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Research Articles

The negative impact of the psychiatric model of chronic fatigue syndrome on doctors’ understanding and management of the illness

Pages 167-180 | Received 02 Apr 2020, Accepted 06 Oct 2020, Published online: 28 Oct 2020

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Emma Portch, Rachel L. Moseley, Liam Wignall, Julie M. Turner-Cobb, Zoe Taylor & Mike Gondelle. (2023) ‘Welcome to my world’: a thematic analysis of the lived experiences of people with Myalgic Encephalomyelitis during the UK COVID-19 lockdown. Psychology & Health 0:0, pages 1-18.
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Frances Waite & Dely Lazarte Elliot. (2021) Feeling like ‘a damaged battery’: exploring the lived experiences of UK university students with ME/CFS. Fatigue: Biomedicine, Health & Behavior 9:3, pages 159-174.
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Articles from other publishers (2)

Lotte Habermann-Horstmeier & Lukas M. Horstmeier. (2023) Auswirkungen der Qualität der Arzt-Patient-Beziehung auf die Gesundheit von erwachsenen ME/CFS-ErkranktenImplications of the quality of the doctor-patient relationship on health in adult ME/CFS patients. A qualitative public health study from a patien perspective. MMW - Fortschritte der Medizin 165:S5, pages 16-27.
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Michael J Scott, Joan S Crawford, Keith J Geraghty & David F Marks. (2021) The ‘medically unexplained symptoms’ syndrome concept and the cognitive-behavioural treatment model. Journal of Health Psychology 27:1, pages 3-8.
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