European ME Alliance

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Jump to: navigation, search

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]


The information provided at this site is not intended to diagnose or treat any illness.

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history