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'I am not the kind of woman who complains of everything': Illness stories on self and shame in women with chronic pain

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  • Werner, Anne
  • Isaksen, L.W.Lise Widding
  • Malterud, Kirsti

Abstract

In this study, we explore issues of self and shame in illness accounts from women with chronic pain. We focused on how these issues within their stories were shaped according to cultural discourses of gender and disease. A qualitative study was conducted with in-depth interviews including a purposeful sampling of 10 women of varying ages and backgrounds with chronic muscular pain. The women described themselves in various ways as 'strong', and expressed their disgust regarding talk of illness of other women with similar pain. The material was interpreted within a feminist frame of reference, inspired by narrative theory and discourse analysis. We read the women's descriptions of their own (positive) strength and the (negative) illness talk of others as a moral plot and argumentation, appealing to a public audience of health personnel, the general public, and the interviewer: As a plot, their stories attempt to cope with psychological and alternative explanations of the causes of their pain. As performance, their stories attempt to cope with the scepticism and distrust they report having been met with. Finally, as arguments, their stories attempt to convince us about the credibility of their pain as real and somatic rather than imagined or psychological. In several ways, the women negotiated a picture of themselves that fits with normative, biomedical expectations of what illness is and how it should be performed or lived out in 'storied form' according to a gendered work of credibility as woman and as ill. Thus, their descriptions appear not merely in terms of individual behaviour, but also as organized by medical discourses of gender and diseases. Behind their stories, we hear whispered accounts relating to the medical narrative about hysteria; rejections of the stereotype medical discourse of the crazy, lazy, illness-fixed or weak woman.

Suggested Citation

  • Werner, Anne & Isaksen, L.W.Lise Widding & Malterud, Kirsti, 2004. "'I am not the kind of woman who complains of everything': Illness stories on self and shame in women with chronic pain," Social Science & Medicine, Elsevier, vol. 59(5), pages 1035-1045, September.
  • Handle: RePEc:eee:socmed:v:59:y:2004:i:5:p:1035-1045
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    Cited by:

    1. Rushforth, Alex & Ladds, Emma & Wieringa, Sietse & Taylor, Sharon & Husain, Laiba & Greenhalgh, Trisha, 2021. "Long Covid – The illness narratives," Social Science & Medicine, Elsevier, vol. 286(C).
    2. Weckesser, Annalise & Denny, Elaine, 2017. "Re-working biographies: Women's narratives of pregnancy whilst living with epilepsy," Social Science & Medicine, Elsevier, vol. 185(C), pages 110-117.
    3. Victoria Mailen Arfuch & Rosa Caballol Angelats & Carina Aguilar Martín & Alessandra Queiroga Gonçalves & Noèlia Carrasco-Querol & Gemma González Serra & Maria Cinta Sancho Sol & Immaculada Fusté Angu, 2022. "Patients’ Lived Experience in a Multicomponent Intervention for Fibromyalgia Syndrome in Primary Care: A Qualitative Interview Study," IJERPH, MDPI, vol. 19(20), pages 1-20, October.
    4. Nettleton, Sarah, 2006. "'I just want permission to be ill': Towards a sociology of medically unexplained symptoms," Social Science & Medicine, Elsevier, vol. 62(5), pages 1167-1178, March.
    5. Wamsiedel, Marius, 2020. "Credibility work and moral evaluation at the ED," Social Science & Medicine, Elsevier, vol. 248(C).
    6. Fielding-Singh, Priya & Dmowska, Amelia, 2022. "Obstetric gaslighting and the denial of mothers’ realities," Social Science & Medicine, Elsevier, vol. 301(C).
    7. Ida Björkman & Magnus Simrén & Gisela Ringström & Eva Jakobsson Ung, 2016. "Patients’ experiences of healthcare encounters in severe irritable bowel syndrome: an analysis based on narrative and feminist theory," Journal of Clinical Nursing, John Wiley & Sons, vol. 25(19-20), pages 2967-2978, October.
    8. Pryma, Jane, 2017. "“Even my sister says I'm acting like a crazy to get a check”: Race, gender, and moral boundary-work in women's claims of disabling chronic pain," Social Science & Medicine, Elsevier, vol. 181(C), pages 66-73.
    9. Eaves, Emery R., 2015. "“Just Advil”: Harm reduction and identity construction in the consumption of over-the-counter medication for chronic pain," Social Science & Medicine, Elsevier, vol. 146(C), pages 147-154.
    10. Philip Kinghorn & Angela Robinson & Richard Smith, 2015. "Developing a Capability-Based Questionnaire for Assessing Well-Being in Patients with Chronic Pain," Social Indicators Research: An International and Interdisciplinary Journal for Quality-of-Life Measurement, Springer, vol. 120(3), pages 897-916, February.
    11. Emslie, Carol & Ridge, Damien & Ziebland, Sue & Hunt, Kate, 2006. "Men's accounts of depression: Reconstructing or resisting hegemonic masculinity?," Social Science & Medicine, Elsevier, vol. 62(9), pages 2246-2257, May.
    12. Dassieu, Lise & Kaboré, Jean-Luc & Choinière, Manon & Arruda, Nelson & Roy, Élise, 2020. "Painful lives: Chronic pain experience among people who use illicit drugs in Montreal (Canada)," Social Science & Medicine, Elsevier, vol. 246(C).
    13. Rasmussen, Erik Børve, 2020. "Rhetorical work and medical authority: Constructing convincing cases in insurance medicine," Social Science & Medicine, Elsevier, vol. 264(C).

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