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The role of psychotherapy in the treatment of ME/CFS patients

Tilman and Bettina Grande, with the support of Fatigatio, the German ME/CFS Society, and the WE&ME Foundation (formerly TEMPI Foundation), have published the following article: https://www.mdpi.com/1648-9144/59/4/719

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a post-infectious, chronic disease syndrome that can lead to severe impairment and complete disability. Although the disease has been known for a long time and has been coded in the ICD (G93.3), medical research has not yet reached a consensus on its physiological basis and the best treatment.

Against the backdrop of these shortcomings, psychosomatic disease models were developed and psychotherapeutic treatments derived from them; however, empirical testing of these models has led to sobering results.

According to current research, psychotherapy and psychosomatic rehabilitation have no curative effect in the treatment of ME/CFS. Nevertheless, in practices and outpatient clinics, we see numerous patients who suffer greatly from their illness and whose psychological well-being and coping strategies would benefit from psychotherapeutic help.

In this article, we outline a psychotherapeutic approach that addresses this need and takes into account two fundamental characteristics of ME/CFS: first, the fact that ME/CFS is a physical illness and therefore curative treatment must be physical in nature, and second, the fact that post-exertional malaise (PEM) is a major symptom of ME/CFS and therefore deserves tailored psychotherapeutic treatment.

Together, we are on the path to a better life for ME/CFS patients.

Unfortunately, this takes time and does not happen overnight. ME/CFS patients do not simply wake up one day and return to their normal lives.

But there is hope, and we are here to fight for those who can no longer do so themselves. By funding more research and raising awareness, we will achieve our goal.

Step by step.

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