The MND Association is calling for urgent support for people who care for people with MND after a report revealed more than half provide 75 hours of care every single week. 245 unpaid carers shared
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
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
Members of the United to End MND coalition have met with Minister for Care, Gillian Keegan to discuss the Government’s £50m commitment to fund motor neurone disease (MND) research. Representing the
Leading MND clinicians have written to the Secretary of State for Health and Social Care to express their concern about the Spring Booster vaccine rollout. Unlike previous booster doses, the Spring
After years of campaigning, the Association is pleased to see that as of today the long-awaited changes to the Special Rules for Terminal Illness have been applied to Employment and Support Allowance
After years of campaigning, the Department for Work and Pensions (DWP) is set to begin introducing its long-awaited changes to the Special Rules for Terminal Illness in England and Wales. From 4th
The All-Party Parliamentary Group (APPG) on MND held an online AGM today, with a focus on access to housing adaptations. Speakers included: Alex Massey and Jonathan Collier from the MND Association;
A campaigner who is living with motor neurone disease (MND) has received a Points of Light award from Prime Minister Boris Johnson following her involvement in the United to End MND campaign. Emma
Legislation to increase access to fast-track benefits for terminally ill people in Northern Ireland reached its final stage today (24 January) in the NI Assembly. The Social Security (Terminal