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Get to know the dedicated team behind debra of america, working tirelessly to support individuals and families affected by epidermolysis bullosa (eb). Learn about debra of americas team working to raise eb awareness, and provide eb support to patients and families affected by epidermolysis bullosa (eb). Debra of america is a non-profit organization providing free programs & eb support services to those living with epidermolysis bullosa. Make a donation to debra of america and support our mission to improve the lives of those with epidermolysis bullosa (eb). Debra of america is part of debra international, a worldwide network of national groups working on behalf of all people living with epidermolysis bullosa (eb). Founded in 1980, debra of america is dedicated to improving the quality of life of all people impacted by epidermolysis bullosa (eb) in the u. s. Explore our mentorship programs, eb nurse educator program, new family advocate program, debra care conference & additional support services. Staff@debra. org phone: Please complete our participant request form below and we will respond shortly. For more information or if you have any questions, feel free to contact us at: 833-debraus (833-332-7287) our team is here to support you with any questions or … Make a donation and help fund research for a cure. Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america. For additional questions, email programs@debra. org or call 833-debraus (833-332-7287), ext. Learn more about our work.
