By Deron Hamel It wasn’t long after Sarah Hysenaj had her first seizure that she became an epilepsy awareness advocate. Sarah was 11 years old and on a school field trip when she had her first seizure in front of her classmates. Fortunately for Sarah, her teacher knew exactly what was happening and what to…
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…
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