Inflammation in the brain is not the underlying cause of ME. There are a variety of possible causes, but inflammation of the brain is a likely culprit. More studies are needed to determine if this is the cause, but it is believed that it is. This article discusses the symptoms of ME and some treatment options for this condition. But for now, the most common treatments for ME are the same as for other conditions, so that patients can be cured of their disease.
The U.S. government has consistently mishandled ME, institutionalizing bias against the disease. The Institute of Medicine has not conducted research in original Lake Tahoe epidemic patients and uses a vague term, “chronic fatigue syndrome,” instead. Because of this, many people have been misdiagnosed and their treatment skews because of this. CDC officials have also been unwilling to adopt the ME-ICC definition as the official term for the disease.
While ME has several different definitions, the World Health Organization (WHO) classifies it as a neurological illness. There are numerous biological abnormalities in the disease, making it a difficult diagnosis. Unfortunately, the CDC and NIH have refused to promote or even adopt the CFS-Fukuda criteria. This has led to significant relegation of ME patients. Some families are now being put into care proceedings. However, the CDC and NIH have not yet accepted the ME-ICC diagnosis.
Despite its widespread recognition, medical research into ME is still underfunded. The government and other medical organizations have not adequately researched this illness, and its diagnosis is often ambiguous. Moreover, the lack of funding from federal sources has caused patients to suffer in silence and denial. The result is a lack of proper care for patients with ME. The only way to change this is to improve the awareness of the disease. The more widespread understanding of ME will help improve patient care.
The WHO categorises ME as a neurological illness, which has biological abnormalities that are difficult to cure. The CDC and NIH’s definitions are inconsistent and contradictory. The CDC does not even use the term ME-ICC. While the term has been accepted, the CDC has yet to approve it. This has been a setback for the patient’s health. But the CDC and NIH are still ignoring it, and neither the patient nor their family should be forced to suffer.
The lack of research into ME has made the disease even more confusing. The CDC and NIH refuse to adopt ME-ICC as a formal diagnosis. Moreover, the CDC and NIH refuse to adopt the term. They instead use the term CFS-Fukuda. This term was used by researchers in the 1990s to help distinguish between different types of me. There are other factors that are causing confusion in the diagnosis of ME.