Jeff has chopped off his lockdown locks for MDUK thanks to barbers King & Captain of Thirsk.
Ronit Himatlal, aged 23, has Spina Bifida and Hydrocephalus.
Krishan Solanki, 27, from London, is Muscular Dystrophy UK’s Challenge Events Manager and the cause holds a very special place in his heart.
Jack, 24, from the London Borough of Havering, is on a work experience placement as part of the Muscular Dystrophy UK Moving Up project.
You probably haven’t heard of my favourite football team. They’re called Golden Boot FC.
Last week I tried out the new UberWAVs! I was quite excited to use Uber, but I was also skeptical of Uber’s idea of a wheelchair accessible vehicle
I quickly got my phone out
Tuesday 19 July, 12pm to 3pm, Attlee Suite, Portcullis House, Houses of Parliament, London SW1A 0AA
Is accessing physiotherapy important to you?
Then come and join us at our parlia
Pompe’s disease, a rare, inherited and progressive muscle disorder, affects about only one in 40,000 people.
Jack McLellan, 24, from Havering, has an undiagnosed form of muscular dystrophy.
Luca Fernandes was diagnosed with Duchenne musclar dystrophy aged three years old.
Our son Luca was diagnosed with Duchenne muscular dystrophy in November 2013.
Omar Foster is 22, from Croydon and has Spinal Muscular Atrophy Type III.