debra of America is a national nonprofit organization dedicated to improving the lives of those impacted by Epidermolysis Bullosa (EB). We integrate direct-to-patient programs and services, education, …

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). Our collective vision is to ensure that …

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

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.

Get free wound care supplies through debra of America's Wound Care Distribution Program, providing support for those with Epidermolysis Bullosa (EB).

DEBRA International’s Emergency Management Steps for EB This reference provides information regarding EB skin care management as well as the most common EB related prompts for seeking …

Support Resources No one should face Epidermolysis Bullosa Simplex alone. debra of America offers free programs, personalized support, and trusted online resources to help individuals and families …

Junctional Epidermolysis Bullosa (JEB) is a rare and often severe form of EB caused by mutations in genes that affect the anchoring of the outer layer of skin (epidermis) to the underlying layer (dermis). …

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.