The Angelman Syndrome Foundation (ASF) is the leading source of information about Angelman syndrome research, support, education, and therapies. ASF has funded the most Angelman-specific research of any nongovernmental organization. ASF-funded research has and will continue to fund beneficial treatments and new discoveries to understand, treat and cure Angelman syndrome.
There are many ways of showing your support and staying involved with ASF.
We thank you for considering to support our efforts. The ASF is 100% funded by the generosity of our donors, volunteers, and supporters. Our National Walk and Biennial Conference cannot function without the support of our volunteers.
We are extremely proud of the work being done by the ASF. We are an organization comprised of many dedicated volunteers committed to improving the lives of people with AS. Please join us. Help us give them a reason to smile.
The Angelman Syndrome Foundation Biennial Conference is the largest gathering of Angelman syndrome families, individuals, researchers, medical experts, and resource professionals of its kind. More than 5,500 people have attended ASF Biennial Conferences, which is one of the most fulfilling experiences along your journey with AS.
The 2015 National Walk will be Saturday, May 16! See more information or register now!