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
Hello. My name is Christie Alexander. I have worked as an Early-Childhood educator for 21 years. A few years ago, I was diagnosed with a rare disease called Olivopontocerebellar Atrophy Read More…
The National Ataxia Foundation, a patient advocacy organization for a rare brain disease, is looking for an ambitious, detail-oriented, and fun-to-work-with Database Manager / Development Associate with a passion for Read More…
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