Review of Social Media for Academics

I have written many times on this blog about my own experiences of using social media and other digital tools for academic work and my research focusing on how other academics are doing this.

One of the people I have encountered along the way is Mark Carrigan, an early career British sociologist. Appropriately enough, we first met on Twitter a few years ago, around the time I began experimenting with various digital tools for professional purposes. Since then, we have had many discussions there and on other online forums, as well as by email, about using social media in universities (and a couple of in-person meetings as well). Mark has now written a book on Social Media for Academics. It is the first book I know of to present a ‘how-to’ manual combined with reflections on the wider implications of  academic social media engagement.

Mark is a great example of someone who has strategically used social media while still in the very early stages of his career (completing his doctorate) to create a high profile for his work. He has now built on this experience not only to work in various positions involving promoting academic journals, departments and organisations, but to produce this book. In its chapters, Mark employs a casual, chatty style to painlessly introduce readers to the art of academic social media.

The book is distinctive because Mark’s sociological training allows him to contextualise the social, cultural and political implications of academic social media use. Yes, he offers  a multitude of helpful tips and advice about how best to communicate online, what platforms and tools are the most effective, how to develop your own voice, how online engagement helps in promoting one’s research and reaching wider audiences outside academia, building networks, curating interesting material you have found on the internet, finding time to use social media and so on. But there are also reflections offered on what academic social media means for professional identities and for academic work in general. In addition there are many pithy remarks drawing on Mark’s observations, for example, of the awkwardness that sometimes accompanies the experience of colleagues meeting in the flesh after having developed a hitherto purely online relationship, or the potential pitfalls of live-tweeting conferences or writing a tweet or blog post in haste and anger that then becomes widely circulated well after the initial irritation has subsided.

This book is highly recommended for higher degree students and faculty staff members who are interested in the possibilities of academic social media for both research and teaching, as well as researchers interested in future directions for the university workplace and academic identities.

 

Edited book ‘Beyond Techno-Utopia: Critical Approaches to Digital Health Technologies’ now out

Last year I guest-edited a special issue of the open-access sociology journal Societies that focused on critical perspectives on digital health technologies. The collection includes my editorial and another article I contributed (on the topic of apps as sociocultural artefacts), as well as eight other articles from scholars based in the UK, Australia, Finland, the USA and Sweden. Individual contributions may be accessed on the journal’s website here, and now the whole collection is available as an open access book PDF (or can be purchased as a hard copy), both available here.

The following outline of the special issue/book’s contents, an edited excerpt taken from my editorial, provides an overview of its contents.

The articles in this special issue build on a well-established literature in sociology, science and technology studies and media and cultural studies that has addressed the use of digital technologies in health and medicine… Several of these topics are taken up in the articles published in this special issue. All the authors use social and cultural theory to provide insights into the tacit assumptions, cultural meanings and experiences of digital health technologies. The articles cover a range of digital health technologies: devices used for the self-tracking of body metrics (Ruckenstein; Till; Rich and Miah; Lupton); social media platforms for discussing patients’ experiences of chronic disease (Sosnowy) and experiences of pregnancy and early motherhood (Johnson); health and medical apps (Till; Johnson; Christie and Verran; Lupton); telehealthcare systems (Hendy, Chrysanthaki and Barlow); and a digital public health surveillance system (Cakici and Sanches). While some articles focus on globalised digital media (Cakici and Sanches; Rich and Miah; Till; Lupton), others engage more specifically with a range of sociocultural groups, contexts and locations. These include Aboriginal people living in a remote region of Australia (Christie and Verran) and Australian mothers in urban Sydney (Johnson) as well as research participants in Helsinki, Finland (Ruckenstein), the United States (Sosnowy) and England (Hendy, Chrysanthaki and Barlow).

Understandings and experiences of selfhood and embodiment as they are generated and experienced via digital health devices are central preoccupations in the articles by Ruckenstein, Rich and Miah, Till, Lupton, Sosnowy and Johnson. Ruckenstein’s study of self-trackers found that they often conceptualised their bodies and their physical activities in different ways when these were being monitored and rendered into digital data. The data that were generated by these devices proved to be motivational and to give value to some activities (like housework) that otherwise lacked value or new meaning to functions such as sleep (which when digitised and quantified became viewed as a competence). Ruckenstein found that the digital data tended to be invested with greater validity than were other indicators of bodily wellbeing or activity, such as the individual’s physical sensations.

All of the above authors comment on the ways in which digital health devices such as wearable self-tracking devices, social media platforms, apps and patient support websites work as disciplinary tools. They invite users to conform to the ideals of healthism (privileging good health above other priorities) and the responsible self-management and self-monitoring of one’s health and body, including avoiding exposure to risk. Rich and Miah use the concept of “public pedagogy” to describe the socio-political dimensions of digital health technologies as they are employed to educate people about their bodies and promote self-management. As Johnson notes, for women who are pregnant or have the care of young children, this sphere of responsibility is extended to the bodies of others: the foetus or child. And as Till’s article emphasises, when employees are “encouraged” to engage in self-tracking, the ethos of responsibility extends from personal objectives to those of employers.

Ruckenstein, Till and Sosnowy also highlight the digital labour involved for people who engage with social media or self-tracking apps as part of their personal health or fitness practices. Sosnowy’s interviews with women with multiple sclerosis who blog about their condition emphasise the work involved in such engagement as an “active patient”. Till’s analysis of digital exercise self-tracking points to the appropriations of people’s labour by other actors for commercial reasons.

The article by Hendy, Chrysanthaki and Barlow moves in a somewhat different direction. Using ethnographic cases studies, they look at the managerial issues involved with implementing telehealthcare in English social and health care organisations. Their focus, therefore, is not on the recipients or targets of digital health technologies but rather those who are attempting to institute programs as part of their work as managers. These authors’ contribution highlights the messiness of introducing new systems and practices into large organisations, and the resistances that may emerge on the part of both workers and the targets of telehealthcare programs. Cakici and Sanches’ article also takes an organisational perspective in addressing a European Commission co-funded project directed at syndromic surveillance, or the use of secondary sources to detect outbreaks and patterns in diseases and medical conditions. Digital data are increasingly being use as part of syndromic surveillance: Google Flu Trends is one such example. Cakici and Sanches’ analysis highlights the role played by human decision-making and the affordances of digital technologies in structuring what kinds of data are retrieved for syndromic surveillance and how they are interpreted.

While there are as yet few detailed ethnographic accounts of how people are implementing, adopting or resisting contemporary digital health technologies, there are even fewer that investigate the use of these technologies by members of cultural groups outside the global North. The article by Christie and Verran takes a much-needed diversion from perspectives on white, privileged groups to Aboriginal people living in a remote part of Australia. As they argue, the concepts on health, illness and the body that are held by this cultural group differ radically from the tacit assumptions that are invested in mainstream health and medical apps. Any app that is developed to assist in health literacy that is targeted at this group must incorporate culturally-appropriate modes of communication: positioning people within their cultural and kinship networks of sociality, for example, rather than representing them as atomised actors.

The articles collected here in this special issue have gone some way in offering a critical response to digital health technologies, but they represent only a beginning. Many more compelling topics remain to be investigated. These include research into the ways in which lay people and healthcare professionals are using (or resisting the use) of social media, apps and self-monitoring devices for medicine and health-related purposes; the implications for medical power and the doctor-patient relationship; how citizen science and citizen sensing are operating in the public health domain; the development of new digital health technologies; the implications of big data and data harvesting in medicine and healthcare; the spreading out of health-related self-tracking practices into many social domains; the unintended consequences and ethical aspects of digital technology use and their implications for social justice; and data security and privacy issues.

Digital Sociology now out

Digital Sociology has now been published (click here for the Amazon link and here for the publisher’s link).

 

The publisher’s blurb is below:

Digital Sociology

We now live in a digital society. New digital technologies have had a profound influence on everyday life, social relations, government, commerce, the economy and the production and dissemination of knowledge. People’s movements in space, their purchasing habits and their online communication with others are now monitored in detail by digital technologies. We are increasingly becoming digital data subjects, whether we like it or not, and whether we choose this or not.

The sub-discipline of digital sociology provides a means by which the impact, development and use of these technologies and their incorporation into social worlds, social institutions and concepts of selfhood and embodiment may be investigated, analysed and understood. This book introduces a range of interesting social, cultural and political dimensions of digital society and discusses some of the important debates occurring in research and scholarship on these aspects. It covers the new knowledge economy and big data, reconceptualising research in the digital era, the digitisation of higher education, the diversity of digital use, digital politics and citizen digital engagement, the politics of surveillance, privacy issues, the contribution of digital devices to embodiment and concepts of selfhood and many other topics.

Digital Sociology is essential reading not only for students and academics in sociology, anthropology, media and communication, digital cultures, digital humanities, internet studies, science and technology studies, cultural geography and social computing, but for other readers interested in the social impact of digital technologies.

Chapter abstracts for my Digital Sociology book

I am pleased to announce that my latest book, Digital Sociology, has now gone into production with Routledge, and is due for publication around October this year. Here are the chapter abstracts to give some idea of the book’s contents.

1 Introduction: life is digital
In this introductory chapter I make an argument for why digital sociology is important and why sociology needs to make the study of digital technologies central to its very remit. It is argued that ubiquitous and mobile digital media have changed the ways in which social life is represented, conducted, monitored, managed and analysed. Digital technologies affect social relationships, concepts of identity and embodiment, the monitoring and organisation of people’s movements in space and the creation of and access to information and knowledge. I provide an overview of how digital sociology has developed and outline its four main aspects: professional digital use, analyses of digital technology use, digital data analysis, and critical digital sociology.

2 Theorising digital society
Chapter 2 provides a foundation for the ensuing chapters by reviewing the major theoretical perspectives that are developed in the book. The literature reviewed in the chapter is mainly drawn from sociology but also includes contributions from scholars in media and cultural studies, science and technology studies, surveillance studies, software studies and cultural geography. The perspectives that are discussed include analyses of the global information economy and new forms of power, the sociomaterial perspective on the relationship between humans and digital technologies, prosumption, neoliberalism and the sharing subject, the importance of the archive, theories of veillance (watching) that are relevant to digital society and theories concerning digitised embodiment.

3 Reconceptualising research in the digital era
Chapter 3 focuses on sociological and other social research in the digital era. The aim of the discussion is not to outline how to do digital research in detail. Rather I present an overview not only of some of the approaches that are available and their possibilities and limitations, but also of the more theoretical and critical stances that sociologists are taking to digital social research. I also devote attention to innovative ways of performing digital social research that are part of attempts to invigorate sociological research practice as a way of demonstrating the new and exciting directions in which sociology can extend in response to digital society.

4 The digitised academic
The higher education workplace has become increasingly digitised, with many teaching and learning resources and academic publications moving online and the performance of academics and universities monitored and measured using digital technologies. Some sociologists and other academics are also beginning to use social media as part of their academic work. In this chapter I examine the benefits and possibilities offered by digital technologies but also identify the limitations, drawbacks and risks that may be associated with becoming a digitised academic and the politics of digital public engagement.

5 A critical sociology of big data
Chapter 5 takes a critical sociological perspective on the big data phenomenon. The discussion emphasises that big data sets are systems of knowledge that are implicated in power relations. Big data are both the product of social and cultural processes and themselves act to configure elements of society and culture. They have their own politics, vitality and social life. Following an overview of the ways in which big data discourses and practices have achieved dominance in many social spheres, I discuss how digital data assemblages and algorithms possess power and authority, the metaphors used to describe big data and what these reveal about our anxieties and concerns about this phenomenon, big data hubris and rotted data and the ethical issues related to big data.

6 The diversity of digital technology use
Chapter 6 reviews research that has studied the use of digital technologies in different areas of the globe and how socioeconomic, cultural and political factors shape, promote or delimit the use of these technologies. I move from a discussion of the findings of large-scale surveys involving large numbers of respondents from specific countries or cross-nationally to in-depth qualitative investigations that are able to provide the detailed context for differences in internet use. The chapter shows that digital social inequalities are expressed and reproduced in a range of ways, including cultures of use as well as lack of access. Social inequalities and marginalisation may also be perpetuated and exacerbated online.

7 Digital politics and citizen digital public engagement
In Chapter 7 I examine the politics of digital veillance, activism, privacy debates, calls for openness of digital data and citizen digital public engagement. It is argued that while digital activism and moves to render digital data more open to citizens can be successful to some extent in achieving their aims, claims that they engender a major new form of political resistance or challenge to institutionalised power are inflated. Indeed digital technologies can provide a means by which activists can come under surveillance and be discredited by governments. Other negative aspects of citizen digital public engagement are outlined, including the ways in which the internet can incite discrimination and vigilantism and promote the dissemination of false information.

8 The digitised body/self
Chapter 8 addresses the ways in which digital software and hardware are becoming part of our identities as they store more data about our experiences, our social relationships and encounters and our bodily functioning. Digital sociologists and other digital media researchers have recognised the ways in which human embodiment and concepts of selfhood are represented and configured via digital technologies, digital data and digital social networks. It is not only the data or images produced via digital technologies that are important to research and theorise, but also how the objects themselves are used in practice. This chapter examines the incorporation of digital technologies into everyday lives across a range of contexts.

My two new books on unborn humans

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Last month both my new books on the topic of the unborn (human embryos and foetuses) were published. One is an authored book, part of the Palgrave Pivot series, entitled The Social Worlds of the Unborn. The other, The Unborn Human, is an open access book that I edited as part of the Living Books about Life series published by the Open Humanities Press.

Both books deal with very similar issues and theoretical perspectives, and therefore complement each other nicely. The Social Worlds of the Unborn has five substantive chapters. The first chapter examines what I call ‘contingencies of the unborn’, drawing on sociological, anthropological, bioethical, philosophical and historical perspectives to highlight the dynamic nature of the ways we think about foetuses and embryos and the debates over the extent of their humanness and personhood. I then go on in the next chapter to discuss technologies for visualising the unborn, such as foetal photography and computer imaging and obstetric ultrasound. These have been particularly important technologies in opening up the uterus to the gaze so that we can see the previously mysterious entities that inhabit this space. I argue that visualising technologies have worked to represent unborn entities as already persons in their own right, autonomous from the maternal body, and indeed as already infants. These images also represent the unborn as beautiful, fragile and vulnerable entities requiring our utmost love and protection, and thus are powerful agents in anti-abortion politics.

In the third chapter of this book I focus on pregnant women’s perspectives on the unborn entities growing within their own bodies. I highlight the ambivalence that pregnant women often feel about this Other body inhabiting their own, as well as their difficulty in coming to terms with their ‘two-in-one’ bodies that depart so radically from the contained, unitary bodily norm. The concept of the ‘good mother’ often precludes acknowledgement that pregnant women may sometimes feel as if their unborn is antagonistic and even parasitic. Yet these feelings are not uncommon in pregnant women, in addition to the more culturally accepted notions of the unborn as precious proto-infants.

The next chapter goes on to examine the dead unborn, including discussion of abortion practices, policies and politics, decisions about the disposal of surplus IVF embryos and the mourning and memorialisation of unborn entities lost in miscarriage or stillbirth. It also looks at bioscientific definitions of the unborn and how working practices in the medical clinic or stem cell laboratory operate to deal with using matter from dead unborn entities. Here again issues concerning judgements about the humanness and status of personhood of various unborn entities are to the fore. I demonstrated that the context in which these entities are created and grow (or fail to develop) is vital to concepts of their value and vitality.

The final substantive chapter examines the concept of the endangered unborn, particularly in relation to how pregnant women are represented as posing a threat to their unborn through ignorance or deliberate negligence. I argue that the increasing humanisation and personalising of the unborn and their representation as precious, vulnerable and as already infants with full human privileges work to position them as more important than the women who bear them, who increasingly as positioned as vessels rather than as individuals with their own rights and needs that may differ from those of their unborn.

The edited book, The Unborn Human, takes up many of these issues. I review the contents of the book in my Introduction (‘Conceptualising and configuring the unborn human‘), showing how each item in the collection contributes to various ways of thinking about, treating, representing, creating or destroying unborn entities. Like the other books in the Living Books about Life series, The Unborn Human is a curated collection of material that is available as open access publications. Some of this material can be viewed via links to the website embedded in the book, while others can be directly accessed under the Creative Commons Attribution licence. This means that all of the articles and other materials included in the book, which range from historical documents to scientific, medical, bioethical, policy, sociological, anthropological and cultural studies articles as well as social and other digital media material such as websites, blog posts and YouTube videos, can be accessed for free (including my introduction using the link supplied above).

My new book: Risk, 2nd edition

My latest book was published recently. It is the second, fully revised edition of  Risk, a volume I contributed to Routledge’s Key Ideas in Sociology series. The first edition appeared in 1999, so it was interesting to see how much had changed in the theoretical and empirical landscape of the sociology of risk in the ensuing years.

In the first edition of Risk, I identified three major theoretical perspectives on risk in social and cultural theory. The first approach draws upon the work of Mary Douglas to articulate the ‘cultural/symbolic’ perspective on risk. The second approach is that of the ‘risk society’ perspective, based on the writings of Ulrich Beck and Anthony Giddens. The third approach covered is that of the ‘governmentality’ perspective, which builds on Michel Foucault’s work.

No major theoretical perspectives have emerged since the first edition, but there have been some extensions of these established perspectives. The second edition adds discussion of new work by Beck and Giddens and governmentality writers in relation to the newly emerging threats of the twenty-first century, such as climate change, extreme weather events, terrorism and global financial crises. Beck’s recent writings on cosmopolitanism and world risk society are incorporated, as are those by Giddens on fundamentalism in relation to terrorism, and climate change politics.

New thoughts by governmentality scholars such as Mitchell Dean on precautionary risk are also covered. Precautionary risk is an approach that has recently emerged in neoliberal societies to deal with apparently incalculable and unpredictable risks. This strategy attempts to deal with great uncertainty about how to calculate and manage catastrophic risks, to govern the ungovernable threats of this new century that challenge neoliberalist ideals of progress, rational management and control.

As well as these theoretical directions, the book also includes discussion of many empirical research studies on risk published since the first edition, undertaken by researchers in the UK, USA, Canada, Australia and Scandinavia. One change in the second edition is that I place more of a focus on the notion of risk and suffering, an aspect that did not receive much attention in the first edition. Scholarly and policy representations of risk often tend not to acknowledge the emotional dimensions  of feeling threatened by risk: the anxiety, fear and despair that  may accompany such experiences.

The new edition also includes discussion of the writings of my colleague and co-author John Tulloch (see Tulloch and Lupton, 2003), who was a victim of the 7 July 2005 London bombings. John has written about his unique position as a well-known scholar of risk and as someone who became the ‘face of the London bombings’ in the news media. He found himself in the difficult position of being used by Tony Blair’s government to support its anti-terrorist legislation even though he trenchantly opposed it. As such, John was able to critique political attempts to contain and control risk and media conventions of portraying risk.

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My new book ‘Fat’


My latest book Fat has just been published as part of Routledge’s Shortcuts series.

In contemporary western societies the fat body has become a focus of stigmatizing discourses and practices aimed at disciplining, regulating and containing it. Despite the fact that in many western countries fat bodies outnumber those that are thin, fat people are still socially marginalized and treated with derision and even repulsion. Medical and public health experts insist that an ‘obesity epidemic’ exists and that fatness is a pathological condition which should be prevented and controlled.

Fat is a book about why the fat body has become so reviled and viewed as diseased, the target of such intense discussion and debate about ways to reduce its size down to socially and medically acceptable dimensions. It is also about the lived experience of fat embodiment: how does it feel to be fat in a fat-phobic society? Deborah Lupton explores fat as a cultural artefact: a bodily substance or body shape that is given meaning by complex and shifting systems of ideas, practices, emotions, material objects and interpersonal relationships.

Fat reviews current scholarship and research into obesity discourse and politics, drawing upon critical perspectives offered in the humanities and social sciences and by fat activism and the size acceptance movement. It will be an engaging introduction for the interested general reader, as well as for students across the humanities and social sciences.

New book: (Re)thinking Violence in Health Care Settings

This comprehensive volume explores various forms of violence in health care settings. Using a broad range of critical approaches in the field of anthropology, cultural studies, gender studies, political philosophy and sociology, it examines violence following three definite yet interrelated streams: institutional and managerial violence against health care workers or patients; horizontal violence amongst health care providers and finally, patients’ violence towards health care providers. Drawing together the latest research from Australia, Canada, the UK, and the US, (Re)Thinking Violence in Health Care Settings engages with the work of critical theorists such as Bourdieu, Butler, Foucault, Latour, and Žižek, amongst others, to address the issue of violence and theorise its workings in creative and controversial ways.  As such, it will be of interest to sociologists and anthropologists with research expertise in health, medicine, violence and organisations, as well as to health care professionals.

  • Contents:   Foreword, Dave Holmes; Introduction: (re)thinking violence in health care settings, Dave Holmes, Trudy Rudge, Amélie Perron and Isabelle St-Pierre; Part I Institutional and Managerial Violence: A critical reflection on the use of behaviour modification programs in forensic psychiatry settings, Dave Holmes and Stuart J. Murray; The violence of tolerance in a multicultural workplace: examples from nursing, Trudy Rudge, Virginia Mapedzahama, Sandra West and Amélie Perron; Changing discourses of blame in nursing and healthcare, Hannah Cooke; Hospital policies regarding violence in the workplace: a discourse analysis, Penny Powers; Exploring violence in a forensic hospital: a theoretical experimentation, Amélie Perron and Trudy Rudge; Nurses’ failure to report elder abuse in long-term care: an exploratory study, Gloria Hamel-Lauzon and Sylvie Lauzon. Part II Horizontal Violence: Foucault and the nexus between violence and power: the context of intra/inter professional aggression, Isabelle St-Pierre; Examining nurse-to-nurse horizontal violence and nurse-to-student vertical violence through the lens of phenomenology, Sandra P. Thomas; The rise of violence in HIV/AIDS prevention campaigns: a critical discourse analysis, Marilou Gagnon and Jean Daniel Jacob; Bullying in the workplace: a qualitative study of newly licensed registered nurses, Shellie Simons and Barbara Mawn; Sexual health nursing assessments: examining the violence of intimate exposures, Patrick O’Byrne and Cory Woodyatt; Bullying on the back-channels: everyday interpersonal communicative relations in telephone talk as a space for covert forms of professional manipulation, Jackie Cook and Colette Snowden. Part III Patients’ Violence: Assessment of risk and special observations in mental health practice: a comparison of forensic and non-forensic settings, Elizabeth Mason-Whitehead and Tom Mason; Policing pornography in high-secure care: the discursive construction of gendered inequality, David Mercer; Warning – this job contains strong language and adult themes: do nurses require thick skins and broad shoulders to deal with encounters involving swearing?, Teresa Stone and Margaret McMillan; Prison nursing: managing the threats to caring, Elizabeth Walsh; The mentally ill and civil commitment: assessing dangerousness in law and psychiatry, Cary Federman; Working in a violent environment: the pitfall of integrating security imperatives into forensic psychiatry nursing, Jean Daniel Jacob; Index.

About the Editor:  Dave Holmes is Professor and University Research Chair in Forensic Nursing, School of Nursing, Faculty of Health Sciences, University of Ottawa, Canada and co-editor of both Critical Interventions in the Ethics of Healthcare and Abjectly Boundless: Boundaries, Bodies and Health Work. Trudy Rudge is Professor at Sydney Nursing School, University of Sydney, Australia, and co-editor of Abjectly Boundless: Boundaries, Bodies and Health Work. Amélie Perron is Assistant Professor, School of Nursing, Faculty of Health Sciences, University of Ottawa, Canada.

New book: Bio-Objects: Life in the 21st Century

Increasing knowledge of the biological is fundamentally transforming what life itself means and where its boundaries lie. New developments in the biosciences – especially through the molecularisation of life – are (re)shaping healthcare and other aspects of our society. This cutting edge volume studies contemporary bio-objects, or the categories, materialities and processes that are central to the configuring of ‘life’ today, as they emerge, stabilize and circulate through society.

Examining a variety of bio-objects in contexts beyond the laboratory, Bio-Objects: Life in the 21st Century explores new ways of thinking about how novel bio-objects enter contemporary life, analysing the manner in which, among others, the boundaries between human and animal, organic and non-organic, and being ‘alive’ and the suspension of living, are questioned, destabilised and in some cases re-established.

Thematically organised around questions of changing boundaries; the governance and regulation of bio-objects; and changing social, economic and political relations, this book presents rich new case studies from Europe that will be of interest to scholars of science and technology studies, social theory, sociology and law.

  • Contents:   Introduction: bio-objects: exploring the boundaries of life, Andrew Webster; Part 1 Changing Boundaries of Human, Nonhuman and Society: Challenging bio-objectification; adding noise to transgenic silences, Tora Holmberg and Malin Ideland; Pluripotent promises: configurations of a bio-object, Lena Eriksson; Water – an exploration of the boundaries of bio-objects, Ragna Zeiss; Bio-objectification of clinical research patients: impacts on the stabilization of new medical technologies, Conor M.W. Douglas. Part 2 Governing Bio-Objects: Beasting biology: interspecies politics, Nik Brown; Comparing public engagement with bio-objects: implementing co-existence regimes for GM crops in Denmark, the UK and Germany, Janus Hansen; Governing hereditary disease in the age of autonomy: mutations, families and care, Aaro Tupasela; At the margins of life: making fetal life matter in trajectories of first trimester prenatal risk assessment (FTPRA), Nete Schwennesen. Part 3 Generative Relations: The fruit of love: the German IVF-embryo turning from abject into bio-object, Bettina Bock von Wülfingen; On why states still matter: in vitro fertilization embryos between laboratories and state authorities in Italy, Ingrid Metzler; Growing a cell in silico: on how the creation of a bio-object transforms the organisation of science, Niki Vermeulen; Genetic discrimination 2.0: the un/differentiating gene in insurance, Ine Van Hoyweghen; Still life? Frozen gametes, national gene banks and re-configuration of animality, Sakari Tamminen; Index.

About the Editor:  Niki Vermeulen, is Wellcome Research Fellow at the University of Manchester, Centre for the History of Science, Manchester, UK, Sakari Tamminen is an Academy of Finland postdoctoral researcher at the University of Helsinki, Finland and Andrew Webster is Professor of the Sociology of Science & Technology and Director of the Science and Technology Studies Unit at the University of York, UK.

New book: Medicine as Culture: Illness, Disease and the Body

Medicine as Culture: Illness, Disease and the Body is unlike any other sociological text on health and medicine. It combines perspectives drawn from a wide variety of disciplines including sociology, anthropology, social history, cultural geography, and media and cultural studies. The book explores the ways in which medicine and health care are sociocultural constructions, ranging from popular media and elite cultural representations of illness to the power dynamics of the doctor-patient relationship.

The Third Edition has been updated to cover new areas of interest, including:

– studies of space and place in relation to the body

– actor-network theory as it is applied in research related to medicine

– The internet and social media and how they contribute to lay health knowledge and patient support

– complementary and alternative medicine

– obesity and fat politics.

Contextualising introductions and discussion points in every chapter makes Medicine as Culture, Third Edition a rigorous yet accessible text for students.

SAGE: Medicine as Culture: Illness, Disease and the Body: Third Edition: Deborah Lupton: 9781446208953.