What is Myalgic Encephalomyelitis (ME)?


ME is an unpredictable condition that affects one million or more people in the United States alone. Although the condition tends to be more common in women than in men, it can affect people of all ages and from all socioeconomic backgrounds. In fact, more than half of people with ME do not even know they have it. In fact, many medical providers are unaware that their patients suffer from ME, which makes diagnosing the disorder a difficult task. Fortunately, there are many resources that can help you with your ME diagnosis.

The hallmark symptom of ME is post-exertional malaise, also known as “post-exercise neuroimmune exhaustion.” This is often studied in relation to physical activity, but it can also be initiated by sensory overload and cognitive overexertion. The person with ME will experience significant physical and cognitive dysfunction and often spends most of their days bedridden. Further, patients with severe ME can experience seizures and other symptoms that may make them unable to continue working or playing sports.

The cause of M.E. is still unknown, but some researchers believe that a virus can trigger the disease. The Epstein-Barr virus (the virus that causes chickenpox, shingles, and M.E.), enteroviruses, and hepatitis A, B, and C infections are among the potential triggers of the disease. In addition, a particular type of bacteria known as Ross River virus is known to cause M.E.

The disease has been called several different things throughout history. It has also been called Atypical Polio, Icelandic disease, Benign Myalgic Encephalomyelitis, Epidemic Neuromyasthenia, and Chronic Fatigue Syndrome. However, the most commonly used term for ME/CFS is ME/CFS. While many researchers and doctors are still unsure of the exact cause of the illness, it is still a controversial subject.

While it is possible to get a diagnosis of ME from a variety of sources, it is important to seek medical advice from a health professional if you suspect that you are suffering from this disorder. In the UK, most doctors accept the condition as a disabling illness. The World Health Organisation classifies ME as neurological, and it affects between 15 and 30 million people in the world. Most sufferers cannot work due to their symptoms, which can range from mild to severe.

There is no known cause of ME/CFS, and the symptoms of ME/CFS do not respond well to specific laboratory tests. Therefore, a physician must evaluate the severity of your symptoms, as well as your medical history, to determine if you have the disorder. There is no cure for ME/CFS, but some symptoms can be treated. The most effective method of treatment for ME/CFS is a specialized exercise program, such as yoga or cycling.

Despite the numerous treatments for ME/CFS, many patients do not get relief. In fact, they may even need to be tube-fed to survive. Although the symptoms of ME/CFS are often sufficient to make a diagnosis, blood tests may be necessary to rule out underlying medical conditions such as anaemia, an underactive thyroid gland, and liver and kidney issues. Ultimately, a patient’s overall health is the best way to determine the exact cause of ME/CFS.