The UK Government has published a new plan, which aims to enhance care for patients living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) in England.

Affecting an estimated 390,000 individuals across the UK, the condition presents with symptoms such as severe fatigue, sleep disturbances, and cognitive issues.

The government's plan lays out a strategy for substantial improvements in the care of ME/CFS patients, who often face challenges in accessing care suited to their complex needs.

As part of this strategy, National Health Service (NHS) healthcare professionals will receive new training and updated learning resources to better understand ME/CFS and avoid misdiagnosis, addressing the stigma associated with the condition.

Public Health and Prevention Minister Ashley Dalton said: “Today’s plan will help tackle the stigma and lack of awareness of this condition through improved training for NHS staff.”

In line with the government's 10-Year Health Plan, the launch of neighbourhood health services will enable ME/CFS patients to receive care closer to home.

These services will be staffed by specially trained individuals who can cater to those with complex needs.

In addition, the plan promises increased funding allocation for research into potential treatments for ME/CFS through the National Institute for Health and Care Research.

The move also focuses on the unique requirements of children and young people with ME/CFS, providing necessary support within educational environments.

The plan encompasses broader government efforts to improve the benefit assessment processes and assist those with long-term conditions and disabilities in finding and maintaining employment.

The government commits to ongoing collaboration with stakeholders and plans to continue building upon this foundation to create an NHS that is prepared for the future.

This announcement follows the government's recent reforms to the NHS dentistry contract earlier this month.