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Feeling like ‘a damaged battery’: exploring the lived experiences of UK university students with ME/CFS, 2021, Waite, Elliot

Discussion in 'PsychoSocial ME/CFS Research' started by Wyva, Nov 25, 2021.

  1. Wyva

    Wyva Senior Member (Voting Rights)

    Messages:
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    Location:
    Hungary
    ABSTRACT

    Introduction: Research regarding students with myalgic encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS) has been limited. This study aimed to understand how their subjective well-being had been affected by their condition by exploring their experiences and sense-making processes.

    Methods
    Semi-structured interviews were conducted with eight students using video-calling software and were enriched by asking participants to think of a metaphor to describe their illness. Interpretative Phenomenological Analysis was used to analyze the interviews.

    Results
    Three themes were developed: University as (de)legitimizing, Negotiating disclosure and Loss and adaptation. Rosenberg’s conceptualization of self-esteem was used as a framework to explore the findings as it reflected participants’ accounts and provided an insight into their subjective well-being. Participants discussed their reduced self-esteem through experiences of delegitimization and stigma at their universities, as well as how they became more accepting of their illness and increased their self-esteem.

    Conclusion
    This study provides an understanding of how the lives of students with ME/CFS have been affected by their condition, including their experiences at university and in their social context. Participants raised potential avenues in which universities can act in a supportive manner to be empowering and enhance self-esteem, which is important due to the debated nature of the illness.

    Open access: https://www.tandfonline.com/doi/full/10.1080/21641846.2021.1969800
     

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