When a 20-year-old man living with complex seizure disorder was recently denied funding for new medication from the Ministry of Health and Long-Term Care’s Exceptional Access Program (EAP), after having a severe reaction to EAP-approved medication, he and his family lodged a complaint with Ontario’s ombudsman’s office. Once investigated by the ombudsman, it was discovered…
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.…
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…
While a provincial epilepsy strategy would help people affected by the neurological disorder access services in a timely manner, it would be especially beneficial to people living in northwestern Ontario, who often must travel long distances to receive treatment, says Trevor Lewis. Lewis and his 18-year-old daughter Katie live in Thunder Bay. They are both…
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