is an international non-profit association whose 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.
Hand in hand, we work towards the following objectives:

- To drive forward research and treatment of the ataxias

- To encourage the free flow of information between members on the latest research

- To foster and improve contacts between practitioners interested in the ataxias, and people with ataxia

- To investigate social, political and cultural matters connected to the welfare of people with ataxia, and promoting and improving the exchange of this information

- To promote co-operation on an international level between national ataxia organisations

- To raise awareness of ataxia among clinicians, scientists and society

To view the Euroataxia leaflet which includes this information in a printable format, click here.