DonateWith help from supporters like you, Debra of America continues to provide programs and services to people with Epidermolysis Bullosa and their families, and to support EB research.
|The mounting cost of bandages is most often not covered by an EB family's health insurance.||86.4¢ of every dollar donated goes directly to EB patients, families, and research.|
Founded over 30 years ago, debra of America is the only national, non-profit organization that provides direct services for children and families affected by EB. As part of an international network, Debra is a leading force behind EB research and care methods. Debra is dedicated to finding a cure for EB and to providing medical, emotional and financial support for families struggling with the day to day hardships of living with this disease.
Connect With Others
By connecting with others who's lives have been affected by EB you have the opportunity to gain strength, become better informed and offer much needed support to others who's lives are similarly affected. Debra offers many opportunities for families to connect with each other as well as with medical professionals, researchers and other health care providers in both formal and informal settings. Together we can conquer this disease.
Special events help raise needed funds for care and support of families affected by EB. To plan an event,inquire about an upcoming event or purchase tickets for an event, visit the Plan A Supporter Led Event page.
View Supporter Led Events View Debra Hosted Events