NAF has launched a petition on Change.org calling on the FDA to prioritize treatment options for rare diseases with urgent unmet needs, including Spinocerebellar Ataxia (SCA). SIGN THE PETITION
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Contact us for general information about Ataxia, genetic testing, research and clinical trials, neurologists or Ataxia Centers in your area, or support group information. NAF does not offer financial assistance to individuals or medical advice. We look forward to hearing from you.