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
CENTRAL TIME ZONE
The Dallas Walk N’ Roll will bring together families, friends, co-workers, neighbors, and the community to support NAF’s mission to accelerate the development of treatments and improve the lives of people living with Ataxia. Join us for a fun event!
Start a Team or Donate: www.ataxia.org/WalkDallas
TW Richardson Park Pavillion
333 E. Interstate Highway 635
Irving, TX 75060
10AM – 12PM
Have questions or want to help? Great! We’d love to hear from you!
Event Organizers:
NAF Contact: Rich McCutchen
Email: rich@ataxia.org
Phone: 763-285-6359
