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Robert Meadowcroft - Chief ExecutiveRobert Meadowcroft, Chief Executive

Robert leads Muscular Dystrophy UK’s core campaigns and our work to improve access to treatment for rare diseases. He is available to discuss and comment on all aspects of the charity’s work and issues affecting people with muscle-wasting conditions and other rare diseases.

Dr Marita Pohlschmidt, Director of Research

Marita specialises in [neuromuscular genetics] and oversees Muscular Dystrophy UK’s wide-reaching and ambitious research programme. Marita is available to discuss and comment on research funded by the charity and other studies that could benefit people affected by muscle-wasting conditions.

Nic Bungay, Director of Campaigns, Care and Information

Nic oversees Muscular Dystrophy UK’s campaign work in the four UK Parliaments, our information and support team, advocacy service and work with the NHS to improve expert care for muscle-wasting conditions. He is available to discuss and comment on key charity reports, muscle-wasting conditions and health and social care issues affecting people living with rare diseases.

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