Sociology of Health and Illness

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Drawing from the Evidence for Equality National Survey (EVENS), this book presents new evidence of ethnic inequalities and sheds new light on underlying racisms, opening them up to debate as crucial social concerns.

Extending the ideas developed in the previous volumes in the Social Determinants of Health series, this book reviews the impact of COVID-19 on local and national governance from the perspectives of public health, social care and economic development.

Drawing on international perspectives and research, this book explores the experiences of sex and sexuality in individuals and groups living with HIV in later life (50+).

This interdisciplinary activist research project shows the health and well-being impacts of transnational migration on Ecuadorean families. Roberta Villalón documents the intersection of social inequalities and migration and health policies, and how individual and collective action challenges marginalising structures and fosters social justice.

This book showcases the impact of state responses to COVID-19 on marginalized communities. The authors analyse the lockdowns, immigration and border controls, vaccine trials, income support and access to healthcare across eight countries in Australasia, North America, Asia and Europe to reveal the internal inequities within and between countries.

Can the social sciences explain the emergence of mental disorders in societies or in individuals? This book presents a critical look at sociological explanations of mental illnesses, making the case for their renewal.

This transdisciplinary collection engages with key issues of social exclusion, inequality, power and knowledge in the context of COVID-19 for a more equitable and inclusive human future.

Health and legal experts from England and Canada consider the influence of medical doctors on reforms in this comparative study. With reflections on participation since the inception of publicly-funded healthcare systems, they show how the status of doctors affects change.

With dementia care shifting from institutional to home settings, this book considers the intersections of formal health and social care strategies and family experiences. Drawing on case studies from Canada, it enhances the understanding of good policy and practice in dementia care and the potential for better outcomes for all those concerned.

Establishing a critical and interdisciplinary dialogue, this text engages with the typically disparate fields of social gerontology and disability studies. It investigates the experiences of two groups rarely considered together in research – people ageing with long-term disability and people first experiencing disability with ageing.

This crucial contribution exposes the misconception that health research and health services are equally effective for all and highlights their failures in engaging with Black and Minority Ethnic (BME) groups. It provides essential case study examples on recruitment, engagement and partnerships with BME groups in research and public engagement.

This book presents a poignant account of the current policy approaches to self-determining sex and gender in the UK and beyond, showing how legal, medical and pedagogical policy developments are interconnected, and how policy is affected by transgender and diverse gender experiences and activism.