Category Archive

Supporting Agencies (Canada & Ontario)

Thesis examines disclosure among young women with epilepsy

January 14, 2016

By Deron Hamel When searching for a topic for her master’s thesis at Brock University, Suzanne McGuire noticed a lack of published information about how young women living with epilepsy disclose their condition. Epilepsy, McGuire notes, is one of the oldest documented medical conditions, yet, there is little information about how people disclose their condition.…

Theatre group provides life-changing experience for man with Dravet syndrome

January 7, 2016

By Deron Hamel Since Brock Welton began participating in a North Bay theatre group last year he has become more independent and social, says his mother, Jo-Anne. Brock, 22, has Dravet syndrome, a catastrophic form of intractable epilepsy, as well as an intellectual disability stemming from the condition. Last year Brock joined TOROS, a progressive…

Cannabidiol the Voices of Epilepsy’s hottest topic of 2015

December 10, 2015

By Deron Hamel Epilepsy Ontario’s weekly column, the Voices of Epilepsy, saw strong readership in 2015, and of all the issues covered this year one received more buzz on the organization’s social-media platforms than any other: cannabidiol (CBD). CBD is a substance derived from the marijuana plant. It is the most abundant, non-psychoactive chemical compound…

Summerfest Camp registration begins Dec. 4 GIVE YOUR CHILD A SUMMER TO REMEMBER

December 3, 2015

By Deron Hamel Summerfest Camp is going into its 22nd year in 2016 and families can register their children for a session in this unique, two-week camping experience starting Dec. 4. Each year Summerfest Camp, which is sponsored by Epilepsy Ontario, has an average of 20 to 40 children and youths who have epilepsy attend…