The ASF is proud to partner with groups and organizations whose values and services align with our mission to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for the community.
Supporting the Angelman community in Canada.
Advocacy for the global rare disease community.
Advocacy for the rare disease community.
Angelman Syndrome News helps us share news and information about AS.
Helping underinsured patients get the medication they need.
Provide resources to families with rare epilepsy diagnosis.
Cofund LADDER Learning Network and Research Symposium
Facilitates and supports research that uses the precious gift of donated brain tissue.
Education and support
Education and support
Global Community Advisory Board
Advocacy, Research and Education
Education and support
ASF Family Fund
Support families with money, meals, and more in one place
