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Understanding the experiences of caring for a partner with myalgic encephalopathy: a qualitative study of men in Norway, Torp, 2022 (Master’s Thesis)

Discussion in 'ME/CFS research' started by Dolphin, Sep 24, 2022.

  1. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    5,084
    Source: Inland Norway University
    Date: September 20, 2022
    URL: https://brage.inn.no/inn-xmlui/handle/11250/3019314


    Understanding the experiences of caring for a partner with myalgic encephalopathy: a qualitative study of men in Norway
    -----------------------------------------------
    Elise Torp
    - Inland Norway University


    Abstract

    Background
    Informal caring is expanding in many countries as populations age. There
    is a lot of research on how to care responsibilities are experienced by
    next of kin, but there is little research on men, which is the focus of
    this study. This specific focus is Myalgic Encephalopathy (ME), which is
    a condition that often affects women. This means that it is men who
    often find themselves in a caring role.

    Aim
    This project aims to explore what it was like for Norwegian men to have
    a caring role toward a partner with ME and how it affects everyday life.

    Method
    A qualitative approach was used. Ten semi-structured interviews were
    conducted, and the participants were recruited from different places in
    Norway. All were between the ages of 30 to 60 years old and were caring
    for a partner for several years. To analyze the data, thematic analysis
    was used, to find different patterns in the data.

    Results
    A data emerged two main themes and seven under the themes “experiencing
    the impact of caring for a partner with ME on everyday life “and
    providing different kinds of support. The experience around the role of
    caring was influenced by several factors, such as changes in finances
    and family dynamics as well as accessing formal support. Overall, the
    mean men felt that being in a caring role meant that life was being put
    on hold.

    Conclusion
    Findings from this study help to strengthen previous research. Having a caring role for a sick partner with ME was demanding and greatly affects everyday life. Men found the role of care challenging and it could
    negatively affect the person psychologically. For most people in a caring role, there was potential for better support both emotionally and financially.
     
    MEMarge, Simon M, Sean and 5 others like this.
  2. Andy

    Andy Committee Member

    Messages:
    21,914
    Location:
    Hampshire, UK
    I assume "mean men" is a mis-translation issue, and should be something like "average man".
     
    MEMarge, Simon M, Tia and 11 others like this.
  3. RedFox

    RedFox Senior Member (Voting Rights)

    Messages:
    1,245
    Location:
    Pennsylvania
    It's even funnier when you consider the context of the whole sentence:
     

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