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debra of America is a non-profit organization providing free programs & EB support services to those living with Epidermolysis Bullosa. Make a donation and help nd 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. Get to know the dedicated team behind debra of America, working tirelessly to support individuals and families affected by Epidermolysis Bullosa (EB). Its mission is to help patients, families, and doctors in countries where there is no DEBRA structure to support them and to ist new groups to form and develop. Explore our Mentorship programs, EB Nurse Educator Program, New Family Advocate Program,
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