Emerging evidence suggests that the historical trauma associated with settler colonialism affects the sexual and reproductive health (SRH) of American Indian (AI) communities today. This article examines how one AI community narratively frames the influence of historical trauma within the context of community-based participatory research (CBPR) and the implications of this framing for health behaviours

In the past few years, self-tracking technologies have been celebrated for the possibilities they offer to ‘optimize’ fitness and wellbeing, yet also criticized for being rigid and isolating. In this article, we identify complex tracking arrangements that consist of a variety of data and multiple modalities of tracking emplaced within arrangements of actors and objects (digital/analog tracking devices

Non-rare thrombophilia (NRT) are hereditary predispositions to thromboembolism, the most severe side effect of combined hormonal contraception. In the mid-1990s, the identification of NRT stirred up a controversy over the possibility of investigating these genetic variants in women wishing to use contraception. Through a review of literature, this article reconstructs the debate over whether and how

For two decades, New Zealand has been placed consistently at the foot of OECD rankings for state expenditure on pharmaceuticals. In this article, we explore New Zealand's containment of pharmaceutical spending as a ‘divergent’ case of pharmaceutical policy in a liberal democracy. To elucidate the likely institutional mechanisms and interests behind this phenomenon, we conducted a case study of New

Drawing on interviews with civil society actors in the AIDS Service Organization (ASO) sector in Canada, this article explores how these actors contribute to shaping the illness identities of people living with HIV/AIDS in the shadow of efforts to criminalize exposure to HIV. While the biographically disruptive qualities associated with an HIV diagnosis have been addressed in the medical sociology

Deaths related to drug ‘misuse’ remain at an all-time high in the United Kingdom (UK). Older heroin consumers are particularly at risk, with the highest rates of deaths among people aged 40–49 and the steepest rises in the over-fifty age bracket. Accordingly, a popular theory for the UK’s increase in drug-related deaths, made by the government, and propelled in the media, is that there is an ageing

In Denmark, parents have needed to deal with inconsistent presentations of risk regarding the human papillomavirus (HPV) vaccination. This has complicated the parents' task of making a decision about having their daughters vaccinated. In this article, I analyse how Danish parents engage with digital media when making this decision. The results are based on interviews with 18 Danish parents of girls

Stress-induced mental illnesses have become the focus of increasing international attention, particularly in Japan since the 1990s, where judiciary cases and welfare-state initiatives established causal links between work stress and mental illness. However, how individuals retrospectively construct this causality remains a marginal topic in the literature. This ethnographic article explores the ways

In the present study, we examine socio-cultural and practical aspects of human papillomavirus vaccination (HPVV) through a multi-sited study of framings. We ask how HPVV is framed in the daily lives of vaccination-aged Finnish girls and in school nurses’ everyday work. We then mirror these framings against both each other and Finland's official vaccination campaign. Based on analysis of interviews

The reduced physical activity of women when they become mothers is a public health priority. Existing studies show that mothers have little time for leisure, or time that is fragmented and requiring negotiation with others. However, the temporal features of mothering are undertheorised and qualitative studies tend to focus on how mothers can skilfully construct physically active identities and balance

In this article, we draw on Michael Lipsky's work on street-level bureaucrats and discretion to analyse a real case setting comprising an interview study of 30 Swedish doctors regarding their experiences of changes in clinical work following patients being given access to medical records information online. We introduce the notion of invisibility work to capture how doctors exercise discretion to preserve

In randomised controlled trials (RCTs), ‘therapeutic optimism’ describes a participant's belief they will benefit from the study treatment, despite the express goal of RCTs to test unknown aspects of interventions. Harbouring such expectations may interfere with RCT participation experiences, particularly among marginalised populations, such as people with substance use disorders (PSUD) who may experience

This paper takes a critical look at the role of chronobiology in society today, with particular reference to its entanglements with health and medicine and whether or not this amounts to the (bio)medicalisation of our bodily rhythms. What we have here, we show, is a complex unfolding storyline, within and beyond medicine. On the one hand, the promises and problems of these circadian, infradian and

This article explores the emergence and development of Death Certificates as a means of establishing the cause of death for individuals and populations. The difficulty in choosing which disease caused death when several are described on the Certificate explains why the number of COVID-19-related deaths has been difficult to determine. This problem also draws attention to the dominant biomedical explanation

In this article, we conduct an empirical ethics approach to unravel the different perspectives on good care that are present in a community mental health team (CMHT) in Utrecht. With the deinstitutionalisation of mental health care, the importance of a close collaboration between the social and medical domains of care on the level of the local community is put in the foreground. Next to organisational

In efforts to control disease, mathematical models and numerical targets play a key role. We take the elimination of a viral infection as a case for exploring mathematical models as ‘evidence-making interventions’. Using interviews with mathematical modellers and implementation scientists, and focusing on the emergence of models of ‘treatment-as-prevention’ in hepatitis C control, we trace how projections

In 2008, Timmermans and Haas called for a ‘sociology of disease’ to develop and challenge the sociology of health and illness. A sociology of disease, they argued, would take seriously the biological and physiological processes of disease in theorising health and illness. Building on two decades of Science and Technology Studies and feminist work on biological actors such as hormones and genes, we

Biographical disruption positions the onset of chronic illness as a major life disruption in which changes to body, self and resources occur (Sociology of Health & Illness, 4, 1982, 167–182). The concept has been used widely in medical sociology. It has also been subject to critique and development by numerous scholars. In this paper, we build on recent developments of the concept, particularly those

The prevalence of obesity and related health problems has increased sharply in recent decades. Dominant medical, economic, psychological, and especially epidemiological accounts conceptualise these trends as outcomes of individuals’ lifestyles – whether freely chosen or determined by an array of obesogenic factors. As such, they rest on forms of methodological individualism, causal narratives, and

Mothers’ alcohol consumption has often been portrayed as problematic: firstly, because of the effects of alcohol on the foetus, and secondly, because of the association between motherhood and morality. Refracted through the disciplinary lens of public health, mothers’ alcohol consumption has been the target of numerous messages and discourses designed to monitor and regulate women's bodies and reproductive

Despite its prevalence, men's anxiety is arguably under-researched and poorly understood. The present study explores the reasoning provided by male posters to an online discussion forum about the source of their anxiety. Posts were collected from an Australian anxiety online discussion forum. This study utilises discursive psychology, informed by principles of membership categorisation analysis, to

Sociological concern for rehabilitation remains limited. This paper aims to contribute to rehabilitation theory. It examines two units of a specialist rehabilitation hospital in the UK (amputee and neurological services) by focusing on the key actors involved – families, patients, staff – and the parameters shaping their relationships. The findings extend previous theoretical understandings of rehabilitation

In Burnett and Veenstra (2017), the link to the three-dimensional model has been updated. The new link is https://www.sociologix.ca/margins-freedom.html.

Materiality has become an increasingly important topic in sociological studies of health care. How objects support the identity of people with dementia in care homes is an emerging area. While early research has tended to focus on sentimental or cherished items (such as photographs or keepsakes), the present study focused on functional objects (such as curling tongs or a hairdryer) as a mechanism to

Contemporary sociological work has emphasised that family is not static, but actively shaped by ideas of who and what makes family. Disclosure of an illness, including diagnosis of stigmatised infections such as HIV, hepatitis B virus and hepatitis C virus, can change the dynamics of family relationships. This paper draws on 61 qualitative semi-structured interviews conducted between 2017 and 2019

Health research concerning Indigenous peoples has been strongly characterised by deficit discourse—a ‘mode of thinking’ that is overly focused on risk behaviours and problems. Strengths-based approaches offer a different perspective by promoting a set of values that recognise the capacities and capabilities of Indigenous peoples. In this article, we seek to understand the conceptual basis of strengths-based

This paper is a narrative review of the use of collective terminology in relation to race and health in Britain, with particular reference to the ‘Black African’ community. ‘Black Africans’ have been categorised in the 1991–2011 censuses with added free-text in 2021 in response to user demand. However, the UK government is increasingly reporting data for the ‘Black’ pan-ethnicity, especially in the

Divided Bodies is an excellent book for scientists, clinicians and the layperson interested in the phenomenon of disease, particularly meanings of disease and illness, and cures and healing, in the context of an increasingly bureaucratic system of administration. It draws attention to the limitations of laboratory testing as arbiter of illness and shows how the dogmatic belief in evidence-based medicine

In healthcare settings, patient participation is increasingly adopted as a possible remedy to ill people suffering from ‘epistemic injustices’ – that is to their unfair harming as knowers. In exploring and interpreting patient participation discourses within the 2013–2018 Dutch Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS) Health Council advisory process, this paper assesses the epistemological

Forensic psychiatric institutions are tasked with both containment and transformation, with securely policing the border between institution and society and readying patients for return to the community. Forensic institutions can thus be theorised as a form of ‘rite of passage’, engaged in a process of transformation which both navigates and demarcates social limits. This article contributes to literature

Analysing data from a nationally representative sample of 3442 interviews conducted in Egypt in 2020, this study examines the influence of four sets of factors in predicting compliance with the advice of healthcare professionals to combat the spread of COVID-19: demographics, knowledge and values, fear of the disease and denial, and the pandemic as a foreign invasion. The findings show that a higher

The substantial literature in political economy and sociology has shown that the increasing importance of financial activities (financialisation) exhibits significant effects on many socioeconomic conditions. While these conditions are relevant to public health, the dominant focus of the literature has been centred on the impact of financial markets on health services and health-care systems. This

A change would be civil rights, which are rights you are due by law… [H]uman rights, if they're honored, would be the rights you are due by your very birth. That is transformation. – Ericka Huggins, former Black Panther Party Leader, quoted on p. 219. Reproductive Rights as Human Rights: Womenof Color and the Fight for Reproductive Justice offers an in-depth account of how and why the reproductive

Based on her reflexive ethnography and building on a feminist perspective, Mahima Nayar sensitively presents the experiences of women living in Jahangirpuri: an urban setting located in north-west Delhi, characterized as heterogeneous in regard to ethnic, caste, religion and socioeconomic status. In her monograph, the author focuses on the challenges of mental health among women from poor households

In Taking Care of Our Own: When Family Caregivers Do Medical Work Sherry Mong draws on feminist, medical sociology and care work theories to illuminate the hitherto sequestered world of people who provide medical care for family members at home focusing on the skilled yet unpaid work that carers undertake in terms of ‘labour processes’. Mong's inspiration to undertake the research underpinning the

Published during the COVID-19 pandemic, where western society's approach to older people is being scrutinised, this book is a timely call to articulate a distinct purpose and meaning to later life in a way that embraces the complexities of ageing as a corporeal process of decline and limitation. Juxtaposing individualism and autonomy alongside the ethics of dependency, human temporality and our fundamentally

Universal health coverage (UHC) has been elevated to the status of a global policy target, but this was at the expense of losing its aspirational meaning. As a case in point, Turkey has been one of the countries that has achieved UHC, according to the technocratic definition. This article employs a combination of deductive and inductive thematic analysis methods to explore patient organisation (PO)

Support Workers and the Health Professions in International Perspective. The invisible providers of healthcare, offers a unique sociological/social science-based analysis of the unsung roles and responsibilities of support workers and social workers in a global context. The text's aims and objectives are to make visible the challenges and opportunities ‘shadow’ workers face within the health employment

Despite the ubiquity of the body mass index (BMI) in discourse on health, there is ambiguity in its use as a biomarker of current abnormality versus future risk. This distinction is consequential for knowledge of the relationship between body size and health, as well as for individuals deemed to have abnormal and ‘unhealthy’ bodies. Consequently, the purposes of this review are threefold. The first

This paper contributes to the debate on the patient–doctor relationship by focussing on a specific chronic disease: type 1 diabetes. This field is characterised by an increasing use of technology, specifically therapeutic devices and a significant requirement of patient self-management. This paper presents the main findings of research conducted in Italy in 2018. It is argued that this relationship

Action = Vie is the first comprehensive study of Act Up Paris for Anglophone audiences. It thus makes a significant contribution to the recent uptick in analyses of AIDS activist groups across the Global North. Specifically, the book expands our understanding(s) of the political underpinnings of sexual liberation strategies, activist mobilisation and historical health promotion. Action = Vie excels

At first sight, this is a promising book on HIV/AIDS, taking an interesting and unusual angle to its topic. Indeed, the author is well versed on the issues he discusses. HIV/AIDS is an important topic in its right, having rather fallen from policy view by having been ‘normalised’ by the development of medical treatments, even though no biomedical cure has been found. As the author also rightly says

Pre‐Exposure Prophylaxis (PrEP) is a novel HIV prevention tool. PrEP stigma is a frequently reported barrier, while social disclosure of PrEP use may be an important facilitator. We explored how PrEP users managed PrEP use disclosure using a symbolic interactionist approach. We interviewed 32 participants from two PrEP demonstration projects (Be‐PrEP‐ared, Antwerp; AMPrEP, Amsterdam). We validated

While some sociologists of health and illness might consider the commissioning of healthcare to be of only marginal relevance to their work, this book demonstrates that nothing could be further from the truth. There is a danger that the ‘Context’ chapter, full of the abbreviated jargon of CCGs, PCTs, PBCs, SHAs, LESs, DESs and more that flourishes in the NHS, could confirm their suspicions that such

Writing in this journal 18 years ago, Clive Seale posed—and answered—the question, ‘why should medical sociologists study the media?’. He argued that ‘we must … understand popular media if we are to understand experience [including of health and illness] and its rendering in narrative forms’. He bemoaned a separation between the fields of media studies and the sociology of health and illness (Seale

The murder of George Floyd has reinvigorated the call for anti‐racism across the Global North, and mental health bodies have joined this political moment. Yet, discussions of racism in mental health are nothing new (Bailey et al., 2017; Fernando, 2017; Fernando et al., 1998; McKenzie & Bhui, 2007; Nazroo et al., 2020; Richards, 1997). Certainly, the COVID‐19 pandemic has revealed the extent to which

In this paper, we contrast two emergences of the concept of ‘uninfectious’ (that pharmaceuticals can render someone living with HIV non-infectious) in HIV. First, using Novas’ framing of ‘political economies of hope’, we describe the deployment of ‘uninfectious’ as part of global health campaigns. Second, we draw on Raffles’ (International Social Science Journal, 2002, 54, 325) concept of ‘intimate

Antimicrobial resistance control programmes often aim to “fix” the behaviour of antibiotic users and prescribers. Such behavioural interventions have been widely criticised in social science literature for being inefficient and too narrow in scope. Drawing on these criticisms, this article analyses how political programmes for fixing antibiotic behaviours were adapted into the practices of health‐care

To understand the complexities of managing long‐term conditions and develop appropriate responses, micro‐, meso‐ and macrolevels must be considered. However, these levels have not been combined in a single analytical framework of long‐term condition management (LTCM). This article aims to describe a framework of LTCM practice and research that combines societal levels and key agents. The actor‐level

This qualitative study focuses on self‐medication with antibiotics as it relates to gender roles and traditions in the Arab society in Israel, a collectivist minority with defined traditional gender norms. Its findings draw on the analysis of 116 face‐to‐face interviews with 60 pharmacists, 27 primary care physicians and 29 community members, mainly mothers and unmarried women, from different geographical

The decommissioning of a health‐care service is invariably a highly complex and contentious process which faces many implementation challenges. There has been little specific theorisation of this phenomena, although insights can be transferred from wider literatures on policy implementation and change processes. In this paper, we present findings from empirical case studies of three decommissioning

Although patients who undergo weight‐loss surgery (WLS/bariatric surgery) must follow severe eating restrictions in a manner similar to that of dieting, professionals strive to demarcate distinctions between the approaches and methods of WLS and diet. Drawing from ethnographic research, this study focuses on the content and interpretative dimensions of professionals' boundary work as well as its meaning

Alongside other Nordic countries, the Norwegian government has introduced Cancer Patient Pathways (CPPs) for faster diagnostic assessment and timely treatment to improve the quality of cancer care. A key aspect of CPPs is the introduction of time limits for each phase of the diagnostic investigation. Occurring simultaneously are ongoing advances in medical technology, complicating the process of diagnosing