National Ataxia Foundation

The National Ataxia Foundation was founded in 1957 as a non-profit, charitable organization, organized to combat all types of hereditary ataxia (HA). The N A F is also concerned with closely related conditions, such as peroneal muscular atrophy (Charcol -Marie - Tooth disease), hereditary spastic paraplegia, and ataxia telangieclasia. Hereditary tremor, a common neurological disorder, is also included.

Objectives of N A F :
An estimated 150,000 people in the United States are affected by the hereditary & sporadic ataxias.
To help these ataxia patients and their families in your area and throughout the nation, we need your help.
The following methods are provided for your consideration:
NAF membership entitles you to all publications and information on hereditary ataxia.
National Ataxia Foundation National Headquarters
2600 Fernbrook Lane, Suite 119
Plymouth, Minnesota 55447
  763-553-0200         Fax 763-553-0167
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N. A. F. Official Web Siteis located at http;//
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