicide signal eventually acknowledged in black box warnings. On identity capture around psychiatric diagnosis, see Four Causes, Seventy Thousand Diseases.
  4. Pfizer BNT162b2 Phase 3 trial data as summarised in the Pfizer Document Analysis Report (War Room/DailyClout, December 2022). The 95% relative risk reduction figure was calculated from 170 total COVID cases in a trial of approximately 40,000 participants.
  5. CDC and FDA advisory communications on post-vaccination myocarditis, 2021–2022, including the June 2021 ACIP meeting that concluded benefits outweighed risks for adolescents and young adults. Critical account: Peter McCullough, MD, and Nicolas Hulscher’s published work on vaccine-associated myocarditis.
  6. Pfizer Document Analysis Report, War Room/DailyClout (December 2022), summarising the FDA-released Pfizer clinical trial documents obtained through court order after the FDA requested 75 years to release them.
  7. Turtles All the Way Down: Vaccine Science and Myth (2019). The 2013 Institute of Medicine report acknowledged that the childhood vaccination schedule as a whole has not been properly studied for safety.
  8. Peter Gøtzsche, Deadly Medicines and Organised Crime (2017); Marcia Angell, The Truth About the Drug Companies; Richard Horton, The Lancet, 2015. Aggregated in Extraction: The Middle Class as Colony.
  9. Lazarus R et al., “Electronic Support for Public Health–Vaccines Adverse Event Reporting System (ESP:VAERS),” Harvard Pilgrim Health Care, funded by AHRQ, 2010. Finding: fewer than 1% of vaccine adverse events are reported.
  10. Abramson J and Starfield B on the purpose of commercially funded clinical research. FDA revolving door: nine of the last ten FDA commissioners as of 2019 joined pharmaceutical companies after leaving the agency. Congressional capture: more than two-thirds of Congress took money from the pharmaceutical industry in 2020.
  11. Missouri v. Biden (2023) and related federal court findings on federal coordination with social media platforms to suppress COVID-related speech, including first-person vaccine injury accounts. Twitter Files disclosures, December 2022 – March 2023.
  12. Patrick Radden Keefe, Empire of Pain: The Secret History of the Sackler Dynasty (2021); Barry Meier, Pain Killer: An Empire of Deceit and the Origin of America’s Opioid Epidemic (updated edition, 2018); internal Purdue Pharma documents released through multi-state litigation and the 2020 Department of Justice settlement.

April 18, 2026 Posted by | Deception, Full Spectrum Dominance, Science and Pseudo-Science, Timeless or most popular | , , , , | Comments Off on The Gratitude of the Captured

REWRITING THE RISK? INSIDE THE GOVERNMENT’S VACCINE SAFETY MESSAGING

The HighWire with Del Bigtree | April 2, 2026

Jefferey examines newly surfaced internal communications suggesting that messaging around potential stroke risks following COVID-19 vaccination may have been altered at the highest levels of government, including the Joe Biden White House. Drawing on reported emails from federal health agencies, the segment explores how language describing a “moderately elevated” safety signal was revised to “slightly elevated,” raising serious questions about transparency, public health communication, and risk disclosure during the vaccine rollout.

The analysis also highlights how terminology shifts, from “potential risk” to “preliminary signal”, may have softened public perception of adverse events at a critical moment when booster doses were being distributed to tens of millions of Americans. With coordinated messaging efforts involving the CDC, FDA, and select media and expert networks, the discussion frames these developments as part of a broader strategy to manage public response rather than fully inform it.

Beyond stroke-related concerns, the conversation expands into other reported safety signals, including myocarditis and cardiovascular stress markers observed in certain populations following vaccination. Internal deliberations and delayed public warnings are presented as evidence of systemic gaps in adverse event reporting and physician awareness, potentially impacting early detection and response to emerging risks.

Framed within the larger debate over censorship, government accountability, and medical transparency, Jefferey raises critical questions about how public health decisions are communicated—and who ultimately controls that narrative. As scrutiny intensifies over pandemic-era policies, the discussion underscores the importance of open scientific dialogue, rigorous safety monitoring, and restoring trust in public health institutions moving forward.

April 6, 2026 Posted by | Deception, Timeless or most popular, Video | , | Comments Off on REWRITING THE RISK? INSIDE THE GOVERNMENT’S VACCINE SAFETY MESSAGING

Britain’s Lebanon surveillance network: A digital map for war

By Kit Klarenberg | The Cradle | April 3, 2026

On 7 March, the British government contractor Siren Associates unveiled Monitor Lebanon, a “real-time situational awareness platform” framed as a public safety tool “designed to help individuals and organizations understand and navigate Lebanon’s rapidly evolving security environment.”

The tool sifts vast swaths of “open-source information” from “news agencies, verified social media accounts, Telegram channels, conflict monitoring initiatives, and traffic data systems.”

Presented as a lifeline for journalists, humanitarian workers, businesses, and civilians during Israel’s ongoing war on Lebanon, the platform carries a far more operational intelligence function. Behind the humanitarian branding lies a sophisticated surveillance infrastructure embedded deep within the Lebanese state.

At the core of Monitor Lebanon is a live interactive incident map tracking “reported security events and key operational information.” The data is highly detailed, including information on “affected areas, road conditions, hospital locations, and other indicators that help users understand how developments may affect movement and access.”

press release announcing the platform’s launch asserts Monitor Lebanon was initially constructed to provide Siren Associates staff with “a clearer view” of local events, before being rolled out for general public use.

“Already, team members displaced by the ongoing hostilities have been using it to check for reported strikes near their homes and to track evacuation orders. But many more people are navigating the same uncertainty, so we want to make this tool available to anyone who may benefit from clearer, real-time information.”

How did a British contractor produce such a detailed, nationwide surveillance platform instantly as the occupation state escalated its assault on Lebanon?

The answer lies in nearly two decades of British-backed penetration.

As The Cradle revealed in September 2021, Siren has received tens of millions of pounds from London to “professionalize” Lebanon’s Internal Security Forces (ISF). Staffed by former British military, intelligence, and policing officials, the company operates in Lebanon’s security sector in plain sight, yet largely beyond scrutiny.

Embedding control through ‘reform’

Siren’s footprint inside Lebanon’s state apparatus is extensive. The company maintains close ties with senior ISF officers, political figures, ministries, and intelligence branches. It has also cultivated future leadership within the ISF through training and recruitment programs.

In May 2019, Siren established Lebanon’s Command and Control Center with British funding. The installation provides the ISF with “state-of-the-art equipment, information and communication technology systems, [and] an analysis and planning room,” purportedly to strengthen the security forces’ intelligence capabilities.

In practice, it embedded a direct channel for British intelligence into Lebanon’s internal security infrastructure.

Such access grants London visibility over investigations, operations, and internal data flows. Over time, this has enabled the systematic accumulation of sensitive information on Lebanese citizens.

The scale of this data collection expanded dramatically during the COVID-19 pandemic. Siren quietly built COVAX, the digital backbone of the Lebanese government’s COVID19 vaccine rollout. Users could register, schedule appointments, and receive vaccine certificates. Over four million people used the service, logging extraordinary amounts of personal information in the process.

What appeared as public health infrastructure operated as a mass data capture system.

From welfare to surveillance architecture

COVAX became the foundation for broader digital penetration. In 2021, the World Bank allocated $246 million to Lebanon for social assistance. Siren used its existing infrastructure to launch DAEM, whereby citizens could apply for social assistance “in record time.”

Carole Alsharabati, Siren’s longtime research chief, has explained that “the idea [was] to deploy a system that was fully digitized from A to Z, just like we did for the vaccine.”

“The registration, the selection, then the payment, the cash transfer, the verification, the dashboard, etcetera. Everything was digitized. And we used the same framework, the same ecosystem, the same machines, the same security protection, the same data governance approach we used in the vaccine.”

Alsharabati described Lebanon at the time as a “very difficult environment,” with the experience of building DAEM “a wild journey.” After all, the country lacked a unique ID system, digital identification, or any established data governance rules, procedures, or even cybersecurity.

However, “nothing stood in the way of Siren’s determination to tackle these and many other challenges.” Evidently, the British and Lebanese governments were happy with the results. It was just the beginning of Siren’s new role in Beirut, constructing deeply intrusive databases on citizens.

This work has been replicated in multiple fields over the years, culminating in Monitor Lebanon’s recent launch. Much of this activity passed entirely under the public radar. It was not until December 2024 that Siren’s central COVAX role was openly admitted on the company’s official website, for example. That same month, Siren announced it had built a bespoke resource for the ISF, collating “operational data to inform decision making around mission planning, resourcing and management.”

Under the project’s auspices, British intelligence created a network of six separate Command and Control Centers across the country, linked digitally to 22 regional operation rooms. A “digital platform that enables the capture and analysis of crime and operational data” was also developed.

In December 2024, too, Siren disclosed how it had introduced “e-governance tools connecting more than 20 ministries, 1,000 municipalities and 1,500 mukhtars [local governments].” Unmentioned was a major scandal that erupted over this effort upon its rollout two years prior.

According to Lebanese daily Al-Akhbar, the platforms produced by Siren were not secure, and permitted the firm to harvest the data of millions of users. Dubbed IMPACT, the resource allowed citizens to access a variety of government services, including applying for welfare payments.

The British embassy in Beirut, which funded the platform to the tune of $3 million, denied any wrongdoing, as did Siren. Nonetheless, local digital rights group SMEX expressed grave concerns over the security of private information stored by IMPACT, which was highly sensitive in nature.

Mapping a society for war

That Siren hoards an enormous amount of invasive information as a result of its work for and with the ISF is underlined by an April 2025 study, funded by Britain’s International Development wing. It probed “irregular maritime migration from Lebanon over the past three years,” placing the phenomenon in the context of Beirut’s “ongoing political, socio-economic, and security crises.”

The research sought to ascertain “who is migrating, why they are choosing to leave by sea, and what risks they face – particularly across gender lines.”

In September 2025, London renewed Siren’s ISF contract, allocating £46.3 million (around $61.3 million) – a significant increase. The timing raises serious questions about how much of that funding went into building Monitor Lebanon ahead of renewed Israeli escalation.

Since Operation Al-Aqsa Flood in October 2023, British activity in West Asia has pointed toward deeper involvement in a wider war effort targeting Iran and its allies.

In November that year, London attempted to secure unrestricted military access to Lebanese territory under the pretext of “emergency missions.” The proposal would have allowed British forces to operate freely, armed and immune from prosecution.

Public backlash forced Beirut to reject the plan. But the infrastructure remained.

Through Siren, Britain has built a digital panopticon spanning Lebanon’s institutions and population. This system provides real-time intelligence with clear military applications.

From Tel Aviv’s perspective, the benefits are obvious. Such data can be used to identify, track, and target members of Hezbollah and their support networks. It can also map civilian environments in ways that facilitate precision strikes.

The parallel to Palantir’s predictive surveillance platforms is clear.

Targeting the Axis of Resistance

Siren’s projects consistently overlap with services provided by Hezbollah. This is not accidental.

For years, British intelligence has worked to undermine the resistance movement’s social base by constructing parallel state structures.

For example, under the terms of a Foreign Office-funded youth radicalization effort, London sought to create an alternative to Beirut’s Hezbollah-run Ministry of Youth and Sport. It was hoped that “young, talented students and graduates” would thus reject the group.

There is little sign of these initiatives having borne fruit. A promptly deleted 23 March Daily Telegraph report documented how Lebanese Christians wholeheartedly embrace Hezbollah, and are determined to resist western-inspired efforts by Beirut’s army to disarm the resistance faction. “How can we as Christians in this area not be with Hezbollah?” a local citizen asked the newspaper perplexedly.

“They protect our churches. They helped us fight ISIS. During COVID, they gave us free care in their hospitals. When there was no electricity, they gave us generators. They even put up a Christmas tree at Christmas. How can we not be with them now?”

Despite the practical impossibility of disarming Hezbollah, it is a fantasy long harbored by western powers, which has gained in ever-mounting urgency since Israel’s genocide of Palestinians in Gaza commenced.

A British parliamentary briefing in September 2025 expressed optimism that the election of former Lebanese Armed Forces (LAF) commander Joseph Aoun as president would weaken Hezbollah’s military wing.

That same month, US special envoy to Syria Tom Barrack openly proposed equipping the LAF “so they can fight their own people.”

He acknowledged that Israel’s aggression since October 2023 had only increased Hezbollah’s popularity, while offering “zero” incentive for disarmament.

Aoun’s presidency has not dismantled Hezbollah. Israeli military escalation continues, with mounting losses on the battlefield and rising civilian casualties across Lebanon.

While its catastrophic military losses accumulate daily, innocent Lebanese civilians are being killed in significant numbers. The line of responsibility for their deaths may lead directly back to London, courtesy of Siren Associates.

April 3, 2026 Posted by | Ethnic Cleansing, Racism, Zionism, Full Spectrum Dominance | , , , , | Comments Off on Britain’s Lebanon surveillance network: A digital map for war

UK Government Secretly Tracked 25 Million People as Potential EV Owners

By Cindy Harper | Reclaim The Net | March 2, 2026

The UK government spent two years tracking 25 million mobile devices to build a picture of who drives electric cars. Not suspects or criminals. Just ordinary people whose browsing history mentioned EVs often enough to flag them as worth following.

The Department for Transport paid telecoms company O2 £600,000 ($809,000) to run the operation. According to the Telegraph, O2 trawled through its customers’ web browsing histories and app records, flagging anyone who visited an EV-related site at least once a month across two or more months.

That pool extended beyond O2’s own customers to include people on Tesco Mobile, GiffGaff, and Virgin Mobile, networks that run on O2’s infrastructure and whose users had no idea their data was being packaged and sold to a government agency.

Once flagged as a “potential EV owner,” your physical movements were traced across the country. London, the North-West, and the East of England received particular attention.

The techniques are standard in serious organized crime investigations. The DfT applied them to people buying environmentally friendly cars.

Andy Palmer, former executive at Nissan and Aston Martin, put it plainly: “I’m told it’s anonymized and aggregated, and that may well satisfy legal thresholds. But legality and legitimacy are not the same thing.” He added: “If you erode public trust in how that data is gathered, you undermine the very transition you are trying to accelerate.”

The idea of “anonymized” data means very little.

The surveillance ran for two years before the DfT quietly admitted defeat in April 2024, conceding that “mobile data cannot directly be used to provide information around charging behaviour or travel time.”

The program ended not because anyone questioned whether mass tracking of innocent people was appropriate, but because the data turned out to be useless for its stated purpose.

Civil servants from the DfT and Treasury were simultaneously exploring new EV taxes to replace fuel duty revenue. The people being surveilled were doing exactly what government policy encouraged them to do.

Conservative MP Sir David Davis drew the obvious conclusion: “It’s an object lesson in why you can’t trust the state with unfettered access to people’s information, because they’ve obviously taken this information without people’s permission with the objective of disadvantaging them, either by tax or other policy matters. If they’ll do it on this, with people who are doing what the government wants in policy terms, namely, pursuing green policies, what on Earth will they do elsewhere?”

The EV surveillance program wasn’t a one-off. During the earlier days of the COVID saga, the government ran a parallel operation, this time tracking people who showed up to get vaccinated.

Researchers funded through the Scientific Pandemic Influenza Group on Behaviors used mobile phone location data covering one in ten British people, without their knowledge or consent, to analyze behavioral changes after vaccination.

From that pool, they selected over 4,200 vaccinated individuals and tracked their movements through call data records, analyzing how far they traveled on vaccination day and whether they went straight home afterward.

The government was monitoring where citizens went after receiving a government-administered medical intervention, and chose not to tell anyone.

March 3, 2026 Posted by | Civil Liberties, Deception, Full Spectrum Dominance | , , | Comments Off on UK Government Secretly Tracked 25 Million People as Potential EV Owners

Project Artichoke: 70 Years Ago, CIA Discussed Hiding Mind-Control Drugs in Vaccines

By Michael Nevradakis, Ph.D. | The Defender | February 24, 2026

In the 1950s, the CIA brainstormed ways to secretly perform mind control on humans — including concealing drugs in vaccines and widely consumed food products, a newly unearthed CIA document revealed. The Daily Mail first reported the story on Monday.

The seven-page document, “Special Research for Artichoke,” is dated April 23, 1952. It describes a series of ideas for how to develop chemicals designed to alter human behavior and thought.

The proposals contained in the document were part of the CIA’s top-secret Project Artichoke, which ran from 1951 to 1956, according to the Daily Mail.

The document, declassified in 1983, recently circulated on social media. However, it was not published in the CIA’s online reading room until last year.

“Some of the suggestions are controversial,” the document states. The proposals included administering drugs in secret as part of a “long-range approach to subjects.”

According to the document:

“This study should include chemicals or drugs that can effectively be concealed in common items such as food, water, coca cola, beer, liquor, cigarettes, etc.

“This type of drug should also be capable of use in standard medical treatments such as vaccinations, shots, etc.”

CIA experimented on humans as part of Project Artichoke

The document also included a special field of research for “bacteria, plant cultures, fungi, poisons of various types, etc.,” that are “capable of producing illnesses which in turn would produce high fevers, delirium, etc.”

This included “species of the mushroom” that “produce a certain type of intoxication and mental derangement.”

Also among the proposals was a suggestion to research “diet” or “dietary deficiencies” on prisoners and on people undergoing interrogation, including using “specially canned foods having elements removed.”

The document included proposals for both short-term and long-term use on humans. Drugs deemed most suitable for long-term use would be designed to produce an “agitating effect (producing anxiety, nervousness, tension, etc.) or a depressing effect (creating a feeling of despondency, hopelessness, lethargy, etc.).”

According to The Daily Mail, the CIA experimented on humans as part of Project Artichoke. The experiments often involved “vulnerable subjects, including prisoners, military personnel and psychiatric patients.” The experiments were usually performed “without informed consent.”

According to Ben Tapper, a Nebraska chiropractor who was included in the “Disinformation Dozen” list in 2021 for questioning vaccine safety, the document exposes “a disturbing reality that government agencies have historically explored ways to manipulate human behavior through chemical and biological means, including concepts involving food and medical interventions.”

“This is not speculation or conspiracy, and it should deeply concern every American who values bodily autonomy and informed consent,” Tapper said.

Precursor to the CIA’s MK-Ultra mind control experiments?

The Daily Mail cited CIA documents suggesting that U.S. intelligence agencies were concerned that enemy nations had developed their own mind and behavioral control techniques. This led the agency to prioritize the development of its own methods.

Project Artichoke “served as a precursor” to the MK-Ultra program, which the CIA launched in 1953. That program “broadened mind-altering experiments on a larger scale,” the Daily Mail reported.

Many of the documents related to this type of experimentation were destroyed in 1973, “leaving the full extent of the research and how far it progressed unknown.”

Naomi Wolf, Ph.D., CEO of Daily Clout and author of “The Pfizer Papers: Pfizer’s Crimes Against Humanity,” told The Defender that the documents further confirm a long history of intelligence agency research targeting human thought and behavior.

“Sadly, it’s long been established that our intelligence agencies, and those of our enemies, have sought to alter human consciousness and behavior, often without the subjects’ consent. The existence of MK-Ultra, the clandestine project into which Project Artichoke evolved, is well documented,” Wolf said.

John Leake, vice president of the McCullough Foundation and author of the forthcoming book, “Mind Viruses: America’s Irrational Obsessions,” said, “Researchers have long suspected that the Church Committee’s revelation of the CIA’s notorious MK-Ultra mind control experiments, mostly using LSD, had the effect of obscuring the agency’s much larger Project Artichoke.”

Leake cited evidence suggesting that a 1951 mass poisoning in Pont-Saint-Esprit, France, in which 250 residents experienced severe hallucinations and seven people died, was a Project Artichoke experiment. The outbreak was officially attributed to contaminated bread from a local bakery.

Leake said the 1952 document is “consistent with the suspicion that the CIA was seeking to discover mind control methods for even large populations.”

In 2024, a Reuters investigation revealed that the CIA operated a secret propaganda campaign involving vaccines in the Philippines. The campaign attacked what the agency perceived as China’s “growing influence” in the country by targeting the Chinese-made Sinovac COVID-19 vaccine through the use of phony online accounts spreading “anti-vax” messaging.

Michael Rectenwald, Ph.D., author of “The Great Reset and the Struggle for Liberty: Unraveling the Global Agenda,” said the Project Artichoke revelations “make it clear that the CIA has posed an enormous threat to U.S. citizens, in addition to the horrors it unleashes on non-U.S. target governments and populations.”

Project Artichoke wanted to enlist help from Army’s Chemical Warfare Service

The 1952 Project Artichoke document also included a recommendation to involve the U.S. Army Chemical Warfare Service in the project’s efforts, citing its experience with “exhaustive studies along these lines.”

This proposal bears a resemblance to recent suggestions that COVID-19 — and the response to the pandemic — were coordinated at high levels of government, military and intelligence agencies.

Last year, former pharmaceutical research and development executive Sasha Latypova and retired science writer Debbie Lerman released the “Covid Dossier,” presenting evidence of the “military/intelligence coordination of the Covid biodefense response in the US, UK, Australia, Canada, the Netherlands, Germany, and Italy.”

According to Latypova and Lerman, “Covid was not a public health event” but “a global operation, coordinated through public-private intelligence and military alliances and invoking laws designed for CBRN (chemical, biological, radiological, nuclear) weapons attacks.”

Leake said “it is far from clear” that the Church Committee hearings of 1975 “put a complete end to CIA covert programs.” He cited the possible laboratory development of the SARS-CoV-2 virus as an example.

“The laboratory creation of SARS-CoV-2 with gain-of-function techniques developed at the University of North Carolina-Chapel Hill, and the U.S. military’s involvement in developing and distributing of mRNA COVID-19 vaccines, should … be regarded as possible outgrowths or even continuations of Project Artichoke,” Leake said.

Experts question similarities between Project Artichoke, COVID vaccines

In a Substack post today, epidemiologist Nicolas Hulscher drew a potential connection between Project Artichoke and the development of COVID-19 vaccines. Hulscher cited recent peer-reviewed studies that identified the vaccines’ adverse impact on neurological health and “surging rates of cognitive decline.”

Hulscher wrote:

“Disturbingly, since 2021, over 70% of humanity received a neurotoxic agent masquerading as a ‘vaccine.’ The same goals outlined in the CIA document (vaccines/drugs capable of covertly inducing anxiety, depression, and lethargy) are now being observed in COVID-19 vaccinated populations. …

“… If the CIA was secretly discussing covert methods to alter human behavior in the 1950s, it would be no surprise if similar classified projects emerged in the decades that followed.”

A 2024 paper published in the journal Molecular Psychiatry investigated psychiatric adverse events among over 2 million people in South Korea. The study found that “COVID-19 vaccination increased the risks of depression, anxiety, dissociative, stress-related, and somatoform disorders, and sleep disorders while reducing the risk of schizophrenia and bipolar disorder.”

A 2025 study published in the International Journal of Innovative Research in Medical Science found “alarming safety signals regarding neuropsychiatric conditions following COVID-19 vaccination, compared to the influenza vaccinations and to all other vaccinations combined.”

This included increases in schizophrenia, depression, cognitive decline, delusions, violent behavior, suicidal thoughts and homicidal ideation.

“The fact that mRNA vaccines were designed to cross the blood-brain barrier and inflame the brain — or at least, they were known to do so, during their manufacture and distribution — should give us pause in light of this news,” Wolf said.

Wolf said the latest revelations, “while shocking, provide all the more reason for us to be critical of opaque, coercive or untested vaccination programs, additives in food and water, and toxic or opaque geoengineering programs.”

Tapper said the revelations reinforce “the urgent need to protect individual liberty, medical freedom, and ethical boundaries in science and public health.”

“The lesson here is simple: vigilance is necessary when governments claim authority over the human body and mind,” Tapper 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.

February 24, 2026 Posted by | Civil Liberties, Deception, Full Spectrum Dominance | , , , , , , , , , , , | Comments Off on Project Artichoke: 70 Years Ago, CIA Discussed Hiding Mind-Control Drugs in Vaccines

Israeli FOIA Data Reveals Massive Heart Injury Spike in Children Immediately After mRNA Shot Rollout

By Nicolas Hulscher, MPH | Focal Points | February 20, 2026

For years, the public was told that COVID-19 mRNA injection–induced cardiac injury in children was rare. That reassurance formed the backbone of adolescent vaccination campaigns across the world. But what if the underlying safety data were never fully processed or disclosed?

What if hundreds of adverse event reports submitted by frontline clinicians were simply left unanalyzed during the very period when policymakers were declaring the injections safe for teens?

According to Israel’s State Comptroller, approximately 279,300 adverse event reports submitted during the vaccination campaign by Clalit Health Services — Israel’s largest health provider — were never processed by the Ministry of Health.

These reports were not publicly examined during mid-2021, when vaccine eligibility was expanded to adolescents. They were not incorporated into real-time risk–benefit assessments. They were not disclosed to parents deciding whether to vaccinate their children.

Only years later, following repeated Freedom of Information Act (FOIA) requests, the raw dataset — containing 294,877 adverse event reports — was released.

We analyzed that dataset using a deliberately conservative methodology. Our findings have now been peer-reviewed and published in the International Journal of Cardiovascular Research & Innovation, in a study titled, Cardiovascular safety signals in Israeli adolescents following COVID-19 Vaccination: Evidence from an unprocessed FOIA datasetauthored by Yaakov Ophir, Yaffa Shir-Raz, David Shuldman, Nicolas Hulscher (myself), and Peter A. McCullough.

The results reveal a concentrated surge of cardiovascular injury among teenagers that occurred immediately after vaccine authorization was expanded to ages 12–16.

Using strict de-duplication criteria to avoid overcounting, we identified 277 unique cardiovascular injury cases among individuals under 18 years old in 2021. Of those, 98% occurred in teens aged 12–16. Nearly every one of these cases was reported within a narrow six-week window between June 28 and August 8, 2021.

The timing is critical. On June 21, 2021, Israel’s Ministry of Health expanded mRNA vaccine eligibility to adolescents under 16. Within days, cardiovascular injury reports began to pile up. The clustering is unmistakable.

The types of events recorded were not trivial. Within the COVID-specific follow-up category, 646 reports were coded as “Acute Cardiovascular Injury.” Notably, the original Hebrew term used in the reporting system translates literally to “Acute Myocardial Infarction.” That is the scientific name for a heart attack. Additional reports included myocarditis, pericarditis, stroke, and thromboembolic events.

To contextualize the scale, we applied conservative population assumptions. Clalit covers approximately 51.6% of Israel’s population. Based on national vaccination dashboard data, about 63.5% of adolescents aged 12–15 received at least one dose during the study period. This yields an estimated vaccinated adolescent population of approximately 254,347 individuals within the dataset’s coverage.

Even under highly conservative assumptions — assuming all vaccinated adolescents received their doses within the same six-week window and that reporting capture was complete — the observed clustering corresponds to a minimum estimated risk of roughly 1 cardiovascular event per 939 vaccinated adolescents.

That figure stands in stark contrast to known background rates of acute myocardial infarction in adolescents, which are measured in single digits per million person-years in U.S. data. Even without annualizing the rate, the difference is substantial.

Equally important is how these findings diverge from the narrative that dominated the early literature. In 2021, published studies largely characterized vaccine-associated myocarditis as a rare complication, predominantly affecting adolescent males, typically after the second dose, and occurring within a narrow post-vaccination window of several days.

The FOIA dataset tells a different story. In our analysis, cardiovascular events were nearly evenly distributed between girls (145 cases) and boys (132 cases). Events occurred after the first dose, within 21 days of the second dose, and more than 21 days following the second dose. The risk pattern appears broader, more heterogeneous, and less confined than initially portrayed.

Following identification of this clustering, we contacted Clalit Health Services to verify whether the number of adolescents reported with “acute myocardial infarction” differed from our findings or whether reporting errors had been identified.

The response we received was stark: “The data do not exist.”

Yet the reports clearly existed. They were submitted by healthcare professionals, entered into the national reporting system, and archived — but not processed during the critical period when adolescent vaccination policy was being determined.

In conclusion, the newly disclosed FOIA data from Israel — now published in peer-reviewed form — document a major cardiovascular injury surge in teenagers that was neither processed nor publicly communicated at the time it occurred.

SUMMARY:

  • In Israel, approximately 279,300 adverse event reports were never processed during the COVID-19 vaccine rollout.
  • Newly released Israeli FOIA data revealed 277 unique cardiovascular injury cases in minors using conservative de-duplication methods.
  • 98% of cases occurred in Israeli adolescents aged 12–16 within a narrow six-week window following eligibility expansion in June 2021.
  • Hundreds of entries were coded in Israel’s national reporting system as “Acute Cardiovascular Injury,” a category that in the original Hebrew terminology corresponds to acute myocardial infarction. When we contacted Clalit Health Services to clarify these adolescent entries, we were told that “the data do not exist.”
  • Cardiovascular events in Israeli teens were distributed across both sexes and across doses — not limited to the narrow “rare male, second-dose” profile emphasized in the literature and by public health agencies.
  • The reports existed within Israel’s national surveillance system — but were not processed or publicly analyzed during the critical 2021 policy window.

Nicolas Hulscher, MPH

Epidemiologist and Foundation Administrator, McCullough Foundation

Support our mission: mcculloughfnd.org

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

February 22, 2026 Posted by | Deception | , | Comments Off on Israeli FOIA Data Reveals Massive Heart Injury Spike in Children Immediately After mRNA Shot Rollout

REDFIELD REWRITES THE RECORD

The HighWire with Del Bigtree | January 29, 2026

Former CDC Director Robert Redfield’s recent, startling admissions about the COVID-19 mRNA vaccines raise a critical question: how different might the COVID era have been if the public had been told early on that these shots were never designed to stop transmission and were not appropriate for children?

February 1, 2026 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, Video | , | Leave a comment

UK Health Officials Covered Up Reports of Heart Damage Linked to AstraZeneca Vaccine

By Michael Nevradakis, Ph.D. | The Defender | January 29, 2026

Newly released U.K. public health data show that in 2021 and 2022, thousands of people filed cardiac-related adverse event reports after receiving the AstraZeneca COVID-19 vaccine.

The data confirm the findings of a study by Children’s Health Defense (CHD) researchers. The study was published on Preprints.org.

GB News last week reported on the data, obtained from the U.K.’s Medicines and Healthcare products Regulatory Agency (MHRA). The data showed that in 2021 alone, the MHRA received 48,472 reports of cardiac-related adverse events linked to the AstraZeneca vaccine.

Of these, 23,914 cardiovascular events had already been reported by late March 2021 — which means the reports were filed within the first three months after the COVID-19 vaccines were rolled out to the public.

A total of 6,175 reports of blood-clotting events were reported during the same period, according to MHRA data.

The adverse event reports were being filed even as U.K. public health authorities told the public that the AstraZeneca vaccine — a non-mRNA vaccine developed in conjunction with Oxford University and licensed under the name Vaxzevria — was safe and effective.

Oxford researchers, Drs. Tom Jefferson and Carl Heneghan obtained the data through a freedom of information request submitted to the MHRA in October 2025. The request sought information on cardiovascular and thromboembolic (blood-clotting) events connected to the AstraZeneca shot between February 2021 and January 2024.

MHRA responded to the request a month later, providing the researchers with data, which Jefferson and Heneghan analyzed and published in a series of Substack posts.

“To the best of our knowledge, this is the first time anyone (outside the powerful) has seen the reports submitted to the MHRA regarding serious potential harms during the first period of the rollout,” the researchers wrote in a Substack post.

CHD Senior Research Scientist Karl Jablonowski said the MHRA “used non-public data from one of the best medical record systems in the world” to craft “a narrative opposite to what the data reflect.”

“Instead of showing the cardiovascular catastrophe that unfolded in those injected with the Oxford-AstraZeneca COVID-19 vaccine, health officials instead wrote that the results of their analysis offer ‘reassurance regarding the cardiovascular safety of COVID-19 vaccines.’ … The word ‘fraud’ may actually be too kind,” Jablonowski said.

Informed consent ‘compromised’

The MHRA contained discrepancies. According to GB News, MHRA dismissed its own figures after the researchers published them on Substack. Instead, they said the number of heart conditions linked to the AstraZeneca shot during the period in question was 13,010 — nearly four times lower than the original figure.

An MHRA spokesperson told GB News that the agency is “currently reviewing previously released figures in more detail to identify any potential discrepancies.”

In its analysis of the MHRA data, TrialSite News suggested that such significant data discrepancies call the MHRA’s credibility into question.

“While adverse-event reporting systems are designed to detect signals rather than prove causation, large unexplained gaps weaken confidence in risk communication,” TrialSite News wrote.

The researchers also asked the MHRA to provide data on the number of AstraZeneca shots administered in the U.K. The UK Health Security Agency initially refused, explaining that the information was “commercially sensitive” and that releasing it “would not be in the public interest.”

The agency later released the data after the researchers appealed. According to the researchers, the data showed a strong correlation between doses administered and adverse events reported. However, even after the AstraZeneca vaccine was withdrawn, adverse event reports were still being filed, suggesting “a long-term dose effect.”

TrialSite News founder and CEO Daniel O’Connor told The Defender that “the MHRA disclosures highlight a core failure of pandemic-era regulation: safety signals were managed rather than transparently communicated.”

“The issue is not only the adverse events themselves, but why their full scale emerged only through freedom of information requests,” O’Connor said. “When critical risk information reaches the public years late, informed consent is compromised and trust in the regulatory system is inevitably eroded.”

CHD study found evidence linking AstraZeneca shot to heart conditions

The data in the MHRA documents support the findings of a preprint study published by CHD and Brownstone Institute scientists last year.

The researchers reanalyzed data used in earlier studies that concluded the COVID-19 vaccines were safe. By comparing relative risks from different vaccines — which the original studies failed to do — the new research revealed evidence linking the Pfizer and AstraZeneca COVID-19 vaccines to significant health dangers.

The study also found that the risks for cardiovascular disease and death from the AstraZeneca vaccine were significantly higher than those of the Pfizer vaccine.

The preprint, which is undergoing review, also suggested that some earlier COVID-19 vaccine safety studies were “biased by design.”

Brian Hooker, Ph.D., CHD chief scientific officer, drew parallels with similar findings that he and Jablonowski discovered about safety signals connected to the Pfizer-BioNTech COVID-19 vaccine and a subsequent cover-up of those signals by U.S. public health agencies.

Hooker said:

“The Pfizer vaccine was released on Dec. 11, 2020, and by January 2021, there were 23 reports of military service personnel with diagnoses of myocarditis following receiving the shot. At this point, less than 5% of U.S. adults had received the jab.

“The evidence regarding the Pfizer shot and myocarditis very quickly unfolded in front of these agencies, but no warning was given until May 27, 2021, when the CDC [Centers for Disease Control and Prevention] trotted out a website that indicated there might be an issue with myocarditis and pericarditis due to VAERS reports. At that point, over 50% of those eligible in the U.S. had received the jab.

“The point was clear: lie and hide until we can get lots of shots in arms.”

UK continued to recommend AstraZeneca shot despite safety signals

According to GB News, at the same time that the MHRA data were showing evidence of cardiac conditions and blood clots linked to the AstraZeneca vaccine, “internal discussions were taking place” about how to manage public messaging about the shot’s safety.

GB News cited minutes from a U.K. government task force on COVID-19 vaccine risks. The minutes, published in 2024, showed that concerns about the link between the AstraZeneca shot and blood clots were discussed as early as April 2021, and that safety issues were known by March 2021.

Throughout 2021, stories about people who died of blood clots after getting the AstraZeneca shot began appearing in the media.

Yet, the task force minutes recorded discussions of “concerns that public alarm over the vaccine could make it harder to vaccinate the population by increasing ‘vaccine hesitancy,’” GB News reported.

During this period, the mainstream press in the U.K. continued to promote the AstraZeneca shot as safe and effective. A March 2021 report by The Guardian claimed, “There’s no proof the Oxford vaccine causes blood clots.”

In April 2021, the U.K.’s Joint Committee on Vaccination and Immunisation advised that adults under 30 should be offered an alternative COVID-19 vaccine. The European Medicines Agency issued similar guidance that month.

Yet, by March 2021, several European countries had withdrawn the AstraZeneca shot, citing the risk of blood clots. Research published that month also found a link between the shot and blood clots.

The AstraZeneca shot was never authorized or licensed in the U.S., but clinical trials for the vaccine were conducted in the U.S. with American participants. TrialSite News cited the case of Brianne Dressen, “who developed severe, long-term neurological symptoms after participating in the U.S. trial.”

AstraZeneca contractually agreed to provide medical care to trial participants for research-related injuries. However, in an ongoing federal lawsuit, Dressen alleges that the company reneged on that promise. AstraZeneca argued it is immune from legal prosecution.

In 2021, Dressen founded React19, an advocacy group for the vaccine-injured.

“These events underscore that even vaccines halted before approval can produce lasting human consequences — and unresolved accountability questions,” TrialSite News wrote.

‘A move to quiet the public, to pacify would-be critics’

AstraZeneca withdrew its COVID-19 vaccine from the market in 2024, citing “commercial reasons.” However, the company admitted in 2024 U.K. court documents that its shot could, in “very rare cases,” cause blood clots.

“This admission is now central to a growing class action lawsuit brought by individuals who say they suffered life-changing injuries,” GB News reported.

“The timing of events is interesting. AstraZeneca requested the withdrawal of the vaccine from EU markets in March 2024. It was effective May 2024. The study decrying its ‘cardiovascular safety’ was published in July 2024,” Jablonowski said.

According to Jablonowski, this suggests that these actions were “not for the betterment of public health nor vaccine uptake, since the vaccine was no longer available,” but were instead “a move to quiet the public, to pacify would-be critics.”

GB News reported that a U.K. parliamentary inquiry into the MHRA’s handling of vaccine safety issues is “very likely” to occur.

“These agencies, both in the U.S. and the U.K., need to be held to account for their felonious lies and those individuals who were harmed need to be compensated,” Hooker 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.

January 30, 2026 Posted by | Deception, War Crimes | , | Leave a comment

The UK Covid Inquiry: Propaganda to protect the ‘pandemic’ narrative

By Gary L. Sidley | Propaganda In Focus | January 9, 2026

On the 20th of November, 2025, the UK Covid Inquiry published a report on Module 2 of its ongoing review titled, ‘Core decision-making and political governance’. Despite, to date, spending around £192 million of taxpayers’ money on an in-depth investigation into the management of the 2020 ‘pandemic’, this 800-page tome indicates that the overarching conclusion of the Inquiry will most likely be that the unprecedented and net harmful government responses (lockdowns, mask mandates, vaccine coercion) were all necessary, and the only problems related to the timings of the interventions and process failures. As such, this Module 2 report can be reasonably construed as a propaganda exercise primarily intent on preserving the core elements of the dominant, fundamentally flawed, covid narrative.

In the words of the oft-quoted Edward Bernays, propaganda involves ‘the conscious and intelligent manipulation of the organized habits and opinions of the masses’. It is clear that this Module 2 report, and the UK Covid Inquiry as a whole, strive to do just that. With the primary goal of protecting the ‘pandemic’ story – that in early 2020, a uniquely lethal pathogen spread carnage across the world, and unprecedented and draconian restrictions on our day-to-day lives were essential to prevent Armageddon – the inquiry has incorporated a range of manipulation techniques designed to promulgate this state-sanctioned ideology. The two most prominent opinion-shaping strategies deployed by the Inquiry have been the suppression of dissenting perspectives, and a narrowing of the Overton window.

Suppression of dissenting perspectives

In her initial selection of ‘core participants’ for the Inquiry, Chairperson Baroness Hallett signalled her intention to marginalise voices that were likely to be critical of the official covid narrative. Those granted core status benefitted from the opportunity to make opening and closing statements, and to suggest lines of questioning to the witnesses, whereas those groups excluded were limited to submitting written evidence in the hope that it would be considered by the Inquiry team. Organisations who had been openly opposed to the mainstream public health responses during the covid event – for example, Us For Them (who repeatedly highlighted the devastating impact of the restrictions on our nation’s children) and the Health Advisory & Recovery Team (a group of scientists and clinicians concerned about ‘pandemic’ policy and guidance recommendations) – were unsuccessful in their applications.

Consideration of those groups who were permitted to be core participants for Module 2 clearly shows a preponderance of stakeholders who were highly likely to be on board with the central tenets of the official covid narrative. In addition to the expected establishment figures (representatives from various government departments, the Office of the Chief Medical Officer, the UK Health Security Agency) and four ‘Covid-19 Bereaved Families for Justice’ groups, it is difficult not to conclude that other core participants were selected on account of their fervour for more and earlier restrictions. For instance, despite ‘long covid’ being a highly contested concept, three groups representing the victims of this assumed malady were awarded core status. Similarly, the British Medical Association (who energetically campaigned for longer lockdowns and stricter mask mandates) also managed to secure a place in Baroness Hallett’s inner circle.

Despite this crude censorship, a significant amount of critical commentary did reach the Inquiry, in the form of both live testimony and written statements. Crucially, however, these counter narratives were de-emphasised by the Inquiry team and – subsequently – were not reflected in its conclusions. One blatant example of a dissenting voice being prematurely curtailed was the interview with Carl Heneghan, Professor of Evidence-Based Medicine and longstanding critic of the dominant covid narrative. When Heneghan asserted that expert interpretation of published research constitutes valid evidence for the Inquiry, Hallett retorted, ‘Not in my world it doesn’t … if there is anything further, please submit it in writing’. This abruptness contrasts sharply with the deferent, sometimes sycophantic, way establishment witnesses were managed by the Inquiry team.

Narrowing the Overton window

It was apparent from the start of the UK Covid Inquiry that Baroness Hallett and her legal team had decided which public health decisions made during the covid event were open to critical scrutiny and which were not. This contraction of the Overton window ensured that crucial elements of the official narrative were shielded from critical analysis.

To illustrate, three pre-determined assumptions – foundational to the official covid story – seemed to fall into this protected category:

1. Lockdowns were necessary

The headline-grabbing conclusion in the Module 2 report was that locking down a week earlier would have saved 23,000 lives. This absurd deduction was not based on robust science or real-world studies, but drawn from the fantasy realm of mathematical modelling. An in-depth analysis of covid-era decision making (which is what the Inquiry was supposed to be) would have given prominence to a detailed cost-benefits evaluation of lockdowns, a process that would have revealed the substantial harms of this unparalleled pandemic restriction. The key reason for the omission of this vital analysis was the Inquiry’s premature assumption that lockdowns were an effective public health tool, essential for the containment of a – purportedly – novel virus.

More specifically, Baroness Hallett and her team adopted a classic propaganda strategy, commonly referred to as ‘unanimity’. With the presumption that all right-thinking people recognise that lockdowns save lives, the Overton window was squeezed to become merely a question of timing; any testimony straying outside of this range of acceptability was ignored – or, at best, reduced to background noise – while, in contrast, speculations about the life-saving benefits of an earlier societal shutdown were amplified.

2. The mass vaccination programme was a great success

Despite increasing recognition that the covid vaccines were less efficacious, and more harmful, than initially claimed, the Inquiry appears to have adopted the foundational assumption that these novel products were safe and effective, and anyone who believed otherwise must constitute a deviant minority at odds with the unanimous opinion of right-thinking people. Indications for the constant presence of this guiding notion are brazen. Thus, Hugo Keith KC (the lead counsel to the Inquiry) has, at various points during his interactions with witnesses, described the vaccines as ‘entirely effective… undoubted successes… with lifesaving benefits that vastly outweighed the very rare risk of serious side effects’. Similarly, Baroness Hallett – at the press conference announcing the findings of Module 2 – hailed the vaccine programme as a ‘remarkable achievement’.

3. Community masking was not associated with any appreciable negative consequences

It was evident at an early stage in the Inquiry that another untouchable premise was that the masking of healthy people in community settings was a sensible precaution that could only have net benefits. Thus, when Professor Peter Horby, the chair of NERVTAG (a high-profile SAGE advisory group), gave evidence in October 2023 he reiterated his group’s 2020 conclusion that the evidence for mask effectiveness in reducing viral transmission was ‘weak’; Lady Hallett interjected, saying, ‘I’m sorry, I’m not following … if there’s a possible benefit, what’s the downside? Horby responded to this challenge by suggesting that respect for institutional science was at stake – in keeping with the majority of the establishment scientists, he failed to highlight the considerable harms associated with routine masking.

The Inquiry’s pre-formed assumption that compelling people to wear face coverings was a public health intervention free of negative consequences was confirmed by the Module 2 report with its emphatic conclusions that:

‘The experience of the Covid-19 pandemic has shown that wearing a face covering has minimal disadvantage for the majority of the population.’

‘In any future pandemic where airborne transmission is a risk, the UK government and devolved administrations should give real consideration to mandating face coverings for the public in closed settings.’ (p. 288)

In conclusion, the overarching take-home message from the Inquiry to date is that public health strategy adopted by the government in response to the emergence of a novel virus in 2020 was essentially the correct one, and any criticism of the official covid narrative should be confined to process issues, such as the timing of restrictions. Devoid of any forensic analysis of their costs and benefits, Lady Hallett and her team have concluded that lockdowns, mRNA vaccines, and mask mandates all achieved positive outcomes and should therefore be repeated when we encounter the next ‘pandemic’. By amplifying voices supportive of the official covid narrative, while marginalising critical viewpoints, the Inquiry has succeeded in strengthening its – apparently pre-determined – perspective that, irrespective of any harms caused, the restrict-and-jab approach was, ultimately, for the greater good.

Most commentators who have been sceptical of the official covid narrative will not be surprised by the Inquiry’s conclusions. Given that the political elites, along with prominent public health mandarins, enthusiastically endorsed the calamitous restrictions and vaccine rollout (and continue to do so) the damage to the establishment of drawing different, more condemnatory, inferences would have been immense. From the perspective of our global leaders, the Inquiry to date is – no doubt – serving its primary purpose of concealing the true ramifications of the covid response from the general population.


Gary Sidley, PhD, is a former NHS consultant clinical psychologist with over 30-years’ experience of clinical, professional and managerial practice in adult mental health. In 2000, he obtained his PhD for a thesis exploring the psychological predictors of suicidal behaviour and has multiple mental health publications to his name, including academic papers, book chapters, and his own book, ‘Tales from the Madhouse: An insider critique of psychiatric services). Since the start of the covid event, he has written many articles critiquing the government’s nudge-infused messaging and mask mandates, including pieces for the Spectator, the Critic and Self & Society. More of his articles can be found on his ‘Manipulation of the Masses’ Substack.

January 30, 2026 Posted by | Deception, Science and Pseudo-Science | , , | Leave a comment