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A new role which is set to improve motor neurone disease (MND) care in the West Midlands will launch in October thanks to funding from the MND Association. The MND Care Coordinator post will provide
MND Association volunteers Lee Millard and Dave Setters have been honoured for their leading role in the United to End MND campaign at the prestigious Third Sector Awards The pair were recognised in
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
Reforms that allow people living with motor neurone disease (MND) to access their benefits more quickly and sensitively have been passed into law after years of campaigning by the MND Association and
The Motor Neurone Disease Association is saddened by the news that Her Majesty Queen Elizabeth II has died aged 96. A message of condolence will be sent to our Royal Patron, HRH The Princess
We are so sad to hear of the death of former footballer Len Johnrose, five years after his diagnosis of motor neurone disease (MND). Len lived with this brutal disease in the public eye after choosing
Families affected by motor neurone disease (MND) are being given free access to personalise and record beautifully illustrated digital stories, poems or greetings cards thanks to an innovative
MND Association patron Kevin Sinfield OBE and the creators of the Spennylympics have been shortlisted at the 2022 JustGiving Awards. Kevin’s fundraising for the Association in honour of his friend
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