Throughout the year, the Angelman Syndrome Foundation hosts, participates in and receives support from events across the country. Below find a list of upcoming events.
Through October, Sloomoo Institute is donating profits from their cloud slime, Hope, to ASF.
Take pictures and interact with 12 of your favorite superheroes and princesses. Stay for food and a DJ dance party AND magic show.
Since 2013, International Angelman Day has been the driving force in uniting AS families and patient organizations around the world for a common purpose – raising awareness of Angelman syndrome. The day is observed by over 50 charitable/support organizations based in over 40 countries around the world.
Angelman syndrome advocates from around the United States meet in Washington, D.C. on Angelman Syndrome Congressional Advocacy Day. Advocates representing their states meet with their Members of Congress to educate their representatives on their personal experiences with Angelman syndrome to accomplish one of our inaugural goals of building relationships and bringing awareness to AS.
Support the Windy City Angels running in the Bank of America Chicago Marathon!
*Our 2025 team is now filled.
ASF and FAST will host a webinar with representatives from MavriX Bio to provide a summary of their Phase 1/2 Clinical Trial (ASCEND-AS) design, requirements, and enrollment criteria.
Join the block party at The Jewish Community Center.
