Health and Social Care - Research

This is the first comprehensive review of dementia research, policy and practice in remote and rural settings. Drawing on case studies from the UK, Australia, Europe and North America, it sets out the unique needs of sufferers and carers in isolated locations, and identifies areas for future research and improvements in dementia services.

This inter-disciplinary study considers the past, present and future of mental health services and community care. From the origins of provision as we know it in the 1960s, it sets out the political, economic and bureaucratic factors behind recent crises and considers what the founding principles of community care tell us about the way forward.

Offering important nuances and crucial insights into diverse gender identities and trans-related healthcare inequalities, this ground-breaking research marks an important contribution to the wider fields of gender studies, LGBTQ scholarship and medical policy.

This original collection analyses the global experience of health care support workers (HSWs) and examines their interface with the health professions, regulatory practice risks, employment challenges and the dilemmas of an ageing population. Crucial future policy recommendations are also made for a world becoming increasingly dependent on HSWs.

This crucial contemporary study reviews the evolving role of local authorities in health, social care and wellbeing. Health and policy experts survey disparities across Britain, share case studies of strategies and consider authorities’ interaction with local and central government.

Putting the spotlight on neoliberalism as a pervasive tool that dictates wellness as a moral obligation, this book critically analyses how users navigate relationships between self-tracking technologies, social media and health management.

The use of fiscal welfare has been growing over the past decades in European welfare states. This book sheds light on the use and effects of fiscal welfare in welfare and labour market reforms in both countries and examines the introduction of a 50% tax deduction on domiciliary care and household services.

This edited collection brings together a range of academics, practitioners and organisations to consider the implications of recent case law around consent in sexual relationships on the day-to-day lives of people with cognitive impairments.

Combining robust evidence with real-life stories, this book reveals the shocking impact of austerity policies on life expectancy and offers an optimistic vision of what can be done to restore life expectancy and reduce health inequality.

Despite being a widely recognised phenomenon, PMS remains difficult to define clinically, with no universally agreed diagnostic criteria or shortlist of deterministic symptoms. This book aims to accurately define and explain cyclical experiences and debunk the myth of the hysterical female, once and for all.

By elevating trans voices and experiences, this book offers a new perspective on transness, medicalization and research methodologies to help trans people, practitioners and policy makers better understand the barriers faced by trans people when seeking healthcare.