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.
MDUK comment on new Government stats on disabled employment
MDUK president awarded MBE
An update on Zolgensma for SMA
The evening of comedy with Jon Richardson of 8 out of 10 Cats.
24 January 2020
26 January 2020
7 February 2020