Go Back
Report Abuse

National Ataxia Foundation

Description

The National Ataxia Foundation (NAF) is the US leading non-profit for hereditary and sporadic ataxias — a group of rare progressive neurological conditions affecting balance, coordination, and speech — including Friedreich's ataxia, spinocerebellar ataxias (SCA1–48+), ataxia-telangiectasia, and multiple system atrophy. Founded in 1957, NAF has invested over $20 million in research, operates the Ataxia Global Initiative biobank and CRC-SCA clinical trial consortium, and runs an Ataxia Clinical Research Network spanning 30+ centres. The Foundation supports patients through annual conferences, 60+ local chapters, and provides educational materials for clinicians and families worldwide.

Video About Us

Contact

Address
600 Highway 169 South, Suite 1725, Minneapolis, MN 55426, USA
Zip/Post Code
55426
600 Highway 169 South, Suite 1725, Minneapolis, MN 55426, USA
Social Info

Rare Disease Watch

Our aim is to make complex information clear, accessible, and trustworthy. With concise reporting and consistent daily coverage, Rare Disease Watch helps professionals, patients, advocates, and families stay informed about what is changing in the rare disease landscape and why it matters.
All Rights Reserved. Rare Disease Watch©. Part of Honnao Ltd, Registered in England and Wales, Company number: 12345498. Trading Address: Highstone House, 165 High Street, Barnet, Herts. EN5 5SU, UK.
linkedin facebook pinterest youtube rss twitter instagram facebook-blank rss-blank linkedin-blank pinterest youtube twitter instagram