A grassroots group of parents of children living with Dravet syndrome is working to form a Canadian branch of Dravet.org, a U.S.-based global collaboration of parents and medical experts dedicated to improving treatments for children with Dravet syndrome spectrum disorders and empowering families to cope with challenges. The parents, most of whom live in the…
Andreea-Oxana Kilin is trying to establish a service in the Ottawa region that would see her and a group of volunteers engage children living with epilepsy through a variety of outings and activities specially suited to meet the needs of those affected by the neurological disorder. Kilin, 29, has had epilepsy since she was 18.…
Trevor Lewis says he hopes the upcoming Run for Epilepsy he and his daughter, Katie, are organizing will help raise awareness about epilepsy in the community and possibly act as a catalyst for establishing an epilepsy agency in his hometown of Thunder Bay. Trevor notes that there’s a great need for more available resources for…
Gerry Cockburn says one of the greatest possibilities that could stem from a provincial epilepsy strategy would be a stronger sense of community created amongst people living with epilepsy and medical professionals who treat the neurological disorder. Cockburn, a 55-year-old retired educator, has had epilepsy since he was 10. He says one of the things…
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