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Genetic and Rare Diseases Information Center (GARD)

Hereditary ataxia


Organizations Supporting this Disease

  • euro-ATAXIA (European Federation of Hereditary Ataxias)
    c/o Mrs. Sue Millman, secretary-general
    Per address Ataxia UK
    Lincoln House
    Kennington Park
    1-3 Brixton Road
    London SW9 6DE,
    Telephone: +44 (0)207 582 1444

  • National Ataxia Foundation
    2600 Fernbrook Lane
    Suite 119
    Minneapolis, MN 55447-4752
    Telephone: 763-553-0020
    Fax: 763-553-0167

Social Networking Websites

  • is a Web site and blog that collects firsthand stories from people facing issues, making tough decisions, and using genomic (DNA) information in their own healthcare. Click on the link to learn from their experiences and/or submit your own story.
  • RareShare is an online social hub dedicated to patients, families and healthcare professionals affected by rare medical disorders.

Organizations Providing General Support