Who we are
The European ME Alliance is a collaboration of ME support
charities and organisations in Europe who intend to provide a common view and
the scientific facts regarding the neurological illness myalgic
The alliance has been
created with a basic set of principles
(see EMEA principles and rules regarding membership).
The members of the European ME Alliance are listed on the left of
this screen by country, in alphabetical order. Click on the name of the country
in order to be directed to the page containing details of
that member group and their website.
The objectives of the European ME Alliance is to provide a correct and
consistent view of myalgic encephalomyelitis (ME/CFS) for healthcare
organisations, healthcare professionals, government organisations, the media and
patients and the public.
Our web site will consist of accurate descriptions of
the illness and details of research which has or is taking place.
The member groups in the alliance will be working together to promote
awareness of ME/CFS and will work closely with organisations and researchers who
are interested in finding treatments and cures for ME/CFS.
The members of the European ME Alliance have agreed the following
That the European ME Alliance has, as an
objective, the preparation and promotion of a common set of documentation,
in all languages, for Alliance use that is supplemented by local
The members of the European ME Alliance are keen to obtain support from
all organisations supporting the principles mentioned above.
The constitution of the European ME Alliance is available here.
Contact us for more info
pages on this web site are offered as a free access information provider.
No medical recommendations are given or implied.
Please consult your own medical practitioner for the treatment of your personal
10 June 2017