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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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VIRTUAL Global Ataxia Support Group Meeting – Time Slot #1

July 21, 2023 @ 3:00 pm - 5:00 pm

Meetings are at 3PM

Click here to register

For more information contact Courtney Ng at courtney@hopeforataxia.org.

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Date:
July 21, 2023
Time:
3:00 pm - 5:00 pm
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