“We’re on a Merry-Go-Round”: Reflections of Patients and Carers after Completing Treatment for Sarcoma
Sarcoma is a rare cancer that has a significant impact on patients’ and carers’ quality of life. Despite this, there has been a paucity of research exploring the diverse experiences of patients and carers following sarcoma treatment. The aim of this study was to explore patients’ and carers’ reflect...
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doaj-687ff69b6a8a4ac8a5982cdc1ecdbb492021-09-20T10:11:34ZengMDPI AGCurrent Oncology1198-00521718-77292021-08-01282633003301410.3390/curroncol28040263“We’re on a Merry-Go-Round”: Reflections of Patients and Carers after Completing Treatment for SarcomaRhys Weaver0Moira O’Connor1Richard Carey Smith2Dianne Sheppard3Georgia K. B. Halkett4Curtin School of Nursing, Faculty of Health Sciences, Curtin University, Perth, WA 6845, AustraliaWA Cancer Prevention Research Unit (WACPRU), School of Population Health, Discipline of Psychology, Faculty of Health Sciences, Curtin University, Perth, WA 6845, AustraliaDepartment of Orthopaedic Surgery, Sir Charles Gairdner Hospital, Perth, WA 6009, AustraliaAccident Research Centre/Office of the Provost and Senior Vice-President, Monash University, Clayton Campus, Melbourne, VIC 3800, AustraliaCurtin School of Nursing, Faculty of Health Sciences, Curtin University, Perth, WA 6845, AustraliaSarcoma is a rare cancer that has a significant impact on patients’ and carers’ quality of life. Despite this, there has been a paucity of research exploring the diverse experiences of patients and carers following sarcoma treatment. The aim of this study was to explore patients’ and carers’ reflections on life after treatment for sarcoma. A qualitative research design with a social constructionist epistemology was used. Participants included patients previously treated for sarcoma (<i>n</i> = 21) and family carers of patients treated for sarcoma (<i>n</i> = 16). Participants completed semi-structured interviews which were analysed using thematic analysis. Three primary themes were identified: “This journey is never going to be over”, “But what happens when I am better?”, and finding a silver lining. Participants represented sarcoma as having a long-term, and sometimes indefinite, threat on their life that they had limited control over. Conclusions: This study highlight the heterogeneous and ongoing needs of sarcoma survivors and their families. Patients and carers strove to translate their experiences in a meaningful way, such as by improving outcomes for other people affected by sarcoma. Parental carers in particular attempted to protect the patient from the ongoing stress of managing the disease.https://www.mdpi.com/1718-7729/28/4/263sarcomasurvivorshiponcologycaregiversqualitative researchrare cancer |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rhys Weaver Moira O’Connor Richard Carey Smith Dianne Sheppard Georgia K. B. Halkett |
spellingShingle |
Rhys Weaver Moira O’Connor Richard Carey Smith Dianne Sheppard Georgia K. B. Halkett “We’re on a Merry-Go-Round”: Reflections of Patients and Carers after Completing Treatment for Sarcoma Current Oncology sarcoma survivorship oncology caregivers qualitative research rare cancer |
author_facet |
Rhys Weaver Moira O’Connor Richard Carey Smith Dianne Sheppard Georgia K. B. Halkett |
author_sort |
Rhys Weaver |
title |
“We’re on a Merry-Go-Round”: Reflections of Patients and Carers after Completing Treatment for Sarcoma |
title_short |
“We’re on a Merry-Go-Round”: Reflections of Patients and Carers after Completing Treatment for Sarcoma |
title_full |
“We’re on a Merry-Go-Round”: Reflections of Patients and Carers after Completing Treatment for Sarcoma |
title_fullStr |
“We’re on a Merry-Go-Round”: Reflections of Patients and Carers after Completing Treatment for Sarcoma |
title_full_unstemmed |
“We’re on a Merry-Go-Round”: Reflections of Patients and Carers after Completing Treatment for Sarcoma |
title_sort |
“we’re on a merry-go-round”: reflections of patients and carers after completing treatment for sarcoma |
publisher |
MDPI AG |
series |
Current Oncology |
issn |
1198-0052 1718-7729 |
publishDate |
2021-08-01 |
description |
Sarcoma is a rare cancer that has a significant impact on patients’ and carers’ quality of life. Despite this, there has been a paucity of research exploring the diverse experiences of patients and carers following sarcoma treatment. The aim of this study was to explore patients’ and carers’ reflections on life after treatment for sarcoma. A qualitative research design with a social constructionist epistemology was used. Participants included patients previously treated for sarcoma (<i>n</i> = 21) and family carers of patients treated for sarcoma (<i>n</i> = 16). Participants completed semi-structured interviews which were analysed using thematic analysis. Three primary themes were identified: “This journey is never going to be over”, “But what happens when I am better?”, and finding a silver lining. Participants represented sarcoma as having a long-term, and sometimes indefinite, threat on their life that they had limited control over. Conclusions: This study highlight the heterogeneous and ongoing needs of sarcoma survivors and their families. Patients and carers strove to translate their experiences in a meaningful way, such as by improving outcomes for other people affected by sarcoma. Parental carers in particular attempted to protect the patient from the ongoing stress of managing the disease. |
topic |
sarcoma survivorship oncology caregivers qualitative research rare cancer |
url |
https://www.mdpi.com/1718-7729/28/4/263 |
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