Hello all, I am working on a project about #ME and looking for physicians who have ME that would be willing to be interviewed about having ME. Dr Lana Dyment, BSc MD CCFP FCFP BC-CLMF

Hey All! The Long Covid Web 4th Canadian Symposium on Long Covid is now open for registration: www.longcovidweb.ca/events/2026-... Join us!

I am not giving up on myself or you! #ME #LC #FM

Am I the only one that noticed Trump say he is “not allowed to drive” yet he runs the USA? Is his licence medically restricted? He has not driven in years he said….

Office conversation: Why don’t you send her to an #ME specialist to get a proper diagnosis?Colleague- What can you do for “those people” anyway? Look him right in the eyes - You know I was in severe ME and here I am working. Give her the respect she deserves. Colleague - Right, where do I send her?

Thanks for posting.

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a disabling chronic illness. People with ME/CFS experience profound fatigue that does not go away with rest, sleep issues, and problems with memory or concentration. Further common symptoms include dizziness, nausea and pain. The hallma

Really appreciate the factual historical documentation which puts in to context our current day experience of #ME in medicine.

Advancing our knowledge base on Long Covid a new dedicated issue of ScienceTM with papers on sex-differences, kids, potential therapies, and more www.science.org/toc/stm/curr...

Hi All, First post. Please tell me what you wanted and needed to hear from your doctor at the beginning of your #LongCovid and or #MyalgicEncephalomyelitis journey. The beginning is the hardest part when approaching a chronic illness that has not yet been addressed.