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
Immerse yourself in the captivating fusion of light and darkness at “Fairies and Shadows – A Performing Arts Party”! This event promises an evening of mesmerizing performances, from the graceful movements of fire dancers to the whimsical allure of bubbles, all set amidst a backdrop of costumes and mysterious shadows.
Beyond the enchanting party lies a deeper purpose: honoring loved ones lost to Ataxia. Every dollar raised supports NAF and their mission to find treatments and a cure. Step into a world of contrast and celebration, where fantasy meets reality, and together, we illuminate the path towards hope and change. Make a difference while indulging in an unforgettable celebration of the arts.
Donate or Buy Tickets: Click here.
VIP Special Ticket- $100 (includes access to the Executive Suite)
VIP Ticket- $75 (includes a ‘thank you’ bag)
General Admission- $50
There will also be a raffle with prizes up to $300
A $25 raffle ticket will enter you into a chance to win!
Have questions or want to help? Great! We’d love to hear from you!
NAF Contact: Jon Wegman, Regional Development Manager
Email: jon@ataxia.org
Phone: 763-231-2747
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.
