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
NAF is proud to have funded millions of dollars of Ataxia research to accelerate treatment development. Each year, we support researchers at every stage of their career. In this webinar series, NAF-funded researchers will present their work and facilitate a discussion about their study. Fellow researchers, clinicians, and industry partners are welcome to participate in scientific discussions or ask questions after the presentation, gaining insights into advancements, methodologies, and findings that are shaping the landscape of Ataxia research. NAF members are also invited to peek into Ataxia research and witness the impact of their generosity!
Register for upcoming sessions or watch past sessions below.
Each month will feature a new speaker presenting their research. Join us for a presentation about their funded project. You will have the opportunity to ask questions after the presentation. Please note that these sessions will include complex scientific information that may be difficult for a lay audience to understand.
Click on a session to learn more about the research being presented and the speaker.
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.
Join for FREE today! Become a part of the community that is working together to find a cure. As a member you will receive access to the latest Ataxia news with our e-newsletter and Generations publication.
