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The European ME Alliance gives a voice for people with ME in Europe and is the European partner for facilitating high-quality biomedical research into Myalgic Encephalomyelitis (ME or ME/CFS)
European ME Alliance (EMEA) - ROUNDTABLE II ME/CFS in EUROPE April 2022
ME/CFS in Europe
EMEA is now arranging the next roundtable - on Myalgic Encephalomyelitis (ME/CFS) in Europe.

The meeting will again bring together a variety of initial stakeholders in Europe, including clinicians, researchers, policymakers, industry and patient representatives from EMEA's members, in order to create a better understanding of the many unmet needs and the devastating impact of ME/CFS on patients and families across generations.

The WHO will be presenting their Global Action Plan for Neorological Diseases and Epilepsy.
The results from EMEA's 2021 patient survey will be presented.
We will have a discussion on data collection using a standard platform.
The meeting will also include discussions on the implications of Long COVID for ME/CFS.

Apr 8, 2022 02:00 PM in Paris

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