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Data were analyzed by direct interpretation and categorical aggregation<\/jats:p><\/jats:sec><jats:sec id=\"S1478951513000333_sec3\"><jats:title>Results:<\/jats:title><jats:p>Various patterns of becoming a caregiver were showed, but family members' willingness to become family caregivers was strongly related to fulfilling the dying persons' wishes to be cared for in their own homes. Important factors for coping with the caregiving situation were their needs of support, the possibility to prepare for death related to a need of communication and planning, the length and predictability of the illness trajectory, and experiences of losses and grief. Sitting service was experienced as supportive for family caregivers when they had possibility to hand over care responsibilities, but as non-supportive when expected help not was received.<\/jats:p><\/jats:sec><jats:sec id=\"S1478951513000333_sec4\"><jats:title>Significance of the research:<\/jats:title><jats:p>Family members' experiences of caregiving and their degree of vulnerability must be different, depending on whether it is a self-selected position or an imposed task. In general, family members in this study were willing to participate in caregiving for end-of life care, but subject to their own conditions. One way to decrease vulnerability is to assess the resources and competence in relation to the responsibility the person is expected to assume. The support and other efforts to help family caregivers must be related to their specific needs and reality, not only to what the care organization can offer as a standard solution.<\/jats:p><\/jats:sec>","DOI":"10.1017\/s1478951513000333","type":"journal-article","created":{"date-parts":[[2013,6,20]],"date-time":"2013-06-20T08:23:26Z","timestamp":1371716606000},"page":"425-437","source":"Crossref","is-referenced-by-count":8,"title":["Family members' caregiving situations in palliative home care when sitting service is received: The understanding of multiple realities"],"prefix":"10.1017","volume":"12","author":[{"given":"Birgitta","family":"Wallerstedt","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Birgitta","family":"Andershed","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eva","family":"Benzein","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"56","published-online":{"date-parts":[[2013,6,20]]},"reference":[{"key":"S1478951513000333_ref26","doi-asserted-by":"publisher","DOI":"10.1136\/bmj.38740.614954.55"},{"key":"S1478951513000333_ref28","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1177\/082585970101700105","article-title":"The emotions and coping strategies of caregivers of family members with a terminal cancer","volume":"17","author":"Grbich","year":"2001","journal-title":"Journal of Palliative Care"},{"key":"S1478951513000333_ref36","doi-asserted-by":"publisher","DOI":"10.1016\/j.jpainsymman.2010.05.006"},{"key":"S1478951513000333_ref48","volume-title":"Tillg\u00e5ng p\u00e5 v\u00e5rdplatser (Available care places).","year":"2010"},{"key":"S1478951513000333_ref41","doi-asserted-by":"publisher","DOI":"10.1007\/s10728-004-6639-6"},{"key":"S1478951513000333_ref14","doi-asserted-by":"publisher","DOI":"10.1016\/j.pec.2007.10.020"},{"key":"S1478951513000333_ref33","doi-asserted-by":"crossref","first-page":"35","DOI":"10.5694\/j.1326-5377.2003.tb05576.x","article-title":"Home-based support for palliative care families: Challenges and recommendations","volume":"179","author":"Hudson","year":"2003a","journal-title":"The Medical Journal of Australia"},{"key":"S1478951513000333_ref21","doi-asserted-by":"publisher","DOI":"10.1089\/jpm.2006.9.196"},{"key":"S1478951513000333_ref39","doi-asserted-by":"publisher","DOI":"10.1177\/1054773803012002002"},{"key":"S1478951513000333_ref19","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1177\/082585970301900107","article-title":"Mapping the journey: Family carers' perceptions of issues related to end- stage care of individuals with muscular dystrophy or motor neuron disease","volume":"19","author":"Dawson","year":"2003","journal-title":"Journal of Palliative Care"},{"key":"S1478951513000333_ref37","doi-asserted-by":"publisher","DOI":"10.1017\/S1478951507070034"},{"key":"S1478951513000333_ref54","volume-title":"Aktuellt p\u00e5 \u00e4ldreomr\u00e5det, 2008","year":"2008"},{"key":"S1478951513000333_ref47","doi-asserted-by":"publisher","DOI":"10.1097\/00002820-200308000-00003"},{"key":"S1478951513000333_ref59","first-page":"312","volume-title":"Palliative care nursing: Principles and evidence for practice","author":"Smith","year":"2004"},{"key":"S1478951513000333_ref44","doi-asserted-by":"publisher","DOI":"10.1007\/s00520-003-0569-y"},{"key":"S1478951513000333_ref56","volume-title":"Socialtj\u00e4nstlag. 2001:453 (The Social Service Act 2001:453). 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