Foundation For Angelman Syndrome
The Angelman Syndrome Foundation (ASF) is dedicated to supporting individuals and families affected by Angelman syndrome, a rare neurodevelopmental disorder impacting approximately one in 15,000 people globally. With a mission focused on increasing awareness and promoting research aimed at finding effective treatments and ultimately a cure, the foundation has been a pillar of support for over 30 years.
Through its various initiatives, including funded research, resource libraries, and community engagement opportunities, ASF fosters a network that connects families and individuals, ensuring they are not alone on their journey. The organization also conducts educational programs and events to enhance understanding of the syndrome and strengthen the global support system.
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