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An interpretative phenomenological analysis of the experience of living with colorectal cancer as a chronic illness

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  • Grant J McGeechan
  • Kerri E McPherson
  • Karen Roberts

Abstract

Aims and objectives The aim of this study was to explore the lived experiences of patients living with cancer as a chronic illness. Background Due to recent advances in detection and treatment, cancer is now regarded as a chronic illness. However, living with cancer as a chronic illness can lead to a number of physical and psychosocial consequences all of which can lead to uncertainty over how patients view and plan for their future. Design A longitudinal qualitative study. Methods Individuals attending oncology follow‐up clinics with their clinical nurse specialist at a hospital in the North East of England were invited to participate in two semistructured interviews over a 6‐month period. A total of six individuals consented to participate, of whom two were women. One participant could not be contacted for the second interview, resulting in 11 interviews. Interviews were audio recorded, transcribed verbatim and analysed using interpretative phenomenological analysis. Results Two super‐ordinate themes emerged from the analysis: physical and psychological consequences of cancer and adapting to life after treatment. Conclusion The experience of future disorientation was common among participants; however, this was impacted on by a number of factors such as functional impairment and fear of recurrence. Furthermore, future disorientation does not appear to be stable and may ease as patients begin to adjust to the uncertainty of living with colorectal cancer as a chronic illness.

Suggested Citation

  • Grant J McGeechan & Kerri E McPherson & Karen Roberts, 2018. "An interpretative phenomenological analysis of the experience of living with colorectal cancer as a chronic illness," Journal of Clinical Nursing, John Wiley & Sons, vol. 27(15-16), pages 3148-3156, August.
    • Handle: RePEc:wly:jocnur:v:27:y:2018:i:15-16:p:3148-3156
    DOI: 10.1111/jocn.14509
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    1. Bloom, Joan R. & Spiegel, David, 1984. "The relationship of two dimensions of social support to the psychological well-being and social functioning of women with advanced breast cancer," Social Science & Medicine, Elsevier, vol. 19(8), pages 831-837, January.
    2. Trusson, Diane & Pilnick, Alison & Roy, Srila, 2016. "A new normal?: Women's experiences of biographical disruption and liminality following treatment for early stage breast cancer," Social Science & Medicine, Elsevier, vol. 151(C), pages 121-129.
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    1. Gloria Ada Adigwe & Rachel Tribe & Folashade Alloh & Patricia Smith, 2022. "The Impact of Stroke on the Quality of Life (QOL) of Stroke Survivors in the Southeast (SE) Communities of Nigeria: A Qualitative Study," Disabilities, MDPI, vol. 2(3), pages 1-15, August.

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