02. Exploring Black British women’s experiences of skin conditions and appearance adjustment

Researchers at Cardiff University would like to interview women who are at least 18 years old, live in the UK, self-identify as Black Caribbean/African or Mixed heritage and have a skin condition that they are willing to discuss.

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Participant information sheet and registration

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DEBRA UK attends Liberal Democrats Autumn Conference in Brighton

Earlier this week we exhibited at the Liberal Democrats Autumn Conference in Brighton. During the two days we were there we engaged with several MPs and members of the party whom we will follow up with to request their support.
06. The Beacon Patient Pairing Scheme 4th September – 30th October 2024
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DEBRA UK supporters, Paul Glover and Martyn Rowley, raise £115,000 for families living with EB

On Tuesday 3rd September, dedicated DEBRA UK supporters Paul Glover and Martyn Rowley were welcomed to DEBRA UK's head office to celebrate their outstanding achievement of raising £115,000 in 2024 to support those living with EB.

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Find a store

Find your nearest DEBRA charity shop and help fight EB. Our stores sell affordable and quality pre-loved clothing, furniture, electrical items, books, homeware and more.
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Donate your unwanted furniture, homewares and electrical items using our free furniture collection service. With safety measures in place, donating your items couldn’t be easier.
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Find out what health and safety standards and labels we require and which items we cannot sell.
What is EB?

Epidermolysis bullosa (EB) is a painful genetic skin blistering condition with no cure. Find out about different types of EB, causes, symptoms and treatments.
Graeme Souness swimming the English Channel to raise £1.1m to stop the pain of EB

Graeme Souness, ex-international footballer, manager, and pundit, is swimming the English Channel this June to raise £1.1m to stop the pain of epidermolysis bullosa (EB).
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If you or a family member live with EB, are a carer or someone who works with people affected by EB, then you can become a DEBRA member. Find out how.
Isla's Story

We’re a normal family. Our children, Isla and Emily, go to school, have their friends round and like to play on the trampoline. But when one of your children has EB, you have to redefine normal.

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