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Una Stenberg, Cornelia
M. Ruland, Mariann Olsson & Mirjam Ekstedt. (2012) To Live Close to a Person With Cancer—Experiences of Family Caregivers. Social Work in Health Care 51:10, pages 909-926.
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Articles from other publishers (22)
Apichat Kardosod, Judith Needham & Elisabeth Coyne. (2023) The experiences and needs of metastatic spinal cancer family caregivers at home: a systematic review. Supportive Care in Cancer 31:5.
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Franziska A. Herbst, Laura Gawinski, Nils Schneider & Stephanie Stiel. (2021) ‘She Can’t Support Me Because She’s so Old’: A Mixed-Methods Study of Support Experiences and Needs in Adult Child–Parent Dyads at the End of Life. OMEGA - Journal of Death and Dying 86:4, pages 1371-1387.
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Semra Ozdemir, Sean Ng, Isha Chaudhry, Irene Teo, Chetna Malhotra & Eric Andrew Finkelstein. (2022) Caregiver-Reported Roles in Treatment Decision Making in Advanced Cancer and Associated Caregiving Burden and Psychological Distress: A Longitudinal Study. Medical Decision Making 43:2, pages 191-202.
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Suzie Y. Rababa’h, Karem H. Alzoubi, Laiali Alquraan, Reema Karasneh, Sayer I Al-azzam & Nasr Alrabadi. (2022) Depression Among the Caregivers of Breast Cancer Patients and its Association with the Quality of Life. Clinical Practice & Epidemiology in Mental Health 18:1.
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Benedicta Owoo, Jerry Paul K. Ninnoni, Evelyn Asamoah Ampofo & Abdul-Aziz Seidu. (2022) “I always find myself very tired and exhausted”: The physical impact of caring; a descriptive phenomenological study of the experiences of prostate cancer caregivers in Cape Coast, Ghana. PLOS ONE 17:7, pages e0268627.
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Rachid Ismaili, Bouchra Haddou Rahou, Ahmed Nejmeddine, Hind Mimouni, Abderraouf Hilali, Rachid Bekkali & Leila Loukili. (2022) Lung cancer and its impact on patient's spouse: A narrative literature review. Annals of Cancer Research and Therapy 30:2, pages 125-130.
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Eylem Pasli Gurdogan, Berna Aksoy & Ezgi Kinici. (2020) The Concept of a Good Death From the Perspectives of Family Caregivers of Advanced Cancer Patients. OMEGA - Journal of Death and Dying 85:2, pages 303-316.
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Sabine Bohnet-Joschko & Katharina Bidenko. (2021) Hochbelastete Gruppen pflegender Angehöriger – Ergebnisse einer Clusteranalyse. Das Gesundheitswesen 84:06, pages 510-516.
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Sharnel Miriam Perera, Clare O’Callaghan, Anna Ugalde, Olinda Santin, Cassandra Beer, G Prue, Katherine Lane, Gerard G Hanna & Penelope Schofield. (2021) Codesigning a supportive online resource for Australian cancer carers: a thematic analysis of informal carers’ and healthcare professionals’ perspectives about carers’ responsibilities and content needs. BMJ Open 11:10, pages e055026.
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Esra ENGİN, Mahire Olcay ÇAM & Hacer DEMİRKOL. (2021) Arafta Bir Yaşam: Kemik İliği Nakli Olan Bir Çocuğun Annesi OlmakA Life in Purgatory: Being the Mother of a Bone Marrow Transplant Child. Psikiyatride Güncel Yaklaşımlar 13:2, pages 282-291.
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Yakubu Salifu, Kathryn Almack & Glenys Caswell. (2020) ‘My wife is my doctor at home’: A qualitative study exploring the challenges of home-based palliative care in a resource-poor setting. Palliative Medicine 35:1, pages 97-108.
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Jane Lowers, Melissa Scardaville, Sean Hughes & Nancy J. Preston. (2020) Comparison of the experience of caregiving at end of life or in hastened death: a narrative synthesis review. BMC Palliative Care 19:1.
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Theresa A. Hastert, Julie J. Ruterbusch, Mrudula Nair, Mirza Ishrat Noor, Jennifer L. Beebe-Dimmer, Kendra Schwartz, Tara E. Baird, Felicity W.K. Harper, Hayley Thompson & Ann G. Schwartz. (2020) Employment Outcomes, Financial Burden, Anxiety, and Depression Among Caregivers of African American Cancer Survivors. JCO Oncology Practice 16:3, pages e221-e233.
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Jae Yop Kim, 황호경, Lim Ji Hye & 성신명. (2016) Cancer Care-giver Burden On The Parents-Children Negative Communication - The Moderating Effect Of Family TSL Attitude -. Korean Journal of Family Social Work null:54, pages 77-106.
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Mauricio Arias Rojas & Cristina García-Vivar. (2015) The transition of palliative care from the hospital to the home: a narrative review of experiences of patients and family caretakers. Investigación y Educación en Enfermería 33:3.
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Jane M. Ussher, Mirjana Sandoval, Janette Perz, W. K. Tim Wong & Phyllis Butow. (2013) The Gendered Construction and Experience of Difficulties and Rewards in Cancer Care. Qualitative Health Research 23:7, pages 900-915.
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J. Armoogum, A. Richardson & J. Armes. (2012) A survey of the supportive care needs of informal caregivers of adult bone marrow transplant patients. Supportive Care in Cancer 21:4, pages 977-986.
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Una Stenberg, Cornelia M. Ruland & Christine Miaskowski. (2009) Review of the literature on the effects of caring for a patient with cancer. Psycho-Oncology 19:10, pages 1013-1025.
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L FunkKI Stajduhar, C Toye, S Aoun, GE Grande & CJ Todd. (2010) Part 2: Home-based family caregiving at the end of life: a comprehensive review of published qualitative research (1998-2008). Palliative Medicine 24:6, pages 594-607.
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Penny E Bee, Pamela Barnes & Karen A Luker. (2009) A systematic review of informal caregivers’ needs in providing home-based end-of-life care to people with cancer. Journal of Clinical Nursing 18:10, pages 1379-1393.
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Deborah P. Waldrop. (2018) Caregiving Systems at the End of Life: How Informal Caregivers and Formal Providers Collaborate. Families in Society: The Journal of Contemporary Social Services 87:3, pages 427-437.
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Deborah P. Waldrop, Robert A. Milch & Judith A. Skretny. (2019) Understanding Family Responses to Life-Limiting Illness: In-depth Interviews with Hospice Patients and Their Family Members. Journal of Palliative Care 21:2, pages 88-96.
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