By Deron Hamel Tyler Herrington is completing his doctoral studies focused on climate-change research, defying the odds a childhood physician gave his parents when asked how epilepsy would impact his life. As a child living with epilepsy, Tyler’s parents were told by the doctor that epilepsy would prevent their son from living a rich and…
By Deron Hamel Alexa Graham has never been one to let epilepsy stand in the way of her dreams. The recent high-school graduate from Timmins, Ont. was diagnosed with the condition as a young child. From that time, Alexa says she and her family were told she would never be able to “lead a normal…
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 epilepsy) to have a say in developing a potential CEA app. We are hoping to develop…
By Deron Hamel Epilepsy Ontario is calling on the Ministry of Health to increase core funding to epilepsy agencies across the province to enhance education and supports to help people living with seizure disorders manage their condition while saving the province money by reducing hospital visits. The organization is launching an e-letter campaign and asking…
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