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debra 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 fund research for a cure
DEBRA International | debra of America 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)
Understanding Epidermolysis Bullosa (EB) | debra of America For more information or if you have any questions, feel free to contact us at: Email: staff@debra org Phone: 833-debraUS (833-332-7287) Our team is here to support you with any questions or concerns regarding EB diagnosis, treatment, and ongoing care
What We Do - debra of America 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 Learn more about our work
Donate to Epidermolysis Bullosa Research Support - DEBRA When there seems to be no way out, there's debra of America, a lifeline for thousands of families living with “The Worst Disease You’ve Never Heard Of,” Epidermolysis Bullosa (EB)
EB Doctor Directory | debra of America Please complete our Participant Request Form below and we will respond shortly For additional questions, email programs@debra org or call 833-DEBRAUS (833-332-7287), ext 104
Dystrophic EB | debra of America No one should face Dystrophic EB alone debra of America offers free programs, personalized support, and trusted online resources to help individuals and families navigate life with EB