Hi, I couldn’t find a general thread to post this so I’m making a new thread. A small but in my opinion cool way to increase advoacy, an...
Solve ME has created an automated tool (meant for folks in the USA) that will contact your Member of Congress (email/phone/twitter) and ask them...
Today, March 15, is Long Covid Awareness Day. I thought there should be a thread for news articles, social media posts (hashtag...
This committee hearing is a pretty big deal and I was kind of waiting for someone to start a thread when it was announced so here we go. Today...
The Ed Yong piece has been going round my head for a while now as it gave me a new perspective on my disease too. I think it's safe to say that...
There have been quite a lot of improvements in the ME/CFS situation in Germany. There are now investment in research, the IQWiG report, political...
From Solve M.E. - a call to action for Advocacy Week: "Ask your Members of Congress to support the CARE for Long COVID Act!"...
I saw this post by @MEFoggyDog on Mastodon so I thought I'd share. This same hashtag - #MPDoYourJobForME - is also being used on twitter so you...
The Solve Newsletter thread has been merged with this thread. Spring 2018 Contents: Page 2 - SMCI This Quarter: A Summary of Our Work Page 5 -...
The ME/CFS patient community has long worked on debunking graded exercise and CBT as treatments for the disease but I am not aware of similar...
Threads about different articles have been merged Article about today's protest at the White House from MedPage Today: "Long COVID, ME/CFS...
Reminder for anyone who wants to help out with the 2022 Millions Missing protest scheduled for Monday, September 19. There's an online training...
In November last year Action for ME invited people with ME to complete a questionnaire describing their experience of ME. The responses were...
A popular YouTuber (149k subscribers), Lex Play, has made a video about an ME island created by Lisa, The Unlikely Gamer. It can be watched here:...
Bit of a mouthful thread title, but I have seen many references in the last few years that explicitly blame the biopsychosocial model of ME/CFS as...
[MEDIA] Great video - one of the best I've seen. Winston has real skill. Maybe we can use it to our advantage. I'd like to see a UK version.
Someone calling themselves Long Covid Patient Action Group UK on Twitter has announced protests calling for more research into long covid outside...
He Was Given 6 Months to Live. Then He Changed D.C. Brian Wallach was diagnosed with ALS the day his daughter came home from the hospital. In the...
As you can see, this is not a new article but I thought it was worth sharing. Written by a family physician. Not really about ME/CFS but this...
I've been seeing many lately and thought a thread could be useful. Either coming from Long Covid advocates or professionals interested in learning...
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