European ME Alliance: Difference between revisions
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
(rv - 'Het Alternatief' is the name of my good friend Frank Twisk's website, nothing else) |
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*[[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 | ||
*[[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 00:31, September 18, 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]
- ME-Vereniging - Belgium
- ME Foreningen - Denmark
- Suomen CFS-Yhdistys - Finland
- Association Française du Syndrome de Fatigue Chronique - France
- Fatigatio e.V. - Germany
- Het Alternatief - Holland (Netherlands)
- ME félag Íslands - Iceland
- Irish ME Trust - Ireland
- Associazione Malati di CFS onlus - Italy
- Hope 4 ME & Fibro NI - Northern Ireland
- Norges ME Forening - Norway
- Liga SFC - Spain
- Riksföreningen för ME-patienter - Sweden
- Verein ME/CFS Schweiz - Switzerland
- Invest in ME Research - United Kingdom