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The lived experience of adults with ulcerative colitis

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  • Jacqueline Sammut
  • Josianne Scerri
  • Rita Borg Xuereb

Abstract

Aims and objectives The purpose of this study was to explore the experiences of adults living with ulcerative colitis. Background Research to date has focused on the impact of inflammatory bowel disease, by analysing the responses of persons with ulcerative colitis and Crohn's disease collectively. This article addresses the dearth in literature by exploring the experiences of adults living with ulcerative colitis. Design An exploratory qualitative phenomenological design was used. Method Semi‐structured interviews were conducted with a purposive sample of 10 adults with ulcerative colitis. Verbatim transcripts were analysed using Interpretative Phenomenological Analysis. Results Three super‐ordinate themes emerged from the analysis: ‘living with physical discomfort’, ‘emotional turmoil in living the experience’ and ‘social interactions’. Conclusion The participants described a fundamental change in their lifestyle, as a result of physical discomfort and emotional turmoil. Misconceptions held regarding the causes of their disease, further compounded their negative emotional experience. Relevance to clinical practice It is of importance that health care professionals understand and explore the unique perspectives of individuals with ulcerative colitis. These perspectives relate to both physical and psychosocial issues. The needs and concerns of persons with ulcerative colitis can then guide the formulation and development of an individualised care plan.

Suggested Citation

  • Jacqueline Sammut & Josianne Scerri & Rita Borg Xuereb, 2015. "The lived experience of adults with ulcerative colitis," Journal of Clinical Nursing, John Wiley & Sons, vol. 24(17-18), pages 2659-2667, September.
  • Handle: RePEc:wly:jocnur:v:24:y:2015:i:17-18:p:2659-2667
    DOI: 10.1111/jocn.12892
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    References listed on IDEAS

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    1. Yunxian Zhou & Weihong Ren & Elizabeth Jan Irvine & Dagan Yang, 2010. "Assessing health‐related quality of life in patients with inflammatory bowel disease in Zhejiang, China," Journal of Clinical Nursing, John Wiley & Sons, vol. 19(1‐2), pages 79-88, January.
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    Cited by:

    1. Kate Muse & Emma Johnson & Annabel L. David, 2021. "A Feeling of Otherness: A Qualitative Research Synthesis Exploring the Lived Experiences of Stigma in Individuals with Inflammatory Bowel Disease," IJERPH, MDPI, vol. 18(15), pages 1-28, July.
    2. Ian Whiteley & Janice Gullick, 2018. "The embodied experience of pregnancy with an ileostomy," Journal of Clinical Nursing, John Wiley & Sons, vol. 27(21-22), pages 3931-3944, November.
    3. Clodagh Byron & Nicola Cornally & Aileen Burton & Eileen Savage, 2020. "Challenges of living with and managing inflammatory bowel disease: A meta‐synthesis of patients’ experiences," Journal of Clinical Nursing, John Wiley & Sons, vol. 29(3-4), pages 305-319, February.
    4. Kjerstin Larsson & Lars Lööf & Karin Nordin, 2017. "Stress, coping and support needs of patients with ulcerative colitis or Crohn's disease: a qualitative descriptive study," Journal of Clinical Nursing, John Wiley & Sons, vol. 26(5-6), pages 648-657, March.

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