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
Our December support zoom call will now be on Sat. Dec.14 at 9:00 am.
The meeting link is: https://us06web.zoom.us/j/82436559728?pwd=AOPeyv4PZogjHXU2hV9kX2kAcKP6dw.1 If you are calling in please use meeting 824 3655 9725 with 975631 as the pass code.
This will be a one hour meeting.
Our generous donors help us fund promising Ataxia research and offer support services to people with Ataxia. Your gift today will help us continue to deliver on our mission to improve the lives of persons affected by Ataxia.
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