mastodon
4.6.4
We are an independent, patient-led, international forum for people with ME/CFS and the carers, clinicians, scientists and advocates who support us.
This account is maintained on a part-time basis by patients.
We are an independent, patient-led, international forum for people with ME/CFS and the carers, clinicians, scientists and advocates who support us. This account is maintained on a part-time basis by patients. #MEcfs #LongCovid
Our latest News in Brief summary has headlines and links to further reading for ME/CFS, Long Covid, and related news for the week of Mar. 16 - 22:
Topics:
News, advocacy and articles
Coming events
Research news and commentary
Published research
https://www.s4me.info/threads/news-in-brief-march-2026.49238/#post-682549
We are an independent, patient-led, international forum for people with ME/CFS and the carers, clinicians, scientists and advocates who support us. This account is maintained on a part-time basis by patients. #MEcfs #LongCovid
Hello 👋
Welcome to the new Mastodon account for the Science for ME forum. Migration to the new server appears to have succeeded and most followers have been transferred.
Our forum is an independent, patient-led, international forum for people with ME/CFS or Long Covid and the carers, clinicians, scientists and advocates who support us.
Anyone can read the public posts on the forum but to join the discussion you must become a forum member.
You can learn more about our forum here:
https://www.s4me.info/threads/welcome.38181/
If you have any questions, just ask! 😁
But please note that this account is run by volunteers who have ME/CFS so replies may be delayed.