This book is open access under a CC BY 4.0 license.
This is the first book-length exploration of the thoughts and
experiences expressed by dementia patients in published narratives over
the last thirty years. It contrasts third-person caregiver and
first-person patient accounts from different languages and a range of
media, focusing on the poetical and political questions these narratives
raise: what images do narrators appropriate; what narrative plot do they
adapt; and how do they draw on established strategies of life-writing.
It also analyses how these accounts engage with the culturally dominant
Alzheimer's narrative that centres on dependence and vulnerability, and
addresses how they relate to discourses of gender and aging. Linking
literary scholarship to the medico-scientific understanding of dementia
as a neurodegenerative condition, this book argues that, first,
patients' articulations must be made central to dementia discourse; and
second, committed alleviation of caregiver burden through social support
systems and altered healthcare policies requires significantly altered
views about aging, dementia, and Alzheimer's patients.