Meet John English, a lifelong Watford fan who is running 496 miles to raise money for the Motor Neurone Disease Association.

The Gesell Assessment System is a research validated and kid-reported “fun” set of screening and assessment tools for educators, parents, pediatricians and other early childhood professionals. Both ...

A retired orthodontist who was diagnosed with motor neurone disease (MND) just over a year ago is organising a fancy dress dip on Brighton beach on Friday. Jon (Joff) Machell, who was diagnosed with ...

The sons of Lewis Moody have spoken of their heartbreak over his MND battle for the first time. The former England rugby captain and his family took part in a new documentary. His wife, Annie, and two ...

When six-year-old Partaap began struggling to stand, climb the stairs and do other everyday activities, his parents knew something was wrong. Over the following months, his family faced a series of ...

Former professional Scottish footballer, Marc Millar has spoken about his personal commitment to Motor Neurone Disease (MND) research after losing his mother to the devastating illness. Despite now ...

Motor neurone disease incidence is more than four times the global estimate in western NSW, while researchers have uncovered an unexpected burden among women. Motor neurone disease is striking people ...

Former rugby league star and fundraiser Kevin Sinfield is aiming to sell 7,777 pairs of sports socks as part of his fundraising mission for motor neurone disease (MND) charities. The Sock It To MND ...

UOW researcher honoured for pioneering work to remove toxic proteins and deliver new treatments to the brain and spinal cord University of Wollongong (UOW) motor neurone disease (MND) researcher Dr ...

Doddie Weir’s charity is offering a training programme for healthcare professionals. Doddie Weir’s foundation is rolling out a new training programme (My Name’5 Doddie Foundation) Dentists, GPs and ...

You have reached your maximum number of saved items. Remove items from your saved list to add more. Over the past four decades, Nicole Lynch has watched motor neurone disease strip her family members ...

Australians living with a rare genetic form of motor neurone disease will have access to a cheaper treatment designed to slow the progression of the condition and help maintain muscle function. From ...