Abstract

Critically assesses recent health and social care policy in Scotland and England in light of the growing body of empirical research into the experiences and perspectives of people with dementia. The author draws on this evidence to consider the particular challenges associated with delivering four key outcomes to people with dementia identified by policy makers as fundamental to well-being. These are: independence, health, choice and social inclusion. The book examines the potential for current policy proposals to meet the needs of people with diverse experiences of dementia and considers the particular issues relating to including people with dementia as partners in policy and practice - a key principle underpinning all health and social care. In so doing the book contributes a much needed policy perspective to the field of dementia, as well as providing a fresh lens through which to consider the difference that proposed policies can make to a diverse range of service users.