Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what actions have been delivered under the Final Delivery Plan on ME/CFS to improve access to healthcare and support for people with severe and very severe ME.

The Department is currently developing a template service specification for mild and moderate myalgic encephalomyelitis, also known as chronic fatigue syndrome (ME/CFS), which also references severe ME/CFS. Further work will need to be undertaken to strengthen support for people with severe ME/CFS, reflecting that people may move between moderate and severe. Future iterations of this document will build on ongoing considerations and emerging insights of severe and very severe ME/CFS.

Departmental and NHS England officials have been working carefully through the steps needed to make a decision on the prescription of a specialised service for very severe ME/CFS. My Rt Hon. Friend, the Secretary of State for Health and Social Care, is responsible for a decision on the prescribing of specialised services, which requires consultation with NHS England.

To support healthcare professionals in the diagnosis and management of ME/CFS, the Department has worked with NHS England to develop an e-learning programme on ME/CFS for healthcare professionals. The final module of this e-learning programme is focussed on managing severe ME/CFS.

Additionally, as set out in the Plan for Change, we are committed to returning to the National Health Service constitutional standard that 92% of patients wait no longer than 18 weeks from referral to consultant-led treatment by March 2029. We delivered 5.2 million additional appointments between July 2024 and June 2025. This will help people with severe ME/CFS to get support sooner. The Plan for Change is available at the following link:

https://www.gov.uk/missions

The 10-Year Health Plan sets out a transformed vision for elective care by 2035, where most interactions no longer take place in a hospital building, instead happening virtually or via neighbourhood services. This will enable patients with severe or very severe ME/CFS who are housebound or bedbound to access support more easily.