Charity registered in Scotland SC039654
DEBRA is the national charity that funds research and healthcare to support individuals and families affected by Epidermolysis Bullosa (EB) – a painful genetic skin blistering condition which, in the worst cases, can be fatal.
We have a vision of a world where no one suffers from the painful genetic skin blistering condition, EB.
DEBRA focuses its work in two areas:
We fund pioneering research to find effective treatments and, ultimately, a cure for EB.
We provide care and support to improve the quality of life for individuals and families living with EB.