Update from the Irish ME/CFS Association for the Hospital Saturday Fund
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME #MyalgicE @mecfs
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Update from the Irish ME/CFS Association for the Hospital Saturday Fund
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME #MyalgicE @mecfs
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A FB memory from 11 years ago. @MEAwarenessHour put together image
It's on each Wednesday.
Some times:
8-9pm (GB and Ireland)
21:00-22:00 (CEST) (i.e. part of Europe)
3-4pm EST (USA).
Use this hashtag: #MEawarenesshour
Dr Amolak S Bansal talk: "What is ME/CFS? Hallmarks of a complex but poorly understood condition" (2026)
YouTube link:
https://www.youtube.com/watch?v=HK3OvIrfTrM
It would be great if more people could subscribe to our channel
#MyalgicEncephalomyelitis #MEcfs #ME #MyalgicE
@mecfs
#PwME #TogetherWeAreStronger
Stigmatisation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) – a scoping review
"not only individuals with ME/CFS can be affected by stigmatisation, but also people in their social circles such as friends & family members"
Stigmatisation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) – a scoping review
"not only individuals with ME/CFS can be affected by stigmatisation, but also people in their social circles such as friends & family members"
From Spain 🇪🇸
Two-timepoint multidomain follow-up of post-COVID condition and ME/CFS: overlapping autonomic, small-fiber, and cognitive changes
https://link.springer.com/article/10.1186/s12967-026-08321-9
Screenshot from Science for ME @s4me weekly update
(Australia)
World Blood Donor Day
Screenshot from June 2026 Emerge Australia email bulletin