[Close]
- This page was created by volunteers like you!
- Help us make it even better. To learn more about contributing to MEpedia, click here.
- Join the movement
- Visit #MEAction to find support or take action. Donate today to help us improve and expand this project.
- Congratulations!
- MEpedia has got over 30 million views as of August 2022!
European ME Alliance
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
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[2] (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[3]
Online presence[edit | edit source]
References[edit | edit source]
- ↑ "EMEA". euro-me.org. Retrieved September 6, 2019.
- ↑ "European ME Alliance - EMEA Holland". euro-me.org. Retrieved September 18, 2019.
- ↑ European ME Alliance. "European ME Alliance Group members". euro-me.org. Retrieved September 18, 2019.
