ME is a neurological and immunological disease that can strike anyone at any age, regardless of gender or race. It typically develops in an acute stage and is characterized by symptoms such as fatigue, cognitive impairment, and muscle weakness. Although it is rare, some patients can even die from the condition. The International Classification of Diseases (ICD) code for ME is G93.3. During the course of the disease, patients with ME often experience a wide range of physical and mental problems.
The CDC maintains a website devoted to ME/CFS and has a brochure that doctors can use to diagnose patients with the disease. The Institute of Medicine’s recommendations for treating ME/CFS form a cornerstone of its ME/CFS information. While the CDC does not yet accept the ME/CFS diagnosis as a separate clinical entity, most physicians recognize it as a debilitating illness. The CDC and NIH have been reluctant to support the ME/CFS diagnosis, citing a 2006 study by Sheffield Hallam University.
The CDC’s web site for ME/CFS is an excellent resource for medical professionals. It contains a summary of the CDC’s recommendations on ME/CFS. Further reading can be found at me.org. Many physicians now recognize ME/CFS as a disabling illness and accept it as a legitimate one. It is important to note that the Institute of Medicine has not yet classified it as a distinct clinical entity.
While most doctors and health care providers have a general understanding of ME/CFS, there is still a long way to go to find a cure. The best way to find a cure for ME is to join an organization that focuses on research. Among the organizations that support ME patients are: the Institute of Medicine and the Open Medicine Foundation. All these organizations provide resources and help with diagnosis and treatment. The Institute of the Americas has a brochure that provides guidelines to healthcare professionals.
While the Institute of Medicine’s NIH website does not specifically state whether it’s a separate diagnosis, most doctors do agree that ME is a disabling neurological disease. The disease is classified as a “chronic debilitating disorder” by the World Health Organisation (WHO). The CDC have no plans to adopt this diagnosis or even promote it as a separate clinical entity. Despite the lack of funding, ME and CFS sufferers are able to find many ways to make their lives better.
ME is a relapsing-remitting condition, which means that its symptoms can change dramatically. The symptoms that make the condition difficult to deal with include fatigue, sleep disturbance, and memory problems. The patient’s condition may also affect one’s ability to concentrate. It’s imperative to have the right treatment plan to address the various aspects of the disease. Fortunately, there are some helpful resources available to help those with ME.