By Deron Hamel The mother of a St. Thomas, Ont. woman with complex-partial seizures is hoping the availability of cannabidiol (CBD), an extract of the cannabis plant, will enhance her daughter’s quality of life. However, Carol Clarke says there needs to be more information available about proper CBD dosages as well as support for people…
By Deron Hamel The Supreme Court of Canada’s landmark decision to legalize all forms of consumption of medicinal marijuana means Mandy McKnight no longer has to break the law in order to stop her young son’s seizures. Mandy’s seven-year-old son, Liam, has Dravet syndrome, a severe form of epilepsy with frequent, prolonged, drug-resistant seizures. He…
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 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…
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