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At our AGM on 8 July, our members have been given a special resolution to vote on. This is a resolution which would allow us to become a UK-wide charity and to operate in Scotland.
To give some context to you, our members, on why we are asking this, we have put together some of the key...
The Minister of State for Care has written to all local councils in England calling for new ‘fast track passports’ to improve the speed of support for people diagnosed with MND. &n...
People affected by motor neurone disease (MND) across England, Wales and Northern Ireland are sharing the moments that mean most to them as part of a new campaign to mark Global MND Awareness Day (21 June).
Alongside birthdays, anniversaries and ...
Keith, from Wrexham, is living with MND but is determined not to let it stop him working or celebrating his son following in his footsteps. Diagnosed in 2024, Keith has continued working as a Production Manager at Solvay, thanks to extensive support from his employer. As his mobility has c...