About EMEA

The European ME Alliance (EMEA) is a grouping of European organisations dedicated to supporting patients suffering from Myalgic Encephalomyelitis (ME, sometimes referred to 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: 8E49.

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.

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Croatia

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Serbia

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Spain

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Advocacy In Action

Some recent and ongoing work in which the European ME Alliance and our partners are involved.


Latest Projects

Check the status of projects organised by EMEA

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Events

What events are being organised by EMEA

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Around Europe

What is happening around Europe with regard to ME

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