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Myalgic Encephalomyelitis (M.E.) is an illness with many names. Within the NHS it is commonly called Chronic Fatigue Syndrome (CFS or CFS/M.E.). Sometimes it is known as Myalgic Encephalopathy or diagnosed as Post Viral Fatigue Syndrome (PVFS). People may also find it crosses over with Fibromyalgia and other conditions.

People with M.E. experience severe, persistent fatigue associated with what’s called post-exertional malaise (the body’s inability to recover after expending even small amounts of energy; sometimes also called ‘payback’) and chronic pain. However, M.E. is also characterised by a range of additional symptoms that may fluctuate or be intermittent and include:

Action for M.E  "Taming the Gorilla".

A guide to living and learning with M.E

Arthritis Research UK booklet on Fibromyalgia questions answered.

Young people with M.E Website AYME

M.E Association Website

Helpline 0844 576 5326

M.E Research UK

Breakthrough Magazine

M.E Support Website

Advice, information and support

Fibromyalgia Action UK


UK Fibromyalgia Website

As the NICE Clinical Guideline says: “The physical symptoms can be as disabling as multiple sclerosis, systemic lupus erythematosus, rheumatoid arthritis, congestive heart failure and other chronic conditions”, and it identifies the following levels of severity:

Mild – where people “are mobile, can care for themselves and can do light domestic tasks without difficulty. Most are still working or in education, but to do this they have probably stopped all leisure and social pursuits. They often take days off, or use the weekend to cope with the rest of the week.”

Pheonix Rising Website and forum

for people with M.E/CFS

Website M.E Support Click Here

Moderate – where people, “have reduced mobility and are restricted in all activities of daily living, although they may have peaks and troughs in their level of symptoms and ability to do activities. They have usually stopped work, school or college and need rest periods, often sleeping in the afternoon for one or two hours. Their sleep at night is generally poor quality and disturbed.”

Severe – where people, “are unable to do any activity for themselves, or can carry out minimal daily tasks only (such as face washing, cleaning teeth). They have severe cognitive difficulties and depend on a wheelchair for mobility. They are often unable to leave the house, or have a severe and prolonged after-effect if they do so. They may also spend most of their time in bed.

M.E. affects an estimated 250,000 people in the UK.

There is much debate about its underlying cause, treatments and what does/doesn’t work and at the time of writing there is still no drug therapy directed specifically at M.E. Current theories about the cause of M.E. include autoimmune deficiencies, viral infections, autonomic/ sympathetic/central nervous system dysfunction and genetic factors, amongst others.

Some people do recover from M.E., often partially and in some cases fully. There isn’t yet clear evidence about who is likely to recover or why. People who have recovered give different reasons, though common themes are:

• stepping back from their busy pre-M.E. lives and taking actions, including resting, to stabilise their condition

• listening to their bodies

• understanding their major symptom triggers

• being resilient to set-backs• finding patience to take very gradual steps towards recovery when able to do so.

Everyone’s experience of M.E. is individual. Even the basic pattern of the illness varies, with some experiencing a sudden onset of symptoms following an infection or accident while others develop the condition gradually over several years. Some people’s condition is relatively constant while others experience cycles of remittance and relapse. There is growing evidence from experts in the field of M.E. that a number of sub-groups exist within M.E. This most probably explains why people with M.E. differ in terms of their illness experience and the course their illness follows

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