- Accessibility
- Advocacy
- Annual Ataxia Conference
- Blog
- Clinical Services
- Clinical Trials
- Education
- Fundraising
- Member Stories
- NAF
- Research
- SCAsource Article Summary
- SCAsource Conference Preview
- SCAsource Project Update
- SCAsource Snapshot
- SCAsource Spotlight
- Special Series: The Discovery
- Support Group News
- Support Groups
- Treatment
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