Category Archive

Diagnosing 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…

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…

Pharmaceutical companies need to explain why drug shortages occur in order to prevent them

February 4, 2016

By Deron Hamel Stakeholders would be better positioned to offer solutions to prevent medication shortages if pharmaceutical companies provided public explanations about why shortages happen, says Suzanne Nurse, Epilepsy Ontario’s director of information and client services. Following public consultation in 2014, the Canadian government announced it would be mandating the country’s pharmaceutical manufacturers to publicly…

Video examines dos and don’ts surrounding tonic-clonic seizures

January 28, 2016

By Deron Hamel When it comes to epileptic seizures, it’s safe to say tonic-clonic seizures are the most recognized – and misunderstood – variety. A new video on Epilepsy Ontario’s website provides insight into what tonic-clonic seizures are, what to do if you see someone having this type of seizure and what not to do.…