Health and Social Care - Research

This book shows researchers how ethnography can be carried out within human service settings, providing an invaluable guide on how to apply ethnographic creativeness and offering a more humanistic and context-sensitive approach to generating valid knowledge about today’s service work.

EPDF and EPUB available Open Access under CC-BY-NC-ND licence. This book examines the unique implications of the pandemic in the Global South. With international contributors from a variety of disciplines, it investigates the pandemic’s effects on development, medicine, gender (in)equality and human rights among other issues.

This book focuses on legal measures to combat disability harassment at work. It sets disability harassment in its international context and confronts the lack of empirical information by evaluating the Irish legal framework in practice.

Re-examining health, healthcare and societal health using the latest data and research, this book addresses definitions of health, changes in health over time and the contribution of healthcare. It also suggests ways of effectively tackling obstacles to improving health and healthcare in 21st century Britain.

Addressing multiple empirical case studies, including COVID-19, this multidisciplinary book explores the relationship between international law and international relations to interrogate how a Public Health Emergency of International Concern (PHEIC) is declared and its role in how we collectively respond to outbreaks.

This book casts light on how the virus has impacted the experience of home and housing through the lens of wider urban processes around transportation, land use, planning policy, racism and inequality, and offers crucial insights for reforming cities to be more resilient to future crises.

Focusing on the flight of women and girls from Venezuela, this book examines the gendered nature of forced displacement and the ways in which the failures of protection regimes to be sensitive to displacement’s gendered character affect women and girls, and their sexual and reproductive health.

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.

This book critiques the popular claim that ‘more information’ equates to ‘better health’ and explores the potential challenges related to people’s changing relationships with traditional health systems as access to, and control over data shifts.

This important book explores the dimensions, dynamics and implications of the emerging pandemic society, shedding new light on how pandemics are socially produced and, in turn, shape societies in governance, work and recreation, science and technology, education, and family life.

This topical and authoritative book examines how the regulation of doctors has been modernised by the introduction of the quality assurance process medical revalidation. In doing so, it questions if there indeed is evidence to support the argument that revalidation serves the public interest by ensuring individual doctors are fit to practice.

This new edition of this bestselling book argues that patients need to develop as active citizens and co-producers of health. This second edition has been entirely rewritten with two new chapters, and includes new material on resistance to that world-wide process.