Reactions, Reality, and Resilience in Adults with Crohn’s Disease: A Qualitative Study

Katherine Jones*, Katherine Baker, Garry A. Tew, Jenni Naisby

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Background
Crohn’s disease (CD) is a lifelong condition that poses unique challenges. This study reports findings from a person’s perspective of living with CD to help enhance the understanding of an individual’s specific care and support needs.

Methods
Semi-structured telephone interviews were conducted with a convenience sample of adults with Crohn’s disease recruited from Newcastle Hospitals NHS Foundation Trust. Data were analysed after data collection using thematic analysis.

Results
Forty-one (68% female) participants aged 49.1±12 years with a disease duration between 1 and 55 years were interviewed. Three overarching themes emerged, along with 12 subthemes: (1) Reactions to presenting symptoms, emotions, and challenges at diagnosis; (2) Reality of living with the condition, seeking information, decision making, psychological challenges, experiencing symptoms/complications during remission and the impact on social life, education, employment, and relationships; (3) Resilience involving emotional adaptations, strategies on self-management, social comparisons as a means of coping and barriers to resilience.

Conclusions
The results highlight the complex health journey and challenges faced by people living with Crohn’s disease and provide health care professionals with a greater insight into the psychological challenges and emotional complexities of the condition to facilitate a more holistic approach to planning care.
Original languageEnglish
Article numberotaf003
Pages (from-to)1-10
Number of pages10
JournalCrohn's and Colitis 360
Volume7
Issue number1
Early online date16 Jan 2025
DOIs
Publication statusPublished - Jan 2025

Keywords

  • Crohn’s disease
  • qualitative
  • health-related quality of life

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