European ME Alliance

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Revision as of 21:44, June 12, 2017 by Kmdenmark (talk | contribs) (typo)

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]