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 ZONE
Support group meetings are a great way to socialize and learn with others who are affected by Ataxia. We welcome you to join us! The discussion is led by our volunteer Support Group Leaders, who are looking forward to helping you connect with others.
Meeting Information
Register in advance for this meeting:
https://us02web.zoom.us/meeting/register/tZYqcuGrrzspH9R2M3NkOTsrH39QBrq76oVP
After registering, you will receive a confirmation email containing information about joining the meeting.
Contact Information
For more information contact Lisa Cole at 772-370-3041 | lisacoleataxia@gmail.com
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