Category Archive

Voices of Epilepsy

Epilepsy Ottawa investing in the future to better serve its community

March 10, 2016

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…

People encouraged to share experiences with first responders after a seizure

March 3, 2016

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…

9-year-old Miah Wheadon getting ready to raise epilepsy awareness ahead of Purple Day

February 25, 2016

By Deron Hamel Purple Day is just around the corner, and one nine-year-old girl and her mother in a small northern Ontario community are gearing up for their annual drive to raise epilepsy awareness. For the past few years, Grade 4 student Miah Wheadon and her mother, Gina, have approached local businesses in Manitouwadge, Ont.…

Seizure medication shortages create anxiety and stress for families

February 18, 2016

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…