Offers a history and mission statement, information and events, research, a message board, links, institutes and doctors and information about the disease.

An IBE project with the objective of giving a voice to young people around the world. Offers a chat room, contacts and information.

Promotes research and education for professionals dedicated to the prevention, treatment and cure of epilepsy.

Provides up-to-date, comprehensive information and interactive resources for living well with this disease.

Promotes, supports and raises money to fund basic and clinical research into the basic causes of epilepsy. It aims to improve the lives of those who suffer from epilepsy and thus the lives of their families, friends and colleagues.

SANEL is a non-government organization dedicated to working with people with epilepsy and their families, to enable them to lead meaningful and enriching lives. The site offers comprehensive information about epilepsy and an Online Counselor.

Information about the organization as well a resource for patients, their families and the community.

National non-profit organization featuring news, information and resources on epilepsy.

Interested in the non-medical aspects, addressing such social problems as education, employment, insurance, driving license restrictions and public awareness. Includes activities, publications and links.

British organization aiming to improve medical treatment, to provide information and to raise awareness about epilepsy among people affected by this disease and among the general public.

Works to promote the welfare and interests of people, and their family, with epilepsy and to increase public awareness. Provides general information, current news and discussion forums.

Provides information, links and support for parents of children with uncontrolled epilepsy. Includes ketogenic diet and food intolerance.

First museum for epilepsy and its history: Causes, diagnosis, therapy, epilepsy in the literature, epilepsy and arts, famous people who suffered from this disease.

A non-profit organization dedicated to improving the lives of people living with epilepsy. Provides also books, videos pamphlets, magazines and other teaching materials.

Provide advice and guidance, education, research and support services in association with allied medical and community agencies.

A charitable, social Service agency established to address community, individual, and family needs related to epilepsy.

Contains details about the association and provides basic information about epilepsy.

Provides information about the organization.

Provides information about the organization and basic information about epilepsies.

Gives information about the organization, offers a discussion forum and a chat session.

Features national epilepsy news and priorities, profiles of everyday Canadians living with seizures, and links to grassroots service organizations for people with epilepsy and their families from coast-to-coast.

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.

A traveling epilepsy awareness bear visits families around the world. His travels are intended to localize and personalize the story of children and adults with Epilepsy. One can request a visit at this site.

Provides peer counseling and information services to people with epilepsy and the parents of children with epilepsy.

Informs about the activities of the association and provides general information about epilepsy.

The private web page offers information about the vagus nerve stimulation and contains a large link list.

Offers evaluation, treatment, and access to the most up-to-date research for children, adolescents, and adults with all forms of epilepsy.

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

Organization dedicated to educate, inform and assist people with epilepsy, their families and those who work with them.

Volunteer-based organization addressing the needs of persons with epilepsy and their care-givers in Singapore.

The not-for-profit membership organization of epilepsy service providers aims to improve the quality of life for citizens affected by epilepsy.

Intents to raise public and political awareness of epilepsy, to promote knowledge and understanding and to dispel stigma based on ignorance and fear.

Not-for-profit community based organization provides information and resources for adolescents and children with epilepsy, as well as support for family members.

Provides up-to-date research and information on epilepsy for all ages and interest groups.

Information about epilepsy, including causes of seizures, treatments and lifestyle issues. Message board, online shop and fundraising events. Details of support, medical and residential care services offered by NSE.

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.

Aims to provide reliable information on epilepsy to people in East Kent in the UK.

This site chronicles the journey of Karla Brown as she walks 9000 miles across America to raise people's awareness of epilepsy.

A traveling epilepsy awareness bear visits families around the world. His travels are intended to localize and personalize the story of children and adults with Epilepsy. One can request a visit at this site.