Joe and Steve Kerrison: How cough assist machines improve quality of life

Brothers Joe and Steve Kerrison, from Derbyshire, have Duchenne muscular dystrophy and have used a cough assist machine since 2015. Now, as Derby and Derbyshire CCG introduces a policy claiming there is not enough evidence to fund this equipment for others, their mum, Trish, shares their story…
Brothers Joe and Steve Kerrison, from Derbyshire, have Duchenne muscular dystrophy and have used a cough assist machine since 2015. Now, as Derby and Derbyshire CCG introduces a policy claiming there is not enough evidence to fund this equipment for others, their mum, Trish, shares their story…

How the new taxi law helped prosecute a driver who tried to overcharge me

The last thing you want during your first week at a new job is to have to ring to say you’re going to be late because you had to call the police about a taxi driver. This is exactly what happened to me when I started working at Muscular Dystrophy UK!
The last thing you want during your first week at a new job is to have to ring to say you’re going to be late because you had to call the police about a taxi driver. This is exactly what happened to me when I started working at Muscular Dystrophy UK!

Making fashion more inclusive

Chloe here! One of the last blogs I wrote for MDUK was a couple of years ago and called “vent about the vent” where I talked about the process I went through to accept the idea of having to use overnight ventilation.
Chloe here! One of the last blogs I wrote for MDUK was a couple of years ago and called “vent about the vent” where I talked about the process I went through to accept the idea of having to use overnight ventilation.

Christmas appeal 2019

My son is really looking forward to Christmas. He’s such an energetic, fun-loving lad, so full of questions and curious about the world. His name is Somhairle (a Gaelic name, pronounced ‘Sorley’) and he was diagnosed with Duchenne muscular dystrophy back in August of 2017, when he was just four years old.
My son is really looking forward to Christmas. He’s such an energetic, fun-loving lad, so full of questions and curious about the world. His name is Somhairle (a Gaelic name, pronounced ‘Sorley’) and he was diagnosed with Duchenne muscular dystrophy back in August of 2017, when he was just four years old.

How the gym shaped my journey towards body positivity

One of my biggest struggles in connection with having Ullrich Congenital muscular dystrophy over the years has been my body image, which has a direct impact on my mental wellbeing.
One of my biggest struggles in connection with having Ullrich Congenital muscular dystrophy over the years has been my body image, which has a direct impact on my mental wellbeing.
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