News

Read real stories from people affected by MND, get inspired by the incredible ways people are supporting our cause and hear more about the latest advancements in research, care and support.​

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LEARN 2025 – Gemma Catton’s blog for MND Scotland

In this blog, Gemma Catton shares her connection to MND, her mother’s journey with the disease, and the importance of MND researchers engaging with individuals living with and affected by the disease during MND Scotland’s LEARN events across Scotland.

LEARN 2025 – Lucy’s blog for MND Scotland

In this blog for MND Scotland, Lucy Lintott-Smith shares her experiences of living with MND and discusses the LEARN (Lived Experience and Researcher Network) events hosted by MND Scotland, which will take place across the country this year. 

Project exploring traumatic brain injury and risk of developing MND publishes results

Researchers at the University of Glasgow have published a large-scale population study examining the relationship between traumatic brain injury and the risk of developing motor neuron disease (MND).  

Dr Jane Haley appointed interim CEO of MND Scotland

“Walk to Work for MND”: Alexander Middleton’s 90 Mile Challenge for MND Scotland

For some people the daily commute to work is a routine part of life. But for Alexander Middleton, a 32-year-old solicitor from Edinburgh, it became an opportunity to raise awareness and vital funds for a charity that supports individuals and families dealing with a motor neuron disease (MND) diagnosis.

LEARN 2025 – Alan Ogg’s blog for MND Scotland

In this blog for MND Scotland, Alan Ogg discusses his connection to motor neuron disease (MND). Alan’s wife, Liz, bravely battled the disease.  Alan talks about the impact MND has had, and why it was important for him to attend MND Scotland’s LEARN (Lived Experience and Researcher Network) event at Celtic Park, Glasgow. 

Running For Purpose: Son-In-Law Of World Class Artist Will Take on Half Marathon for MND Scotland

Next month, Russ Ball will participate in the Bournemouth Half Marathon in support of his father-in-law, Mark Fennell. A former art director turned full-time world-class portrait artist, Mark is living with Frontotemporal Dementia with motor neuron disease (FTD-MND).

“Not Fast, Just Furious”: Friends Rally Together for Mum Living With MND

A group of childhood friends from Hertfordshire are preparing to take on the epic Tough Mudder challenge to help raise funds for MND Scotland, inspired by their friend Callum’s mother, Linda Cruickshank, who was diagnosed with motor neuron disease (MND) in March this year.