Jeff has chopped off his lockdown locks for MDUK thanks to barbers King & Captain of Thirsk.
Joanne Ashton (pictured right) and her eleven-year-old son Liam live in Liverpool.
Being a Trailblazer offers not only an opportunity to share your experiences with others, but to challenge yourself to do something new.
Charcot Marie Tooth disease (CMT) is a group of genetic conditions affecting the peripheral nerves, which connect the brain and spinal cord to the rest of the body.
Fight for the right support: Have your say
Our Advocacy Service helps thousands of people living with muscle-wasting conditions fight for the support they need to live independentl
“If Muscular Dystrophy UK hadn’t put me in touch with other people living with FSH, I doubt that I would ever have had the confidence to continue living my life to the fullest,
Having been part of Trailblazers since the very beginning, I have experienced many years of benefits for the community of young disabled people we represent, but also personal and
Saul Catlin’s school in Walthamstow is inclusive. According to the Year 10 student, Frederick Bremer School also offers everyone the chance to be what they want to be.
“I was so proud I had achieved something I never thought I’d be able to. But I guess that’s what’s great about being in a wheelchair in this modern world.
Muscular Dystrophy UK will be launching vital new condition specific alert cards and a printable online care plan to ensure people with all muscle-wasting conditions can inform hea
Michelle Young’s son, eight-year-old Michael, has Duchenne muscular dystrophy, and is eligible for new drug, Translarna.