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
Your voice matters. Patients, families, and caregivers have the power to improve the lives of people living with Ataxia. NAF is here to help you get started! The resources on this page provide excellent tools to propel your advocacy journey.
Our United Against Ataxia Hill Day training video is a great start. Continue watching the playlist to learn more about the issues that NAF is advocating for.
Check out advocacy resources from our trusted partners.
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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