Dean joined Muscular Dystrophy UK in January 2014.
Before this he worked with Action Duchenne for five years; organising lobbies, conferences and numerous fundraising events, as well as supporting families affected by Duchenne and Becker muscular dystrophy. He is looking forward to continuing this work at Muscular Dystrophy UK.
Dean has a 18 year old son with Duchenne muscular dystrophy and understands the importance of ensuring everyone affected by a muscle-wasting condition receives the best possible care and support to lead independent fulfilling lives.
Get in touch with Dean:
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Contact: 01738 637458 / email@example.com
Contact name: Jim O’Hagan
Contact name: Dean Widd
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