Ahead of the Scottish Parliament election this Spring, MND Scotland is calling on the next Government to deliver timely, fast-tracked support for everyone in Scotland living with motor neuron disease (MND).
MND Scotland is calling on the next government to deliver:
1. Invested in, and fast-tracked, housing and adaptations;
2. Fast- tracked social care;
3. Increased, targeted funding for neuro-progressive conditions.
To support our campaign, over the coming weeks we will share the personal stories of people with experience of issues around social care, housing or research.
You can also support our Manifesto by spreading the word on social media.
Our Open Letter to the First Minister
In Scotland right now, 481 people are living with Motor Neuron Disease (MND). Between now and 2031, we estimate another 1,000 more people will be diagnosed across the country. There is no cure. The average life expectancy is just 18 months from the point of being diagnosed.
MND Scotland is appealing to the next Scottish Government to legislate and recognise the urgent statutory rights and needs of those with terminal illnesses like MND. But we need your support.
With the Scottish Parliament election just two weeks away, the main political parties have launched their Manifestos, setting out what they pledge to do if elected to govern.
With our key asks outlined above, we have reviewed each Manifesto to see what pledges could most benefit people affected by MND.We were pleased to see that the Manifestos published by all of the main political parties reflect a number of our asks, including commitments to review accessible housing; invest in services and ensure better pay for social care staff; better support unpaid carers; and advance understanding and knowledge of terminal illnesses.
We particularly welcome the SNP’s explicit mention of MND in their commitments for fast-tracking social care for people with MND, and investing in MND research. The language used directly reflects our manifesto, which was shared with all parties in January, and through work last year.
ON SCOTLAND’S SIDE: SNP Manifesto 2026k
“A HEALTHY SCOTLAND”: Motor Neurone Disease (MND)
“Our aim is to devise a long term plan to cluster in funding for research and development in rare, neuro-progressive conditions like MND. We will also seek to enable fast tracking of care packages for people who are diagnosed with MND”. (www.snp.org/manifesto)
We are committed to working with the next Scottish government to ensure the urgent statutory rights and needs of those with MND are met.
Our policy news
“It May Be a Job to Them, But It’s My Life” – Nicola’s story
Nicola McFarlane was diagnosed with motor neuron disease (MND) in May 2023 when she was forty-six years old. She worked full-time, stayed fit and active, and lived an independent life.
“I don’t want to see other people go through what we had to” Daughter who lost her mum to MND calls for more investment in MND research
An NHS physiotherapist who lost her mum to motor neuron disease (MND) is urging the government to increase investment into MND research.
“We Don’t Have a Year to Wait” Lynda’s Fight for Home Adaptations for People with Motor Neuron Disease
A woman from the Scottish Borders is demanding change to Scotland’s home adaptations system after being forced to wait more than a year for essential work - despite the average life expectancy following a diagnosis of motor neuron disease (MND) being just 18 months.