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Make a donation and help fund research for a cure. Current therapy is directed toward the prevention of skin trauma, prevention of infection, and the treatment of complications. Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america.
Get to know the dedicated team behind debra of america, working tirelessly to support individuals and families affected by epidermolysis bullosa (eb). At present, there is no specific treatment for eb For more information or if you have any questions, feel free to contact us at
Its mission is to help patients, families, and doctors in countries where there is no debra structure to support them and to assist new groups to form and develop.
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Learn about debra of america's team working to raise eb awareness, and provide eb support to patients and families affected by epidermolysis bullosa (eb). Please contact debra of america's national office with further questions or concerns
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