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A health education resource for children, youth and caregivers that is approved by health-care providers at The Hospital for Sick Children. 

A Canada-wide network of grassroots organizations dedicated to the promotion of independence and quality of life for people with epilepsy and their families, through support services, information, advocacy, and public awareness. 

An organization of medical and basic sciences professionals counting more than 125 members, including physicians, basic scientists, nurses, neuropsychologists, neuroradiologists, students and other health professionals. 

An Epilepsy Research Program of the Ontario Brain Institute. 

 Epilepsy Ontario is the voice of epilepsy in the province. Since 1956, we have been serving the province as a registered health charity incorporated under the statutes of Ontario as a non-profit and non-governmental organization.  

An organization made up of over 120 chapters to:

• Advance and disseminate knowledge about epilepsy
• Promote research, education and training
• Improve services and care for patients, especially by prevention, diagnosis and treatment

An organization that improves the social condition and quality of life of people with epilepsy and those who care for them. We have a vision of the world where everywhere ignorance and fear about epilepsy are replaced by understanding and care. 

A branch of the global charity that promotes the treatment of drug resistant epilepsy and other neurological disorders through ketogenic diet treatment. Established in 2015 to support Canadian families and health professionals with proper evidence based information, support awareness & learning, promote networking of ketogenic families.

 A national alliance of patient organizations with a shared goal of equitable and consistent access for all Canadians to safe and effective medicines that improve patient outcomes.