Current status: Answered by Jenni Minto on 3 March 2025
To ask the Scottish Government what its response is to the report, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Services in Scotland: An updated analysis of Health Board survey data as of July 2024, which was published in November 2024 and (a) suggested that there was a lack of services for children and young people with ME/CFS and (b) noted that only one NHS board reported any provision for children and young people with ME/CFS.
We recognise the importance of good quality care for children and young people living with ME/CFS.
The Scottish Budget 2025-26 includes £4.5 million to deliver specialist support across the country for long COVID, ME/CFS and other similar conditions. We are carefully considering how this new investment can best benefit people with these conditions across Scotland.
ME/CFS can present a broad range of symptoms, and we know there is no ‘one-size fits all’ response. Children and young people with ME/CFS who require investigation or input from secondary care specialities may access this via an appropriate GP referral, according to their needs.
We have funded the dissemination of an online learning module on ME/CFS for GPs and health professionals in Scotland, which is improving participants’ ability to diagnose and manage ME/CFS. NHS Education for Scotland have also published a Practice Based Small Group Learning module about ME/CFS for GPs and Primary Care professionals.
There are a number of national policy and strategic drivers which aim to ensure children and young people receive the best quality care & support. The Maternal and Child Health page on the Scottish Government website outlines the latest pieces of work towards our priorities in supporting children and young people.
The Health and Social Care Standards set out what we should expect when using health, social care or social work services in Scotland. We have also set out guidance regarding health and social care and supporting disabled children, young people and their families.
We want every child and young person in Scotland to reach their full potential. All support and planning for children and young people with ME/CFS should be underpinned by Getting it Right for Every Child (GIRFEC) - the national approach in Scotland to supporting the wellbeing, and to improving outcomes, of our children and young people.