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
CENTRAL TIME ZONE
During this webinar, an expert will join us to take a look at the causes and symptoms of Autosomal Recessive Spinocerebellar Ataxia type 20 (SCAR20)*, the typical diagnostic journey for those affected, what to expect for clinical care, and an overview of current research into the disease.
*This webinar is about Autosomal Recessive Spinocerebellar Ataxia type 20, not Spinocerebellar Ataxia type 20 (SCA20).
Register: Click here.
NAF hosts educational webinars about Ataxia presented by industry experts. Learn about important topics related to living with Ataxia. Webinars are complimentary for NAF members, with new sessions offered each month. Join NAF to receive invitations to upcoming Ataxia webinars. Visit www.ataxia.org/webinars to explore past webinars on a variety of topics.
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