Campaigning
for ME

European
ME Alliance

A Voice for People with ME in Europe SHOP NOW

In Focus
This Month

More
Information
Current

NEWS

in Europe Go

Latest Projects

Check the status of projects organised by EMEA

VIEW MORE

Events

What events are being organised by EMEA

VIEW MORE

Around Europe

What is happening around Europe with regard to ME

VIEW MORE
EMEA
Who We Are

European ME Alliance

The European ME Alliance is a grouping of European organisations who are involved in supporting patients suffering from myalgic encephalomyelitis (ME or ME/CFS) and are campaigning for funding for biomedical research to provide treatments and cures for ME.

The alliance was formed in 2008 by national charities and organisations in Europe.

The Alliance now has representatives from Belgium, Czech Republic, Denmark, Finland, France, Germany, Holland, Iceland, Ireland, Italy, Norway, Spain, Sweden, Switzerland and the UK.

ME/CFS is a debilitating neurological illness classified as such by the World Health Organisation under ICD-10 G93.3.

Our aim is to campaign for appropriate funding of biomedical research into ME/CFS to establish an understanding of the aetiology, pathogenesis and epidemiology of the disease. This should lead to the development of treatments to cure or alleviate the effects of the illness.

Read More