Jeff has chopped off his lockdown locks for MDUK thanks to barbers King & Captain of Thirsk.
Farhan Mian, aged 30, has Duchenne Muscular Dystrophy and lives in Hammersmith and Fulham.
Claire O’Hanlon’s son, Luke (pictured on the right with his cousin, James), has Duchenne muscular dystrophy.
Claire O’Hanlon’s son, Luke, has Duchenne muscular dystrophy.
Following the sad loss of our founder, Lord Walton, on 21 April, a Service of Thanksgiving for his life will be held at St Aidan’s Church, Bamburgh, Northumberland, on Thursday 5
There have been significant developments in the assessment of the Duchenne muscular dystrophy treatment, Translarna, the first therapy available to treat an underlying cause of Duc
Zishan Kinoo, a student aged 20 and with Duchenne Muscular Dystrophy, has been a star member of our Trailblazers Work Experience Scheme since he began in April.
Anthony is part of Muscular Dystrophy UK’s Trailblazers group of young disabled campaigners.
Myotonic dystrophy is one of the most common inherited muscle wasting conditions. It affects individuals of all ages and both sexes and is extremely variable in its presentation.
Seventeen-year old Olivia Lewis lives with juvenile dermatomyositis.
Three-year old Stanley Newman, from Clacton, Essex, lives with Congenital muscular dystrophy (CMD), a progressive muscle-wasting condition which has no treatment or cure.