Our Mission Statement
For people whose skin doesn’t work – we do.
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.
Find out how you can donate below.
Donate to #FightEB
Could pay for healthcare for a week for an EB person, helping to reduce pain
Could pay for a pair of gloves to protect the wounds of someone with EB when playing
Could provide a counselling session for someone with EB struggling with mental health
Could pay for half an hour of vital EB research into reducing itch
“The worst part of my day is having my dressings changed, but I'm a fighter. I've got so much to be happy for, I won't let EB beat me.” - Mason.
We need you to join the #FightEB movement and help raise £482,639 to alleviate the debilitating symptoms of pain, itch, open wounds and mental health difficulties for those living with EB as we drive towards a cure.