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
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
EASTERN TIME ZONE
Big news—our annual Jacksonville Walk N’ Roll for Ataxia is back…
🎯 Location: Winston Family YMCA, 221 Riverside Avenue, Jacksonville, FL 32202
📅 Date: October 4th, 2025
🕘 Time: 8:00 AM – 12:00 PM
Whether you’ve joined us before or are stepping up to the plate for the first time, we’re inviting you to walk, connect, and rally support for those living with Ataxia. Every step we take and every dollar we raise brings us closer to a cure.
To set up an individual or team page visit the Fundraiser Page
Can’t attend? You can still donate or support a team, Donate Here!
Let’s show the world what’s possible when we walk together. Spread the word, bring your friends, and let’s make this year unforgettable.
Have questions or want to help? Great! We’d love to hear from you!
Event Organizer: Jon Wegman, Regional Development Manager
Email: jon@ataxia.org
Phone: 763-231-2747
Our generous donors help us fund promising Ataxia research and offer support services to people with Ataxia. Your gift today will help us continue to deliver on our mission to improve the lives of persons affected by Ataxia.
Join for FREE today! Become a part of the community that is working together to find a cure. As a member you will receive access to the latest Ataxia news with our e-newsletter and Generations publication.
