Trial Report Invisibility and diagnosis stigma: disabling factors for female adults with ME/CFS in a small-scale qualitative study in England, 2023, Khalafbeigi

Discussion in 'ME/CFS research' started by Tom Kindlon, Jul 22, 2023.

  1. Tom Kindlon

    Tom Kindlon Senior Member (Voting Rights)

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    Invisibility and diagnosis stigma: disabling factors for female adults with myalgia encephalomyelitis (ME)/chronic fatigue syndrome (CFS) in a small-scale qualitative study in England


    Free fulltext:
    https://www.emerald.com/insight/content/doi/10.1108/IJOT-08-2022-0032/full/html

    Abstract
    Purpose
    Female adults diagnosed with myalgia encephalomyelitis (ME) and chronic fatigue syndrome (CFS) often are marginalised because their condition is not fully recognised by medical and health-care systems. The purpose of this small-scale study was to explore the lived experiences of adult females with ME/CFS in England in relation to contributing factors that impact their occupational participation.

    Design/methodology/approach
    A qualitative study design using semi-structured interviews was used with nine female adult participants who were selected using a purposive sampling method. A Thematic Networks tool was used to analyse data.

    Findings
    Four organising themes were identified: impairment-, person-, environment- and society-related factors. Two global themes, invisibility and diagnosis stigma, were identified as the overarching issues that female adults with ME/CFS face in occupational participation.

    Originality/value
    Many of the issues that contribute to lack of participation by this population are associated with environmental factors which are secondary to their illness.


     
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