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:
Family funds are a great way for families to fundraise for Muscular Dystrophy UK to keep our vital research moving forward. Family funds in this area are:
Branches and Committees:
Contact name: Marie Kobine
Contact: 01738 637458 / firstname.lastname@example.org
Contact name: Jim O’Hagan
Contact name: Dean Widd
Contact: 01786 812288 / email@example.com
Contact name: Dr Sheonad MacFarlaneContact: firstname.lastname@example.org
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