Health and Social Care - All titles

Drawing on case studies from the UK, China, Japan, New Zealand and the US this text explores policy responses to COVID-19 through the lens of risk. The book considers how different countries framed the pandemic, categorised their populations and communicated risk. It also evaluates the role of the media, conspiracy theories and hindsight.

Drawing on case studies from optometrists, physiotherapists, pedorthists and allied health assistants, this book offers an innovative comparison of allied health occupations in Australia and Britain. Adopting a theory of the sociology of health professions, it explores how the allied health professions can achieve their professional goals.

This book analyses the political and long-term systemic factors associated with the failures to control COVID-19 in England. Exploring the role of key policy actors, it focuses on two policy failings during the first wave: the establishment of a ‘Test, Trace and Isolate’ system and responses to the high death rate in care homes for older people.

EPDF and EPUB available Open Access under CC-BY-NC- ND This accessible, yet authoritative book shows how the pandemic is a syndemic of disease and inequality. It argues that these inequalities are a political choice and we need to learn quickly to prevent growing inequality and to reduce health inequalities in the future.

Adult social care was the first major social policy domain in England to be transferred from the state to the market. This book meticulously charts this shift, challenges the dominant market paradigm, explores alternative models for a post-Covid-19 future and locates the debate within the wider political thinking and policy change literature.

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.

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.

Using Qualitative Comparative Analysis to explore 11 developed countries’ health services, this ambitious text identifies which factors are associated with the strongest outcomes.

Academic experts review the impact of neoliberal politics and ideology on the status of care work in Nordic countries. They explore different understandings of the care crisis, the consequences for gender equality and the long-term sustainability of the Nordic welfare states.

Informed by a case study from the authors’ work with a unique NGO in the UK, this book illustrates what it really means to adopt a strengths approach in practice.

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.

Challenging the ethics of care as a tradeable commodity, this book introduces the concept of ailment as a framework for understanding social care. Providing examples from Britain and Finland, it demonstrates how ailment shapes all societies, and by addressing the marketisation of care, the authors bring to light increasing inequalities in care.