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Reporting the findings of a series of in-depth studies based on diverse groups of students, including early school-leavers, men, Maori, teachers, nurses, midcareer students, and retirees, this book examines these students' patterns of study, their employment status, their motivations, and the decisions they make. It examines how they experience university, how they see their futures, and how educational institutions might better plan, promote, process, and deliver courses to this growing group of older students.
This book comprehensively explores social, political and cultural dimensions of health in contemporary society. It addresses many issues and pertinent questions, including the following: Are we over diagnosed and over medicated? How can patients participate in their own care? Do pharmaceutical companies coerce us into medication regimes? What drives inequalities in health outcomes? What is the experience of health care for indigenous communities? Why do different countries have such different health care systems? How do we respond to life-changing conditions? Can we achieve a ‘good death’? How do new genetics shape our identities? Is public health a force of liberation or disempowerment? The book incorporates the range of levels of influence on health, covering individual patient experiences, the health professions, multinational corporations, the state, global organisations as well as examining trends in social organisation, cultural expression and technological developments. It volume provides an accessible, yet in-depth, overview and discussion of the sociology of health. The chapters include an illustrative case study and further readings relating to the topic.
Later years are changing under the impact of demographic, social and cultural shifts. No longer confined to the sphere of social welfare, they are now studied within a wider cultural framework that encompasses new experiences and new modes of being. Drawing on influences from the arts and humanities, and deploying diverse methodologies – visual, literary, spatial – and theoretical perspectives Cultural Gerontology has brought new aspects of later life into view. This major new publication draws together these currents including: Theory and Methods; Embodiment; Identities and Social Relationships; Consumption and Leisure; and Time and Space. Based on specially commissioned chapters by leading international authors, the Routledge Handbook of Cultural Gerontology will provide concise authoritative reviews of the key debates and themes shaping this exciting new field.
Drawing on over 100 oral histories from men and women who were children in the first three decades of the century, this book explores the work done in those years by men, women and children as members of families and communities. It considers work done for pay and free. Extracts from interviews are used to illustrate various family patterns represented, and the text makes use of historical and demographic literature on family and kinship in the past in New Zealand and elsewhere. A bibliography and an index are provided.
This book focuses on the place sand purpose of emotions in the research process, and explores the appropriate boundaries. Designed to explore how to manage the emotional content of research, the text service as a supplemental to qualitative research method courses, and is an excellent reference for the professional as well.
This book explores the social history of venereal disease and public health in New Zealand in the twentieth-century by re-evaluating existing international scholarship on disease control and issues of morality. By using untapped archival material, this case study highlights the wider importance in international research into the interception of health agencies and targeted groups and the impact of gender, race and class on the venereal disease debate.
Once a synonym for death, cancer is now a prognosis of multiple probabilities and produces a world of uncertainty for carers. Drawing on rich, in-depth interview data and employing interactionist theories, Towards a Sociology of Cancer Caregiving explores carers' lived experiences, paying close attention to the ways in which spouse carers manage the ambiguity that pervades their orientations to the future, their responsibilities and their emotions. A detailed exploration of the temporal and emotional journeys of spouse carers of cancer patients, this volume raises and responds to new questions about how to conceptualise informal caregiving, offering a fresh theorisation of the uncertainty that now characterises cancer. As such, it will appeal to scholars of the sociologies of emotion, time and identity, and all those interested in the question of how to support informal carers.
Bringing together unique international research from the United States, United Kingdom, Canada, Australia and Europe, this book presents a detailed examination of the violence perpetrated by males and females within the context of childhood, adolescence and adulthood. Based on illuminating empirical studies it accurately locates the societal implications of violence against males and females as well as the legal, social and public responses to violence. Combining feminism and a related analysis of power, the book provides an introduction to the study of violence in general, and violence against males and females who know each other in particular. It outlines the major evolutionary, psychological, and sociological theories proposed to explain this social problem and the traditional methods of studying this topic. The book also examines child violence - in the playground, the classroom and the home; adolescent dating violence and adult violence, both male and female, within cohabiting and marital relationships and violence occurring between strangers.
Introduction -- The new normal in American family caregiving -- Caregiving begins -- The costs of care -- Decision-making: with advance direction -- Decision-making: looking for direction -- Mourning rubrics and burial -- The intricacies of wealth transfer -- 21st century caregiving