Provides guidance for parents and caregivers on effectively addressing disagreements with schools regarding their child’s Individualized Education Program (IEP). The presentation covers strategies for resolving disputes, understanding legal rights, and advocating for appropriate educational services for children with Angelman syndrome. It emphasizes the importance of collaboration, communication, and utilizing available resources to ensure the child’s educational needs are met.
The mission of Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.