John R. Houk, Blog Editor
© July 14, 2025
Big Pharma is evil motivated by greedy profits more than the health of its customers. Don’t get me wrong, making a profit ethically is good individuals, Companies and Corporations all alike. BUT when that profit comes at the cost of harming human lives up to and including death, such a profit becomes evil.
Pfizer LIES about mRNA injections as “Safe & Effective” enters the realm of evil profit.
On 7/13 Telegram Natural News reposted its 7/10 website Natural News article by S.D. Wells entitled at the website, “HIGHLY CORRUPT PFIZER won’t release MYOCARDITIS study results because vaccine “safety” claim will obviously get blown out of the water”. Go to the website if you wish to check the source-links. I’m cross posting the Telegram version below.
THEN along the line “Pfizer is evil”, I’m sharing a Telegram Dr. Maria Hubmer-Mogg – MAHUMO post which excerpts 6-Minutes of a Naomi Wolf presentation it entitled, “PFIZER DOCUMENTS REVEAL THE GREATEST CRIME AGAINST HUMANITY”. I uploaded the video excerpt to my Rumble Channel which I share below the Natural News post.
This evil is more and more being exposed in slow-boat released documents and ever increasing peer-reviewed studies abandoning the Globalist-Science Narrative.
JRH 7/14/25
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HIGHLY CORRUPT PFIZER Won’t Release MYOCARDITIS Study Results
July 13, 2025
Telegram Natural News (Pt 1 & 2)
HIGHLY CORRUPT PFIZER won’t release MYOCARDITIS study results because vaccine “safety” claim will obviously get blown out of the water
Pfizer is facing growing scrutiny after delaying the completion of its post-marketing safety study on myocarditis and pericarditis in individuals under 21 who received its COVID-19 vaccine. Originally scheduled to be completed in 2024, the study’s new end date is November 2030 — eight years later than initially planned.
The delay has prompted accusations from medical experts and public health advocates of potential data suppression, especially in light of increasing evidence linking mRNA COVID-19 vaccines to heart inflammation in young people.
• Pfizer has delayed completion of its myocarditis safety study in individuals under 21 to November 2030, sparking criticism over transparency and concern that interim findings — which have not been released — may reveal safety issues with its COVID-19 vaccine.
• The study, involving 300 vaccinated participants and 100 controls, defines myocarditis cases only within seven days of vaccination, a narrow window that experts say could underestimate the true incidence compared to broader definitions used by the CDC and other health authorities.
• Updated FDA vaccine labels now warn of increased myocarditis risk, especially among males aged 16–25, with Pfizer and Moderna both required to include stronger language after mounting evidence from international and U.S. sources linked mRNA shots to heart inflammation.
• Multiple studies and adverse event reports, including VAERS data and international research, continue to show elevated myocarditis risks post-vaccination, fueling calls for greater scrutiny, transparency, and even moratoriums or bans on mRNA vaccines in some U.S. states.
Pfizer pushes deadline for study of myocarditis in kids and adults under 21
Launched in November 2022, the study is a collaborative effort with the U.S. National Heart, Lung, and Blood Institute. It follows 300 participants under age 21 who developed myocarditis or pericarditis after receiving Pfizer’s vaccine, with a control group of 100 individuals who developed similar conditions after a COVID-19 infection or related complications. Despite ongoing data collection, no interim results have been publicly released.
Critics argue that if the findings were positive, Pfizer would likely have already published them. Dr. Clayton J. Baker stated, “If their findings were reassuring, there would be a strong incentive to release them now.” Delaying results until 2030 while continuing vaccine administration, he said, is scientifically irresponsible.
Study design flaws have also been highlighted. Investigative journalist Sonia Elijah criticized the narrow definition of vaccine-related myocarditis — only counting cases diagnosed within seven days of vaccination. This contradicts other health guidelines. The CDC allows a 40-day window, while the Brighton Collaboration recognizes up to six weeks. VAERS data suggests symptoms can emerge up to 120 days post-vaccination. Elijah and others also noted the lack of an unvaccinated control group, making it harder to clearly establish causality.
Enrollment difficulties are another issue. Experts suggest Pfizer may be struggling to recruit enough participants, as noted by Dr. Jane Orient. With only 300 participants, the study lacks sufficient power to detect rare but serious side effects. Additionally, participant dropout over time could further undermine the study’s credibility.
Despite Pfizer’s delay, independent studies continue to link COVID-19 mRNA vaccines to increased heart inflammation risks. A South Korean study published in July 2024 found a 620% higher risk of myocarditis in vaccinated individuals. A 2024 UK study of 1.7 million children found myocarditis and pericarditis occurred only in vaccinated children. Likewise, a 2022 Nordic study involving 23.1 million people confirmed elevated myocarditis risk, especially among males aged 16 to 24.
In response to these findings, the FDA recently required stronger warning labels for Pfizer and Moderna vaccines. Current data show myocarditis occurs in about 8 cases per million doses for people under 65, with the highest rate — 38 per million — seen in males aged 16–25.
The CDC has acknowledged a causal link between mRNA vaccines and myocarditis since 2021. However, critics allege key data were withheld from the public, including early warnings from the Israeli Ministry of Health and redacted U.S. government reports obtained via FOIA.
With growing calls for accountability, some states like Idaho and Florida have moved to ban or restrict mRNA vaccine use. Experts and lawmakers continue to debate whether ongoing vaccination is justified given the known risks—especially as Pfizer’s key safety study remains unfinished for another five years.
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PFIZER DOCUMENTS REVEAL THE GREATEST CRIME AGAINST HUMANITY – Naomi Wolf
July 13, 2025
Telegram Dr. Maria Hubmer-Mogg – MAHUMO
Rumble VIDEO: PFIZER DOCUMENTS REVEAL THE GREATEST CRIME AGAINST HUMANITY – Naomi Wolf
[Posted by SlantRight
Published July 14, 2025]
Dr. Maria Hubmer-Mogg – MAHUMO Description:
Journalist Naomi Wolf claims internal Pfizer files expose massive fraud and cover-up:
👉 Pfizer KNEW by Nov. 2020 – just one month after rollout – that the vaccine had “failure of efficacy” and didn’t stop COVID.
👉 Pfizer’s own docs list COVID itself as the third most common side effect.
👉 By early 2021, Pfizer was so overwhelmed by adverse event reports, it had to hire 2,400 full-time staff just to process them.
👉 In May 2021, Pfizer documented heart damage in 35 minors – but the public wasn’t warned until four months later.
👉 Pfizer and the FDA knew the vaccine components didn’t stay at the injection site. They biodistributed to the brain, liver, spleen, adrenals, and ovaries.
👉 Lipid nanoparticles (industrial fats + polyethylene glycol) accumulate in female ovaries with no known way to remove them.
"The Pfizer documents contain evidence of the greatest crime against humanity in the history of our species."
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