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.
Advocacy In Action
Some recent and ongoing work in which the European ME Alliance and our partners are involved.
WHO-Europe Support for ME in International ME Conference Week
WHO Europe provided a supporting video for people with ME and for delegates to the International ME Conference Weeke events in UK in June
