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
This “One Night Treatment for Ataxia” Comedy Show will bring together 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 with lots of laughs! There will be great gift baskets included in the raffle similar to those at the Walk n’ Roll at Liberty State Park.
Featured comedians- Gina Dee, Mister Direct, and headliner Laz Vic
6:00 pm- doors open with FREE appetizers and a cash bar
7:30 pm- Show starts
Buy Tickets or Donate: Click here.
Have questions or want to help? Great! We’d love to hear from you!
NAF Contact: 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.
