CURRENT ACTION ALERTS

This year's AS Congressional Advocacy Day is on March 5th, where over 145 advocates from 30+ states DC gather on Capitol Hill in Washington, D.C. to advocate on behalf of their loved one(s) living with Angelman syndrome. ASF and FAST thoughtfully developed "asks" to support what matters to our community, caregivers, Medicaid, and research   

For those who could not attend in person, you can take action from home! Please review the 2025 legislative priorities for Angelman syndrome and click below to take action today. 

By clicking below, you will send these AS priorities straight to your congress members' inbox!