SWAlexander
Senior Member
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It is time that we stop accepting ME/CFS as a psychosomatic illness.
https://www.mdpi.com/1648-9144/60/1...kQcqTzfpqWxhC3cZg_X44rRtJSStL8eoc6QaCk2HDLshs
Abstract
Since 1969, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has been classified as a neurological disease in the International Classification of Diseases by the World Health Organization. Although numerous studies over time have uncovered organic abnormalities in patients with ME/CFS, and the majority of researchers to date classify the disease as organic, many physicians still believe that ME/CFS is a psychosomatic illness. In this article, we show how detrimental this belief is to the care and well-being of affected patients and, as a consequence, how important the education of physicians and the public is to stop misdiagnosis, mistreatment, and stigmatization on the grounds of incorrect psychosomatic attributions about the etiology and clinical course of ME/CFS.7. Conclusion: False Psychosomatic Attributions on the Etiology of ME/CFS Hinder Adequate Patient Care
Even though, in recent years, more and more healthcare practitioners view ME/CFS correctly as a somatic illness, there are still widespread views in the medical community of ME/CFS being a psychosomatic illness. These views are detrimental for affected patients as they can result in misdiagnosis and harmful therapies, such as GET, which can result in lasting worsening of symptoms. Moreover, false psychosomatic attributions lead to stigmatization. A correct biomedical understanding of ME/CFS in line with the current state of empirical evidence for treatment is, therefore, essential to providing adequate care to patients with ME/CFS.https://www.mdpi.com/1648-9144/60/1...kQcqTzfpqWxhC3cZg_X44rRtJSStL8eoc6QaCk2HDLshs