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Written by a collection of experts in the field, this important new text provides a critical and constructive analysis of the ways in which service users and carers engage with health and social care services. Covering topics such as the importance of terminology, wellbeing and resilience and the notion of tokenism, and enhanced by a wealth of first-hand experiences and creative work by a range of service users and carers, the text examines how different forms of collaboration, participation and involvement (or lack of it) have contributed, and continue to contribute, to service development and the expansion of participant movements. With a strong focus on retrospective as well as prospective analysis, it encourages the reader to learn from both historical and current developments in service user and carer involvement in order to anticipate and inform future directions. This engaging and inspiring text is key reading for students on undergraduate and postgraduate social work programmes, as well as practitioners looking for a fresh new perspective.
This textbook provides a greater understanding of the lived effect that social policies have on service users and carers. While service user and carer involvement has become more and more prominent in social policy over recent years, it is rarely the case that the perspectives of service users and carers goes beyond consultation to truly meaningful involvement and co-production. This book is unique in that it has ten substantive co-produced chapters with service users and carers who have direct lived experiences of social policies. The chapters include lived experiences of direct payments, domestic violence and abuse, looked after children, being a foster carer, receiving long term health an...
Moving away from clinical, medical or therapeutic perspectives on disability, this book explores disability in India as a social, cultural and political phenomenon, arguing that this `difference' should be accepted as a part of social diversity. It further interrogates the multiple issues of identification of the disabled and the forms of oppressio
Mental health has long been perceived as a taboo subject in the UK, so much so that mental health services have been marginalised within health and social care. There is even more serious neglect of the specific issues faced by different ethnic minorities. This book uses the rich narratives of the recovery journeys of Chinese mental health service users in the UK – a perceived ‘hard-to-reach group’ and largely invisible in mental health literature – to illustrate the myriad ways that social inequalities such as class, ethnicity and gender contribute to service users' distress and mental ill-health, as well as shape their subsequent recovery journeys. Recovery, Mental Health and Inequality contributes to the debate about the implementation of ‘recovery approach’ in mental health services and demonstrates the importance of tackling structural inequalities in facilitating meaningful recovery. This timely book would benefit practitioners and students in various fields, such as nurses, social workers and mental health postgraduate trainees.
This textbook provides a greater understanding of the lived effect that social policies have on service users and carers. While service user and carer involvement has become more and more prominent in social policy over recent years, it is rarely the case that the perspectives of service users and carers goes beyond consultation to truly meaningful involvement and co-production. This book is unique in that it has ten substantive co-produced chapters with service users and carers who have direct lived experiences of social policies. The chapters include lived experiences of direct payments, domestic violence and abuse, looked after children, being a foster carer, receiving long term health an...
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