Chronic fatigue syndrome/ME is a condition where you have long-term disabling tiredness (fatigue). Most people with chronic fatigue syndrome/ME also have one or more other symptoms such as muscular pains, joint pains, disturbed sleep patterns, poor concentration, headaches. The cause is not known. Treatments that may help in some cases (but not all) include a programme of graded exercise therapy (GET) and cognitive behavioural therapy (CBT).
Chronic fatigue syndrome (CFS)/ME is a condition that causes marked long-term fatigue and other symptoms which are not caused by any other known medical condition.
However, there is controversy about the nature of this condition. There is no test to diagnose the condition. The diagnosis is made in people who have a certain set of symptoms (which can vary in their type and severity). There is even controversy about what to call this condition.
Until these issues are resolved, many people now use the umbrella term of CFS/ME.
The cause of CFS/ME is not known. There are various theories - but none has been proved. A popular theory is that a viral infection may trigger the condition. It is well-known that fatigue is a symptom that can persist for a short time after having certain viral infections. For example, infection with the glandular fever virus or the influenza virus can cause fatigue for several weeks after other symptoms have gone. However, most people recover within a few weeks from the fatigue that follows known viral infections.
Even if a viral infection is a trigger of CFS/ME, it is not clear why symptoms persist when there is no evidence of persisting infection. Also, the symptoms of many people with CFS/ME do not start with a viral infection.
Factors that are thought to contribute to some people developing CFS/ME include:
The following factors are thought to make CFS/ME worse:
It is hoped that research will clarify the cause of CFS/ME in the future.
CFS/ME can affect anyone. It is estimated that CFS/ME affects about 1 in 300 people in the UK, possibly more. It is about three times as common in women as in men. The most common age for it to develop is in the early twenties to mid-forties. In children the most common age for it to develop is 13-15 years, but it can develop at an earlier age.
There is no test that proves that you have CFS/ME. A doctor will usually diagnose CFS/ME based on your symptoms. Some tests are usually done to rule out other causes of your fatigue or other symptoms. For example, blood tests may be done to rule out anaemia, an underactive thyroid gland, and liver and kidney problems. All these tests are normal in people with CFS/ME.
The medical definition of CFS/ME states that symptoms should have lasted for at least four months in adults and three months in children and young adults.
The onset of symptoms can be fairly sudden (over a few days or so), or more gradual.
The most common main symptom is persistent fatigue (tiredness). The fatigue is of new onset. That is, it has not been lifelong but started at a point in time and causes you to limit your activities compared with what you were used to. It is often felt to be both physical and mental fatigue, and said to be overwhelming, or to be like no other type of fatigue. For example:
The fatigue is often made worse by activity. This is called post-exertional malaise. However, the post-exertional malaise usually does not develop until the day following the activity. It then takes several days to improve.
In addition to fatigue, one or more of the following symptoms are common (but most people do not have them all). In some people, one of the following symptoms is more dominant than the fatigue and is the main symptom:
Physical or mental exertion will often make your symptoms worse.
The severity of CFS/ME can roughly be divided into three levels:
Mild cases - you can care for yourself and can do light domestic tasks, but with difficulty. You are still likely to be able to do a job, but may often take days off work. In order to remain in work you are likely to have stopped most leisure and social activities. Weekends or other days off from work are used to rest in order to cope.
Moderate cases - you have reduced mobility and are restricted in most activities of daily living. The level of ability and severity of symptoms often varies from time to time (peaks and troughs). You are likely to have stopped work and require rest periods. Night-time sleep tends to be poor and disturbed.
Severe cases - you are able to carry out only minimal daily tasks such as face washing and cleaning teeth. You are likely to have severe difficulties with some mental processes such as concentrating. You may be wheelchair-dependent for mobility and may be unable to leave your home except on rare occasions, and usually have severe prolonged after-effects from effort. You may spend most of your time in bed. You are often unable to tolerate any noise, and are generally very sensitive to bright light.
Note: most cases are mild or moderate.
There is no known cure for CFS/ME although treatment may help to ease symptoms. You are likely to be referred to a specialist who will be able to offer you support and treatment. Treatments that may be considered include the following.
Painkillers may help if muscle or joint pains are troublesome symptoms. Eating little and often may help any nausea. Specific diets have not been shown to be beneficial.
Depression can occur in people with CFS/ME (as it is with many other chronic diseases). Depression can make many symptoms worse. Antidepressants may be prescribed if depression develops.
It is likely you will be given advice about your sleep. Any changes to your sleep pattern (for example, having too little, or even too much, sleep) may actually make your fatigue worse. This includes sleeping in the daytime, which should ideally be avoided. Any changes to your sleep pattern should be done gradually.
Rest (rather than actual sleep) is very beneficial. You should introduce rest periods into your daily routine. These should ideally be limited to 30 minutes at a time and be a period of relaxation.
Relaxation can help to improve pain, sleep problems and any stress or anxiety you may have. There are various relaxation techniques (such as guided visualisation or breathing techniques) which you may find useful when there are built into your rest periods.
It is very important that you have a well-balanced diet. You should try to avoid any foods and drinks that you are sensitive to. Eating small, regular meals which contain some starchy foods is often beneficial.
One or more of the following may be recommended as part of your treatment:
Graded exercise therapy (GET) means a gradual, progressive increase in exercise or physical activity, such as walking or swimming. The level of exercise recommended will depend upon your symptoms and current level of activity. Graded exercise is a structured treatment during which you are closely monitored. It is not the same as going to the gym or doing more exercise by yourself. It should be tailored to suit each individual case. Ideally, it should be supervised by a physiotherapist or occupational therapist who is used to treating people with CFS/ME.
Graded exercise can improve symptoms for some people. However, some people report that they do not find it beneficial.
Cognitive therapy is based on the idea that certain ways of thinking can fuel certain health problems. Behavioural therapy aims to change any behaviours that are harmful or not helpful. Cognitive behavioural therapy (CBT) is a combination of cognitive and behavioural therapy. The use of CBT does not imply that the cause of an illness is psychological. CBT is one of the most effective treatments for CFS/ME.
Although CBT does not aim to cure the condition, it helps to improve symptoms, coping strategies and day-to-day functioning. For people with CFS/ME the core components of CBT would normally include: energy/activity management, establishment of a sleep routine, goal setting, and psychological support.
So which specific treatment is most effective? A large research trial was published in 2011 which compared the two treatment options listed above. 641 people with CFS/ME (but who were not bed-bound) took part in the trial. They were split into four groups. One group received standard medical care alone. The other three groups received standard medical care plus Adaptive Pacing Therapy (APT), or CBT, or GET. Adaptive pacing therapy was invented for the trial and is used as a control, just for comparison. After one year the results showed that 76 in 100 people had markedly improved with CBT, and 80 in 100 people had markedly improved with GET. With normal medical care, 65 in 100 people had markedly improved but this was the same for the APT group. The conclusion of this study was that CBT and GET were the most effective treatments. Also, that APT was unlikely to give any extra benefit to normal medical care.
It was also worth noting in this trial that all the treatments had limited effects. Yes, it was found that a good number of people improved (had less severe symptoms) with each treatment. However, only about 3 in 10 people treated with CBT or GET in this trial (the treatments found to be most effective) recovered fully.
Depending on the severity of illness, other support may be needed. For example, carers, nursing support, equipment and adaptations to the home to help overcome disability.
If you are employed, your doctor will be able to advise you about whether you should take time off work. And, if you take time off work, when you may be ready to go back to work. It may be that you need to work doing slightly different hours or even with different duties. If you have an occupational health department at work, they are likely to be involved with you also regarding work and going back to work if you take time off.
As there is only limited success with conventional treatments, it is understandable that people turn to complementary practitioners. Many people with CFS/ME find various therapies helpful. However, there is not enough research evidence to support the use of complementary therapies for the treatment of CFS/ME.
There is also insufficient evidence to recommend the use of supplements (for example, vitamins).
It can be common to have setbacks when symptoms become worse for a while. These can have various triggers - for example, poor sleep, infection or stress.
Your doctor may discuss with you strategies which may help during a setback. These may include relaxation techniques, talking with your family, and maintaining your activity and exercise levels, if possible. However, it may be necessary for you to reduce or even stop some of your activities and increase the amount of rest you have during a setback.
Following a setback you should usually be able gradually to return to your previous activity level.
In most cases, the condition has a fluctuating course. There may be times when symptoms are not too bad, and times when symptoms flare up and become worse (a setback). The long-term outlook is variable:
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