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
We welcome you to join us for a day of fun and networking!
The Walk N’ Roll to Cure Ataxia campaign is NAF’s largest grassroots fundraising event. Walk N’ Roll began in 2007. It is held in cities across the United States. Thousands of families, friends, co-workers, neighbors, and communities come together each year to support NAF’s mission to accelerate the development of treatments and improve the lives of people living with Ataxia.
Walk N’ Roll events have raised more than $3,000,000 thanks to the tireless commitment from walkers, rollers, runners, volunteers, donors, and sponsors.
Volunteers in the community step up to organize local Walk N’ Roll events to raise awareness and support NAF. Find an event near you to donate, create a team, or attend for a day of fun and networking. If there is not an event near you, join our national virtual Walk N’ Roll!
We are always looking for individuals who are passionate about making a difference for the Ataxia community. Contact Jon Wegman, Regional Development Manager, at (763) 231-2747 or jon@ataxia.org for more information.
Make an impact today by donating to our event.
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.
