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
ARIZONA STANDARD 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
Join NAF’s Community Services Coordinator, Sarah Pilato, as we host a virtual support group meeting for those in Arizona! We hope to see Arizona rebuild it’s Ataxia Support community so please join us if you’d like to connect with others in the area and help us on our search for new support group leadership!
Zoom Link: https://us02web.zoom.us/j/83511385087?pwd=SBj7d0oGi1hi9z48yySfbrWGtG1fui.1
Meeting ID: 835 1138 5087
Passcode: 869341
Contact Information
Sarah Pilato – NAF Community Services Coordinator
Phone #: 763-553-0093
Email: sarah@ataxia.org
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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