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Myalgic encephalomyelitis, also called chronic fatigue syndrome or ME/CFS, is a long-term condition that can affect different parts of the body. The most common symptom is extreme tiredness. The cause of ME/CFS is unknown. ME/CFS can affect anyone, including children. The 4 main symptoms of ME/CFS are:

We estimate that at least 250,000 people in the UK have ME/CFS. In addition, a significant but unknown number of people diagnosed with some form of Long Covid also meet diagnostic criteria for ME/CFS.

2024年9月9日 · Chronic fatigue syndrome (CFS) is defined as persistent or recurrent debilitating fatigue that is not the result of ongoing exertion, not alleviated by rest, not explained by any other condition, and results in a substantial reduction in activity. People with ME/CFS tend to feel unwell with no energy after activities, with a worsening of symptoms.

2021年10月29日 · This guideline covers diagnosing and managing myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome (ME/CFS) in children, young people and adults. It aims to improve awareness and understanding about ME/CFS and when to suspect it, so that people are diagnosed earlier.

Myalgic encephalomyelitis (ME) or chronic fatigue syndrome (CFS) is a long term (chronic) neurological condition that affects the nervous and immune systems. People with ME/CFS experience severe pain and fatigue associated with post-exertional malaise (PEM). This is when the body is not able to recover after using even small amounts of energy.

Treatments for myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS) aim to help relieve your symptoms. Your treatment will be tailored to your symptoms. You may find there are times when your symptoms get better, as well as times when your symptoms are more severe. Treatment plans for ME/CFS

2024年5月13日 · “The lifetime prevalence of ME/CFS for English females and males may be as high as 0.92% and 0.25%, respectively, or approximately 390,000 UK individuals overall. This improved estimate of ME/CFS prevalence allows more accurate assessment of the socioeconomic and disease burden imposed by ME/CFS.”

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We exist to present one voice to anyone keen to know more about Myalgic Encephalomyelitis known as ME, sometimes referred to as Chronic Fatigue Syndrome or CFS, representing a number of UK charities and organisations in an alliance that together unites us in a common cause to ease the suffering of patients, and in time, find a cure.