Each year, the Epilepsy Foundation recognizes SUDEP Action Day — a day devoted to raising awareness around the world about sudden unexpected death in epilepsy (SUDEP) and inspiring action to save lives. On October 19, 2022, join the Epilepsy Foundation and its...
We invite you to share your expectations and opinions regarding the potential development of a Canadian Epilepsy Alliance mobile app. We are asking the epilepsy community (epilepsy agencies, epilepsy partners, people living with epilepsy, and families of people with...
We have learned of an anticipated drug shortage that may affect some epilepsy patients in Canada. The product shortage affects SABRIL (vigabatrin), in the 500 mg powder for oral solution only. Stock of 500 mg SABRIL tablets remains available. The shortage is expected...
The Canadian Epilepsy Alliance (CEA) is 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.