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This complicated disorder may be triggered by an infection. While there's no cure for chronic fatigue syndrome, treatment focuses on easing symptoms.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complicated disorder.
It causes extreme fatigue that lasts for at least six months. Symptoms worsen with physical or mental activity but don't fully improve with rest.
The cause of ME/CFS is unknown, although there are many theories. Experts believe it might be triggered by a combination of factors.
There's no single test to confirm a diagnosis. You may need a variety of medical tests to rule out other health problems that have similar symptoms. Treatment for the condition focuses on easing symptoms.
Symptoms of ME/CFS can vary from person to person, and the severity of symptoms can fluctuate from day to day. In addition to fatigue, symptoms may include:
Some people with this condition have headaches, sore throats, and tender lymph nodes in the neck or armpits. People with the condition also may become extra sensitive to light, sound, smells, food and medicines.
Fatigue can be a symptom of many illnesses. In general, see your doctor if you have persistent or excessive fatigue.
The cause of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is still unknown. A combination of factors may be involved, including:
Factors that may increase your risk of ME/CFS include:
Symptoms of ME/CFS can come and go, and often are triggered by physical activity or emotional stress. This can make it difficult for people to maintain a regular work schedule or to even take care of themselves at home.
Many people may be too weak to get out of bed at different points during their illness. Some may need to use a wheelchair.
There's no single test to confirm a diagnosis of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Symptoms can mimic those of many other health problems, including:
It's also common for people who have ME/CFS to also have other health problems at the same time, such as sleep disorders, irritable bowel syndrome or fibromyalgia.
In fact, there are so many overlapping symptoms between this condition and fibromyalgia that some researchers consider the two disorders to be different aspects of the same disease.
Guidelines proposed by the United States Institute of Medicine define the fatigue associated with ME/CFS as being:
To meet the Institute of Medicine's diagnostic criteria for this condition, a person would also need to experience at least one of these two symptoms:
These symptoms must last for at least six months and occur at least half the time at moderate, substantial or severe intensity.
There is no cure for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Treatment focuses on symptom relief. The most disruptive or disabling symptoms should be addressed first.
Some problems associated with ME/CFS can be improved with certain medicines. Examples include:
People with ME/CFS have a worsening of their symptoms after physical, mental or emotional effort. This is called post-exertional malaise. It usually begins within 12 to 24 hours after the activity, and it can last for days or weeks.
People who have post-exertional malaise often struggle to find a good balance between activity and rest. The goal is to remain active without overdoing it. This is also called pacing.
The goal of pacing is to reduce post-exertional malaise, rather than getting back to the same activity level you had when you were healthy. As you improve, you may be able to safely engage in more activity without triggering post-exertional malaise.
It may help to keep a daily diary of your activities and symptoms, so you can track how much activity is too much for you.
Lack of sleep can make other symptoms more difficult to deal with. Your health care team might suggest avoiding caffeine or changing your bedtime routine. Sleep apnea can be treated by using a machine that delivers air pressure through a mask while you sleep.
Many alternative therapies have been promoted for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), but very few have evidence that they work. Patients with this condition may be sensitive to medications, including herbal products and supplements. Treatments that are expensive or potentially harmful should be avoided.
The experience of ME/CFS varies from person to person. Emotional support and counseling may help you and your loved ones deal with the uncertainties and restrictions of this disorder.
Talking with a counselor can help build coping skills to deal with chronic illness, address limitations at work or school, and improve family dynamics. It also can be helpful if you are dealing with symptoms of depression.
You may find it helpful to join a support group and meet other people with your condition. Support groups aren't for everyone, and you may find that a support group adds to your stress rather than relieves it. Experiment and use your own judgment to determine what's best for you.
If you have signs and symptoms of ME/CFS, you're likely to start by seeing your family's health care professional.
Before your appointment, you may want to write a list that includes:
For chronic fatigue syndrome, some basic questions to ask your health care team include:
Don't hesitate to ask other questions during your appointment as they occur to you.
Your health care team is likely to ask you a number of questions, such as: