Those living with chronic fatigue syndrome (CFS) or myalgic encephalomyelitis (ME) will be able to access better support closer to home, thanks to government plans published today (22nd July).

Around 390,000 people in the UK are affected by ME/CFE, and suffer from debilitating fatigue, sleep problems and difficulties with thinking, concentration and memory. Severe ME/CFE, which is thought to affect a quarter of those diagnosed, leaves patients housebound or unable to work.

A plan published today provides the foundations for significant improvements in all key areas that affect people living with ME/CFS in England, many of whom struggle to access appropriate care tailored to their complex condition.

The plan includes training NHS professionals to increase their understanding of the condition, which will help combat the stigma faced by people living in ME/CFS. ME/CFS patients will also be able to access care closer to the home, thanks to neighbourhood health services.

Minister for Public Health and Prevention, Ashley Dalton, said: “ME/CFS is a debilitating illness that can severely limit patients’ ability to participate in everyday activities, maintain employment, or enjoy family and social life.

“Today’s plan will help tackle the stigma and lack of awareness of this condition through improved training for NHS staff.

“And through our neighbourhood health services, we will ensure patients suffering from the effects of ME/CFS can access quality care, closer to home, as pledged in our 10 Year Health Plan.

“Our Plan for Change is transforming how patients experience care and this plan represents a comprehensive approach to addressing the long-standing gaps I care and support for people with these conditions, with patient access to appropriate care at its heart.”