DYSTROPHIC EPIDERMOLYSIS BULLOSA RESEARCH ASSOCIATION OF CANADA (DEBRA CANADA)
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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OAKVILLE
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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DEBRA is an Australian charity that supports individuals, families & carers affected by Epidermolysis Bullosa (EB), a rare genetic condition which causes the skin to blister at the slightest friction or even spontaneously.
Epidermolysis Bullosa is a protein deficiency that effects the skin and has a domino effect the rest .
“Nossa missão é aliviar o sofrimento das crianças brasileiras com epidermólise bolhosa, aumentando sua qualidade de vida e a daqueles com quem convivem".
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