Category Archive

Information

Epilepsy Action Day continues dialogue with gov’t on important issues

December 4, 2014

The fifth annual Epilepsy Action Day at Queen’s Park on Dec. 1 was successful in its mission of engaging MPPs in the important issues facing people with seizure disorders, says Epilepsy Ontario executive director Rozalyn Werner-Arcé. During the event there were three areas that representatives from Epilepsy Ontario and seven other epilepsy support agencies across…

The continuing success story of Kerry Jenkins

November 27, 2014

In January, Voices of Epilepsy spoke with 45-year-old Peterborough resident Kerry Jenkins, who had lived with epilepsy since age seven. She shared her story of how deep brain stimulation (DBS) surgery cut her seizures in half and eliminated her tonic-clonic seizures. The surgery continues to improve her quality of life. Today, Jenkins says that 75…

Researcher speaks about recent study on neurological conditions and their impact on Canadians

October 23, 2014

On Sept. 11, the results of a first-of-its-kind study examining the impact neurological conditions like epilepsy have on affected people, their families and the greater health-care system, were released.According to the report, more than 3.6 million Canadians are affected by neurological conditions, including 50 per cent of those living in long-term care homes or receiving…

CLAE conference will bring to light latest discoveries in epilepsy research

October 16, 2014

The upcoming Canadian League Against Epilepsy (CLAE) conference will be an opportunity for attendees to learn about the latest discoveries in epilepsy research, says its main organizer. Neurologist Dr. Jorge Burneo, the CLAE’s director of education, says the conference is aimed at bringing together Canada’s epilepsy clinicians and researchers to share information and learn from…