Blog

Shaped by you – our five-year research goals.

2 February 2026
Our Director of Research and Innovation, Mike Rogers, explains our new research strategy.
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News

Royal reveal of our new look.

30 January 2026
The MND Association’s Royal Patron, HRH The Princess Royal attends special event with the MND community to launch our brand.
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Rona and Adrian smiling at the camera
Caregiving

Rona

January 2026
Rona recounts her husband, Adrian's, journey with MND and Frontal Temporal Dementia (FTD). She discusses the emotional and practical challenges, emphasising the importance of making every day matter.
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Martin Ashburn - pwMND - on his bespoke bike
Fundraising

Martin

January 2026
Martin was diagnosed with MND in 2023 and emphasises the importance of support from family and friends. He completed an epic coast-to-coast cycling fundraiser to raise money and awareness for MND. 
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News

Making every day matter.

28 January 2026
We unveil our new look and new approach to drive us faster to a world free from Motor Neurone Disease.
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Blog

Tofersen latest

27 January 2026
Our Chief Executive, Tanya Curry, provides an update on our campaign to get people with SOD1 motor neurone disease access to tofersen.
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Liam with dog
Fundraising

Liam

January 2026
Liam was diagnosed with MND in 2021 and has taken part in fundraising activities. He has had financial support grants from the Association to adapt his home and his MND progresses.
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News

Unlock The Door campaign sees councils adopt MND fast-track motion

20 January 2026
DFGs help people living with a disability to adapt their homes to be safe, suitable and accessible
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British Parliament
News

Have your say on powered mobility devices

19 January 2026
People who rely on powered mobility devices such as electric wheelchairs and mobility scooters are being invited to shape long-overdue changes to the law on their use in public places.
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