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
Please join us for our annual in-person Ataxia Wellness Event that will be focused on mental health and ataxia.
“Coping with Ataxia from a Mental Health Perspective”
Please RSVP no later than April 5.
You are allowed to bring one guest (care partner)
A box lunch will be served
Location: The Meeting House in Columbia
5885 Robert Oliver Place
Room 200
Columbia, Maryland 21045
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.
