Category Archive

Epilepsy Ontario

Pharma companies will be federally mandated to report drug shortages

February 12, 2015

The federal government announced Feb. 10 that Canadian pharmaceutical companies must post all actual and anticipated medication shortages in coming months, a move that is welcomed by the epilepsy advocacy community. Drug shortages have affected the epilepsy community in recent years. In January 2013, it was announced that clobazam, an anticonvulsant medication, was in short…

Neurosurgery gives Cathleen Townsend’s life a ‘360-degree change’

January 29, 2015

One year ago at this time, Cathleen Townsend was having up to 15 seizures per day. Then she had life-changing surgery last April. She’s not had a seizure since. The Casselman, Ont. resident says her life has had a “360-degree change” in the past nine months. Being seizure-free has allowed her to go back to…

Sharing your story about epilepsy can make a difference

January 22, 2015

One of the great things about having the Voices of Epilepsy news program is that Epilepsy Ontario can help people share their inspirational stories about how they’ve conquered their condition and, in some cases, foster positive change. The news program has even demonstrated lifesaving ability. In January 2013, it was announced there was a shortage…

Weekend exhibit will raise awareness of epilepsy and brain research

January 14, 2015

Epilepsy Ontario, Epilepsy Toronto and Epilepsy Durham Region are collaborating this weekend to bring an interactive display about epilepsy to BRAINFest, a family-friendly celebration of brain research at Toronto’s Ontario Science Centre. BRAINFest will also provide an understanding of how people in different aspects of brain-health research are aligning their efforts to raise awareness and…