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DEBRA is the national charity that supports individuals and families affected by Epidermolysis Bullosa (EB) - a rare genetic condition which causes the skin to blister and shear at the slightest friction or even spontaneously.

There are at least 5,000 people living with this devastating condition in the UK and 500,000 people worldwide. DEBRA provides expert nurses and social care staff to work with families and commissions world-leading research with the aim of finding effective treatments and, ultimately, a cure for EB.

DEBRA relies on the generosity of the public to carry out its vital work improving lives and giving hope.

Call: 01344 771961


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