Our members Member directory DEBRA For people whose skin doesn't work - we do. DEBRA is the national charity that supports individuals and families affected by Epidermolysis Bullosa (EB) - a painful genetic skin blistering condition which, in the worst cases, can be fatal. DEBRA was founded in 1978 by Phyllis Hilton whose daughter Debra had EB – the charity was the world's first EB patient support group. Our vision: We have a vision of a world where no one suffers from the painful genetic skin blistering condition, EB. www.debra.org.uk Twitter: @charityDEBRA Primary research areas Cancer, Child health, Infection, Inflammatory and immune system, Neurological, Skin Grant types Clinical trial, Fellowship, Equipment, Programme (typically >4 years), Project (typically <4 years)