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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.

What attendees learned at the Community of Research and lived Experience (CORE) event

17/04/2025

On 3 March 2025, MND Scotland and My Name’s Doddie Foundation welcomed people with and affected by MND from Scotland, and MND researchers from across the UK, to Dynamic Earth in Edinburgh for our inaugural CORE event. It was a wonderful experience which provided a platform for the MND community to come together and share their knowledge, opinions and experience on MND research through our shared goal of a world without MND.

Devoted husband and father of four opens up about life with MND

Mark is bravely sharing his story to raise awareness around motor neuron disease.

MND Scotland statement on low dose interleukin 2

Read MND Scotland's statement on low dose interleukin 2.

Scottish Brothers Take on Edinburgh 7 Summits Challenge in Memory of Late Father

Alan and Andrew Sinclair are preparing to walk 35km to raise money for people affected by MND.

New Research Project to Investigate Link Between Traumatic Brain Injury and Increased MND Risk

MND Scotland is partnering with the MND Association and My Name’5 Doddie Foundation to co-fund a new research project at the University of Glasgow.

A rose in support of MND Scotland launches at RHS Hampton Court Garden Festival

The rose was chosen in memory of Richard Falconer, who sadly passed away in March 2022.

MND Scotland to continue as Hearts shirt sponsor

Heart of Midlothian Football Club confirms that MND Scotland will continue as its front of shirt partner for season 2023/24.

Dad’s MND Symptoms Mistaken for Signs of Aging

Scott Kerr bravely shares his dad's story to raise awareness about people diagnosed with Motor Neuron Disease (MND) later in life.

New programme to move potential MND drugs into clinical trials faster

A ground-breaking programme to screen potential MND treatments faster in people living with MND has been announced.

Tommy’s 26 years with MND

Having originally shared his story in 2017, ahead of Global MND Awareness Day, Tommy opens up about how his life has continued to change over the past six years.

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