Our @gijn Guide Investigating Health and Medicine is out! 90 pages with hundreds of tips to dig deeper on drugs, scientific studies and public health policies. Beautifully illustrated by Marcelle Iouw, @RecheckHealth#GIJNHealthGuide is open access: https://t.co/cnPakECy0i
The 9-question survey many doctors use to diagnose depression was actually created by Zoloft’s manufacturer @pfizer marketing guy.
Too easy and quick for doctors to prescribe antidepressants.
https://t.co/YwMRGFb4bF via @thisisinsider
Several vaccines have been developed and authorised for emergency use (Emergency Use Authorization or EUA) at warp speed. The so-called “Fast Track” process has become the new normal, by @RecheckHealth https://t.co/NlonSsLDxV
Periodismo de investigación y vacunas covid19. Transparencia y más.
Nothing to hide? The quest for transparency on Covid-19 vaccines. And more.
https://t.co/JbZ874NphC
La newsletter de @RecheckHealth site d'information de deux excellentes journalistes, parle des vaccins sous l'angle des risques générés par l'absence de régulation alliée à l'opacité https://t.co/SkZSg4Yytw
We filed a formal Citizen Petition requesting #FDA to update mRNA covid vaccine labelling. The current FDA approved label is SERIOUSLY out of date. Our petition outlines 10 safety and efficacy concerns.
Please share.
@drwasy@MartyMakary@VPrasadMDMPH
https://t.co/nKhRiU68un
EXCLUSIVE: I interview lead author of Cochrane's #mask review, Tom Jefferson
He condemns the pandemic’s overnight experts, the multitude of scientifically baseless health policies & opens up about his disappointment in Cochrane https://t.co/6naOqKW4ps @VPrasadMDMPH@davidemccune
New systematic review (in French) on influence of drug industry over health care professionals. In a nutshell:
1-Influence is very significant over health care professionals.
2-Influence is very underestimated by health care professionals.
https://t.co/KLNqPYluK1
@gmresearchgroup
Finally joining Substack. Here's my first article...the backstory of how I became the Accidental Advocate.
Harms in medicine are often dismissed and just considered "anecdotes" or acceptable collateral damage.
@SurfsBri@Amothersanthem
https://t.co/LU3i55iepc
[UN JOUR, UN GUIDE📚🔎] Avec la pandémie de Covid-19, des journalistes du monde entier ont dû s’improviser du jour au lendemain journalistes spécialisés dans la santé...
Voici le guide @gijn@RecheckHealth pour enquêter sur la santé et la médecine.
https://t.co/zd3eflwN7P
1. THREAD:
THE TWITTER FILES: HOW TWITTER RIGGED THE COVID DEBATE
– By censoring info that was true but inconvenient to U.S. govt. policy
– By discrediting doctors and other experts who disagreed
– By suppressing ordinary users, including some sharing the CDC’s *own data*
Interested in behind-the-scene corporate strategies to influence science, opinion, and policy-makers? Check out our website on Ghost-Management for publications, events, resources and relevant news 🗞️ Please help us spread the word 👻❤️ @MA_Gagnon https://t.co/M0a1UEw9sx
After Fauci & Collins spent $5B on long-Covid research, a new JAMA study finds that long-haul symptoms happen after Covid just as they do with other common respiratory infections.
Add this to the long list of studies Dr. Fauci should have funded 2yrs ago
https://t.co/U5IZEhqNQi
.@BBC pandemic coverage has strictly followed what is now known as official science. No questions asked; just report what you are told.
By @carlheneghan https://t.co/Ynl6FlbY9U
📢Read our new paper:
Analysis suggests Covid-19 boosters likely to cause a net clinical harm to young adults(18-29 yr), where total severe adverse events (SAEs) will outweigh Covid hospitalizations averted
Booster mandates are unethical because:1/13🧵
https://t.co/QNmF8rIneH
Based on available resources aimed at doctors and journalists about the proper reporting of observational research, we identified 5 thematic categories that we employed as minimum reference standard to evaluate the quality of medical reporting in the news articles.
This FDA FOIA release is heavily redacted but paints a clear-ish picture of why FDA officials Krause & Gruber resigned last year. They wanted to require clinical studies before approving the booster, but the CDC wanted the booster approved without a trial.
https://t.co/kOivfj2NsL