We are here for you, and your child, at the point of diagnosis and at every stage thereafter, and can:
- give you accurate and up-to-date information about Duchenne muscular dystrophy, and keep you updated about progress in research
- give you tips and advice about day-to-day life, written by people who know exactly what it’s like to live with Duchenne muscular dystrophy
- put you in touch with other families living with Duchenne muscular dystrophy, who can share their experiences with you tell you about – and help you get – the services, equipment and support you’re entitled to.
Muscular Dystrophy UK’s Trailblazers worked with Heid
NHS long term plan published
Four UK sites are expected to open in the next few months
One man's inspirational fundraising challenge