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, …

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).

Learn More debra Care Conference This multi-day biennial conference is designed specifically for EB families and the professional community to access the best information, discover new ideas, and …

Epidermolysis Bullosa (EB) is a group of rare genetic disorders that cause the skin and mucous membranes to be extremely fragile. Even minor friction, heat, or trauma can result in painful blisters …

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).

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.

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.

Dystrophic Epidermolysis Bullosa Research Association of America (debra of America) es a la unica organización nacional sin fines de lucro dedicada a promover la investigación para encontrar nuevos …