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
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
We invite you to share your story with the Ataxia community! Join the courageous individuals and families who have contributed their personal accounts of living with Ataxia. Help us make sure that nobody faces Ataxia alone, until no one faces Ataxia, period.
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To view other member stories, visit www.ataxia.org/members.
Any questions can be emailed to naf@ataxia.org. Thank you!
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