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What it means to be a palliative care volunteer in eight European countries: a qualitative analysis of accounts of volunteering

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What it means to be a palliative care volunteer in eight European countries: a qualitative analysis of accounts of volunteering. / Scott, Ros; Goossensen, Anne; Payne, Sheila et al.
In: Scandinavian Journal of Caring Sciences, Vol. 35, No. 1, 01.03.2021, p. 170-177.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Scott, R, Goossensen, A, Payne, S & Pelttari, L 2021, 'What it means to be a palliative care volunteer in eight European countries: a qualitative analysis of accounts of volunteering', Scandinavian Journal of Caring Sciences, vol. 35, no. 1, pp. 170-177. https://doi.org/10.1111/scs.12832

APA

Vancouver

Scott R, Goossensen A, Payne S, Pelttari L. What it means to be a palliative care volunteer in eight European countries: a qualitative analysis of accounts of volunteering. Scandinavian Journal of Caring Sciences. 2021 Mar 1;35(1):170-177. Epub 2020 Mar 6. doi: 10.1111/scs.12832

Author

Scott, Ros ; Goossensen, Anne ; Payne, Sheila et al. / What it means to be a palliative care volunteer in eight European countries : a qualitative analysis of accounts of volunteering. In: Scandinavian Journal of Caring Sciences. 2021 ; Vol. 35, No. 1. pp. 170-177.

Bibtex

@article{0df24d50a07c427483074e1a7cad160b,
title = "What it means to be a palliative care volunteer in eight European countries: a qualitative analysis of accounts of volunteering",
abstract = "This paper addresses the stories of volunteers in hospice and palliative care (HPC) from eight European countries. The aims of the paper are to explore the experiences of volunteers in HPC from their insider perspective, to understand why volunteers choose to work in this field and to understand what it means to them to be involved in palliative care in this way. Stories were collected by the European Association for Palliative Care (EAPC) Task Force for Volunteering contacts in each of the eight countries. The majority of stories (n = 32) came from volunteers involved in different settings including adult patient{\textquoteright}s homes, hospices, hospitals and care homes. Twenty volunteers were female, six were male, and ten did not give their gender. Stories were translated into English, and a qualitative framework analysis was performed. Volunteers were asked two questions: {\textquoteleft}What do you do as a volunteer?{\textquoteright} {\textquoteleft}What does volunteering mean to you?{\textquoteright} Three themes were identified from the data: (i) What volunteers do (ii) How volunteers approach their work and (iii) What working in HPC means to volunteers. The analysis revealed that common approaches to addressing and describing HPC volunteering in terms of tasks and roles could be expanded. To volunteers, it is not about tasks, but about a part of their life, the impact upon which can be significant. The results of this paper, therefore, add to the understanding of volunteers, in the sense of giving attention, being with, and of compassion as a community resource to patients and families in difficult situations. Theories about presence and presencing might have value in further underpinning this contribution to palliative care. Understanding the extent and depth of the volunteers{\textquoteright} experience will help to prevent the undervaluing of their contribution and increase the impact of their involvement.",
keywords = "activities, hospice and palliative care, meaning, narratives, stories, volunteer, volunteering",
author = "Ros Scott and Anne Goossensen and Sheila Payne and Leena Pelttari",
year = "2021",
month = mar,
day = "1",
doi = "10.1111/scs.12832",
language = "English",
volume = "35",
pages = "170--177",
journal = "Scandinavian Journal of Caring Sciences",
issn = "0283-9318",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - What it means to be a palliative care volunteer in eight European countries

T2 - a qualitative analysis of accounts of volunteering

AU - Scott, Ros

AU - Goossensen, Anne

AU - Payne, Sheila

AU - Pelttari, Leena

PY - 2021/3/1

Y1 - 2021/3/1

N2 - This paper addresses the stories of volunteers in hospice and palliative care (HPC) from eight European countries. The aims of the paper are to explore the experiences of volunteers in HPC from their insider perspective, to understand why volunteers choose to work in this field and to understand what it means to them to be involved in palliative care in this way. Stories were collected by the European Association for Palliative Care (EAPC) Task Force for Volunteering contacts in each of the eight countries. The majority of stories (n = 32) came from volunteers involved in different settings including adult patient’s homes, hospices, hospitals and care homes. Twenty volunteers were female, six were male, and ten did not give their gender. Stories were translated into English, and a qualitative framework analysis was performed. Volunteers were asked two questions: ‘What do you do as a volunteer?’ ‘What does volunteering mean to you?’ Three themes were identified from the data: (i) What volunteers do (ii) How volunteers approach their work and (iii) What working in HPC means to volunteers. The analysis revealed that common approaches to addressing and describing HPC volunteering in terms of tasks and roles could be expanded. To volunteers, it is not about tasks, but about a part of their life, the impact upon which can be significant. The results of this paper, therefore, add to the understanding of volunteers, in the sense of giving attention, being with, and of compassion as a community resource to patients and families in difficult situations. Theories about presence and presencing might have value in further underpinning this contribution to palliative care. Understanding the extent and depth of the volunteers’ experience will help to prevent the undervaluing of their contribution and increase the impact of their involvement.

AB - This paper addresses the stories of volunteers in hospice and palliative care (HPC) from eight European countries. The aims of the paper are to explore the experiences of volunteers in HPC from their insider perspective, to understand why volunteers choose to work in this field and to understand what it means to them to be involved in palliative care in this way. Stories were collected by the European Association for Palliative Care (EAPC) Task Force for Volunteering contacts in each of the eight countries. The majority of stories (n = 32) came from volunteers involved in different settings including adult patient’s homes, hospices, hospitals and care homes. Twenty volunteers were female, six were male, and ten did not give their gender. Stories were translated into English, and a qualitative framework analysis was performed. Volunteers were asked two questions: ‘What do you do as a volunteer?’ ‘What does volunteering mean to you?’ Three themes were identified from the data: (i) What volunteers do (ii) How volunteers approach their work and (iii) What working in HPC means to volunteers. The analysis revealed that common approaches to addressing and describing HPC volunteering in terms of tasks and roles could be expanded. To volunteers, it is not about tasks, but about a part of their life, the impact upon which can be significant. The results of this paper, therefore, add to the understanding of volunteers, in the sense of giving attention, being with, and of compassion as a community resource to patients and families in difficult situations. Theories about presence and presencing might have value in further underpinning this contribution to palliative care. Understanding the extent and depth of the volunteers’ experience will help to prevent the undervaluing of their contribution and increase the impact of their involvement.

KW - activities

KW - hospice and palliative care

KW - meaning

KW - narratives

KW - stories

KW - volunteer

KW - volunteering

U2 - 10.1111/scs.12832

DO - 10.1111/scs.12832

M3 - Journal article

VL - 35

SP - 170

EP - 177

JO - Scandinavian Journal of Caring Sciences

JF - Scandinavian Journal of Caring Sciences

SN - 0283-9318

IS - 1

ER -