A voice for ME in Europe
Membership in EMEA
Help Us Influence ME Policies in European
About EMEA
The European ME Alliance (EMEA) is a grouping of European organisations dedicated to supporting patients suffering from Myalgic Encephalomyelitis (ME), also known as ME/CFS.
Founded in 2008 by national patient organisations and charities across Europe, the alliance is committed to improving the lives of those affected by ME. This debilitating neurological illness is classified by the World Health Organisation under ICD-11 Code: 8.E49.
Our vision is to ensure that all patients have access to accurate diagnosis, compassionate care, and effective treatment, recognising ME as a serious, chronic illness.
EMEA are currently receiving applications for membership.
Use the contact link below to apply if you are a interested in working with EMEA to create a better future for European ME patients.
Last Update: September 2020