ME/CFS and Fibromyalgia International Awareness Day

ME/CFS and Fibromyalgia International Awareness Day

May 12 is ME/CFS and Fibromyalgia International Awareness Day. ME/CFS is not just fatigue. ME/CFS is a serious, long-term illness. Those affected are unable to perform their usual activities and suffer from profound fatigue that is not relieved by rest. A distinguishing feature is post-exertional malaise (PEM), which is the worsening of symptoms after physical or mental activity. Other symptoms include a lack of refreshing sleep, dizziness, problems thinking and concentrating, worsened memory, and pain.

What is ME/CFS?

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a disabling and complex illness.

People with ME/CFS are often not able to do their usual activities. At times, ME/CFS may confine them to bed. They also have overwhelming fatigue that is not improved by rest. ME/CFS may get worse after any activity, whether it’s physical or mental. This symptom is known as exertion malaise (PEM). Other symptoms can include problems with sleep, thinking and concentrating, pain, and dizziness. People with ME/CFS may not look ill.

However:

• People with ME/CFS are not able to function the same way they did before they became ill.
• ME/CFS changes people’s ability to do daily tasks, like taking a shower or preparing a meal.
• ME/CFS often makes it hard to keep a job, go to school, and take part in family and social life.
• ME/CFS can last for years and sometimes leads to serious disability.
• At least one in four ME/CFS patients is bed- or house-bound for long periods during their illness.

Who Gets ME/CFS?

Anyone can get ME/CFS. While most common in people between 40 and 60 years old, the illness affects children, adolescents, and adults of all ages. Among adults, women are affected more often than men. White people are diagnosed more than other races and ethnicities. But many people with ME/CFS have not been diagnosed, especially among people from racial and ethnic minority groups.

A report noted:

• An estimated 836,000 to 2.5 million Americans suffer from ME/CFS.
• About 90 percent of people with ME/CFS have not been diagnosed.
• ME/CFS costs the U.S. economy about $17 to $24 billion annually in medical bills and lost incomes.

Some of the reasons that people with ME/CFS have not been diagnosed include limited access to healthcare and a lack of education about ME/CFS among healthcare providers.

• Most medical schools in the United States do not have ME/CFS as part of their physician training.
• The illness is often misunderstood and might not be taken seriously by some healthcare providers.
• More education for doctors and nurses is urgently needed so they are prepared to provide timely diagnosis and appropriate care for patients.

Researchers have not yet found what causes ME/CFS, and there are no specific laboratory tests to diagnose ME/CFS directly. Therefore, doctors need to consider the diagnosis of ME/CFS based on in-depth evaluation of a person’s symptoms and medical history. It is also important that doctors diagnose and treat any other conditions that can cause similar symptoms. Even though there is no cure for ME/CFS, some symptoms can be treated or managed.

Possible Causes to Know on ME/CFS and Fibromyalgia International Awareness Day

Scientists have not yet identified what causes myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). It is possible that ME/CFS has more than one cause, meaning that patients with ME/CFS could have illness resulting from different causes. In addition, it is possible that two or more triggers might work together to cause the illness.