This is the first book to extend the narrative lens to explore the contribution of narrative to social work values and ethics, social policy and our understanding of the self in social, cultural and political context.
This book considers ethical decisions in the context of relationships, treatment, safety and quality of life. It draws on the experiences of family carers as well as on existing research and emphasizes the importance of empathy and the need to acknowledge different perspectives in order to reach the best decision for the person with dementia
This guide will give practitioners the confidence to deal with the ethical and legal issues which arise in clinical dementia contexts. The standalone chapters cover difficult issues such as abuse, behaviour that challenges, and forced care, and the book contains clinical case vignettes throughout.
Providing a much-needed accessible overview of the complex philosophical and ethical underpinnings of dementia care, this book explores current thinking around the concepts of ageing, personhood, capacity, liberty, best interests and the nature of palliative care, shedding new light on their implications for the caring professions.