Angelman syndrome is a rare neuro-genetic disorder characterized by severe developmental delays, speech impairments, balance issues, seizures, sleep disorders, anxiety, frequent laughter and a happy demeanor. Affecting approximately 1 in 15,000 people, this condition significantly impacts the lives of those diagnosed and their families. Despite the challenges, research and therapeutic interventions hold promise for improved outcomes. Your support can make a difference in funding vital research and providing resources for those affected, offering hope and a better quality of life for individuals living with Angelman syndrome and their families.
Gabe, his sister, & service dogASF Walk 2025FAST Gala 2025Awareness Night at Drexel WBB 2025