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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)
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Month: July 2019

DeCrescenzo Family

DeCrescenzo Family

Ten years ago this month, my husband Joe was diagnosed with hereditary Spinocerebellar Ataxia, SCA2. That marked the day our lives changed and would never again be the same. Since Read More…


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