Mark Millich
@Unstoppable218
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"Discipline Equals Freedom" Fighting/seeking justice for the many lives destroyed by pharmaceuticals. Moral Medicine - https://t.co/JcYE5dhhCy
Joined September 2017
Random internet troll - "Bro, these guys with PFS just have low testosterone and a sedentary lifestyle.". Me - “Okay…”
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RT @RodneyAllebach: I go to the gym to bury the man who rotted in silence for decades. Who wore comfort like a coffin and let time devour h….
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Any other PFS or PSSD sufferers with an INFJ personality type?.
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RT @dsowens17: Any system that requires only short-term company-funded trials to prove benefit, but demands catastrophic, undeniable harm-p….
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We need to get Moral Medicine in front of as many eyes as possible. These are real people, living real nightmares because of Finasteride and SSRIs, and the world is still turning a blind eye. To everyone reading this - share these stories everywhere you.
youtube.com
Your Story Matters! We conduct in-depth interviews with individuals enduring permanent, life-altering side effects from medications such as Finasteride, Accutane (Isotretinoin), SSRIs, Lion’s Mane,...
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RT @DrMcFillin: The foundation of the psychiatric industrial complex is built on lies, manipulation, fraud and systematic deception. Its a….
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RT @MoralMedicine: Had a powerful interview this past weekend with @yassie_pirani on PSSD and iatrogenic harm. We….
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RT @katug05: ⸻. Finasteride is not harmless. It has destroyed lives—physically, mentally, emotionally. Young men seeking help for hair loss….
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RT @katug05: 💔 From a Parent’s Perspective (Revised):. My son didn’t take finasteride for hair loss. They gave it to him for a bladder issu….
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Moral Medicine just hit 500,000 lifetime views. Half a million views on a grassroots platform built from the ground up; no big budget, no corporate backing. Just raw truth, real pain, and the voices of those who refuse to be silenced. Thank you to.
youtube.com
Your Story Matters! We conduct in-depth interviews with individuals enduring permanent, life-altering side effects from medications such as Finasteride, Accutane (Isotretinoin), SSRIs, Lion’s Mane,...
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RT @PSSDNetwork: "Now, these folks who have been exposed to ashwagandha, they're reporting genital numbness and loss of sexual sensation. ….
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RT @i_r_wilson: Mark @MoralMedicine is doing an amazing job with his YouTube channel, but he needs our help. If you or a loved one have b….
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Another warrior has stepped up. In this emotional and eye-opening interview, Matt shares his journey after being prescribed Rexulti; an atypical antipsychotic that led to life-altering consequences. What started as a plea for help turned into years of.
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To dismiss suffering just because it hasn’t been “peer-reviewed” is exactly how real harm gets ignored for decades. That logic was used to downplay smoking related cancer, Vioxx deaths, and Accutane injury; not because no studies existed, but because early harm was denied,.
@Unstoppable218 @0x63726162 @stacycay These anecdotes aren't backed up by any kind of systematic, large-scale, peer-reviewed studies. It describes a constellation of ill-defined symptoms, and it's usually entirely a self-diagnosis.
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Call me crazy, but perhaps mainstreaming and prescribing a potent anti-androgenic drug to masses of healthy, androgenic young men hasn’t been the best idea, especially in a society facing declining testosterone levels and rising infertility rates.
wrote about the link between finasteride (propecia) and male infertility for @nytimes shout out @maxwellstrachan
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🚨 PFS/PSSD Community — Act Now 🚨. The FDA is directly asking the public to submit questions to the Commissioner for their next “FDA Direct” conversation. This is your chance to be heard. It took me less than 30 seconds to submit mine. If you’re a sufferer of Post-Finasteride.
Got a question for the FDA Commissioner?. In our next FDA Direct conversation, we'll be fielding questions from the audience. Click the link below to submit yours!.
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I try to stay out of the politics and avoid anything that could be seen as controversial when it comes to PFS progress, but this needs to be said. PFS charities (or any charity built on researching rare diseases) must understand that periodic updates for their supporters are.
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