DEBRA Canada knows that we all want to give our loved ones the very best of care. The costs associated with Epidermolysis Bullosa can be challenging at times, and the health insurance in our... READ MORE
DEBRA Canada is a voluntary, registered, non-profit organization dedicated to providing support for families affected by Epidermolysis Bullosa (EB) and to increasing Canadians’ awareness of this challenging disease.
Thank you for visiting the DEBRA Canada website. Here you will find information on Epidermolysis Bullosa
– the most painful condition you’ve never heard of.
A Special Thank You to All Who Supported & Attended the 4th Annual Bella’s Ball Charity Open The 4th Annual Bella’s Ball Broomball Charity Open took place on Friday, February 19, 2016 and... READ MORE
Support DEBRA Canada by participating /or supporting the Ottawa Tamarack Ottawa Race Weekend taking place May 28-29, 2016 READ MORE
Calling all EB Wishes! Do you have a special wish that you would like to come true with the help of DEBRA Canada and our supporters? READ MORE
We are happy to report that on April 13, 2015 our DEBRA Canada President Tina Boileau and her son Jonathan Pitre were featured in an amazing news feature entitled “The Butterfly Child – an... READ MORE