Dementia has been widely debated from the perspectives of
biomedicine and social psychology. This book broadens the debate to
consider the experiences of men and women with dementia from a
socio-political perspective. It brings to the fore the concept of
social citizenship, exploring what it means within the context of
dementia and using it to re-examine the issue of rights,
status(es), and participation. The book fills a gap in the global
market for an up-to-date, coherent, and authoritative account on
the present day situation of people with dementia. It offers fresh
and practical insights into how a citizenship framework can be
applied in practice, and it analyzes biographical accounts of
living with dementia from a life course perspective.
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