Participants of Epilepsy Action Day at Queen’s Park Address Issues Facing Ontario’s Epilepsy Community

TORONTO, March 2 /CNW/ – Today, epilepsy organizations across Ontario, led by Epilepsy Ontario and Epilepsy Cure Initiative, launched Epilepsy Awareness Month by hosting Epilepsy Action Day at Queen’s Park. Members from the epilepsy community met with MPPs to discuss key challenges facing the 140,000 Ontarians living with the disorder.

“Today’s activities provided a rare opportunity for us to raise awareness with government about the issues within the epilepsy community,” said Dr. Mac
Burnham, board member, Epilepsy Ontario and director, University of Toronto Epilepsy Research Program. “Our meetings with government representatives highlighted the need for research, standards of care and disability support, and ultimately, our request for an action plan to address these issues.”

Epilepsy, the second most common neurological condition after headache, is a seizure disorder caused by sudden bursts of electrical energy in a person’s brain. Up to one-third of people living with epilepsy do not have seizure control, severely impacting their independence, productivity and overall quality of life. The disorder can cause significant challenges, including difficulty finding employment, loss of driving privileges, cognitive decline and memory impairment and higher mortality rates. People living with epilepsy also live with a significant social stigma associated with seizures.

“Like others with disabilities, people with epilepsy often face barriers to their basic human rights and freedoms,” said Margaret Maye, president, Epilepsy Cure Initiative. “Through advocacy efforts, such as Epilepsy Action Day, we strive to invoke change at the governmental, legal, social, economic and institutional levels.”

Epilepsy Action Day will culminate in a reception at Queen’s Park, featuring remarks by Christine Crosbie, a Torontonian living with epilepsy.

“I am pleased to be able to share my personal story to help bring awareness and understanding to the Ontario government, and advocate for those who feel epilepsy is being kept in the shadows,” said Christine Crosbie. “By addressing the gap in support and raising awareness, we can better assist epilepsy patients and their families in their efforts to live well with this disorder.”

About Epilepsy Ontario

Epilepsy Ontario (EO) is a registered charitable non-profit non-governmental health organization dedicated to promoting independence and optimal quality of life for children and adults living with seizure disorders, by promoting information, awareness, support services, advocacy, education and research. Through a network of local agencies, contacts and associates, Epilepsy Ontario provides client services, counselling, information and referral services, education and advocacy services for children and adults living with seizure disorders, and for their families, friends, co-workers and caregivers.

EO offers long-term programmes to raise standards of care and support medical research into seizure disorders. EO hopes to improve public awareness and education through the Provincial Resource Centre, publications, the EO web site, conferences, and outreach programs.

About Epilepsy Cure Initiative

Epilepsy Cure Initiative (ECI) is a not for profit incorporated organization founded by parents of a child with uncontrolled seizures, inspired by life
experiences and fuelled by a burning desire to make a positive difference for people with epilepsy here and now. ECI is dedicated to creating awareness
and understanding of epilepsy to bring an end to myths, misconceptions and fear of both seizures and the disorder, as well as to discrimination against
people with epilepsy. ECI is also committed to promoting medical dietary therapies, supporting epilepsy research and informing the public about the urgent need for increased efforts in epilepsy research to advance new treatments that offer better seizure control and fewer side effects. As well ECI is advocating for a more effective and improved formalized epilepsy care system being brought to Canada.


For more information and to schedule an interview please contact:

Dita Kuhtey      
Cohn & Wolfe      
Nic Canning
Cohn & Wolfe

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