MND Association on X: ""Rob sharing his story raised the profile of MND, amongst the public, including myself, who were unaware of the devastating effects the disease has." "Without his story, I'm
Inherited motor neurone disease (MND) - John
HuffPost UK on X: "@MNDScotland 'As I watched Eddie Redmayne tripping over his own legs, I became convinced that I too had Motor Neurone Disease. I was given my diagnosis three months
Sports stars speak out about life with motor neurone disease
Motor Neurone Disease (MND) - First symptoms of MND
Businessman, 77, with advanced motor neurone disease takes his own life by removing oxygen mask | Daily Mail Online
I'm dealing with motor neurone disease by becoming a cyborg
Death sits on my Shoulder: Selley, Richard, Selley, George: 9781976751554: Amazon.com: Books
Motor neurone disease: making choices about managing symptoms - Evidently Cochrane
Inherited motor neurone disease (MND) - Harriet
My body was rapidly unravelling': living with motor neurone disease | Motor neurone disease | The Guardian
Motor neurone disease is perfectly captured in this film | British GQ
Motor neurone disease is one of, if not the most, cruellest of diseases
Motor neurone disease: Anger grows at Rishi' refusal not to fund cure | UK | News | Express.co.uk
Rob Burrow: I have no regrets about playing rugby league despite MND battle; 'My kids can play whatever sport they desire' | Rugby League News | Sky Sports
With motor neurone disease (MND), things change so rapidly."
Wollongong professor Justin Yerbury dies from motor neurone disease - ABC News
MNDa
Motor neurone disease is one of, if not the most, cruellest of diseases
The best experience of my life' – woman (60) with motor neurone disease raised €20,000 for charity by walking Camino trail | Independent.ie
Motor neurone disease 'could be spotted in gut 14 YEARS before it takes hold' | Daily Mail Online
Sam Perkins: "This is my chance to take part in triathlon just one more time" - 220 Triathlon
What is motor neurone disease? Government 'fast-tracking' millions to fund research | Evening Standard
Mum with motor neurone disease knows she will never see kids grow up | UK | News | Express.co.uk
Being told I had Motor Neurone Disease felt like a death sentence, but 20 years on, I'm still here'
