ABOUT #MEACTION SCOTLAND

#MEAction Scotland is a volunteer-led group determined to raise awareness of ME in Scotland and campaign for health equality for the patient community. We are an affiliate of #MEAction UK

Responsibility for delivery of  health services and policy decisions in Scotland are devolved to the Scottish Parliament. By being Scotland-specific, #MEAction Scotland can engage directly with Members of Scottish Parliament (MSPs) and NHS Scotland health boards. Where projects affect the whole of the UK, we work closely with the UK team.

Neurological Alliance of Sctoland

Our Work

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Get Involved in Campaigning

To get involved in any aspect of our work in Scotland, click on the image to contact us and arrange a chat with one of our volunteers.

You can also click here to join our #MEAction Scotland Facebook group.

MEET YOUR MSP

#MEAction Scotland has developed a guide to give you the basic tools to help you feel confident in meeting your MSP. Click the photo above to read it now.

Explore OUR RESOURCES

Take a look through the resources our volunteers have created to help you understand our work, as well as factsheets and guides to enable you to take action.

LATEST News

A photo of a blue background with a marker pen drawing of an arrow hitting a target surrounded by the words strategy, plans and goals. A red marker pen is in the bottom right corner and the ME Action Scotland logo is at the top.

#MEAction Scotland publishes refreshed strategic priorities

#MEAction Scotland has refreshed and updated its strategic priorities for the period 2024-2026, in anticipation of the expected Scottish Parliament elections in May 2026. We continue to work towards our vision of a Scotland where health and social care professionals, politicians and policy makers, and the general public understand and support people with ME and

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#MEAction UK’s email/letter to Andrew Gwynne MP

To: Andrew Gwynne, Under Secretary of State for Public Health and Prevention Subject: Treatment of Very Severe ME  email [email protected] Dear Andrew Gwynne,  Thank you for being an ally to people with ME  (myalgic encephalomyelitis) and Long Covid and committing to ensuring publication of the DHSC ME/CFS Delivery Plan without more delay.  We trust your

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Questions to Ask Prospective MPs About ME/CFS

In the next few weeks, candidates will be knocking on doors seeking votes for the upcoming UK Election. It’s important that candidates from all parties are made aware of the challenges facing people with ME and Long Covid. It can be a little daunting to be unprepared so here are some questions you might want

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EXPLORE OUR SCOTTISH RESOURCES

Contact the Scottish team

Looking to contact someone else? Contact the global team here, or the UK team here.

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Donate now to support #MEAction.

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