TIPS FOR RENEWING OR FILLING YOUR PRESCRIPTIONS
EPILEPSY MEDICATIONS Many people are concerned about the possibility of drug shortages as we move...
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Donate Now
The Canadian Epilepsy Alliance is the national voice for people with epilepsy and is comprised of...
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Seizure detection through wearables: Your opinion matters!
We invite you to share your expectations and opinions regarding seizure detection systems in order...
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We need your voice to shape the future of epilepsy research
The Ontario Brain Institute’s (OBI) epilepsy research program (EpLink) is looking to better...
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Saved by a Snow Day
Everyone who has Epilepsy will have at least one seizure story that they can tell you changed...
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Canadian Epilepsy Alliance Statement on Ken Jeong’s Netflix Comedy Special
CANADIAN EPILEPSY ALLIANCE Statement on Ken Jeong’s Netflix Comedy Special Deirdre Floyd,...
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My anxiety held me hostage in my bedroom
As President of the Canadian Epilepsy Alliance , I want to introduce you to Christine Jameison...
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ILAE 2017 — New Classification OF SEIZURE TYPES
The International League Against Epilepsy (ILAE) is a scientific organization devoted to improving...
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Celebrating 20 years of support to people with epilepsy in Canada
My name is Deirdre Floyd, and I am President of the Canadian Epilepsy Alliance. My epilepsy was...
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Letter to Netflix
August 29, 2018 Reed Hastings CEO, Netflix Netflix, Inc. 100 Winchester Circle Los Gatos, CA...
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Statement on Netflix’s Film ‘The After Party’
August 28, 2018 Netflix recently released a movie called The After Party. Deirdre Floyd,...
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Epilepsy Newfoundland and Labrador Member Lisa Pack Shares Her Epilepsy Story”
As President of the Canadian Epilepsy Alliance , I want to introduce you to Lisa Pack from...
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