A statement from the United to End MND coalition following the Roundtable with Health and Social Care Secretary Steve Barclay, which involved leading representatives from across the MND research
Budding MND researchers are being provided a vital stepping-stone to help them continue a career in MND research thanks to funding and support from two MND charities. The four pre-fellowships on
The Motor Neurone Disease Association, LifeArc and My Name'5 Doddie Foundation have jointly awarded £1million to researchers at University College London to progress two cutting-edge therapies for
The first official meeting of the virtual institute focused on MND Research is taking place today (29 November) to lay down plans for the future of collaborative research into motor neurone disease
This research, supported in part by the MND Association and published in Brain, suggests some people with a possible genetic cause of their MND are not currently eligible for genetic testing. Under
Researchers investigating the effectiveness of the drug Tofersen on people with an inherited form of motor neurone disease (MND) have found it can slow progression of the disease if taken over a
The MND Association's Royal Patron HRH Princess Anne joined researchers and people affected by MND at the first MND EnCouRage UK event last month. Organised by the MND Association, the two-day event
On Thursday 21 July Gloucester Rugby Club announced that their lock, 33-year-old Ed Slater, had been diagnosed with motor neurone disease and was retiring from premiership rugby with immediate effect.
A new event to find, keep and encourage the important work of early career researchers is being organised by the Motor Neurone Disease (MND) Association. The exciting new venture, named MND EnCouRage
After months of hard work from the coalition behind the United to End MND campaign, researchers believe they have a solution to access the £50 million funding committed by the Government to motor