ME/CFS: Health Services
The question
To ask the Secretary of State for Health and Social Care, whether his Department plans to allocate (a) new and (b) ring-fenced funding to support the implementation of the Final Delivery Plan for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, published in July 2025.
Answered by Ashley Dalton
We recognise the negative impact that myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) has on patients and their loved ones, and also the cost to health and care services and the wider economy through, for example, loss of work and an increased benefits bill. We, therefore, recently published the ME/CFS final delivery plan, which focuses on boosting research, improving attitudes and education, and bettering the lives of people with this debilitating disease.
There are currently no plans to allocate new or ring-fenced funding specifically to support the implementation of the ME/CFS final delivery plan. However, we continue to commission research on ME/CFS services across the United Kingdom, focussing on the most severely affected. The plan includes increased funding for research, awarded through the National Institute for Health and Care Research, into how existing medicines can be used for post-viral conditions, including ME/CFS. Additionally, there are always opportunities for researchers to bid for and secure research funding for ME/CFS through our open research funding calls.
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