The European ME Alliance is a grouping of European organisations who are involved in supporting patients suffering from myalgic encephalomyelitis (ME or ME/CFS)
European ME Alliance - An Updated Constitution and New Members
A change now allows non-European groups to become Associate members of EMEA and partner with us to improve the future for people with ME and their families
europeanmealliance.org/news-โฆ#mecfs#InternationalMEawarenessDay
10 Dec #HumanRightsDay
Human rights mean recognising suffering, and acting to end neglect
๐๐๐๐จ ๐๐๐ฃ๐ฃ๐ค๐ฉ ๐๐ช๐จ๐ฉ ๐๐ ๐ฌ๐ค๐ง๐๐จ
They must be ๐๐๐๐๐๐๐๐๐๐๐ into actions for people with #mecfs, and their carers
europeanmealliance.org/humanโฆ#DignityForAll#HealthEquity
Building disability-inclusive Europe means acknowledging โinvisibleโ conditions such as #mecfs Ensuring policies, funding, services reflect that reality
Genuine disability-inclusive societies ensure no one is left behind
europeanmealliance.org/news-โฆ#IDPD2025#DisabilityInclusion
3/3
๐ข #YEVienna2025 โ Registration Extended!
Good news: you now have until 7 November to register for our two-day workshop for early career researchers in ME/CFS.
You can still:
๐งโ๐ Attend the workshop
๐ฐ Submit a poster
๐จ Request discounted accommodation
๐ข #YEVienna2025 โ Registration Extended!
Good news: you now have until 7 November to register for our two-day workshop for early career researchers in ME/CFS.
You can still:
๐งโ๐ Attend the workshop
๐ฐ Submit a poster
๐จ Request discounted accommodation