Tireless Tyrone volunteer Claire O’Hanlon hasn’t stopped fundraising for Duchenne charities since her son Luke was diagnosed with the condition, aged 13 months, in 2012 and
Gerry and Jenny met in their early 20s. He was an engineer, she worked in retail. They fell in love and got married, with dreams of starting a family.
In our commitment to giving patients a voice in drug development, Muscular Dystrophy UK is working with pharmaceutical companies, academics, patients, healthy technology assessment
Genome editing is considered to have great potential for treating numerous health conditions, including muscle-wasting conditions.
My name is Neeru Malhotra and I’m the Head of Information and Support Services at Muscular Dystrophy UK. My brother has Duchenne muscular dystrophy.
Clinical trial coordinators play an important role in the successful running of clinical trials.
When one of your children is diagnosed with an incurable muscle-wasting condition, it can have a devastating effect on your whole family.
Teddy Rooks, 24, from Romford, is taking on the Prudential RideLondon-Surrey 100 next summer for Muscular Dystrophy UK as part of the family fund, Moving Muscles for Marcus.
A fundraiser with Becker muscular dystrophy has spent the month ziplining, canoeing and biking to raise money to help children with muscle-wasting conditions.
Hayley Lloyd says making friends with someone who has the same condition as her son has given him a “role model” to look up to.
Amy Cameron’s son Zac, three, was diagnosed with SMA Type 1 in November 2016.