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Author: Roisin Ryan Flood Publisher: Routledge ISBN: 1317555740 Category : Social Science Languages : en Pages : 202
Book Description
Third party conception is a growing phenomenon and provokes a burgeoning range of ethical, legal and social questions. What are the rights of donors, recipients and donor conceived children? How are these reproductive technologies regulated? How is kinship understood within these new family forms? Written by specialists from three different continents, Transnationalising Reproduction examines a broad range of issues concerning kinship and identity, citizenship and regulation, and global markets of reproductive labour; including gamete donation and gestational surrogacy. Indeed, this book seeks to highlight how reproductive technologies not only makes possible new forms of kinship and family formations, but also how these give rise to new, ethical, political and legal dilemmas about parenthood as well as new modes of discrimination and a re-distribution of medical risks. It also thoroughly investigates the ways in which a commodification of reproductive tissue and labour affects the practices, representations and gendered self-understandings of gamete donors, fertility patients and intended parents in different parts of the world. With a broad geographical scope, Transnationalising Reproduction offers new empirical and theoretical perspectives on third-party conception and demonstrates the need for more transnational approaches to third-party reproduction. This volume will appeal to postgraduate students and postdoctoral researchers interested in fields such as Gender Studies, Health Care Sciences, Reproductive Technology and Medical Sociology.
Author: Roisin Ryan Flood Publisher: Routledge ISBN: 1317555740 Category : Social Science Languages : en Pages : 202
Book Description
Third party conception is a growing phenomenon and provokes a burgeoning range of ethical, legal and social questions. What are the rights of donors, recipients and donor conceived children? How are these reproductive technologies regulated? How is kinship understood within these new family forms? Written by specialists from three different continents, Transnationalising Reproduction examines a broad range of issues concerning kinship and identity, citizenship and regulation, and global markets of reproductive labour; including gamete donation and gestational surrogacy. Indeed, this book seeks to highlight how reproductive technologies not only makes possible new forms of kinship and family formations, but also how these give rise to new, ethical, political and legal dilemmas about parenthood as well as new modes of discrimination and a re-distribution of medical risks. It also thoroughly investigates the ways in which a commodification of reproductive tissue and labour affects the practices, representations and gendered self-understandings of gamete donors, fertility patients and intended parents in different parts of the world. With a broad geographical scope, Transnationalising Reproduction offers new empirical and theoretical perspectives on third-party conception and demonstrates the need for more transnational approaches to third-party reproduction. This volume will appeal to postgraduate students and postdoctoral researchers interested in fields such as Gender Studies, Health Care Sciences, Reproductive Technology and Medical Sociology.
Author: Alexander Styhre Publisher: Routledge ISBN: 1317616227 Category : Social Science Languages : en Pages : 202
Book Description
Reproductive medicine has been very successful at developing new therapies in recent years and people having difficulties conceiving have more options available to them than ever before. These developments have led to a new institutional landscape emerging and this innovative volume explores how health and social structures are being developed and reconfigured to take into account the increased use of assisted reproductive technologies, such as IVF treatments. Using Sweden as a central case study, it explores how the process of institutionalizing new assisted reproductive technologies includes regulatory agencies, ethical committees, political bodies and discourses, scientific communities, patient and activists groups, and entrepreneurial activities in the existing clinics and new entrants to the industry. It draws on new theoretical developments in institutional theory and outlines how health innovations are always embedded in social relations including ethical, political, and financial concerns. This book will be of interest to advanced students and academics in health management, science and technology studies, the sociology of health and illness and organisational theory.
Author: Fabienne Portier-Le Cocq Publisher: Routledge ISBN: 1351803255 Category : Social Science Languages : en Pages : 216
Book Description
In Europe, the percentage of lone-parent families has risen from 14% to 19% between 1996 and 2012. Only in Greece and Finland did the rates fall, while in Denmark and the Republic of Ireland the rise has reached or exceeded 10 percent. As of 2017, there are 2.9 million lone parents with dependent children in the UK, and nine out of ten lone parents are women. Sadly, lone parents are known to experience considerable social, financial, and health problems. Fertility, Health and Lone Parenting examines the way in which lone parents live their lives, and how it impacts their health and well-being. Topics explored in these interdisciplinary contributions include lifestyle, nutrition, and the mental health of both parents and children. Unique empirical case studies within a European context help to expand the reader’s understanding, whilst also drawing comparisons between the impacts of lone parenting on young mothers, fathers and their children. A timely volume, this book will appeal to undergraduate and postgraduate students interested in subjects such as Sociology of the Family, Social Policy, Social Work, Gender Studies and Family Policy.
Author: Sallie Han Publisher: Routledge ISBN: 100045598X Category : Social Science Languages : en Pages : 631
Book Description
The Routledge Handbook of Anthropology and Reproduction is a comprehensive overview of the topics, approaches, and trajectories in the anthropological study of human reproduction. The book brings together work from across the discipline of anthropology, with contributions by established and emerging scholars in archaeological, biological, linguistic, and sociocultural anthropology. Across these areas of research, consideration is given to the contexts, conditions, and contingencies that mark and shape the experiences of reproduction as always gendered, classed, and racialized. Over 39 chapters, a diverse range of international scholars cover topics including: Reproductive governance, stratification, justice, and freedom. Fertility and infertility. Technologies and imaginations. Queering reproduction. Pregnancy, childbirth, and reproductive loss. Postpartum and infant care. Care, kinship, and alloparenting. This is a valuable reference for scholars and upper-level students in anthropology and related disciplines associated with reproduction, including sociology, gender studies, science and technology studies, human development and family studies, global health, public health, medicine, medical humanities, and midwifery and nursing.
Author: Virginie Rozée Publisher: Routledge ISBN: 1317393805 Category : Health & Fitness Languages : en Pages : 237
Book Description
Assisted Reproductive Technologies in the Global South and North critically analyses the political and social frameworks of Assisted Reproductive Technology (ART), and its impact in different countries. In the context of a worldwide social pressure to conceive – particularly for women – this collection explores the effect of the development of ARTs, growing globalisation and reproductive medicalization on global societies. Providing an overview of the issues surrounding ART both in the Global South and North, this book analyses ART inequalities, commonalities and specificities in various countries, regions and on the transnational scene. From a multidisciplinary perspective and drawing on multisite studies, it highlights some new issues relating to ART (e.g. egg freezing, surrogacy) and discusses some older issues regarding infertility and its medical treatment (e.g. in vitro fertilisation, childless stigmatisation and access to treatment). This book aims to redress the balance between what is known about Assisted Reproductive Technologies in the Global North, and how the issue is investigated in the Global South. It aims to draw out the global similarities in the challenges that ARTs bring between these different areas of the world. It will appeal to scholars and students in the social sciences, medicine, public health, health policy, women’s and gender studies, and demography.
Author: Cecilia Vindrola Padros Publisher: Routledge ISBN: 1351202014 Category : Health & Fitness Languages : en Pages : 198
Book Description
By taking an ethnographic approach to medical travel, this important book uses critical perspectives to understand inequalities in healthcare access and delivery, including gender, class and ethnicity, and explore how these are negotiated. In this key text Vindrola- Padros presents a comprehensive overview of the work carried out on this topic to date, highlights the gaps that remain and suggests strategies for enriching medical travel research in the future. Drawing from the author’s research on internal medical travel to access pediatric oncology treatment in Buenos Aires, Argentina and other research from across the globe, this book presents four dimensions of medical travel that can be explored through a critical (im)mobilities lens: infrastructures, differential mobility empowerments, culture and affective dimensions of care and travel. Vindrola-Padros encourages the reader to critically explore processes of medical travel by considering the structures that shape travel, individual capacities for travel, the role emotions play in decisions and experiences of movement and service delivery and the ways in which culture(s) influence both travel and care. This book will be important reading for scholars across medical sociology, anthropology and critical health studies.
Author: Shirley Sun Publisher: Routledge ISBN: 1134989199 Category : Social Science Languages : en Pages : 139
Book Description
The second decade of the twenty-first century has witnessed a surging interest in personalized medicine with the concomitant promise to enable more precise diagnosis and treatment of disease and illness, based upon an individual’s unique genetic makeup. In this book, my goal is to contribute to a growing body of literature on personalized medicine by tracing and analyzing how this field has blossomed in Asia. In so doing, I aim to illustrate how various social and economic forces shape the co-production of science and social order in global contexts. This book shows that there are inextricable transnational linkages between developing and developed countries and also provides a theoretically guided and empirically grounded understanding of the formation and usage of particular racial and ethnic human taxonomies in local, national and transnational settings. The Open Access version of this book, available at http://www.taylorfrancis.com/doi/view/10.4324/9781315537177 has been made available under a Creative Commons Attribution-Non Commercial-No Derivatives 4.0 license.
Author: Sabrina Ching Yuen Luk Publisher: Routledge ISBN: 1315516276 Category : Business & Economics Languages : en Pages : 150
Book Description
China’s current social medical insurance system has nominally covered more than 95 per cent of 1.4 billion population in China and is moving towards the ambitious goal of universal health insurance coverage. Challenges posed by a rapidly ageing population, an inherently discriminatory design of the health insurance system, the disorder of drug distribution system and an immature legal system constrain the Chinese government from realizing its goal of universal health insurance coverage in the long run. This book uses a refined version of historical institutionalism to critically examine China's pathway to universal health insurance coverage since the mid-1980s. It pays crucial attention to the processes of transforming China's healthcare financing system into the basic social medical insurance system alongside rapid socio-economic changes. Financing Healthcare in China will interest researchers and government and think-tank officials interested in the state of healthcare reforms in China. Healthcare specialists outside of East Asia may also be interested in its general study of healthcare in developing countries. Scholars and students interested in the healthcare field will also find this useful.
Author: Simon M. Dyson Publisher: Routledge ISBN: 1351580841 Category : Social Science Languages : en Pages : 242
Book Description
Sickle cell disease (SCD) is a severe chronic illness and one of the world’s most common genetic conditions, with 400,000 children born annually with the disorder, mainly in Sub-Saharan Africa, India, Brazil, the Middle East and in diasporic African populations in North America and Europe. Biomedical treatments for SCD are increasingly available to the world’s affluent populations, while such medical care is available only in attenuated forms in Africa, India and to socio-economically disadvantaged groups in North America and Europe. Often a condition rendered invisible in policy terms because of its problematic association with politically marginalized groups, the social study of sickle cell has been neglected. This illuminating volume explores the challenges and possibilities for developing a social view of sickle cell, and for improving the quality of lives of those living with SCD. Tackling the controversial role of screening and genetics in SCD, the book offers a brief thematic history of approaches to the condition, queries the role of ethnicity and includes a discussion of how the social model of disability can be applied, as well as featuring chapters focusing on athletics, prisons and schools. Bringing together a wide range of original research conducted in the USA, the UK, Ghana and Nigeria, Sickle Cell and the Social Sciences is anchored in the discipline of sociology, but draws upon a diverse range of fields, including public health, anthropology, social policy and disability studies.
Author: Gaynor Macdonald Publisher: Routledge ISBN: 1351241796 Category : Social Science Languages : en Pages : 234
Book Description
A diagnosis of dementia changes the ways people engage with each other – for those living with dementia, as well their families, caregivers, friends, health professionals, neighbours, shopkeepers and the community. Medical understandings, necessary as they are, provide no insights into how we may all live good lives with dementia. This innovative volume brings together an interdisciplinary group of researchers and practitioners to focus on dementia as lived experience. It foregrounds dementia’s social, moral, political and economic dimensions, investigating the challenges of reframing the dementia experience for all involved. Part I critiques the stigmas, the negativity, language and fears often associated with a dementia diagnosis, challenging debilitating representations and examining ways to tackle these. Part II examines proactive practices that can support better long-term outcomes for those living with dementia. Part III looks at the relational aspects of dementia care, acknowledging and going beyond the notion of person-centred care. Collectively, these contributions highlight the social and relational change required to enhance life for those with dementia and those who care for them. Engaging in a critical conversation around personhood and social value, this book examines the wider social contexts within which dementia care takes place. It calls for social change, and looks for inspiration to the growing movement for relational care and the caring society. Dementia as Social Experience is important reading for all those people who, in various ways, are living with dementia, as well as for those working in this area as clinicians, researcher and carers.
Author: Roisin Ryan Flood
Author: Roisin Ryan Flood
Author: Alexander Styhre
Author: Fabienne Portier-Le Cocq
Author: Sallie Han
Author: Virginie Rozée
Author: Cecilia Vindrola Padros
Author: Shirley Sun
Author: Sabrina Ching Yuen Luk
Author: Simon M. Dyson
Author: Gaynor Macdonald