Promotes research and education for professionals dedicated to the prevention, treatment and cure of epilepsy. Offers professional development, publications and events calendar.

The Foundation was established in 1994 in order to raise awareness about the ketogenic diet as a treatment for childhood epilepsy. The Foundation's role is to facilitate investigation, educate professionals, and inform families about the current status of the ketogenic diet.

Dravet syndrome is also known as Severe Myoclonic Epilepsy of Infancy (SMEI). The organization raises funds for research of Dravet syndrome and related conditions, while spreading awareness and offering support for afflicted individuals and families.

A not-for-profit organization supporting pediatric epilepsy research and programs for children with epilepsy. Part of the NYU Medical Center, New York, USA.

With the goal of no seizures and no side effects, the NAEC strives to make high quality care available and affordable for epilepsy patients. Find care providers and care centers.

A non profit organization founded in 1966 by a group of parents. Offers summer camps for kids, epilepsy information and providing grants for research and other epilepsy related activities.