DEBRA UK
Mike Jaega serves as Chairman of the Board of Trustees at DEBRA UK since May 2013, also holding multiple committee positions related to governance, finance, and charitable activities within the organization, which supports research and advocacy for Epidermolysis Bullosa. Additionally, Mike is the President of DEBRA International, contributing to a global network dedicated to those affected by this genetic skin condition. Previous experience includes roles at the British Association of Dermatologists, CliniSupplies, and Halton Disability Partnership, focusing on research support, patient representation, and providing advice to disabled clients. Mike holds a Diploma in Counselling from Liverpool Community College.
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DEBRA UK
DEBRA is the national charity and patient support group for people living with the extremely painful, genetic skin blistering condition, epidermolysis bullosa (EB). Please help us #StopThePain of EB.