Abstract
Background: Radiotherapy for pelvic cancers can affect any organ within the pelvis, including the gastrointestinal tract. These late effects, or consequences of treatment, can have a significant impact. These symptoms are collectively known as pelvic radiation disease (PRD). Aims: To identify and consider the experiences of people affected by PRD, including both the patient and their family and friends. Methods: Exploratory interviews were conducted with patients and their carers. The transcripts underwent framework analysis to identify key themes. Findings: Three main areas of concern were feelings of stigma, experiences of contact with healthcare services and the need, and occasional lack, of support from family and friends. Conclusion: PRD has a significant physical, psychological and social impact on quality of life for those affected, as well as their carers.
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