By Deron Hamel Canadian children living with epilepsy say it’s their need for social and emotional support from friends and family – not their seizures – that concerns them most about their quality of life. This is the main finding from a recent study that surveyed 480 children aged eight to 14 who are living…
By Lisa Bailey With involvement at the local, provincial and national level of epilepsy agencies, Paul Raymond has gained new perspective on the realities and challenges for people living with the seizure disorder. Now, as Epilepsy Ontario’s new executive director, he’s energized by the prospect of helping to change the landscape and enhance the lives…
By Deron Hamel Parents of children attending Summerfest Camp say the annual camping experience enhances independence, builds self-confidence and drives personal development. Speaking with Voices of Epilepsy in 2014, Philippa Howell recalled how she had concerns when her daughter, Georgina, went to her first Summerfest Camp in 2010. Georgina, then eight, had never been away…
By Deron Hamel The third phase of a study examining the impact of cannabidiol (CBD) on people living with severe, drug-resistant forms of epilepsy will paint a clearer picture as to whether or not the cannabis extract has any side effects, says epilepsy researcher Dr. McIntyre Burnham. Phase 2 of the multi-centre study, which was…
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