Pub Date : 2023-10-01Epub Date: 2023-12-01DOI: 10.1080/15524256.2023.2262157
Jennifer DiBiase
Palliative care social workers are trained to identify how trauma manifests over the course of serious and chronic illness. This expertise can guide patients and team members to ensure a trauma-informed experience of care. This paper identifies the growth of outpatient palliative care clinics as an opportunity for palliative care social workers to emphasize this clinical skill set and assume a leadership role in the implementation of trauma-informed practices early in the trajectory of serious illness.
{"title":"Social Workers as Leaders for Facilitating Trauma-Informed Palliative Care in the Outpatient Palliative Care Clinic.","authors":"Jennifer DiBiase","doi":"10.1080/15524256.2023.2262157","DOIUrl":"10.1080/15524256.2023.2262157","url":null,"abstract":"<p><p>Palliative care social workers are trained to identify how trauma manifests over the course of serious and chronic illness. This expertise can guide patients and team members to ensure a trauma-informed experience of care. This paper identifies the growth of outpatient palliative care clinics as an opportunity for palliative care social workers to emphasize this clinical skill set and assume a leadership role in the implementation of trauma-informed practices early in the trajectory of serious illness.</p>","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":" ","pages":"296-308"},"PeriodicalIF":1.6,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41152098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01Epub Date: 2023-07-11DOI: 10.1080/15524256.2023.2229034
Ginu George Powathil, Anish Kr
The prevalence of End-Stage Renal Disease (ESRD) has been rising over time and substantially affects morbidity and mortality. ESRD requires lifelong treatment, and as a result, patients experience multiple physical and psychosocial stressors. ESRD patients struggle to retain their jobs, social lives, financial flexibility, and diet restrictions of liquids and solid foods. The present study aims to understand the experiences of ESRD patients undergoing hemodialysis. The study was conducted at Eldho Mor Baselious Dialysis Center in Perumbavoor, Kerala, in the hemodialysis outpatient unit. The Biopsychosocial model was used as the theoretical framework of the study. As the goal of the study was to investigate the inner experiences of ESRD patients, a qualitative research approach was employed. Twelve respondents were selected for the study using purposive sampling, and the data were organized and analyzed using Colaizzi's descriptive phenomenological method. Four theme categories emerged from data analysis: decline in physical function, psychosocial distress, economic hardships, and impact on the support system. The study shows that ESRD patients experience significant psychosocial and health-related issues. The role of the clinical social worker is vital as there is a need for social work interventions to resolve the psychosocial issues of patients with ESRD.
终末期肾病(ESRD)的患病率随着时间的推移而上升,并对发病率和死亡率产生重大影响。ESRD需要终身治疗,因此,患者会经历多种身体和心理压力。ESRD患者很难保住自己的工作、社交生活、经济灵活性以及液体和固体食物的饮食限制。本研究旨在了解ESRD患者进行血液透析的经验。这项研究是在喀拉拉邦佩伦巴沃的Eldho Mor Baselious透析中心血液透析门诊部进行的。生物心理社会模型被用作研究的理论框架。由于本研究的目的是调查ESRD患者的内心经历,因此采用了定性研究方法。采用有目的的抽样方法选择了12名受访者进行研究,并使用Colaizzi的描述性现象学方法对数据进行了组织和分析。数据分析得出四个主题类别:身体功能下降、心理痛苦、经济困难和对支持系统的影响。研究表明,ESRD患者经历了重大的心理社会和健康问题。临床社会工作者的作用至关重要,因为需要社会工作干预来解决ESRD患者的心理社会问题。
{"title":"The Experience of Living with a Chronic Illness: A Qualitative Study among End-Stage Renal Disease Patients.","authors":"Ginu George Powathil, Anish Kr","doi":"10.1080/15524256.2023.2229034","DOIUrl":"10.1080/15524256.2023.2229034","url":null,"abstract":"<p><p>The prevalence of End-Stage Renal Disease (ESRD) has been rising over time and substantially affects morbidity and mortality. ESRD requires lifelong treatment, and as a result, patients experience multiple physical and psychosocial stressors. ESRD patients struggle to retain their jobs, social lives, financial flexibility, and diet restrictions of liquids and solid foods. The present study aims to understand the experiences of ESRD patients undergoing hemodialysis. The study was conducted at Eldho Mor Baselious Dialysis Center in Perumbavoor, Kerala, in the hemodialysis outpatient unit. The Biopsychosocial model was used as the theoretical framework of the study. As the goal of the study was to investigate the inner experiences of ESRD patients, a qualitative research approach was employed. Twelve respondents were selected for the study using purposive sampling, and the data were organized and analyzed using Colaizzi's descriptive phenomenological method. Four theme categories emerged from data analysis: decline in physical function, psychosocial distress, economic hardships, and impact on the support system. The study shows that ESRD patients experience significant psychosocial and health-related issues. The role of the clinical social worker is vital as there is a need for social work interventions to resolve the psychosocial issues of patients with ESRD.</p>","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":"19 3","pages":"190-208"},"PeriodicalIF":1.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10450329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01Epub Date: 2023-06-18DOI: 10.1080/15524256.2023.2223772
Ian M Johnson, Michael A Light
The shifting age demographics of those experiencing homelessness in the United States expose shortcomings and barriers within homelessness response services and safety-net healthcare to address serious illness. The purpose of this study is to describe the common trajectories of patients concurrently experiencing homelessness and serious illness. As a part of the Research, Action, and Supportive Care at Later-life for Unhoused People (RASCAL-UP) study, the study uses patient charts (n = 75) from the only specialty palliative care program in the U.S. specifically for people experiencing homelessness. Through a thematic mixed-method analysis, a four-point typology of care pathways taken by people experiencing homelessness while seriously ill is introduced: (1) aging and dying-in-place within the housing care system; (2) frequent transitions during serious illness; (3) healthcare institutions as housing; and (4) housing as palliation. Implications of this exploratory typology include targeted, site-specific interventions for supporting goal-concordant patient care and assisting researchers and policy makers in appreciating heterogeneity in experience and need among older and chronically ill people experiencing homelessness and housing precarity.
{"title":"Pathways of Individuals Experiencing Serious Illness While Homeless: An Exploratory 4-Point Typology from the RASCAL-UP Study.","authors":"Ian M Johnson, Michael A Light","doi":"10.1080/15524256.2023.2223772","DOIUrl":"10.1080/15524256.2023.2223772","url":null,"abstract":"<p><p>The shifting age demographics of those experiencing homelessness in the United States expose shortcomings and barriers within homelessness response services and safety-net healthcare to address serious illness. The purpose of this study is to describe the common trajectories of patients concurrently experiencing homelessness and serious illness. As a part of the Research, Action, and Supportive Care at Later-life for Unhoused People (RASCAL-UP) study, the study uses patient charts (<i>n</i> = 75) from the only specialty palliative care program in the U.S. specifically for people experiencing homelessness. Through a thematic mixed-method analysis, a four-point typology of care pathways taken by people experiencing homelessness while seriously ill is introduced: (1) aging and dying-in-place within the housing care system; (2) frequent transitions during serious illness; (3) healthcare institutions as housing; and (4) housing as palliation. Implications of this exploratory typology include targeted, site-specific interventions for supporting goal-concordant patient care and assisting researchers and policy makers in appreciating heterogeneity in experience and need among older and chronically ill people experiencing homelessness and housing precarity.</p>","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":"19 3","pages":"209-228"},"PeriodicalIF":1.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10064858","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01Epub Date: 2023-06-29DOI: 10.1080/15524256.2023.2229037
Michael R Bennett, Carly Charron, Patricia Valcke
The literature pertaining to community-based hospice wellness centres, especially concerning program evaluation, is sparse. This article describes the development and implementation of a mixed-method, rapid needs assessment for a nonprofit community-based hospice wellness centre in Ontario, Canada. As part of the needs assessment, a survey and focus groups were performed to elicit responses from service users. Individuals registered for services and wellness centre attendees were asked about their needs, opinions, and preferences to help guide future program and service options. Findings and recommendations are presented for programming and service options, and implications for future program evaluation projects are discussed. The methodology of this time and cost-efficient evaluation provides insights that can be utilized by other hospice wellness centres facing similar challenges of time, money, and program evaluation expertise constraints. The findings and recommendations may inform program and service offerings at other Canadian hospice wellness centres.
{"title":"Stretching a Penny: Completing a Rapid Needs Assessment for a Nonprofit Community-Based Hospice Wellness Center in Ontario, Canada.","authors":"Michael R Bennett, Carly Charron, Patricia Valcke","doi":"10.1080/15524256.2023.2229037","DOIUrl":"10.1080/15524256.2023.2229037","url":null,"abstract":"<p><p>The literature pertaining to community-based hospice wellness centres, especially concerning program evaluation, is sparse. This article describes the development and implementation of a mixed-method, rapid needs assessment for a nonprofit community-based hospice wellness centre in Ontario, Canada. As part of the needs assessment, a survey and focus groups were performed to elicit responses from service users. Individuals registered for services and wellness centre attendees were asked about their needs, opinions, and preferences to help guide future program and service options. Findings and recommendations are presented for programming and service options, and implications for future program evaluation projects are discussed. The methodology of this time and cost-efficient evaluation provides insights that can be utilized by other hospice wellness centres facing similar challenges of time, money, and program evaluation expertise constraints. The findings and recommendations may inform program and service offerings at other Canadian hospice wellness centres.</p>","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":"19 3","pages":"229-251"},"PeriodicalIF":1.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10077965","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01Epub Date: 2023-06-02DOI: 10.1080/15524256.2023.2219407
Aline Demerjian
{"title":"Bearing Witness: The Power of Presence.","authors":"Aline Demerjian","doi":"10.1080/15524256.2023.2219407","DOIUrl":"10.1080/15524256.2023.2219407","url":null,"abstract":"","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":"19 3","pages":"171-173"},"PeriodicalIF":1.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10129998","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01DOI: 10.1080/15524256.2023.2248808
Ellen L Csikai
Welcome to another issue! In a look ahead to the final issue of this volume, the issue will contain reflections and practice concepts and innovations manuscripts that were submitted in response to a “call” pertaining to trauma-informed practice within endof-life and palliative care. This issue begins with the thoughtful reflections of three authors: Demerjian, Abrams and Olsen. I am always impressed with these reflections that definitely give pause to spur on our own reflection or to learn a new or different way to view. This issue’s “Practice Concepts and Innovations,” brings awareness to a vital part of communication and quality of life and near the end of life: the ability to hear. Hughes describes a hearing aid loan program that provided hearing aids to individuals to their benefit as well as their caregivers. The author discusses the intervention, partnerships formed and challenges identified in implementing this type of program. Social workers may wish to consider designing a similar problem with partners as a resource for hearing loss within hospice and palliative care settings. The first of the research articles, highlights the prevalence of end-stage renal and the experiences of individuals in hemodialysis. Because ESRD is a chronic illness with deterioration in kidney function over time, even with following treatment plans, it often comes with many physical and psychosocial stressors. Powathil & AR describe a qualitative study conducted in a dialysis center in India. The participants described their decline in physical functioning and psychosocial concerns, including social support system changes and economic hardships. The authors place these results within their cultural context. What remains similar is the need for social work interventions to help individuals and families cope with the stressors of this end stage disease. When someone has a serious illness, it seems most would assume that treatment of the illness should bring about at least some relief from symptoms that may be causing distress. It is often not widely acknowledged by health care professionals that there are other factors that could interfere with treatment, such as homelessness. Johnson and colleagues present a study examining the common experiences that people who have unstable housing and a concurrent serious illness may face while living with the illness and seeking treatment. The authors then craft these common experiences found into a typology of pathways that may be seen. These include aging and dying within the housing care system, frequent transitions, “use” of health facilities as housing and stable housing seen as palliative (providing comfort). Practitioners and policy advocates can utilize this typology to bring further attention to this growing problem. Next, Bennett and colleagues share a methodology utilized for a rapid needs assessment that was used for a nonprofit community-based hospice wellness center. Multiple methods of data collection was used
{"title":"Editor Introduction.","authors":"Ellen L Csikai","doi":"10.1080/15524256.2023.2248808","DOIUrl":"10.1080/15524256.2023.2248808","url":null,"abstract":"Welcome to another issue! In a look ahead to the final issue of this volume, the issue will contain reflections and practice concepts and innovations manuscripts that were submitted in response to a “call” pertaining to trauma-informed practice within endof-life and palliative care. This issue begins with the thoughtful reflections of three authors: Demerjian, Abrams and Olsen. I am always impressed with these reflections that definitely give pause to spur on our own reflection or to learn a new or different way to view. This issue’s “Practice Concepts and Innovations,” brings awareness to a vital part of communication and quality of life and near the end of life: the ability to hear. Hughes describes a hearing aid loan program that provided hearing aids to individuals to their benefit as well as their caregivers. The author discusses the intervention, partnerships formed and challenges identified in implementing this type of program. Social workers may wish to consider designing a similar problem with partners as a resource for hearing loss within hospice and palliative care settings. The first of the research articles, highlights the prevalence of end-stage renal and the experiences of individuals in hemodialysis. Because ESRD is a chronic illness with deterioration in kidney function over time, even with following treatment plans, it often comes with many physical and psychosocial stressors. Powathil & AR describe a qualitative study conducted in a dialysis center in India. The participants described their decline in physical functioning and psychosocial concerns, including social support system changes and economic hardships. The authors place these results within their cultural context. What remains similar is the need for social work interventions to help individuals and families cope with the stressors of this end stage disease. When someone has a serious illness, it seems most would assume that treatment of the illness should bring about at least some relief from symptoms that may be causing distress. It is often not widely acknowledged by health care professionals that there are other factors that could interfere with treatment, such as homelessness. Johnson and colleagues present a study examining the common experiences that people who have unstable housing and a concurrent serious illness may face while living with the illness and seeking treatment. The authors then craft these common experiences found into a typology of pathways that may be seen. These include aging and dying within the housing care system, frequent transitions, “use” of health facilities as housing and stable housing seen as palliative (providing comfort). Practitioners and policy advocates can utilize this typology to bring further attention to this growing problem. Next, Bennett and colleagues share a methodology utilized for a rapid needs assessment that was used for a nonprofit community-based hospice wellness center. Multiple methods of data collection was used ","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":"19 3","pages":"169-170"},"PeriodicalIF":1.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10076884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01Epub Date: 2023-06-30DOI: 10.1080/15524256.2023.2229036
Patricia Dobríková, Regina Scheitel, Audrey Roulston
In addition to addressing nursing and medical needs, the social needs of patients within hospice care require assessment (i.e., relationships, isolation, loneliness, societal inclusion or exclusion, negotiating adequate formal and informal support, or living with a life-limiting condition). The objectives of this scoping review are to examine the challenges of adult patients in receipt of hospice care during the COVID-19 pandemic and to identify innovative changes to care during the pandemic. The methodology of the scoping review follows the Joanna Briggs Institute framework developed in 2015. The context included hospice services (inpatient, outpatient and community). In August 2022, PubMed and SAGE journals were searched from 2020 onwards for studies published in English, which focused on COVID-19, hospice, social, support and challenges. Titles and abstracts were independently screened by two reviewers against agreed criteria. Fourteen studies were included. Data were independently extracted by authors. Emerging themes were loss due to COVID-19 restrictions, challenges for staff, barriers to communication and transition to Telemedicine, and positive effects of the pandemic. Pivoting to Tele-medicine and restricting visitors reduced the risk of spreading coronavirus but resulted in patients being socially isolated from loved ones, and a reliance on technology to have sensitive conversations.
{"title":"Challenges and Innovations in Hospice Care during the COVID-19 Pandemic: A Scoping Review.","authors":"Patricia Dobríková, Regina Scheitel, Audrey Roulston","doi":"10.1080/15524256.2023.2229036","DOIUrl":"10.1080/15524256.2023.2229036","url":null,"abstract":"<p><p>In addition to addressing nursing and medical needs, the social needs of patients within hospice care require assessment (i.e., relationships, isolation, loneliness, societal inclusion or exclusion, negotiating adequate formal and informal support, or living with a life-limiting condition). The objectives of this scoping review are to examine the challenges of adult patients in receipt of hospice care during the COVID-19 pandemic and to identify innovative changes to care during the pandemic. The methodology of the scoping review follows the Joanna Briggs Institute framework developed in 2015. The context included hospice services (inpatient, outpatient and community). In August 2022, PubMed and SAGE journals were searched from 2020 onwards for studies published in English, which focused on COVID-19, hospice, social, support and challenges. Titles and abstracts were independently screened by two reviewers against agreed criteria. Fourteen studies were included. Data were independently extracted by authors. Emerging themes were loss due to COVID-19 restrictions, challenges for staff, barriers to communication and transition to Telemedicine, and positive effects of the pandemic. Pivoting to Tele-medicine and restricting visitors reduced the risk of spreading coronavirus but resulted in patients being socially isolated from loved ones, and a reliance on technology to have sensitive conversations.</p>","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":"19 3","pages":"252-274"},"PeriodicalIF":1.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10077968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01Epub Date: 2023-06-27DOI: 10.1080/15524256.2023.2229038
M Courtney Hughes, Diane ScheckLong, King Chung
This article describes a hearing aid loan program to provide free amplification devices for patients at the end of life to help them communicate more effectively at this critical time. It includes steps for establishing such a program, addressing challenges, and the role of the informal caregiver throughout the intervention. Healthcare professionals and social workers are encouraged to develop similar programs and use the information here as helpful suggestions to consider for their programs.
{"title":"Hearing Aid Loan Program for Hearing Loss at the End of Life.","authors":"M Courtney Hughes, Diane ScheckLong, King Chung","doi":"10.1080/15524256.2023.2229038","DOIUrl":"10.1080/15524256.2023.2229038","url":null,"abstract":"<p><p>This article describes a hearing aid loan program to provide free amplification devices for patients at the end of life to help them communicate more effectively at this critical time. It includes steps for establishing such a program, addressing challenges, and the role of the informal caregiver throughout the intervention. Healthcare professionals and social workers are encouraged to develop similar programs and use the information here as helpful suggestions to consider for their programs.</p>","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":"19 3","pages":"182-189"},"PeriodicalIF":1.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10077960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01Epub Date: 2023-06-02DOI: 10.1080/15524256.2023.2219411
Elizabeth Abrahams
{"title":"Agency as a Key to Identity.","authors":"Elizabeth Abrahams","doi":"10.1080/15524256.2023.2219411","DOIUrl":"10.1080/15524256.2023.2219411","url":null,"abstract":"","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":"19 3","pages":"174-178"},"PeriodicalIF":1.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10129997","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01Epub Date: 2023-07-04DOI: 10.1080/15524256.2023.2231160
Catherine Olsen
{"title":"Sitting with Helplessness.","authors":"Catherine Olsen","doi":"10.1080/15524256.2023.2231160","DOIUrl":"10.1080/15524256.2023.2231160","url":null,"abstract":"","PeriodicalId":45992,"journal":{"name":"Journal of Social Work in End-of-Life & Palliative Care","volume":"19 3","pages":"179-181"},"PeriodicalIF":1.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10072355","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}