120 research outputs found

    The place of volunteering in palliative care

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    This chapter discusses the place and development of volunteering in palliative care in the context of hospice service provision in the UK. It draws on recent qualitative research undertaken in a large hospice in England. The research explored a range of issues connected to the process and experience of voluntary work in this setting including who volunteers, what roles volunteers take up, how they are trained and supported and the ways in which role boundaries are established and maintained. The research revealed that hospice volunteering is rewarding but often emotionally challenging and is now highly routinised and closely monitored in ways paralleling practices in the paid labour market. Although volunteers freely give their time to the work of hospice, their activities are subject to significant management prescription, with hospices increasingly adopting sophisticated business models to underpin their operation and, in many cases, their expansion (Watts, 2010)

    Teaching a distance higher education curriculum behind bars: challenges and opportunities

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    The provision of education that is both effective and relevant to the needs of students within prison is challenging on a number of levels. The uniqueness of prison culture with a regime characterised by a focus on security measures such as lock-downs and head counts constrains the possibilities for learning. The absence of a supportive learning environment together with an emphasis on punishment rather than rehabilitation has the effect of marginalising education in prison so that ‘education’ has come to be seen by some as ‘off limits’. Education in basic skills such as literacy and numeracy that contributes to ‘life skills’ is given priority. In contrast, access to higher education is more problematic with this generally perceived by both prisoners and prison staff as an ‘elite’ activity. This article adopts a case study approach to consider the barriers to higher education distance learning in the prison setting. It focuses on the practical and organisational constraints faced by educators in their efforts to help students in prison negotiate the different worlds of prison and higher education. It also highlights the value of one-to-one tutorial support in facilitating learning in less than optimum teaching conditions

    To publish or not to publish before submission? Considerations for doctoral students and supervisors

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    Postgraduate research education is multi-faceted incorporating the teaching of a range of skills and study behaviours. A key skill for doctoral students is that of scholarly writing that Aitchison (2009) argues is often difficult to teach, with students unclear about the standards required for doctoral work. One benchmark of standards of academic literacy is published outputs, with Kamler (2008) pressing for greater pedagogical attention to be given to writing for publication within doctoral education. However, the case for pursuing publication as part of doctoral research experience is subject to a number of variables. This discussion paper debates some of these variables to consider writing for publication within diverse doctoral education. Features of difference will be discussed to reveal that the choice of whether or not to “publish as you go” (Taylor & Beasley, 2005: 130) is influenced by the personal, disciplinary and institutional context that frames the doctoral undertaking

    Spiritual care at the end of life: whose job is it?

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    Interest in and recognition of the function of religious and spiritual coping in adjustment to serious illness has been growing. In particular, there has been increasing interest in the importance of understanding and valuing patients' individual spirituality as a function of providing appropriate support, particularly as part of nursing practice. This stems partly from the influence and application of palliative care principles in a range of care settings and not just hospices. Four decades of professional rhetoric have emphasised the importance of care for the 'whole' person in terms of spiritual as well as psychological, physical and social needs, without evaluating its impacts on patients or considering whether this approach is realistic in every case. Professional ideology within palliative care has been dominant in influencing a culture of openness between professional health workers and dying patients in their care, with attention to spiritual needs an increasing part of professionals' remit. New ways to both assess and address spiritual concerns as part of overall quality of life are being developed by health care practitioners as part of a package of support for people with critical and terminal illness (Randall and Downie, 2006; Watts, 2008). For this support to be meaningful, however, it is necessary to determine which dimensions of spirituality are relevant and the ways in which the human spirit can be celebrated in the face of life-threatening illness (Cobb and Legood, 2008). The ultimate value of such exploration is to make it possible for us to die the way we live (Hockey, 2002)

    Cancer, life review and the boundary between the 'personal' and academic research

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    Much social research and commentary derives from the personal position and interest of the writer with, in recent years, a marked increase in the use of case histories, vignettes and auto ethnography, as legitimate methodological research tools. This article, drawing on that tradition, is a reflective commentary on the author's experience of supporting a friend through a critical life-threatening illness, highlighting the dual aspects of personal engagement and academic reflection. The ways in which the 'personal' can be opportunity for methodological and empirical reflection, but also serve as ethical constraint, are considered. An underpinning concern is the requirement for ethical probity, both in maintaining confidentiality within the account and in considering the issue of consent, in reporting the personal details of the author and those of the friend whose critical health episode is central to the discussion. Attention is also drawn to the importance of life review on the part of those who face life-limiting illness. Discussion focuses on the experience of life review from the perspective of both the author and friend, suggesting that this may be a more meaningful support in the form of intimate exchange rather than as clinical therapeutic intervention. The article argues that the personal, rather than disrupting critical social research, particularly in the field of health and well-being, can contribute positively to shaping new understandings and insights

    An integrated literature review of death education in pre-registration nursing curricula: key themes

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    Recent policy has raised the profile of end-of-life care internationally, with the aim of increasing access to quality care for everyone experiencing life-limiting illness. This reflects an international shift in the provision of palliative care to encompass chronic conditions other than cancer. Nurses have an important role in delivering this care and need to be equipped with particular knowledge and skills. However, pre-registration nursing curricula have traditionally had a limited emphasis on death and dying and nurses report feeling unprepared to care for dying patients. This has led to claims that death education in pre-registration curricula is inadequate. This integrated review explores published literature that reports on death education within pre-registration nurse education. Presenting an international overview, the aim of the review is to contribute to knowledge about the nature and extent of death education in pre-registration curricula. In the context of this paper, death education encompasses both palliative and end-of-life care. Electronic searches of major bibliographic databases found inconsistencies across educational provision with variations in quantity, content and approach. Despite an increasing amount of death education in pre-registration curricula, there remains a deficit in key areas such as knowledge, skills, organisation of care and teamwork
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