Drivers from Arriva North East’s Darlington depot raised almost £750 towards a £50,000 target to find a cure for six year old Ryan Chidzey’s rare and fatal muscle-wast
St Brigid’s school in Denbigh, joined in with our Bake a Difference fundraiser this year and managed to successfully raise some dough to help MDUK in its work.
Gemma Godrey, who has Limb girdle muscular dystrophy, has recently solved issues with constant sickness by having a PEG feed fitted straight into her stomach.
Please help ensure families like mine have the support we need at Christmas – and all year round – with a gift today.
My son is really looking forward to Christmas.
Seated water-skiing, indoor skydiving and a mammoth zipwire are just a few of the amazing new challenges for 2019 on Rich Copson’s list of inclusive sports and activities he’s
Jon Powton lives in Burnley, Lancashire, with his wife and two foster children.
When Barry needed to find new accessible accommodation, he turned to Muscular Dystrophy UK.
Muscular Dystrophy UK’s support inspired Peter Neville to cook up a plan which has united and helped over a thousand Charcot Marie Tooth (CMT) ‘warriors’.
Mairi Leitch has no fewer than eight family members living with limb girdle muscular dystrophy.
2019 has been the ‘busiest year since diagnosis’ yet for Martin Hywood, 46, from Buckinghamshire who has become a leading and respected fundraiser for Muscular Dystrophy UK.
Ellie Renton (pictured here with her brother William) is a nine-year-old girl from Kirkby Malzeard who has SMA Type 2.