Living with epilepsy — or supporting someone who does — can raise many questions. This page was created to help individuals, families, caregivers, educators, and community members access trusted information, services, and educational resources related to epilepsy. These resources offer helpful starting points for learning, connection, and support.
A U.S.-based national nonprofit organization dedicated to improving the lives of people affected by epilepsy and seizure disorders. Founded in 1968, it leads public education, advocacy, research funding, and community services to support the approximately 3.4 million people living with epilepsy nationwide.
The Epilepsy Foundation Nevada provides programs and services that support people and families impacted by epilepsy. With the strength of a national organization and network of epilepsy experts, EFN provides national scope and local impact.
(AES) is a professional organization dedicated to advancing research and education in epilepsy and seizure disorders. It serves as a central hub for clinicians, scientists, and allied health professionals seeking to improve understanding, diagnosis, and treatment of epilepsy worldwide.
The United States’ leading public health agency, operating under the Department of Health and Human Services. It focuses on protecting public health through disease surveillance, research, outbreak response, and health education.
(ILAE) is a global professional organization uniting physicians, scientists, and health professionals dedicated to improving the lives of people with epilepsy.
A US-based nonprofit research organization focused exclusively on funding scientific research to find cures for the epilepsies. It is parent-founded and has become one of the leading nongovernmental funders of epilepsy research worldwide.
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