Access to treatment shouldn’t depend on how common your disease is. That’s why we’ve launched the #LetsFindAWay campaign to raise awareness of Spinocerebellar Ataxia and other rare diseases that currently have no FDA-approved treatment options. This is a call for change, and you can help. Sign and share the petition urging the FDA to prioritize treatment access for people living with rare diseases: ataxia.org/letsfindaway #SCAawareness #RareDisease #Ataxia #Advocacy | National Ataxia Foundation
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