DEBRA UK (Dystrophic Epidermolysis Bullosa Research Association)
Long-term Conditions · Charity · National service
DEBRA UK supports people with the rare skin condition Epidermolysis Bullosa via a community support team, grants and free membership.
DEBRA UK is the national charity for people living with Epidermolysis Bullosa (EB), a rare and painful genetic skin condition. Its Community Support Team (01344 771961, Mon-Fri 9am-5pm) provides free information, practical, financial and emotional support, advocacy and grants. Free membership gives access to events, discounted respite breaks and an online support community. DEBRA also funds EB research and supports specialist NHS centres. Membership queries: membership@debra.org.uk.
Contact
Phone: 01344 771961
Website: https://www.debra.org.uk/
Email: debra@debra.org.uk
Address: The Capitol Building, Oldbury, Bracknell, Berkshire, RG12 8FZ
Opening hours: Mon-Fri 9am-5pm
Who it's for
Who they help: EB patients of all ages, carers and families across the UK.
Eligibility: People living with Epidermolysis Bullosa and their families.
Not suitable for: Specialist support focused on people affected by Epidermolysis Bullosa.
Information last verified June 2026. Printed from https://www.socialprescriber.co.uk/charities/debra-uk