DEBRA

We provide care and support to individuals and families affected by EB

Your support can change lives

£15

buys a special needs feeder system for babies who have blistered mouths

£50

could fund an additional home visit by the EB team

£168

could pay for one hour of research to bring us closer to a cure

£5

monthly

buys a special toothbrush which makes a real difference to delicate gums

£10

monthly

buys a pair of specialist socks that promote comfort and reduce blistering

£15

monthly

buys a special needs feeder system for babies who have blistered mouths

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Charity Registration No. 1084958

www.debra.org.uk

fundraising@debra.org.uk

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About us

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. We fund pioneering research and provide care and support to individuals and families living with EB.

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