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
We need more voices! Contact your elected officials today and urge them to support our 2025 AS Legislative Prorities. Every email makes a difference!