DEBRA International is a worldwide network of national groups working on behalf of those affected by the genetic skin blistering condition, Epidermolysis Bullosa (EB).

On our site you will find information about the condition EB, appropriate medical care, research into EB and living with EB as well as links to the national DEBRA groups around the world.

Our Vision is to ensure that people living with EB have access to the best quality support and medical care, whilst driving the development of effective treatments and cures for EB.

DEBRA International documents including patient information booklets (in several languages) and updates on research