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
EASTERN TIME
Guest Speaker: Lori Shogren, National Ataxia Foundation Programs Director
Topic: United Against Ataxia Hill Day 2023
Join Zoom Meeting
https://us02web.zoom.us/j/84872580415?pwd=R09hRnNpVVNPeHhUa0tPYXZXVnJYQT09
Meeting ID: 848 7258 0415
Passcode: 429848
For more information contact Lisa Cole at 772-370-3041 | lisacoleataxia@gmail.com
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