“Case 17”: Perfectly healthy 83-year-old woman dies 10 days after Pfizer vaccine with massive histological damage across multiple organs

I’m going to share with you the ChatGPT autopsy report on “Case 17” which is one of over 75 deaths of people investigated by German pathologist Arne Burkhardt at the request of family members who thought the death was suspicious.

In 77% of the referred cases, Burkhardt could confirm the association between the vaccine and death. What that implies is that the family members are correctly assessing causality about 80% of the time. This is about 80% better than medical doctors who are right about 0% of the time.

I want you to see for yourself just how incredibly damaging the COVID vaccines are.

They can kill you in just a matter of days (sometimes years) and the damage can be so widespread it’s hard to tell exactly what you died from. It’s like dying from multiple stab wounds; it’s hard to tell which one killed you.

Even ChatGPT who normally tries to gaslight people into believing the shots are safe was horrified.

Here’s how ChatGPT described the cause of death:

It’s a bit like seeing a ship sink—not because one hole blew it open, but because 10 small-to-medium breaches overwhelmed the hull at once.

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The Media Playbook for Measles Looks a Lot Like Its COVID Playbook — This Time, Kids Are the Pawns

There are moments in the history of a movement that test its resolve. For the medical freedom movement, this is one of those moments.

We are in the midst of another full-on attack by the pharmaceutical-industrial complex, aided and abetted by a beholden mainstream media united around its allegiance to a $69 billion vaccine industry.

Five years ago, we fought back as our government, Big Media and Big Pharma orchestrated and executed a COVID-19 fear campaign — a campaign built on lies, deception and censorship — and then parlayed the public’s fear into dangerous and deadly medical mandates and hospital protocols that continue to cause profound harm.

The upside to COVID-19 global disaster?

It opened the eyes of millions more people to the dangers of shoddily tested vaccines, regulatory agency hubris and one-size-fits-all “medicine.”

As our movement has grown exponentially, so has our threat to Big Pharma.

In response, we’re seeing the same tactics rolled out again. This time, it’s measles. This time, children are the pawns in pharma’s playbook.

Children’s Health Defense (CHD) stood strong and stayed true to our mission during COVID. We’re standing just as strong now. We remain just as committed now to the truth, informed consent and medical freedom as we were during the pandemic.

As pharma ramps up its measles playbook, our No. 1 job is to dismantle the vaccine industry’s lies — broadcast far and wide through the industry’s most reliable and faithful megaphone: mainstream media.

The media would have you believe that measles is a “deadly” disease. But any suggestion that MMR (measles-mumps-rubella) vaccines are safer than measles infection isn’t supported by facts.

In fact, between 2000 and 2024, nine measles-related deaths were reported to the CDC. During the same period, 141 deaths following MMR or MMRV vaccination were reported in the U.S. to the Vaccine Adverse Event Reporting System (VAERS) — suggesting the MMR vaccine can be deadlier than measles.

The media echo the same familiar refrain: The MMR vaccine is “overwhelmingly safe.”

In fact, the MMR vaccine is associated with serious health risks. The package insert for Merck’s MMRII says, “M-M-R II vaccine has not been evaluated for carcinogenic or mutagenic potential or impairment of fertility.”

Research also shows the MMR vaccine causes febrile seizures, anaphylaxis, meningitisencephalitis, thrombocytopeniaarthralgia and vasculitis. In 2004, researchers at the Centers for Disease Control and Prevention found that boys vaccinated with their first MMR vaccine on time were 67% more likely to be diagnosed with autism compared to boys who got their first vaccine after their 3rd birthday.

The media insist there’s no viable treatment for measles — hence prevention, with the MMR vaccine, is the sole solution.

In fact, as CHD reported, doctors in West Texas are successfully treating measles with budesonide and vitamin A. Even the World Health Organization recommends vitamin A.

Yet some hospitals and doctors are refusing to treat measles patients with budesonideTexas health officials rejected pleas by a treating physician to endorse the treatment and get the word out to hospitals about its effectiveness.

Sound familiar?

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85-Million-Person Study Finds Increased Risks of Stroke, Heart Attack, Coronary Artery Disease, and Arrhythmia Following COVID-19 Vaccination

This comprehensive Bayesian multivariate meta-analysis included 15 studies, with 11 controlled observational studies forming the basis of the primary analysis. In total, the analysis evaluated over 85 million individuals, including nearly 46 million vaccinated individuals (with first, second, or third doses) and nearly 40 million unvaccinated or control participants. Vaccines studied included BNT162b2 (Pfizer), mRNA-1273 (Moderna), and ChAdOx1 (AstraZeneca), spanning multiple countries across Asia, Europe, and North America. Moderna (mRNA‑1273) was not prominently featured in the primary risk estimates due to limited availability of controlled studies specifically isolating its cardiovascular effects. As a result, the main metrics focus on outcomes associated with Pfizer, AstraZeneca, and dose-specific pooled data.

Here’s what they found:

Increased Risks Following COVID-19 Vaccination

(Compared to unvaccinated/control group)


Coronary Artery Disease (CAD)

  • Overall: OR 1.70 (95% CrI: 1.11–2.57) → 70% increased risk
  • BNT162b2 (Pfizer): OR 1.64 (95% CrI: 1.06–2.55) → 64% increased risk
  • Second dose (all vaccines): OR 3.44 (95% CrI: 1.99–5.98) → 244% increased risk

Myocardial Infarction (MI)

  • Second dose (all vaccines): OR 3.86 (95% CrI: 2.28–6.60) → 286% increased risk
  • BNT162b2 (Pfizer): OR 1.87 (95% CrI: 1.22–2.89) → 87% increased risk
  • Second dose of BNT162b2: OR 3.84 (95% CrI: 2.21–6.66) → 284% increased risk

Stroke

  • BNT162b2 (Pfizer): OR 2.09 (95% CrI: 1.36–3.21) → 109% increased risk
  • First dose of BNT162b2: OR 3.69 (95% CrI: 2.13–6.37) → 269% increased risk
  • First dose (any vaccine): OR 3.40 (95% CrI: 1.98–5.86) → 240% increased risk

Arrhythmia

  • First dose (any vaccine): OR 2.99 (95% CrI: 1.20–7.44) → 199% increased risk
  • ChAdOx1 (AstraZeneca): OR 8.11 95% CrI: 3.67–17.99) → 711% increased risk
  • First dose of ChAdOx1: OR 4.89 (95% CrI: 1.21–19.38) → 389% increased risk

This large-scale analysis of over 85 million individuals shows that COVID-19 vaccines are associated with significantly increased risks of stroke, heart attack, coronary artery disease, and arrhythmia. Pfizer’s mRNA injections (BNT162b2) were specifically linked to substantial increases in stroke, myocardial infarction, and coronary artery disease—particularly following the first and second doses. Arrhythmia risk was elevated following the first dose of any vaccine, with the strongest signal observed after AstraZeneca’s ChAdOx1.

As each day passes, a new study is published that reveals the serious harms of the COVID-19 genetic countermeasures. They must be removed from global markets immediately.

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NEW STUDY – Flu Vaccination Linked to 27% Increased Risk of Flu

The Cleveland Clinic study titled, Effectiveness of the Influenza Vaccine During the 2024-2025 Respiratory Viral Seasonwas just uploaded to the MedRxiv preprint server:

Background The purpose of this study was to evaluate the effectiveness of the influenza vaccine during the 2024-2025 respiratory viral season.

Methods Employees of Cleveland Clinic in employment in Ohio on October 1, 2024, were included. The cumulative incidence of influenza among those in the vaccinated and unvaccinated states was compared over the following 25 weeks. Protection provided by vaccination (analyzed as a time-dependent covariate) was evaluated using Cox proportional hazards regression.

Results Among 53402 employees, 43857 (82.1%) had received the influenza vaccine by the end of the study. Influenza occurred in 1079 (2.02%) during the study. The cumulative incidence of influenza was similar for the vaccinated and unvaccinated states early, but over the course of the study the cumulative incidence of influenza increased more rapidly among the vaccinated than the unvaccinated. In an analysis adjusted for age, sex, clinical nursing job, and employment location, the risk of influenza was significantly higher for the vaccinated compared to the unvaccinated state (HR, 1.27; 95% C.I., 1.07 – 1.51; P = 0.007), yielding a calculated vaccine effectiveness of −26.9% (95% C.I., −55.0 to −6.6%).

Conclusions This study found that influenza vaccination of working-aged adults was associated with a higher risk of influenza during the 2024-2025 respiratory viral season, suggesting that the vaccine has not been effective in preventing influenza this season.

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Why Did The FDA Hide Vaccine Injuries?

A frequent criticism of corporations (which I believe also applies to governmental bureaucracies) is that their organizational structure encourages sociopathic behavior. This is because members of these entities are shielded from legal or personal accountability for their actions, with any wrongdoings being attributed to the corporation as a whole. In contrast, the main form of accountability most members face is the pressure to advance the institution’s mission (e.g., make more money), leading to the proliferation of increasingly unethical methods to achieve that goal.

To illustrate, consider this quote from Peter Rost, a former executive at Pfizer and one of the few pharmaceutical leaders to speak out against the industry:

It is scary how many similarities there are between this industry and the mob. The mob makes obscene amounts of money, as does this industry. The side effects of organized crime are killings and deaths, and the side effects are the same in this industry. The mob bribes politicians and others, and so does the drug industry … The difference is, all these people in the drug industry look upon themselves – well, I’d say 99 percent, anyway – look upon themselves as law-abiding citizens, not as citizens who would ever rob a bank … However, when they get together as a group and manage these corporations, something seems to happen … to otherwise good citizens when they are part of a corporation. It’s almost like when you have war atrocities; people do things they don’t think they’re capable of. When you’re in a group, people can do things they otherwise wouldn’t, because the group can validate what you’re doing as okay.

In looking through what went awry with the COVID-19 response, while Fauci was commonly blamed for all that went amiss, I kept running into another less-known individual who, while hidden within the FDA bureaucracy, I believe was directly responsible for many of the mishaps that happened

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Who Needs Vaccine Data When You Have Vaccine Mandates?

FDA Gene-Editing mRNA Vaccine Chief – Peter Marks – has always been a strong proponent of vaccine mandates. Marks also has as a history of overruling large expert panels for FDA approval of gene therapies at the agency.

STAT News reported that “Marks was one of the architects of Operation Warp Speed, the $18 billion U.S. effort to speed development of Covid-19 vaccines. He regularly embraced regulatory flexibility. And he spoke not infrequently about the importance of accelerated approval for next-generation treatments, including with those whose potential benefits weren’t always crystal-clear in clinical trial data.”

“Vaccine Mandates Are Not Going to Get Us THERE. It’s Got to Be Compelling Evidence.” – Vaccine Chief Peter Marks

During a 4-hour Public Health Workshop hosted by Duke University on March 20, 2025, Marks alluded to having contentious disputes with the higher-ups of the new Health & Human Services (HHS) administration (aka – Secretary Kennedy) over ‘the need for vaccine efficacy and vaccine safety data’ when FDA-approved vaccines can just be mandated.

“How We Generate Evidence Going Forward”

Throughout the 4-hour workshop, Marks and his colleagues strategically avoided discussing retrospective data analyses (i.e. analyzing the adverse events of vaccines in the US government databases) and the specifics on how to measure safety data going forward.

“By Definition, Vaccines Are Very Safe Medical Products”

“By definition, when we are developing vaccines for broad use, one of their direct benefits has to be that they are very safe medical products. That just goes without saying, because that goes to getting acceptance for the individual’s direct benefit.”

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Ex-CDC Director Pushes Extra MMR Shot For Babies, As Arizona Reports Suspected Measles Case Was ‘Rare’ Vaccine Reaction

Some infectious disease experts — including the Centers for Disease Control and Prevention’s (CDC) former director, Dr. Rochelle Walensky — are pushing health officials to recommend an extra dose of the MMR vaccine for babies ages 6-11 months who live in or travel to areas of the U.S. with measles outbreaks, according to Medpage Today.

The news comes as a suspected measles case in a 1-year-old child in Pima County, Arizona, this week turned out to be a reaction to the measles-mumps-rubella (MMR) vaccine — not measles.

According to a Pima County news release, reactions to the MMR vaccine are “rare and do not carry the same risk as community-acquired measles.”

The Pima County Health Department did not specify the toddler’s symptoms but said state and county health authorities — and the local hospital where the child was treated — “took precautions in the child’s treatment as if it were an infectious case.”

Arizona has not reported any measles cases so far in 2025, the release said.

The CDC’s current Child and Adolescent Immunization Schedule recommends children receive their first dose of the MMR vaccine between the ages of 2-15 months, and their second dose between ages 4-6 years.

Infants 6-11 months old who are about to travel internationally are advised to get an extra dose before traveling.

Walensky and colleagues argued in op-eds published in the Journal of the American Medical Association (JAMA) and STAT News that the recommendation should be changed due to the uptick in U.S. measles cases.

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Canadian Cop Disciplined for Investigating Post-Vax Infant Deaths

A Canadian police detective has been found guilty of “discreditable conduct” for investigating a surge of sudden deaths among babies who died after receiving Covid mRNA ‘vaccines’

Ottawa Police Service Detective Helen Grus was charged after she started to investigate a large number of cases of Sudden Infant Death Syndrome (SIDS) in December 2021.

Grus found that SIDS cases skyrocketed after the “vaccines” were rolled out for public use that year.

The cop believed that the sudden deaths were linked to Covid injections, which all of the victims had received, however, Grus found herself at the center of an official probe over her investigations.

Following an investigation into her actions, Grus was called before a disciplinary hearing.

In a March 25 decision, Grus was found guilty of “discreditable conduct.”

Retired superintendent Christopher Renwick, who presided over the proceedings, ruled that Detective Grus brought “discredit upon the reputation of the Ottawa Police Service” when she investigated a potential link between sudden deaths of several infants and the Covid mRNA “vaccines” they received.

The OPS alleged that Grus “self-initiated an unauthorized project, wherein she accessed nine child and/or infant death cases in which she had no investigative role/responsibility, and failed to then record her involvement or finding in the files.”

Beginning in December 2021, Grus began questioning if Covid injections played a role in the increasing number of infant deaths she was reportedly witnessing. Accordingly, she attempted to determine if either the babies or their parents had received the experimental “vaccine.”

After it was revealed that Grus was conducting these investigations, she was suspended from performing her duties by the Ottawa Police Service’s professional standards unit.

Officials then filed a disciplinary charge against Grus and forced her to defend her actions in front of a tribunal.

OPS alleges that Grus transgressed a professional boundary by looking into the infant deaths for cases in which she had no investigative role. One incident occurred in January 2022 when Grus allegedly contacted the father of an infant who suddenly died.

Grus sought to inquire into the vaccination status of the baby’s mother. Along with her lawyer, Bath-Sheba van den Berg, Grus argued that the probe into the deaths was within the detective’s sphere of authority as a member of the sex assault and child abuse (SACA) unit.

SACA is tasked with investigating deaths of children under five. Additionally, the protocol for SIDS (Sudden Infant Death Syndrome) includes gathering information regarding the medical history of parents.

Information gathering includes all street, over-the-counter, and prescription drug use. During the hearing, van den Berg argued that Grus had taken “reasonable steps” after noticing a “doubling or tripling” of infant deaths since the Covid “vaccine” rollout.

Furthermore, Grus “saw it as her duty to investigate criminal negligence on the part of the government.”

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Tucker Carlson Horrified as Dr. Mary Talley Bowden Drops Chilling COVID Statistic

Dr. Mary Talley Bowden left Tucker Carlson visibly shaken after dropping a chilling COVID-19 vaccine statistic that’s impacting millions of children right now.

Before her appearance on Carlson’s show, Dr. Bowden, a Texas-based ENT specialist, rose to prominence in the medical freedom movement by speaking out against vaccine mandates and advocating for early treatment options like ivermectin.

She gained national attention after she was suspended by Houston Methodist Hospital for challenging the prevailing COVID narrative.

Despite the backlash, Bowden has remained committed to the Hippocratic Oath, successfully treating an impressive total of over 6,000 COVID patients without a single death.

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Jenny McCarthy Reveals Chilling Encounter After Challenging Vaccine Narrative

Jenny McCarthy is once again speaking out about the emotional and professional toll she endured after her son was diagnosed with autism—and why sharing her story, she says, came with serious consequences.

This time, she pulled back the curtain on a private conversation so disturbing, it changed the way she saw everything.

Appearing on Maria Menounos’s podcast, McCarthy revisited the painful journey that changed her life forever—a horrifying health crisis involving her 2½-year-old son.

Before Evan, her son, was diagnosed with autism, McCarthy said the signs started with something far more terrifying—seizures that came out of nowhere and escalated fast.

“He started having seizures,” she said, “and they were life-threatening seizures. Like cardiac arrest.” They weren’t the kind of thing you expect in a toddler, and the severity made it clear something was deeply wrong.

She recalled one of the worst days of her life, when Evan went into cardiac arrest and turned blue. “At one point, my heart sank into my toes,” she said, describing the panic as she waited for paramedics to arrive. “There’s nothing worse,” she added. “He’s two and a half years old, he’s turning blue.”

Calling 911, she screamed for help, but time felt like it stood still. She compared herself to a mother in Terms of Endearment, pleading and shouting with everything she had.

Evan was revived not once but twice—first in the house, then again in the ambulance. During that chaos, McCarthy said she was bargaining with God. “Bring back my boy first… or I’ll kill myself,” she admitted. “He had to survive.”

He did. But what followed shortly after, she said, was an autism diagnosis. The emotional toll was crushing. “I hit such a low,” she said, remembering how she broke down in the shower, crying uncontrollably and feeling completely helpless.

What shook her most was the suddenness of it all. Evan had been a typical child—smiling, talking, hitting all his milestones. “How did my son get diagnosed,” she asked, “when he was a normal, typical child?” Though he had a few minor signs like eczema, she believed the real change came after his MMR shot.

McCarthy is convinced the vaccine triggered encephalitis, a type of brain inflammation, which she notes has been “clinically in published science” linked to autism. “And my son was one of them,” she said. “Because it was after his MMR, when his encephalitis… leads to autism.”

She first shared her story publicly on The Oprah Winfrey Show in 2007 during the release of her book, Louder Than Words: A Mother’s Journey in Healing Autism.

“That’s when I really outed myself,” she said. Oprah had long been pressed by parents to cover the link between vaccines and autism. “So, so many… were pounding Oprah to do a story on the association.”

Though the network initially resisted, Oprah eventually gave Jenny a live platform, insisting that recording it in advance would risk censorship. “She told me I had to go on live… so we had to go live.” Even then, Oprah had to read what Jenny called a “giant long page disclaimer.”

But despite the warning label, McCarthy said her message got through. “People heard me… parents heard me.”

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