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The Scottish Motor Neurone Disease Association exists to help all those affected by Motor Neurone Disease (MND) within Scotland; those living with the disease, their families, carers and those health and social care professionals who contribute to the care of people with MND.
Our vision is ‘to make Scotland a place where people are aware of MND, where those living with MND can expect consistently high standards of care and where we can work towards finding a cure’.
Our aims are to:
Our History
Find out about the history of the Association, when it was formed and some significant milestones along the way.
Our Organisation
Find out how the Association is managed, who are our trustees and what is their role.
Our People
Meet the staff that work for the Association
Local Branches
Find out about our branches, where they are, how to contact them and what they do.
Working for SMNDA
View current job vacancies.
Income and Expenditure
See a breakdown of where our money comes from and how we spend it.
Press Support
Find out what support we can offer to the press.
The Scottish Motor Neurone Disease Association is a registered charity. All of our services are free to people living in Scotland with MND and their families. Often, we are the only source of support.
Our services and support will cost more than £700,000 this year, meaning we need to raise almost £13,500 every week.
We receive little financial support form the NHS or government.
None of our work would be possible without the generous support of our donors and fundraisers.