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
Guest Author: Donna Gorzela, Boston Ataxia Support Group Co-Leader Over time, actual support groups change and evolve but the many memories and friendships we’ve made persist. Isn’t that what support Read More…
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