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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)
 SIGN THE PETITION

Day: September 16, 2021


Mary M.

Most of my career I lived in Texas and worked as a secretary.  After I retired, I moved to Maryland to be closer to relatives.  I’m so grateful that I didn’t Read More…


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