Europe: European ME Alliance (EMEA) (also EMECC and EMERG)

ME/CFS and post Covid in the Balkans

"The next roundtable webinar on Myalgic Encephalomyelitis (ME/CFS) in Europe will be held on Friday 27 May 14:00 CET.

This webinar will try to begin the process of raising awareness of ME in Slovenia, Croatia and Serbia, and the Balkan countries in general, in order to improve research and services for people with ME, and thereby overcome the inherent stigma and misinformation about the disease that still exists."

https://www.europeanmealliance.org/news-Q22022-001.shtml
 
ME/CFS IN THE NORDIC COUNTRIES

"Status of Health Care and Research and Suggestions for Joint Actions and Policies

In November 2021 the Medical Association of ME/CFS in Finland (SLME) organised an online conference with the purpose to assess the existing Nordic ME/CFS health care and research resources and discuss how best to put them into good use. A report was produced from this conference."

https://www.europeanmealliance.org/emea-nordic-web.shtml
 
Wonderful presentation and question answering by Gracemarie Bricalli - approx 10 minutes all up.:thumbup: I hope that we have Gracemarie as a member here.

There's an interesting discussion about pain that follows, there's a mention of fibromyalgia and gender issues. Also a discussion of the importance of patient involvement in research.
 
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