Ignored for years, Canada’s vaccine-injured finally get their day in Parliament

The idea of two solitudes in Canada is typically understood as the great divide between Anglophones and Francophones who cannot see eye-to-eye due to cultural and linguistic differences, the latter preventing any meaningful communication to bridge the gap.

But in the post-COVID era, “two solitudes” could just as easily describe the chasm between lawmakers, legacy media and its subscribers who remain uninterested in the suffering that COVID vaccines caused, and the camp of vaccine-injured, their advocates and members of the public who saw through the “safe and effective” lies, understand the damage caused and now want accountability.

While any accountability for the human toll that experimental COVID vaccines wrought has been non-existent in Canada, on Tuesday, Conservative MP Dean Allison’s COVID vaccine injury hearings – dubbed The Allison Inquiry – began on Parliament Hill in Ottawa. Whether it will bring Canada’s two COVID solitudes any closer together remains to be seen.

Legacy media journalists were absent, as were any MPs from the governing Liberal Party, which bears ultimate responsibility for these injuries. Of the four Conservative MPs who attended, Mike Dawson (Miramichi–Grand Lake, NB) told the Inquiry he believed his daughter-in-law’s baby died in the womb following a COVID vaccination in the second trimester, and Essex MP Chris Lewis (Ontario) said he believed his mother suffered from turbo esophageal cancer after taking the COVID shot.

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U.S. Supreme Court Rejects New York Healthcare Workers’ Bid to Revive COVID Vaccine Mandate Lawsuit

The U.S. Supreme Court today declined for a second time to take up a case brought by New York healthcare workers who lost their jobs after the state denied their requests for religious accommodations from its COVID-19 vaccine mandate, SCOTUSblog reported.

The justices rejected a petition asking them to reconsider their June decision not to hear Does 1-2 v. Hochul, the lawsuit healthcare workers brought against the state. The court denied the request without asking New York Gov. Kathy Hochul to respond.

“This ruling is definitely a sad day for the workers who stood up and said no,” said Michael Kane, Children’s Health Defense (CHD) director of advocacy and member of New York’s Teachers for Choice, which also challenged New York’s vaccine mandate in the courts.

Kane said he was “not surprised” by the decision.

The plaintiffs represented a handful of healthcare workers, he said. “But over 30,000 were fired in New York state because of this horrendous policy from Gov. Hochul. The policy didn’t allow for any religious exemption from vaccination. On its face, it is illegal. It is unconstitutional, but the politics of the thing seems to be playing out instead.”

The workers filed their lawsuit in 2021, challenging a now-repealed New York state law mandating that workers in some healthcare-related positions get the COVID-19 vaccine.

In 2022, a federal court dismissed the lawsuit, and in 2024, the 2nd U.S. Circuit Court of Appeals upheld the dismissal. In 2025, the workers appealed to the U.S. Supreme Court.

In an unusual move, the Supreme Court asked the U.S. Department of Justice solicitor general to weigh in. In May 2026, Solicitor General D. John Sauer wrote an amicus brief recommending the court deny the appeal.

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Italian Police in Schools: Hunt for Lists of Unvaccinated Kids

Starting on the first day of school, carabinieri will enter preschools and elementary schools in northern Palermo to identify pupils who are not up to date with mandatory vaccinations. Officers will obtain enrollment lists and, together with the schools and the ASP (Azienda Sanitaria Provinciale, or Provincial Health Authority), verify the children’s health status. The intervention, described as “extremely urgent,” was ordered by the minors’ prosecutor Claudia Caramanna following the death of Anna Rosa Bartolotta, the four-year-old unvaccinated child who was given a diagnosis of diphtheria. Before all aspects of the case have been clarified, the tragedy has become the pretext for launching an emergency operation.

The operation will begin on September 15, the date set by the Sicilian Region for the start of classes. Enrolled students are registered on the ministerial Sidi portal; schools transmit the lists to the ASP, and the health authority cross-checks them against the vaccination registry, returning the names of those not in compliance. Attention will initially focus on northern Palermo, but the ASP holds data for the entire metropolitan area. Also under scrutiny by the prosecutor’s office is a system used by some families to delay compliance: submitting an appointment booking, not having the child vaccinated, and then repeating the procedure later. “It may work at preschool, but in first grade the checks are strict,” explained Giusto Catania, principal of the Giuliana Saladino comprehensive institute. The Lorenzin law stipulates that compliance with vaccination requirements is a condition for access to nurseries and preschools; from age six onward, the pupil may attend classes, while parents face administrative fines ranging from €100 to €500 (approximately $110 to $550). If forms of “serious negligence” are established, such as failure to undergo pediatric check-ups, the consequences could extend as far as loss of parental custody. The checks, therefore, will not concern only the regularity of vaccination certificates but will also serve to identify possible situations of “health abandonment.”

The climate that developed during the pandemic thus seems to be reemerging, this time in school classrooms, through procedures that also find full support from part of the press. La Repubblica, for example, presents the initiative using a formula that closely echoes the language of the Covid emergency: “A virtuous machine has been set in motion to counter no-vax conspiracy theories in the protection of public health.” Giovanna Perricone, the regional ombudsman for children and adolescents, speaks of a “comprehensive and strategic operation”: from the checks, she explains, may follow reports on parents, fines, and the taking into care of families. Since “we cannot close social media,” she adds, it would also be necessary to counter their influence by disseminating messages on vaccines in a widespread manner, even through videos projected in supermarkets. The goal, in short, goes beyond verifying compliance with the law: it is about policing public space, re-educating parents so as to crack “conspiracy ideas.”

The Palermo case thus reproduces the polarization mechanism already tested during the pandemic. Diverse situations are folded into the undifferentiated category of “no-vax conspiracy theories.” Beyond the specific incident, the label allows attention to shift from the merits of individual cases to the alleged irresponsibility of families and to present as necessary an operation involving schools, the ASP, the prosecutor’s office, and law enforcement. Anna Rosa’s death has become the starting point for blanket checks and a cultural campaign extended even to supermarkets. The entry of carabinieri into schools is thus normalized as a tool of health protection, while the invocation of “conspiracy theories” once again serves to preemptively neutralize doubts and possible objections regarding the proportionality of the measures adopted.

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FDA’s Botched Review of Moderna’s Flu mRNA Vaccine

When the FDA licensed Moderna’s new mRNA flu vaccine last week, legacy media coverage focused almost exclusively on efficacy.

The pivotal trial reported that the vaccine was “26.6% more effective” than a conventional flu vaccine at preventing protocol-defined influenza-like illness.

What received far less scrutiny was a much more serious problem in the trial data published in The New England Journal of Medicine—much of it relegated to an appendix behind a paywall.

An analysis of that appendix alongside the FDA’s own briefing document exposes clear regulatory malfeasance.

A statistically significant safety signal from the pivotal trial was systematically diluted until it disappeared from the official story.

The Safety Signal

Moderna’s pivotal Phase 3 trial (P304) enrolled roughly 40,000 adults aged 50 and older, randomised 1:1 to either the company’s mRNA-1010 vaccine or a traditional trivalent flu vaccine.

This study evaluated an “optimised” version of Moderna’s vaccine after earlier versions produced disappointing efficacy results.

Even with this updated formulation, the headline “26.6% relative efficacy” figure was misleading. In absolute terms, the vaccine reduced the risk of illness by just 0.8%.

Most concerning, however, were the serious adverse event (SAE) data.

The six-month data show that 449 participants in the mRNA group experienced at least one SAE, compared with 389 in the conventional group—an excess of 60 people.

So, while the pivotal trial showed there were 4 fewer influenza hospitalisations in the mRNA group, 60 additional people experienced an SAE.

SAEs are not mild events—they are usually severe enough to require hospitalisation, threaten life, cause significant disability, or result in death.

The imbalance of SAEs in Moderna’s pivotal trial was statistically significant—meaning it was unlikely to be a random fluke.

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The Politics Of Measles

By the middle point of 20th-century American history, measles was widely considered a rite of passage for kids. You get it and you shake it off. You earn lifetime immunity. This was true of every generation just before mine.

For the previous century, measles had become ever less dangerous with sanitation and nutrition. By the time the vaccine came along, it was fully controlled and only very rarely led to hospitalization. The protocols were taught in every school and understood by all classes.

I was apparently part of the first generation to receive the inoculation. It was convenient, but not necessary simply because society had systems and traditions in place to manage it well. How much difference did the shot make in driving infection to zero? Some, surely, and this added to the prestige of vaccines.

That said, I did get chicken pox as a natural infection and recall well what it was like. That no longer happens except in a few communities. I was the last to experience this and I’m happy to share the experience.

My parents came to me excitedly and said we were going to a party. I found myself among a group of kids I did not know and we played and played for hours. Then we left. That was fun, I thought, but a bit confusing. The next day, I woke up with itchy red spots.

My parents cheered. Their plan had worked. I recalled feeling great confusion. Why were my parents celebrating my sickness? It seemed very odd. They had their reasons. They knew the science.

They explained to me how the immune system works and why it is best that I get this when I’m young rather than old. My immunity would be durable and be boosted later in life as my own kids caught the normal childhood infections, which in turn would protect me from the related infection of shingles.

There is this tendency now to treat these strategies as paleolithic as compared with syringes and fluids in the childhood vaccination schedule. Actually, we should look back on these days as the height of serious science. My parents knew exactly what they were doing and it taught me a valuable lesson as a kid. I learned about the high complexity of the immune system that needs exposure as training.

Eventually, of course, the chicken pox vaccine came along and many others as well, resulting in a vast mixture of combined shot after shot. Industry profited. Human health suffered. The Trump administration is trying to fix the problem. Industry doesn’t like that. It is calling in favors from politicians to stop the return to science.

This takes us to the wild drama now playing itself out in Pennsylvania. In April of this year, the media and the governor’s office started going on about a measles outbreak. It was centered in Lancaster and Lebanon counties – both with sizable Amish and Mennonite populations.

The framing here matters. The Amish and Mennonite communities routinely expose children, just as my parents did. It is not an “outbreak” but an application of sophisticated science.

The health of this community ranks among the highest. The most common health issues affecting children in the United States are nearly absent among the Amish, including autism, obesity, diabetes, ADHD, and so on.

Nonetheless, Pennsylvania set up 91 pop-up clinics around the infected community and jabbed kids with more than 4,000 doses using the MMR shot that many people connect to the rise of autism. Forty more clinics are planned.

In science, you have the control group and the tested group. The Amish are the control and keep revealing that there might be a better way. Eliminate the control and you eliminate the embarrassment. This is precisely what both Pfizer and Moderna did after their own tests of the COVID shot: they pushed it on the saline group following first results.

In Pennsylvania, opposition arose to this push for industrial inoculation, and understandably so. In the post-COVID era, trust in public health is depleted to near zero.

Here is where the current drama picked up. On Aug. 14, a newborn child died in Strasburg Township, Lancaster County. The cause of death was later given by the county coroner: lacerated/ruptured spleen, massive blood loss. The postmortem used the PCR test (which detects presence, not infection) and found measles in utero. Obviously, this baby could not otherwise have been vaccinated. It is pointless to call a baby unvaccinated for measles, just as it is ridiculous to observe the infant is illiterate.

A week later, the Pennsylvania Department of Health announced two “measles-associated” deaths in Lancaster County: unvaccinated residents, they said. They claimed these were the first measles-related deaths in Pennsylvania in 35 years. There were no other details given: nothing about the cause of death, nothing about ages, nothing about anything.

Governor Josh Shapiro announced two deaths caused by measles. Not merely associated or related, but caused. The media ran with the story, using the language of causation. He called the deaths preventable and tied them to lack of immunization. He highlighted his clinic campaign and told reporters that Secretary Kennedy had called to offer help with the outbreak to which he responded:

“I was very, very blunt with him, and I made very clear that his actions and the rhetoric that’s coming from this administration are having a negative impact on communities across America, particularly right here in Pennsylvania.”

It was at this point that the narrative fell apart. The CDC called. The governor’s office could give no more information. The Lancaster County Commissioner Josh Parsons spoke out and said that the coroner’s office has zero deaths with measles listed as immediate cause; one person died with measles, not from it.

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Where Is the Outrage? Profound Autism Didn’t Used to Exist — Now It’s Everywhere

If I had walked into my fourth-grade classroom in 1978 and told my teacher that one day virtually every school district in America would have multiple classrooms dedicated to children who could not speak, who required one-on-one aides, who wandered, who self-injured, who had seizures, who would require lifelong care, she would have assumed I was describing some dystopian science fiction novel. Yet here we are. Why are we just accepting it?

Country artist Tyler Hudson came bombing through the U.S. last week (he’s a Texan living in Australia), and one of his Instagram posts about autism did something that really doesn’t happen to me anymore after 22 years as an autism dad: it choked me up.

His post was a read-aloud excerpt from his new book, “The Missing Lyrics,” that discussed a poem written by his NT (neurotypical) daughter about his teenage son with profound autism, whose name is Lyric.

I was fine until these words:

“He’s never been to a party, never walked into a friend’s house … if I could cure him I would. Acceptance looks really nice on a T-Shirt until he bites himself so hard he bleeds. If I could cure him I would … It’s love that makes us fight for a cure, a life.”

I want to personally thank Tyler Hudson and his family for reigniting something in me that’s faded with time and with my focus on optimizing my son’s life: outrage.

I’m 57 years old, which means I have one advantage in this conversation that many people don’t: I remember the world before profound autism became commonplace.

That’s not nostalgia talking. It’s memory.

I went to elementary school in the 1970s. I played Little League. I rode my bike around the neighborhood until the streetlights came on. I went to church, summer camp, birthday parties, county fairs, airports, shopping malls and movie theaters.

I sat in packed gymnasiums and crowded cafeterias. I stood in line for the Scrambler at the fair behind a hundred kids I’d never met. I was surrounded by children everywhere I went, constantly, for my entire childhood.

Looking back, I can remember many of them. The kid who always picked his nose. The kid who couldn’t stop talking. The class clown, the bully, the shy girl, the future valedictorian. I even remember the girl in my sister’s grade with Down syndrome, because there was exactly one.

What I cannot remember — not a single time, not once, not anywhere — is a child who couldn’t speak. A child who wore a helmet because he smashed his head into concrete.

A child who shrieked uncontrollably for hours. Parents wrestling a teenage son twice their size to keep him from hurting himself. A mother scanning a parking lot in a panic because her nine-year-old bolted and can’t say his own name.

I’ve asked hundreds of people my age the same question, and I get the same answer every time, usually after a long pause and a puzzled look. They don’t remember it either. (Ask a former nurse or teacher over the age of 70, and you’ll get the same response, too.) If those children existed in our world, they were so extraordinarily rare that none of us ever encountered them.

Today, they are everywhere. And the most astonishing part isn’t that our world changed. It’s that we’ve stopped acting like it did.

Think about that for a minute. If I had walked into my fourth-grade classroom in 1978 and told my teacher that one day virtually every school district in America would have multiple classrooms dedicated to children who could not speak, who required one-on-one aides, who wandered, who self-injured, who had seizures, who would almost certainly require lifelong care, she would have assumed I was describing some dystopian science fiction novel.

She would have asked what happened. She would have wanted to know what we did about it. Any reasonable adult in 1978 would have.

Yet here we are. We built an entire infrastructure around this new reality — special education departments, behavioral therapy franchises, sensory gyms, respite care agencies, Medicaid waivers, sibling support groups, adult residential services, a whole professional class of people whose careers exist because of it.

We did it fast, and we did it without ever really pausing to say out loud what the construction of that infrastructure implies. You do not build all of that for a population that has always been there. And somewhere along the way we collectively decided to stop asking the most obvious question in the world:

How the f*&^ did this happen?

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MMR Vaccine-Linked Deaths Outnumber Measles Deaths in 2026

So far in 2026, there have been ZERO confirmed measles deaths and at least THREE MMR vaccine-linked deaths in the United States.

Yet Americans hear virtually nothing about deaths occurring after MMR vaccination. Instead, the captured mass media blasted out headlines claiming that two children in Pennsylvania had died from measles—claims that have since fallen apart under scrutiny. Meanwhile, three highly concerning MMR-linked deaths have already appeared in VAERS this year:

2026 U.S. MMR VACCINE DEATH REPORTS (VAERS): 3

1-year-old boy: fatal cardiac arrest just ONE DAY after MMR

The first case involves a 1-year-old boy who suffered fatal cardiac arrest just one day after receiving MMR. The extraordinarily short interval makes the report impossible to simply dismiss as some distant event occurring long after vaccination. Along with MMR, he was also subjected to a battery of four additional vaccines—Varivax, Havrix, Vaxelis, and Prevnar 20—for five vaccines total at the same visit. The child was hyper-vaccinated and died the following day.

1-year-old girl: died from disseminated rubella after MMR

The second case is even more biologically concerning. A 1-year-old girl died from disseminated rubella after receiving MMR. She reportedly had an undiagnosed primary immunodeficiency when she was vaccinated.

This matters because MMR does not contain an inert rubella antigen. It contains a live attenuated rubella virus designed to replicate in a controlled manner and generate immunity. In a person with severe immune dysfunction, however, the immune system can fail to adequately contain or eliminate the attenuated virus. Instead of remaining limited, vaccine-strain virus can persist and disseminate into tissues throughout the body leading to multi-organ failure.

76-year-old woman: vaccine-strain measles detected during fatal pneumonia

The third case may be the most remarkable of all. A 76-year-old woman developed measles vaccine-associated pneumonia after receiving MMR, progressed to severe respiratory failure, and died after a 16-day hospitalization.

Critically, vaccine-strain measles was detected in her respiratory tract, including pulmonary samples. In other words, this was not simply a patient who happened to test positive for measles after vaccination. Molecular testing identified the vaccine strain itself.

The measles component of MMR is also a live attenuated virus. In immunocompromised individuals, the weakened virus can escape normal immune control, continue replicating, and produce serious systemic disease. When that process involves the lungs, it can produce measles pneumonitis or pneumonia, impair oxygen exchange, and progress to respiratory failure.


2026 U.S. MEASLES DEATHS: 0

Now contrast those three reports with what happened in Pennsylvania.

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US Army doctor claims 28 troops died from Covid vaccines – Politico

A US Army doctor has testified that she knows of 28 US military deaths caused by Covid-19 vaccines, Politico has reported citing a court deposition. The US government is investigating 2,544 deaths reported following the jabs, the official has said.

Theresa Long, who also serves as an adviser to US Health Secretary Robert F. Kennedy Jr., reportedly gave the testimony during an August 14 deposition in a federal court case in Virginia. Neither her testimony nor her role at the Department of Health and Human Services (HHS) had previously been reported.

Long allegedly said that the 2,544 unverified deaths were reported to the department’s Vaccine Adverse Event Reporting System (VAERS).

Former US President Joe Biden ordered all US military staff to be vaccinated or be discharged from service, resulting in over 9,000 dismissals. After returning to office, President Donald Trump ordered the Pentagon to offer reinstatement to those who had been discharged for refusing a vaccine.

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Two CDC studies on vaccines and autism using the same data find opposite conclusions. Both cannot be correct

Two US Centres for Disease Control and Prevention (“CDC”) studies of the autism rate in Denmark in the 90s: the first one, produced by admitted felon Poul Thorsen, says the autism rate increased from 1995 to 2000, which was then used to claim there is no connection between giving infants mercury in vaccines and autism; the second study found that the autism rate in Denmark not only decreased from 1995 to 2000, but was more than 10 times higher than the rate claimed by Thorsen. At least one of these studies is bogus. 

Thorsen was a Danish researcher hired by the CDC in 1999 to do a series of studies, including several on the role of vaccines causing autism. He was indicted for embezzling more than $1 million from the CDC and other crimes by a US federal court in 2011.  He lived openly in Denmark, where he was an instructor at Aarhus University, but was finally arrested and extradited to the US in 2025. Yesterday he pleaded guilty.

The first study, ‘Thimerosal and the Occurrence of Autism: Negative Ecological Evidence from Danish Population-Based Data’, a widely publicised and highly influential study released in 2003, claimed that mercury in vaccines played no role in causing autism because the rate of autism in Danish children increased after mercury was removed from Danish-produced vaccines in 1992. 

Another CDC study, ‘Recurrence of Autism Spectrum Disorders in Full- and Half-Siblings and Trends Over Time: A Population-Based Cohort Study’, led by Therese K. Gronborg and released in 2013, however, shows the exact opposite: that the rate of autism in Danish children decreased after mercury was removed. And if the increasing rate of autism claimed in the earlier study showed that mercury had no role in causing autism, then logic would also require that the rate of autism going down, as shown in the current study, indicates that mercury in vaccines may very well have a great deal to do with causing autism. 

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FDA Approves Moderna XFG COVID Vaccines 81 Days Before Teen/Adult Safety Study, 126 Days Before Children’s Study

The U.S. Food and Drug Administration approved Moderna’s new XFG-formulated COVID-19 vaccines on August 27, 81 days before a human study specifically designed to evaluate the safety and immune response of the new formulations was scheduled to begin.

Pfizer’s XFG COVID vaccine formulation was approved on the same day, equally without safety data for its new formulation.

FDA approved the 2026–2027 formulas for Moderna’s SPIKEVAX and mNEXSPIKE vaccines, which are claimed to contain genetic instructions corresponding to the alleged JN.1-lineage XFG subvariant.

But FDA’s own Aug 27 approval letters show that a Phase 3b/4 human study specifically evaluating the “Immunogenicity and Safety of MNEXSPIKE and SPIKEVAX 2026-2027 Formula” is not scheduled to begin until November 16.

The first interim results are not due until March 26, 2027.

For younger children eligible to receive the new SPIKEVAX formulation, a separate human safety and immunogenicity study is scheduled to begin even later.

In other words, FDA approved Moderna’s new XFG vaccines first.

The human studies specifically evaluating the new formulations come afterward.

The regulatory pathway allows FDA to rely on claimed evidence from previously licensed formulations rather than require a new human safety trial of every updated formulation before approval.

But that raises consequential health, informed-consent, regulatory, and accountability questions:

  • How can FDA determine that a newly reformulated vaccine is safe before formulation-specific human safety data exist?
  • What evidence justifies carrying earlier safety findings forward to a changed product?
  • And why is FDA requiring a Phase 3b/4 study specifically to evaluate the new formulas’ “Safety” only after Americans are permitted to receive them?
  • And most fundamentally, if FDA is approving a newly reformulated vaccine before human safety data specific to that formulation exist, is the agency fulfilling its responsibility to independently establish that products are safe before Americans receive them, or shifting that uncertainty onto the public and collecting the answers afterward?

Congressional committees have confirmed that the FDA “is not meeting important federal safety requirements to protect its employees and the public while also failing to prioritize scientific data quality delivered from FDA laboratories.”

You can contact the FDA here.

And Moderna here.

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