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      • Trusted Partner
        Feeling the strain
        Humanities & Social Sciences
        July 2019

        Feeling the strain

        A cultural history of stress in twentieth-century Britain

        by Jill Kirby, Keir Waddington, David Cantor

        Examining the popular discourse of nerves and stress, this book provides a historical account of how ordinary Britons understood, explained and coped with the pressures and strains of daily life during the twentieth century. It traces the popular, vernacular discourse of stress, illuminating not just how stress was known, but the ways in which that knowledge was produced. Taking a cultural approach, the book focuses on contemporary popular understandings, revealing continuity of ideas about work, mental health, status, gender and individual weakness, as well as the changing socio-economic contexts that enabled stress to become a ubiquitous condition of everyday life by the end of the century. With accounts from sufferers, families and colleagues it also offers insight into self-help literature, the meanings of work and changing dynamics of domestic life, delivering a complementary perspective to medical histories of stress.

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      • Trusted Partner
        Beautyscapes
        Humanities & Social Sciences
        June 2019

        Beautyscapes

        Mapping cosmetic surgery tourism

        by Ruth Holliday, Meredith Jones, David Bell

        Beautyscapes explores the global phenomenon of international medical travel, focusing on patient-consumers seeking cosmetic surgery outside their home country and on those who enable them to access treatment abroad, including surgeons and facilitators. It documents the journeys of those who travel for treatment abroad, as well as the nature and power relations of the IMT industry. Empirically rich and theoretically sophisticated, Beautyscapes draws on key themes of interest to students and researchers interested in globalisation and mobility to explain the nature and growing popularity of cosmetic surgery tourism. Richly illustrated with ethnographic material and with the voices of those directly involved in cosmetic surgery tourism, Beautyscapes explores cosmetic surgery journeys from Australia and China to East-Asia and from the UK to Europe and North Africa.

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      • Trusted Partner
        Beautyscapes
        Humanities & Social Sciences
        June 2019

        Beautyscapes

        Mapping cosmetic surgery tourism

        by Ruth Holliday, Meredith Jones, David Bell

        Beautyscapes explores the global phenomenon of international medical travel, focusing on patient-consumers seeking cosmetic surgery outside their home country and on those who enable them to access treatment abroad, including surgeons and facilitators. It documents the journeys of those who travel for treatment abroad, as well as the nature and power relations of the IMT industry. Empirically rich and theoretically sophisticated, Beautyscapes draws on key themes of interest to students and researchers interested in globalisation and mobility to explain the nature and growing popularity of cosmetic surgery tourism. Richly illustrated with ethnographic material and with the voices of those directly involved in cosmetic surgery tourism, Beautyscapes explores cosmetic surgery journeys from Australia and China to East-Asia and from the UK to Europe and North Africa.

        More
      • Trusted Partner
        Beautyscapes
        Humanities & Social Sciences
        January 2020

        Beautyscapes

        Mapping cosmetic surgery tourism

        by Ruth Holliday, Meredith Jones, David Bell

        Beautyscapes explores the global phenomenon of international medical travel, focusing on patient-consumers seeking cosmetic surgery outside their home country and on those who enable them to access treatment abroad, including surgeons and facilitators. It documents the journeys of those who travel for treatment abroad, as well as the nature and power relations of the IMT industry. Empirically rich and theoretically sophisticated, Beautyscapes draws on key themes of interest to students and researchers interested in globalisation and mobility to explain the nature and growing popularity of cosmetic surgery tourism. Richly illustrated with ethnographic material and with the voices of those directly involved in cosmetic surgery tourism, Beautyscapes explores cosmetic surgery journeys from Australia and China to East-Asia and from the UK to Europe and North Africa.

        More
      • Trusted Partner
        Feeling the strain
        Humanities & Social Sciences
        July 2019

        Feeling the strain

        A cultural history of stress in twentieth-century Britain

        by Jill Kirby, Keir Waddington, David Cantor

        Examining the popular discourse of nerves and stress, this book provides a historical account of how ordinary Britons understood, explained and coped with the pressures and strains of daily life during the twentieth century. It traces the popular, vernacular discourse of stress, illuminating not just how stress was known, but the ways in which that knowledge was produced. Taking a cultural approach, the book focuses on contemporary popular understandings, revealing continuity of ideas about work, mental health, status, gender and individual weakness, as well as the changing socio-economic contexts that enabled stress to become a ubiquitous condition of everyday life by the end of the century. With accounts from sufferers, families and colleagues it also offers insight into self-help literature, the meanings of work and changing dynamics of domestic life, delivering a complementary perspective to medical histories of stress.

        More
      • Trusted Partner
        Balancing the self
        Medicine
        February 2020

        Balancing the self

        Medicine, politics and the regulation of health in the twentieth century

        by Mark Jackson, Martin D. Moore, David Cantor

        Balancing the Self explores the diverse ways in which balanced and unbalanced selfhoods have been subject to construction, intervention and challenge across the long twentieth century. Chapters on diabetes, `sensible drinking', obesity control, dietetic regulation, fatigue, heart disease, physical and emotional extremes, Parkinson's disease and other conditions understood in terms of disordered balance analyse the ways in which the mechanisms and meanings of balance have been framed historically. Together, contributions examine the positive narratives that have been attached to the ideals and practices of `self-help', and the extent to which rhetorics of empowerment and responsibility have been used for a variety of purposes, from disciplining bodies to cutting social security provision.

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      • Trusted Partner
        Balancing the self
        Medicine
        February 2020

        Balancing the self

        Medicine, politics and the regulation of health in the twentieth century

        by Mark Jackson, Martin D. Moore, David Cantor

        More
      • Trusted Partner
        Balancing the self
        Medicine
        March 2020

        Balancing the self

        Medicine, politics and the regulation of health in the twentieth century

        by Mark Jackson, Martin D. Moore, David Cantor

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      • Trusted Partner
        Trust in the system
        Science & Mathematics
        December 2020

        Trust in the system

        Research Ethics Committees and the regulation of biomedical research

        by Adam Hedgecoe, Des Fitzgerald, Amy Hinterberger

        Based on extensive observations, interviews, and archival research, this book provides an in-depth insight into one of the most crucial forms of regulation around medical research: Research Ethics Committees. Every month, groups of people from all over the United Kingdom decide what kind of research should be carried out on patients within the National Health Service. These groups - Research Ethics Committees (RECs) - made up of doctors, nurses, researchers, and members of the general public - help shape the future of medicine, and play a crucial role in the regulation of a wide range of research from social science to epidemiology, vaccine and drugs trials, and surgery. In providing one of the first empirical examinations of this kind of regulation, this book highlights how, despite the trappings of a modern regulatory system, REC decision making revolves around outdated aspects of social life. Hedgecoe argues that an accurate understanding of this kind of regulation requires an acceptance of the inherently social nature of the processes involved. In placing trust at the centre of ethics decision making, this book challenges the impersonal, de-socialised, and mechanical models of REC decision making that dominate mainstream accounts, and documents the subtle, messy, and complex way in which these bodies decide what kind of research should take place.

        More
      • Trusted Partner
        Trust in the system
        Science & Mathematics
        December 2020

        Trust in the system

        Research Ethics Committees and the regulation of biomedical research

        by Adam Hedgecoe, Des Fitzgerald, Amy Hinterberger

        Based on extensive observations, interviews, and archival research, this book provides an in-depth insight into one of the most crucial forms of regulation around medical research: Research Ethics Committees. Every month, groups of people from all over the United Kingdom decide what kind of research should be carried out on patients within the National Health Service. These groups - Research Ethics Committees (RECs) - made up of doctors, nurses, researchers, and members of the general public - help shape the future of medicine, and play a crucial role in the regulation of a wide range of research from social science to epidemiology, vaccine and drugs trials, and surgery. In providing one of the first empirical examinations of this kind of regulation, this book highlights how, despite the trappings of a modern regulatory system, REC decision making revolves around outdated aspects of social life. Hedgecoe argues that an accurate understanding of this kind of regulation requires an acceptance of the inherently social nature of the processes involved. In placing trust at the centre of ethics decision making, this book challenges the impersonal, de-socialised, and mechanical models of REC decision making that dominate mainstream accounts, and documents the subtle, messy, and complex way in which these bodies decide what kind of research should take place.

        More
      • Trusted Partner
        Trust in the system
        Science & Mathematics
        December 2020

        Trust in the system

        Research Ethics Committees and the regulation of biomedical research

        by Adam Hedgecoe, Des Fitzgerald, Amy Hinterberger

        Based on extensive observations, interviews, and archival research, this book provides an in-depth insight into one of the most crucial forms of regulation around medical research: Research Ethics Committees. Every month, groups of people from all over the United Kingdom decide what kind of research should be carried out on patients within the National Health Service. These groups - Research Ethics Committees (RECs) - made up of doctors, nurses, researchers, and members of the general public - help shape the future of medicine, and play a crucial role in the regulation of a wide range of research from social science to epidemiology, vaccine and drugs trials, and surgery. In providing one of the first empirical examinations of this kind of regulation, this book highlights how, despite the trappings of a modern regulatory system, REC decision making revolves around outdated aspects of social life. Hedgecoe argues that an accurate understanding of this kind of regulation requires an acceptance of the inherently social nature of the processes involved. In placing trust at the centre of ethics decision making, this book challenges the impersonal, de-socialised, and mechanical models of REC decision making that dominate mainstream accounts, and documents the subtle, messy, and complex way in which these bodies decide what kind of research should take place.

        More
      • Trusted Partner
        Understanding baby loss
        Humanities & Social Sciences
        November 2023

        Understanding baby loss

        The sociology of life, death and post-mortem

        by Kate Reed, Julie Ellis, Elspeth Whitby

        This book offers a detailed and sensitive account of how parents experience different forms of baby loss, and subsequently make decisions about post-mortem examination. It also analyses some of the challenges professionals face when working in this highly sensitive field of medicine. It draws on data from an ESRC award-winning UK based study on the development of minimally invasive post-mortem to examine a range of sociologically pertinent issues relating to: 'trauma' 'emotions', 'decisions', 'care' 'technology' 'memory' and the role of 'social and biological relationships'. By shedding light on this taboo aspect of healthcare, the book provides a highly original contribution to sociology, offering a comprehensive analysis of some of the most pressing concerns in the field to date.

        More
      • Trusted Partner
        Understanding baby loss
        Humanities & Social Sciences
        November 2023

        Understanding baby loss

        The sociology of life, death and post-mortem

        by Kate Reed, Julie Ellis, Elspeth Whitby

        This book offers a detailed and sensitive account of how parents experience different forms of baby loss, and subsequently make decisions about post-mortem examination. It also analyses some of the challenges professionals face when working in this highly sensitive field of medicine. It draws on data from an ESRC award-winning UK based study on the development of minimally invasive post-mortem to examine a range of sociologically pertinent issues relating to: 'trauma' 'emotions', 'decisions', 'care' 'technology' 'memory' and the role of 'social and biological relationships'. By shedding light on this taboo aspect of healthcare, the book provides a highly original contribution to sociology, offering a comprehensive analysis of some of the most pressing concerns in the field to date.

        More
      • Trusted Partner
        Personalised cancer medicine
        Medicine
        January 2021

        Personalised cancer medicine

        Future crafting in the genomic era

        by Anne Kerr, Choon Key Chekar, Emily Ross, Julia Swallow, Sarah Cunningham-Burley

        This electronic version has been made available under a Creative Commons (BY-NC-ND) open access license. What does it mean to personalise cancer medicine? Drawing on an ethnographic study with cancer patients, carers and practitioners in the UK, this book traces their efforts to access and interpret novel genomic tests, information and treatments as they craft personal and collective futures. Exploring multiple experiences of new diagnostic tests, research programmes and trials, advocacy and experimental therapies, the authors chart the different kinds of care and work involved in efforts to personalise cancer medicine, as well as the ways in which benefits and opportunities are unevenly realised and distributed. Comparing these experiences with policy and professional accounts of the 'big' future of personalised healthcare, the authors show how hope and care are multi-faceted, contingent and, at times, frustrated in the everyday complexities of living and working with cancer. This book is available as an open access ebook under a CC-BY-NC-ND licence.

        More
      • Trusted Partner
        Personalised cancer medicine
        Medicine
        January 2021

        Personalised cancer medicine

        Future crafting in the genomic era

        by Anne Kerr, Choon Key Chekar, Emily Ross, Julia Swallow, Sarah Cunningham-Burley

        This electronic version has been made available under a Creative Commons (BY-NC-ND) open access license. What does it mean to personalise cancer medicine? Drawing on an ethnographic study with cancer patients, carers and practitioners in the UK, this book traces their efforts to access and interpret novel genomic tests, information and treatments as they craft personal and collective futures. Exploring multiple experiences of new diagnostic tests, research programmes and trials, advocacy and experimental therapies, the authors chart the different kinds of care and work involved in efforts to personalise cancer medicine, as well as the ways in which benefits and opportunities are unevenly realised and distributed. Comparing these experiences with policy and professional accounts of the 'big' future of personalised healthcare, the authors show how hope and care are multi-faceted, contingent and, at times, frustrated in the everyday complexities of living and working with cancer.

        More
      • Trusted Partner
        Personalised cancer medicine
        Medicine
        January 2021

        Personalised cancer medicine

        Future crafting in the genomic era

        by Anne Kerr, Choon Key Chekar, Emily Ross, Julia Swallow, Sarah Cunningham-Burley

        What does it mean to personalise cancer medicine? Drawing on an ethnographic study with cancer patients, carers and practitioners in the UK, this book traces their efforts to access and interpret novel genomic tests, information and treatments as they craft personal and collective futures. Exploring multiple experiences of new diagnostic tests, research programmes and trials, advocacy and experimental therapies, the authors chart the different kinds of care and work involved in efforts to personalise cancer medicine, as well as the ways in which benefits and opportunities are unevenly realised and distributed. Comparing these experiences with policy and professional accounts of the 'big' future of personalised healthcare, the authors show how hope and care are multi-faceted, contingent and, at times, frustrated in the everyday complexities of living and working with cancer. This book is available as an open access ebook under a CC-BY-NC-ND licence.

        More
      • Trusted Partner
        Embodiment and everyday cyborgs
        Medicine
        June 2021

        Embodiment and everyday cyborgs

        Technologies that alter subjectivity

        by Gill Haddow

        This electronic version has been made available under a Creative Commons (BY-NC-ND) open access license. Your organs are failing and require replacement. If you had the choice, would you prefer organs from other humans or non-human animals, or would you choose a 'cybernetic' medical implant? Using a range of social science methods and drawing on the sociology of the body and embodiment, biomedicine and technology, this book asks what happens to who we are (our identity) when we change what we are (our bodies)? From surveying young adults about whether they would choose options such as 3-D bioprinting, living or deceased human donation, or non-human animal or implantable biomechanical devices, to interviewing those who live with an implantable cardiac defibrillator, Haddow invites us to think about what kind of relationship we have with our bodies. She concludes that the reliance on 'cybernetic' medical devices create 'everyday cyborgs' who can experience alienation and new forms of vulnerability at implantation and activation. Embodiment and everyday cyborgs invites readers to consider the relationship between personal identity and the body, between humans and non-human animals, and our increasing dependency on 'smart' implantable technology. The creation of new techno-organic hybrid bodies makes us acutely aware of our own bodies and how ambiguous the experience of embodiment actually is. It is only through understanding how modifications such as transplantation, amputation and implantation make our bodies a 'presence' to us, Haddow argues, that we realise our everyday experience of our bodies as an absence.

        More
      • Trusted Partner
        Embodiment and everyday cyborgs
        Medicine
        June 2021

        Embodiment and everyday cyborgs

        Technologies that alter subjectivity

        by Gill Haddow

        This electronic version has been made available under a Creative Commons (BY-NC-ND) open access license. Your organs are failing and require replacement. If you had the choice, would you prefer organs from other humans or non-human animals, or would you choose a 'cybernetic' medical implant? Using a range of social science methods and drawing on the sociology of the body and embodiment, biomedicine and technology, this book asks what happens to who we are (our identity) when we change what we are (our bodies)? From surveying young adults about whether they would choose options such as 3-D bioprinting, living or deceased human donation, or non-human animal or implantable biomechanical devices, to interviewing those who live with an implantable cardiac defibrillator, Haddow invites us to think about what kind of relationship we have with our bodies. She concludes that the reliance on 'cybernetic' medical devices create 'everyday cyborgs' who can experience alienation and new forms of vulnerability at implantation and activation. Embodiment and everyday cyborgs invites readers to consider the relationship between personal identity and the body, between humans and non-human animals, and our increasing dependency on 'smart' implantable technology. The creation of new techno-organic hybrid bodies makes us acutely aware of our own bodies and how ambiguous the experience of embodiment actually is. It is only through understanding how modifications such as transplantation, amputation and implantation make our bodies a 'presence' to us, Haddow argues, that we realise our everyday experience of our bodies as an absence.

        More

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