by tim » Fri Oct 10, 2025 8:44 am
https://www.midwesterndoctor.com/p/the- ... ikes-again
The Revolving Door Strikes Again
Why did the FDA relentlessly suppress all evidence of vaccine injuries?
Many individuals I’ve spoken to believe Peter Marks is the government official most directly responsible for the entire COVID catastrophe, and those I know who directly interacted with him despise him. For that reason, six months ago, I published a detailed exposé of his conduct throughout the pandemic, both to highlight the systemic issues within our healthcare bureaucracy that must be fixed and to disincentivize other health officials from following in his footsteps. Since that time:
•Despite immense industry pushback, he was replaced with MAHA appointee Vinay Prasad
•Marks has made statements on the national media which display either a profound degree of ignorance of vaccines or a cult-like devotion to them, such as telling CBS the MMR vaccine absolutely does not cause encephalitis—despite this specific injury being one of the only vaccine injuries the Federal Government acknowledged as real and eligible for compensation when it created the the National Childhood Vaccine Injury Act of 1986.
Note: the primary reason DMSO (a safe and affordable substance with remarkable therapeutic applications against a wide range of “incurable” ailments) never entered mainstream medical practice was because the FDA, feeling DMSO’s broad therapeutic potential threatened their control of American medicine, waged a multi-decade war against it despite widespread opposition from the public, Congressmen, scientists and physicians across the country. One journalist who interviewed the successive FDA commissioners throughout this saga was struck by how “lacking [they were] in solid information about the most spectacular and controversial drug of our time” and how often they simply quoted nonsensical misinformation the FDA had previously put out about the drug without a basic understanding of it—something I would argue also applies to Peter Marks.
•Yesterday, it was announced that Peter Marks had started working with Eli Lilly, where he will oversee molecule discovery and infectious diseases at Lilly. While his salary has not been publicly announced, the AI systems I queried said given the existing precedent, he would likely get 2-6 million this year (a big upgrade from his roughly $200,000.00 FDA salary)—and possibly much more (e.g. 10-15 million).
This understandably enraged the vaccine injured parties who directly interacted with Marks over the last four years, so I felt it was important to revisit exactly what Marks did and discuss the broader revolving door in regulatory medicine.
Note: last year, the FDA approved Eli Lilly’s anti-amyloid monoclonal antibody for the treatment of Alzheimer’s disease (granting the application Fast Track, Priority Review, and Breakthrough Therapy designations). I showed in last weekend’s article, that these costly drugs do close to nothing (they may slightly slow the progression of Alzheimer’s disease) while simultaneously creating a variety of severe symptoms including giving over a quarter of recipients brain bleeds and brain swelling—yet remarkably, safer and much more effective Alzhemier’s therapies have languished in obscurity.
[url]https://www.midwesterndoctor.com/p/the-revolving-door-strikes-again[/url]
[quote]The Revolving Door Strikes Again
Why did the FDA relentlessly suppress all evidence of vaccine injuries?[/quote]
[quote]Many individuals I’ve spoken to believe Peter Marks is the government official most directly responsible for the entire COVID catastrophe, and those I know who directly interacted with him despise him. For that reason, six months ago, I published a detailed exposé of his conduct throughout the pandemic, both to highlight the systemic issues within our healthcare bureaucracy that must be fixed and to disincentivize other health officials from following in his footsteps. Since that time:
•Despite immense industry pushback, he was replaced with MAHA appointee Vinay Prasad
•Marks has made statements on the national media which display either a profound degree of ignorance of vaccines or a cult-like devotion to them, such as telling CBS the MMR vaccine absolutely does not cause encephalitis—despite this specific injury being one of the only vaccine injuries the Federal Government acknowledged as real and eligible for compensation when it created the the National Childhood Vaccine Injury Act of 1986.
Note: the primary reason DMSO (a safe and affordable substance with remarkable therapeutic applications against a wide range of “incurable” ailments) never entered mainstream medical practice was because the FDA, feeling DMSO’s broad therapeutic potential threatened their control of American medicine, waged a multi-decade war against it despite widespread opposition from the public, Congressmen, scientists and physicians across the country. One journalist who interviewed the successive FDA commissioners throughout this saga was struck by how “lacking [they were] in solid information about the most spectacular and controversial drug of our time” and how often they simply quoted nonsensical misinformation the FDA had previously put out about the drug without a basic understanding of it—something I would argue also applies to Peter Marks.
•Yesterday, it was announced that Peter Marks had started working with Eli Lilly, where he will oversee molecule discovery and infectious diseases at Lilly. While his salary has not been publicly announced, the AI systems I queried said given the existing precedent, he would likely get 2-6 million this year (a big upgrade from his roughly $200,000.00 FDA salary)—and possibly much more (e.g. 10-15 million).
This understandably enraged the vaccine injured parties who directly interacted with Marks over the last four years, so I felt it was important to revisit exactly what Marks did and discuss the broader revolving door in regulatory medicine.
Note: last year, the FDA approved Eli Lilly’s anti-amyloid monoclonal antibody for the treatment of Alzheimer’s disease (granting the application Fast Track, Priority Review, and Breakthrough Therapy designations). I showed in last weekend’s article, that these costly drugs do close to nothing (they may slightly slow the progression of Alzheimer’s disease) while simultaneously creating a variety of severe symptoms including giving over a quarter of recipients brain bleeds and brain swelling—yet remarkably, safer and much more effective Alzhemier’s therapies have languished in obscurity.[/quote]