Angelman Syndrome Foundation
The Angelman Syndrome Foundation (ASF) is dedicated to advancing awareness and treatment for Angelman syndrome, a rare neurodevelopmental disorder affecting approximately one in 15,000 people worldwide. With over 30 years of experience, ASF provides critical support to families and individuals navigating the challenges associated with the condition.
ASF not only focuses on education, advocacy, and research, but also invests in global care initiatives and resources, ensuring families are equipped with the information and support they need. Their mission emphasizes collaboration within the Angelman community to drive research and treatment efforts toward an ultimate goal of finding a cure.
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