important notice
Please note that our office remains physically closed.
The best way to reach us is by email at info@epilepsyyork.org.
You can also contact us by calling
905-640-8000 and leaving a message.
Phone messages are picked up daily and calls will be returned within 48 hours.
we are looking for new board members!
EYR is in need of individuals to join our Board of Directors who are looking to give back to our community in a meaningful way.
Our Board of Directors are a group of volunteers who currently meet one evening a month (virtually) to evaluate, develop, and make decisions on current programming and initiatives while supporting the growth of our organization. Attendance to various events (such as community awareness, support programming, and fundraising) are always welcome!
Additional information and/or interested applicants are to send questions/a resume to Claudia Cozza, ccozza@epilepsyyork.org.
Take A Chance for Epilepsy 50/50 Raffle
2nd Annual Glimmer of Hope Golf Tournament
2nd Annual Glimmer of Hope Golf Tournament
Tickets are 3 for $5
10 for $10 or 60 for $20.00
Grand Prize Draw date: January 31
2nd Annual Glimmer of Hope Golf Tournament
2nd Annual Glimmer of Hope Golf Tournament
2nd Annual Glimmer of Hope Golf Tournament
Thank you to everyone who volunteered and/or participated!
Learn about the people in our community!
2nd Annual Glimmer of Hope Golf Tournament
Learn about the people in our community!
Read stories from members of the EYR community.
Sign the letter: tell the Minister of Health to fund Community Epilepsy Programs.
Community Epilepsy Agencies provide health education programs for people with seizures that improve quality of life and reduce pressure on hospitals. Mental health programs support people living with epilepsy who are also facing issues like depression. The Ministry of Health needs to help fund these programs!
Sign your name to Epilepsy Ontario's letter to the Minister of Health
here!
Donate to Our Cause!
Your donation will help us provide services, advocacy and assistance to those living with epilepsy and their families.
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