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
Meetings are at 3PM Click here to register For more information contact Amy DeLeon at amy@hopeforataxia.org.
Meetings are at 6PM EST Click here to register For more information contact Amy DeLeon at amy@hopeforataxia.org.
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