Chronic fatigue syndrome / myalgic encephalomyelitis
International CFS/ME Patients Day
Chronic fatigue syndrome / myalgic encephalomyelitis
International CFS/ME Patients Day
The AMCFS association, which is part of the Rare Disease Alliance, celebrates World Chronic Fatigue Syndrome Patient Day. The difficulties of diagnosis and the shortcomings of the healthcare system make it difficult to recognize the pathology and take care of patients, whose number is constantly increasing, also due to the consequences of Covid.
The AMCFS association, which is part of the Rare Disease Alliance, celebrates World Chronic Fatigue Syndrome Patient Day. The difficulties of diagnosis and the shortcomings of the healthcare system make it difficult to recognize the pathology and take care of patients, whose number is constantly increasing, also due to the consequences of Covid.
Chronic Fatigue Syndrome: Why Diagnosis is Difficult
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Dr. Lorenzo Lorusso
CFS/ME, comparison with Long Covid. The absence of biological markers
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Dr. Lorenzo Lorusso
The Impact of CFS/ME on the Patient's Daily Life
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Roberta Beretta Ardino
Difficulties in diagnosis in CFS/ME, what are the consequences for the patient?
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Roberta Beretta Ardino
Treatment of CFS/ME: what are the criteria?
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Dr. Lorenzo Lorusso
Treatment of CFS/ME, the cognitive behavioral approach
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Dr. Lorenzo Lorusso
The problem of taking charge of the CFS/ME patient
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Roberta Beretta Ardino
CFS/ME Patients Association, Results and Perspectives
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Roberta Beretta Ardino