National Ataxia Foundation
2024 Member
About National Ataxia Foundation
The National Ataxia Foundation (NAF) was founded in 1957 to search for a cause and cure for Ataxia. This continues to be at the heart of the organization today. Ataxia is a devastating disease that negatively impacts peoples’ lives. NAF is a world leader in the Ataxia research field, using national and global collaboration to further research efforts. NAF exists to improve the quality of life for persons with Ataxia and their caregivers. NAF strives to build connections in the Ataxia community and empower people to make the best choices possible to live better with Ataxia. NAF serves as a credible source for quality educational materials about Ataxia, news about Ataxia, community support, and information about research and resources.
Related Rare Diseases:
- Subacute Cerebellar Degeneration
- Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Lactate Elevation
- Spinocerebellar Ataxia with Axonal Neuropathy
- Kennedy Disease
- Cerebellar Agenesis
- Marinesco-Sjögren Syndrome
- Autosomal Dominant Hereditary Ataxia
- Ataxia with Vitamin E Deficiency
- Olivopontocerebellar Atrophy
- Ataxia Telangiectasia
- Multiple System Atrophy
- Machado-Joseph Disease
- Friedreich’s Ataxia
- Ataxia con deficiencia de vitamina E
- Agenesia cerebelar
- Enfermedad de Kennedy
- Ataxia Telangiectasia