European federation of hereditary ataxias

a European non profit association whose member organisations work together
to give people with hereditary ataxia as normal a life as possible.

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Working together!

euro-ATAXIA is an international non profit association who’s member organisations work together to give people with hereditary ataxia as normal a life as possible. We do this by building a strong organisation that represents people with hereditary ataxia throughout Europe, by encouraging scientific research into causes and treatments, and by campaigning for treatments to be made available.

Legal information

Registered in Belgium
Name: Europese federatie van erfelijke ataxieën IVZW
Enterprise number 446.797.050.
Granted legal personality by H.M. Baudouin, King of Belgium, 25 February 1992.
Statutes (articles of association) and board members registered at the clerk of the court of commerce in Brussels and published in the gazette of the federal state of Belgium.
Type: International non-profit association.
Statutory address: Avenue du Général Médicin Derache 36, B-1050 Bruxelles / Laan van Generaal Geneesheer Derache 36, B-1050 Brussel.

We are member of

Eurordis, the European organisation for rare diseases: www.eurordis.org.
EFNA, the European federation of neurological associations: www.efna.net.
EDF, the European Disability Forum: www.edf-feph.org.