Welcome to DebRA

DebRA is the national charity working on behalf of people in the UK with the genetic skin blistering condition Epidermolysis Bullosa (EB).

This site is your first port of call for reliable information on EB whether you or your child has EB, you want to support the charity, or you simply want to find out more.

What is EB?

Epidermolysis Bullosa (EB) is a very rare genetic condition in which the skin and internal body linings blister at the slightest knock or rub.

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Latest News

EB News
DebRA to benefit from forthcoming “Dallaglio Cycle Slam”: 

Gold Bond Marathon runner hopes to raise £26,000 for DebRA!: 

I’m a celebrity come trade with me!: 

DebRA founder Phyllis Hilton dies: 

Amateur sailor, Della Parsons, sets sail around the world in aid of DebRA: 

 

Research

The funding of research into the cause and possible treatment of epidermolysis bullosa is one of DebRA UK's main activities.

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DebRA Events Diary

See a list of events that you could take part in and raise money for DebRA.

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Get Involved

See how you can get involved and raise money for DebRA.

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