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.

Explore our Mentorship programs, EB Nurse Educator Program, New Family Advocate Program, debra Care Conference & additional support services.

Get to know the dedicated team behind debra of America, working tirelessly to support individuals and families affected by Epidermolysis Bullosa (EB).

Learn about Epidermolysis Bullosa (EB), a rare genetic disorder, its symptoms, treatments, and personal stories from the EB community at 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).

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.

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.

Make a donation to debra of America and support our mission to improve the lives of those with Epidermolysis Bullosa (EB). Employer matching. Tax-deductible.

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).

DEBRA Chile publicó recientemente un manual en español sobre el tratamiento de los pacientes con EB para ayudar a los pacientes que hablan español y sus familias, cuidadores y …