European ME Alliance: Difference between revisions

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
m (→‎Member organisations: revert false information added by Guido den Broeder - Het Alternatief remains a member for Holland and there are NO listings for Netherlands)
(rv - 'Het Alternatief' is the name of my good friend Frank Twisk's website, nothing else)
Line 7: Line 7:
*[[Association Française du Syndrome de Fatigue Chronique]] - France
*[[Association Française du Syndrome de Fatigue Chronique]] - France
*[[Fatigatio e.V.]] - Germany
*[[Fatigatio e.V.]] - Germany
*[[Het Alternatief]] - Holland (Netherlands)
*[[ME félag Íslands]] - Iceland
*[[ME félag Íslands]] - Iceland
*[[Irish ME Trust]] - Ireland
*[[Irish ME Trust]] - Ireland
*[[Associazione Malati di CFS onlus|Associazione Malati di CFS]] onlus - Italy
*[[Associazione Malati di CFS onlus|Associazione Malati di CFS]] onlus - Italy
*[[Stichting ME-de-patiënten]] - Netherlands
*[[Hope 4 ME & Fibro NI]] - Northern Ireland
*[[Hope 4 ME & Fibro NI]] - Northern Ireland
*[[Norges ME Forening]] - Norway
*[[Norges ME Forening]] - Norway

Revision as of 00:55, September 17, 2019

The European ME Alliance is a group of European patient groups for myalgic encephalomyelitis (ME or ME/CFS).[1] It was formed in 2008 and set up to lobby for increased funding for biomedical research to lead to for patients. It now has representatives from Belgium, Denmark, Germany, Holland, Ireland, Italy, Norway, Spain, Sweden, Switzerland and the UK.

Member organisations[edit | edit source]

Online presence[edit | edit source]

References[edit | edit source]

  1. "EMEA". www.euro-me.org. Retrieved September 6, 2019.