DYSTROPHIC EPIDERMOLYSIS BULLOSA RESEARCH ASSOCIATION OF CANADA (DEBRA CANADA)

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Creating awareness about EB & support for families and people suffering from EB. DEBRA Canada is a voluntary, registered charitable organization dedicated to providing support for families affected by Epidermolysis Bullosa (EB) and to increasing Canadians' awareness of this challenging disease.

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868336751

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OAKVILLE

Address: 1500 UPPER MIDDLE ROAD UNIT 3, OAKVILLE, OAKVILLEWeb: Sign in to see organisation websiteFacebook: DEBRACanadaEBX (Twitter): DEBRACanadaICO: 868336751

DEBRA Canada Just added to your cart Become a Member Become an Ambassador Become a SupporterVolunteer DEBRA Butterfly Nike Ball Cap Get your DEBRA Butterfly Ball Cap CLICK HERE Understanding EB Epidermolysis Bullosa EB is the name for a group of painful genetic skin conditions that cause the skin to tear and blister at the slightest touch. The name comes fromepiderm the outer layer of skinlysis the breakdown of cells andbullosa blisters. People with EB have a faulty gene which means the skin cannot bind together so any trauma or friction can cause painful blisters which results in open wounds and scarring. It can also affect internal liningsmucous membranesand organs.

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Victor

2. What innovative fundraising strategies could DEBRA Canada implement to sustain its programs and support for individuals living with EB?

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Catherine

1. How can we effectively raise awareness about Epidermolysis Bullosa (EB) within local communities to ensure better understanding and support for affected families?

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George

Just ordered my DEBRA Butterfly Ball Cap! 🦋 Can't wait to wear it and show my support for all those living with Epidermolysis Bullosa. Every little bit helps! 💪✨

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Marcella

❤️ Grateful for DEBRA Canada and all the amazing work you do to support families affected by EB! Together, we can spread awareness and make a difference. Let's keep fighting! 🌟

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