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Press release
Spinraza – the only treatment available for people with spinal muscular atrophy – has not been…
Publication
It is only through your help that we are able to fund vital research, and offer care and support to…
Blog
Jamie Hale is a writer and disability activist currently interning with Muscular Dystrophy UK's…
Press release
The Changing Places Consortium is calling for a facility in all large railway stations, and for law…
Press release
The survey found that:
Only 3% of UK adults think all tourist attractions provide easy access for…
Your story
I absolutely loved RideLondon last time, there is such a buzz about the event, and after a year…
Press release
People with muscle-wasting conditions in Birmingham who need special cough assist machines to avoid…
Press release
Nic Bungay, Director of Campaigns, Care and Information and Muscular Dystrophy UK, which co-…
Your story
Today is FSHD Awareness Day – find out more about the day and the condition here.
Ann Blake, a…
Press release
A £35,000 investment into a rare genetic condition at St Andrews University will ‘bring hope’ to…