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Total raised so far

22%

£1,080,346.00 of £5,000,000 target +£1,104.00 Gift Aid See breakdown

Recent donations

2 hours ago

Anonymous

£10.00 + £2.50 Gift Aid

15 hours ago

Emma Sawyer

£5.00 + £1.25 Gift Aid

yesterday

DIANNE

£5.00 + £1.25 Gift Aid

hope this helps

yesterday

Debz

£10.00

yesterday

Anonymous

£10.00 + £2.50 Gift Aid

yesterday

Anonymous

£50.00 + £12.50 Gift Aid

yesterday

katie marsh

£10.00

2 days ago

Anonymous

£10.00 + £2.50 Gift Aid

3 days ago

Suzanne Anderson

£5.00

About us

DEBRA is the national charity supporting those directly affected by, and working with, Epidermolysis Bullosa (EB), a potentially fatal skin condition that causes constant pain due to unstoppable internal and external blistering. DEBRA provides lifelong care and support to the entire EB Community. Visit www.DEBRA.org.uk or call 01344 771961 to learn more.

Charity number: 1084958

A Life Free of Pain

A life free of pain is what we all want. Unfortunately for people living with EB, excruciating pain is something they must live with, every day.

EB is an incredibly painful genetic skin blistering condition. It causes the skin to blister and tear at the slightest touch. With skin as fragile as a butterfly’s wings, it’s often referred to as ‘Butterfly Skin’. EB can affect the hands and feet only or in the most severe cases any part of the body, including blistering on the eyes and internal organs. People living with EB live in constant debilitating pain and in severe cases it can be fatal.

There is hope though.

There are drugs already available within the NHS to treat other inflammatory skin conditions such as Psoriasis and Atopic Dermatitis which could significantly improve blistering and overall quality of life for people living with EB.

With your help we can test these drugs, with your help we can find treatments that will enable people to live free from the pain of EB.

Thank you.


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