We’re calling for people living with a muscle wasting and weakening condition to get faster, better and more equitable access to NHS services and treatments.
By ellen moye
Enjoying nature as a disabled family
By ellen moye
Being a mum is the most rewarding experience of my life
By ellen moye
Courageous Carmela is On A Roll
By ellen moye
“We spend so much of our lives wishing we were in someone else’s shoes that we often forget to enjoy what we have right now”
By ellen moye
“Sometimes, having the heating on is the only way I can stop my muscles hurting – so what happens when people like me can’t afford the energy bill?”
By ellen moye
“I’ll just do it the Josie way!”: What it’s like living with muscular dystrophy as a five-year-old
By ellen moye
“It’s getting to a breaking point – a lot of disabled people are already living in poverty”
By ellen moye
My parents were told that I wouldn’t make anything of my life
By ellen moye
You have to change and adapt the way you think about everything
By ellen moye