We are DEBRA. We were established in 1978 by Phyllis Hilton, whose daughter Debra had epidermolysis bullosa (EB), as the world’s first EB patient support organisation. Today we are national charity that supports over 4k members, which includes people living with all forms of EB, their families, and carers, plus healthcare professionals and researchers who work with EB. We are also one of the world’s largest investors into EB research. We employ over 300 colleagues and can count on the support of over 1200 volunteers who support us across our network of charity shops located throughout England and Scotland. Will you join us on our journey to a world where no one suffers with EB?

Our mission

is a world where no one suffers with epidermolysis bullosa

Our vision

is that we live in a world where no one suffers with epidermolysis bullosa (EB) and we provide life-long care, while seeking cures, for all those affected/impacted by living with EB.

Our values

Our values are based around care, inclusivity, and making a difference. These values are the foundation of our culture are help make DEBRA a great place to work

Rewards & benefits

We offer a competitive salary, along with rewards & benefits which include

Auto Enrolment Pension with DEBRA contribution

Life Assurance Scheme

Employee Assistance Program

Personalised Recognition Awards

Opportunities for Apprenticeships and Internships

Testimonials