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WHAT CRUCIAL COMPONENTS SHOULD BE INTEGRATED INTO BEREAVEMENT PROGRAMS FOR THE LATINO POPULATION?Blanco, Aida 01 June 2019 (has links)
The purpose of the study is to provide an understanding of the emotional and cultural needs Latinos experience when grieving the loss of a loved one. Current research shows that the Latino community is less likely to seek mental health treatment including end of life and bereavement services. This study uses a qualitative approach examining participant’s experiences during the bereaved phase focusing on emotional needs. The study reveals that Latinos experience emotional distress during bereavement and grief. It also identifies a scarcity of programs designed to meet the needs of the bereaved of Latino communities in the Inland Empire where this study takes place. The study explores different barriers that prevent Latinos from accessing and utilizing bereavement services among Latino communities, social work professionals, and organizations focusing on emotional and mental health. The study reveals that Latinos have a need for culturally sensitive programs to help them process feelings of grief and loss; language, values, and traditions are identified as main cultural characteristics including family and religion. The study identifies support groups, counseling, home visits, and phone calls as the top bereavement services needed in Latino communities as well as professionals who can understand their cultural needs.
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The impact of peer death on adolescent girls : an efficacy study of the Adolescent Grief and Loss groupMalone, Pamela Ann 14 December 2010 (has links)
Many adolescent girls experience the death of a peer, which is often sudden and at times violent. These deaths are typically viewed as preventable, which can complicate the grief reactions of adolescent girls. The impact of peer death on adolescent girls involves a number of physical, emotional, social, and cognitive grief responses. Negative outcomes include school problems, depression, substance abuse, and suicidal ideation.
This study examines the efficacy of the Adolescent Grief and Loss (AGL) group, a six-week group designed to address the needs of adolescent girls who have experienced the death of a peer within the past two years. The goal of the AGL group was to reduce or lessen physical, emotional, social, and cognitive responses to grief, and to foster mutual support and connection to others via various tasks associated with each group session. The AGL group was conducted in four different public high schools in Central Texas, with a sample size of 20 girls.
A mixed methods design was utilized for this study, integrating both quantitative and qualitative research designs. The quantitative component employed a non-experimental simple time-series design, using two pre-test and three post-test time points. The qualitative component was based on a phenomenological analysis of adolescent grief and loss response, which included open-ended questions developed to capture each adolescent girl’s individual experience of peer death. Questions were also asked to elicit the girls’ experience of participating in the AGL group.
The quantitative results of the study indicate that adolescent girls benefited from participation in the AGL group as evidenced by significantly reduced scores on the Loss Response List for all domains of physical, emotional, social, and cognitive grief responses. The qualitative findings yielded five overarching themes of experience of peer death: the story, physical reactions, emotional reactions, social reactions, and cognitive reactions. Integration of the quantitative and qualitative findings of this research study strongly support the benefits of providing a grief and loss group to adolescent girls who have been impacted by the experience of peer death. / text
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Constructing a life after death: Writing my younger experiences of grief and lossCragg, Carys Margaret 19 August 2008 (has links)
In a series of performative and narrative pieces, readers of this autoethnographic text are invited into the story of a young girl experiencing grief and loss, as expressed through her journals, poetry, and letters, and their corresponding events, written between the ages of 11-18 years. From present day, back through time, and forward again, encircled with clinical practice accounts, an alternative perspective of younger people’s experience of grief and loss is taken up, emphasizing one young girl’s construction of a life after her father’s sudden death.
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Constructing a life after death: Writing my younger experiences of grief and lossCragg, Carys Margaret 19 August 2008 (has links)
In a series of performative and narrative pieces, readers of this autoethnographic text are invited into the story of a young girl experiencing grief and loss, as expressed through her journals, poetry, and letters, and their corresponding events, written between the ages of 11-18 years. From present day, back through time, and forward again, encircled with clinical practice accounts, an alternative perspective of younger people’s experience of grief and loss is taken up, emphasizing one young girl’s construction of a life after her father’s sudden death.
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You and Me, AlwaysNguyen, Frenci Maxine 19 July 2021 (has links)
No description available.
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Career Termination: The Collegiate Athletes' Self-Identity with the Transition Through the Grief and Loss CycleStreet, Dylan B 01 January 2022 (has links)
The research seeks to understand and explain the impact, if any, on the transition out of sport, based on the level of commitment to sport being a Collegiate Athlete. Interest for this study came from personal experience as an athlete, as well as knowing numerous athletes who have gone or are going through, questioning their Identity once their playing days came to an end. This study includes extant literature discussing Athletic Identity. It offers a different perspective than other studies working through grief and loss after losing the ability to play a sport.
The purpose of this study is to offer possible explanations and resources to deal with the problem of Identity Crisis in a post-athletic career. Here, Identity Crisis will be defined as a “personal psychosocial conflict, especially in adolescence that involves confusion about one's social role and often a sense of loss of continuity to one's personality” (Merriam-Webster's dictionary). This is currently being brought to light with the COVID-19 pandemic. The results of this study will describe the effects of transitioning out of sport through the Kübler-Ross “Grief and Loss cycle” of an athlete. This study is intended to be a resource for collegiate athletes, coaches, trainers, administrators, parents, and counselors to be better prepared to help athletes with this transition.
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Beyond Telling: A Phenomenology of Adoptive Parents' Adoption Communication Openness with Early AdolescentsSamuel, Jane D. 01 January 2019 (has links)
Despite calls for increased Adoption Communication Openness (ACO) within the adoptive family, research indicates that families still struggle to accomplish the recommended elements and levels of openness. What could be holding families back from this key process? Three focus groups comprised of 17 adoptive parents of early adolescents (aged 10-14) who were age 0-2 at the time of placement were thematically coded. This inductive analysis revealed the complexity rooted in being —sometimes successfully and sometimes not—communicatively open. Four key themes emerged painting a vivid and rich picture of: a) the breadth and depth of this experience; b) the work entailed; c) the emotionality of it; and d) the grief and loss embedded in it. These results strengthen the understanding of the lived-experience of the adoptive parent thus magnifying the call for not only further research into what drives ACO in the family, but also consistent and supportive pre- and post-adoption services and clinical work.
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A study of the integration of health promotion principles and practice in palliative care organisationsRosenberg, John Patrick January 2007 (has links)
The modern hospice movement emerged in the 1960s as a grassroots social movement that attempted to restore an holistic and contextualised approach to the care of people at the end of life. This approach embraced the lived experience of the dying person at the centre of care across physical, emotional, social and spiritual domains of life. To achieve this, the care of dying people was largely removed from mainstream health care systems to promote more holistic and socially contextualised dying. In recent decades, the evolution of palliative care demonstrates the gradual return of palliative care services to the mainstream. It has been asserted that, in this process, palliative care services have progressively abandoned the social context of dying people, increasing instead an emphasis on "physical care [while] simultaneously de-emphasizing psychological, social and spiritual care" (Kellehear, 1999a, p.76). Kellehear and others have proposed that the repositioning of palliative care within mainstream health care systems has increased a focus upon illness and disease at the expense of health and wellbeing. Subsequently, conventional palliative care services have been criticised for not adequately locating end of life care within the social contexts in which death and dying take place. In an attempt to address this problem, Australian sociologist Allan Kellehear proposed an approach to end of life care that brought together the core concerns of palliative care with the principles and practices of health promotion (Kellehear, 1999b). Whilst their congruence is not immediately apparent, these two fields have been increasingly examined for their potential benefits in the provision of end of life care. In the current policy climate in Australia, there is an imperative to consider how end of life support services might be improved through adopting a health promoting palliative care approach. The aim of this study has been to investigate the integration of health promotion principles and practice by a selected palliative care service by examining the qualitative impact of this change on the organisation. Specifically, it endeavoured to identify the factors that advanced or impeded this integration by examining how the structures and processes of, and outcomes for, the organisation reflected a health promoting approach. To meet these aims, this study undertook an in-depth examination of the implementation of a health promoting palliative care model by a community based palliative care organisation. Based in a constructionist-interpretivist paradigm, a mixed-method (QUAL+quant), instrumental case study research design was utilised to capture multiple perspectives of the implementation process. Data collection comprised examination of 127 organisational documents, 32 in-depth interviews with staff, volunteers and consumers, 5 focus groups with staff and volunteers, and 25 carer questionnaires. Qualitative data were subject to thematic analysis, with supplementary quantitative data analysed to generate descriptive statistics. The findings demonstrated a large number of complex and interrelated enabling and impeding factors to the implementation in the case study site. These factors have been grouped into four key themes which have been examined in light of the aims of this study and the issues identified in a comprehensive review of the literature. This study found that: ◦ Conceptual congruence between health promotion and palliative care was a fundamental starting point in the implementation of a health promoting palliative care model. ◦ Where conceptual congruence was clear, activities associated with the model that were regarded as beyond conventional approaches to palliative care core business were viewed favourably by stakeholders and were less likely to encounter resistance within the organisation. ◦ When systematic approaches to organisational change, such as quality improvement systems, were rigorously applied, the impact of the transition upon stakeholders was qualitatively less. ◦ Where this transition had been effectively made, consumers, staff, volunteers and members of the wider community were seen to benefit. This study adds to the current discourse regarding the intersection between end of life support and health promotion, and provides insight into how palliative care organisations might undertake the transition from conventional models to a health promoting palliative care approach.
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My Journey with Prisoners: Perceptions, Observations and OpinionsBriney, Carol E. 08 July 2013 (has links)
No description available.
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