<p/><br></br><p><b> About the Book </b></p></br></br>Launching the dementia debate into new and exciting territory, this book applies a human rights lens to interrogate the lived experience and policy response to dementia.<p/><br></br><p><b> Book Synopsis </b></p></br></br>Launching the dementia debate into new and exciting territory, this book applies a human rights lens to interrogate the lived experience and policy response to dementia.<p/><br></br><p><b> Review Quotes </b></p></br></br><br>"Recommended. . .Powerfully advocates for person-centered principles of participation, accountability, non-discrimination, empowerment, and legality. A worthwhile addition to health policy and ethics collections."-- "Choice"<br><br>"This book is a down to earth, accessible translation of complex legal, sociological, and ethical subjects and as such will appeal to undergraduate and post-graduate students of dementia, practitioners, and policy makers alike." -- "Kate Irving, Dublin City University"<br><p/><br></br><p><b> About the Author </b></p></br></br><b>Suzanne Cahill</b> is national director of the Dementia Services Information and Development Centre and research associate professor in the Department of Medical Gerontology, Trinity College Dublin, where she is also adjunct associate professor of social work and social policy.
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