Despite its commonity, ME still has no definite cure or universal treatment. Doctors generally focus on relieving symptoms and restoring normal functioning in ME patients. While the symptoms of ME vary between patients, different treatments and medical facilities have varied results. Overall, ME patients have lower health-related quality of life (QOL) than people with other chronic conditions. As many as 25% of patients are housebound, which makes it difficult to pinpoint a single cause for the illness.
Inflammation of the brain is not part of the official definition of ME, but it may contribute to the disease. More research is needed to piece together the full biological understanding of ME. It’s important to note that the diagnosis of ME varies across the world, as the symptoms are so variable. Moreover, there are twenty different case definitions for chronic fatigue syndrome (CFS), making it difficult to find the proper diagnostic criteria for each person with the illness.
Because the cause of ME/CFS remains unclear, some doctors rely on their own clinical judgment to diagnose patients. The most recent research on the illness used the Fukuda criteria. Some clinicians use the 2003 Canadian criteria. The Canadian criteria was created by a multidisciplinary group of doctors and emphasizes neuroimmune dysfunction. There are no definite cures for ME/CFS, but there are many treatments for ME/CFS.
The WHO has issued a brochure on the condition, and most medical professionals accept the disease as a disabling condition. A recent WHO report classified ME/CFS as a neurological disease. However, the diagnostic criteria are becoming more complex. Over 20 criteria are used for ME, some for clinical and others for research purposes. While a single diagnostic criteria is sometimes enough to rule out the disease, the best way to ensure that you’re getting the correct treatment is to get medical help.
While the disease is rare, its impact on health and productivity is large. Many individuals with ME are unable to work. This has a disproportionate impact on their quality of life. The disease affects people of all ages, races and socioeconomic groups. The number of suicides in people with ME is rising. It is estimated that the medical care system costs the nation approximately $100 billion annually. However, no one knows why people suffer from it, and the treatments vary between individuals.
If you are experiencing any of the symptoms of ME/CFS, it is recommended that you consult a specialist. They can diagnose the disease and help you develop a treatment plan. If you are experiencing symptoms of ME/CFS but can’t take your usual medication, your doctor may suggest a new medicine for you. It is also a good idea to consult with a mental health professional. A psychiatrist will help you make the correct diagnosis, as it’s important for you to be able to get the right treatment for your condition.