Deron Hamel Epilepsy Ottawa is working to strengthen the agency to enhance its sustainability to better serve the thousands of people living with a seizure disorder in the Ottawa region and their families. Diversifying the agency’s funding model, building upon strengths in its volunteer program and supporting ongoing initiatives are some of the ways Epilepsy…
By Deron Hamel Epilepsy Ontario is embarking on an outreach strategy with first responders to build relationships between epilepsy support agencies and police, firefighters and paramedic teams to create training opportunities and encourage appropriate responses to people who may have had a seizure. The first step in this process is gathering people’s stories – both…
By Deron Hamel Tina Smith has seen the negative impact seizure medication shortages have on people living with epilepsy and their families – she and her son, Nicholas, have lived through it more than once. Fifteen-year-old Nicholas had his first tonic-clonic seizure at seven. In 2009, Nicholas was diagnosed with epilepsy. During the next several…
By Deron Hamel The scene is a play rehearsal. Two high-school students, a boy and a girl, are practising their parts. Suddenly, the girl pauses. She stares blankly, appearing lost in her thoughts. Several seconds pass. She then she resumes speaking, as though nothing has happened. One of the students asks another if a teacher…
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