DEBRA is a UK national medical research charity and patient support organisation for people living with the rare, extremely painful, genetic skin blistering condition, epidermolysis bullosa …

DEBRA UK partners with the NHS to deliver an enhanced EB healthcare service which is vital for people living with all types of EB as it aims to reduce the risk of further skin damage and …

DEBRA UK exists to provide community care and support services to improve quality of life for people living with all types of inherited and acquired EB. We also fund pioneering research to …

Shop with DEBRA online or in one of our charity shops, and experience excellent customer service, discover quality pre-loved items and know you are supporting people living with EB. …

We are the UK's EB patient support organisation with almost 4,000 members. Every year, over 1,000 of our members access our support services.

We are the UK's EB patient support organisation with almost 4,000 members. Every year, over 1,000 of our members access our support services.

DEBRA UK is the largest UK funder of epidermolysis bullosa (EB) research. We have invested over £22m and have been responsible, through funding pioneering research and working …

DEBRA UK is the largest UK funder of Epidermolysis Bullosa (EB) research. We have invested over £22m and have been responsible, through funding pioneering research and working …

We are the national charity for people with epidermolysis bullosa (EB) in the UK. Become a member and access our services and benefits.

Shop with DEBRA online or in one of our charity shops, and experience excellent customer service, discover quality pre-loved items and know you are supporting people living with EB. …