Category Archive

Supporting Agencies (Canada & Ontario)

Unable to get clobazam? Work with your doctor, pharmacist

January 10, 2013

If people who take clobazam to control their seizure disorder are unable to obtain the medication, they need to be working with their doctor and pharmacist to develop an alternative drug-therapy program. This is the message Karen Sullivan, Shoppers Drug Mart’s director of pharmacy professional affairs for Western Canada, recently shared with the Voices of…

Conference an opportunity to share Cdn survey findings, learn about latest research

January 3, 2013

Epilepsy information specialist Suzanne Nurse says attending a recent U.S. conference was an opportunity to share a Canadian survey’s findings with colleagues across North America, as well as a chance to learn about new epilepsy research developments that will help her better serve Epilepsy Ontario’s stakeholders. Nurse attended the American Epilepsy Society’s (AES) 2012 meeting,…

2012 a successful year for epilepsy advocacy

December 20, 2012

  The announcement of a proposed provincial epilepsy strategy, funding for epilepsy research and bringing in an epilepsy information specialist are some of the major successes Epilepsy Ontario saw in 2012, says Epilepsy Ontario executive director Rozalyn Werner-Arcé. Perhaps the biggest news impacting Ontario’s epilepsy community in 2012 was the announcement of a proposed provincial…

Epilepsy Ontario donations are gifts that keep on giving

December 13, 2012

Are you struggling for gift ideas this holiday season? Don’t know what to get for those hard-to-buy-for family members and friends? If so, consider making a donation in a loved one’s name to help provide supports for people living with epilepsy, a neurological disorder affecting one in 100 Canadians. Why is donating to Epilepsy Ontario…