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.

Email: [email protected] 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.

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

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

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

About debra of America We are dedicated to improving the lives of those impacted by EB, or what we call “The Worst Disease You’ve Never Heard Of.” We integrate direct-to-patient programs …

debra of America is here to guide you in making informed decisions surrounding proper EB care. How To: Care for Wounds Acute and chronic wounds may occur very frequently in individuals …

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).