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.
The annual research symposium is a chance for leading researchers, scientists and doctors to discuss the latest research in the world of AS.
Take pictures and interact with 12 of your favorite superheroes and princesses. Stay for food and a DJ dance party AND magic show.
On this global day of doing good, consider donating, creating an online fundraiser, random acts of kindness or sharing your time through volunteerism. This year, Giving Tuesday donations to the ASF will be matched up to $50,000! Help us raise $100,000 in one day.
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.
Through October, Sloomoo Institute is donating profits from their cloud slime, Hope, to ASF.
