Debra International is a global organization dedicated to supporting individuals affected by Epidermolysis Bullosa (EB), a rare genetic skin condition. The organization focuses on raising awareness, providing education, and funding research to improve the quality of life for those living with EB. Founded in 2008, Debra International connects various national EB organizations to share resources and best practices. It aims to create a united front in advocating for better treatments and support systems for patients and their families worldwide.