• This is how life feels to people with EB

  • This is how life feels to people with EB

  • This is how life feels to people with EB

Welcome

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.

Medical Assistance Fund

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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

EB Ambassador Wish Campaign

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EB Ambassador Wish Campaign – Help our Butterfly Ambassadors Spread their Wings! We are highlighting DEBRA Canada Ambassadors to help spread awareness and educate Canadians to the daily struggles and amazing perseverance it... READ MORE

EB Awareness Social Media Campaign

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People with Epidermolysis Bullosa (commonly referred to as EB) are born with an extremely rare genetic condition making their skin as fragile as a butterfly’s wing. Those affected live with constant pain and... READ MORE