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04829nam a2200421Ii 4500 |
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9781351241816 |
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180813s2018 fluab ob 001 0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
9781351241816 |
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(e-book : PDF) |
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(OCoLC)1032290087 |
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RC523 |
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WM 220 |
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SOC |
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MED |
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| Classification number |
616.8/31 |
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23 |
| 245 00 - TITLE STATEMENT |
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| Title |
Dementia as social experience : |
| Remainder of title |
valuing life and care / |
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edited by Gaynor Macdonald and Jane Mears. |
| 250 ## - EDITION STATEMENT |
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| Edition statement |
First edition. |
| 300 ## - PHYSICAL DESCRIPTION |
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| Extent |
1 online resource (234 pages) : |
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6 illustrations |
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| Topical term or geographic name as entry element |
Dementia. |
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Sociological Factors. |
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Dementia |
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| Topical term or geographic name as entry element |
Sociological Factors |
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MEDICAL / Geriatrics. |
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| Topical term or geographic name as entry element |
SOCIAL SCIENCE / Anthropology / General. |
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| Personal name |
Macdonald, Gaynor |
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editor. |
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| Personal name |
Mears, Jane, |
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editor. |
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| Corporate name or jurisdiction name as entry element |
Taylor and Francis. |
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| Uniform Resource Identifier |
https://www.taylorfrancis.com/books/9781351241816 |
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Boca Raton, FL : |
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Routledge, an imprint of Taylor and Francis, |
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2018. |
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text |
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rdacontent |
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computer |
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online resource |
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rdacarrier |
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part, PART I Challenging social constructions of ageing and dementia -- |
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chapter 1 Reframing dementia: the social imperative / |
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GAYNOR MACDONALD JANE MEARS -- |
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chapter 2 Negative positioning of 'dementia' in an environment of competition for resources / |
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TRACEY McDONALD -- |
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chapter 3 'Nobody cares about me': older women, caring and dementia / |
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JANE MEARS -- |
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chapter 4 Feeling invisible and ignored: families' experiences of marginalisation living with younger onset dementia / |
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KAREN HUTCHINSON CHRIS ROBERTS -- |
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chapter 5 Generational perceptions of dementia in the public sphere: public health, age- othering and generational intelligence / |
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SIMON BIGGS IRJA HAAPALA ASHLEY CARR -- |
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part, PART II Autonomy and dignity -- |
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chapter 6 Developing a relational approach to decision- making in healthcare settings / |
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SUZANNE JARRAD -- |
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chapter 7 'We've always thought of one another': relational perspectives on autonomy and decision- making among people with dementia and their family carers / |
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CRAIG SINCLAIR, ROMOLA S. BUCKS, MEREDITH BLAKE, -- |
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chapter 8 Planning for the rest- of-life, not end- of-life: reframing advance care planning for people with dementia / |
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GAIL YAPP CRAIG SINCLAIR ADELE KELLY -- |
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part, PART III Persons in relationship: the dynamics of care -- |
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chapter 9 The critical importance of adopting a 'personhood lens' in reframing support and care for those with dementia / |
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LYNETTE R. GOLDBERG, ANDREA D. PRICE, -- |
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chapter 10 Emotional labour, person- centred care and problem solving in regulating dementia care / |
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ASHLEY CARR SIMON BIGGS -- |
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chapter 11 Why 'person- centred' care is not enough: a relational approach to dementia / |
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GAYNOR MACDONALD. |
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A diagnosis of dementia changes the ways people engage with each other - for those livingwith dementia, as well their families, caregivers, friends, health professionals, neighbours, shopkeepers and the community. Medical understandings, necessary as they are, provide no insights into how we may all live good lives with dementia.This innovative volume brings together an interdisciplinary group of researchers and practitioners to focus on dementia as lived experience. It foregrounds dementia's social, moral, political and economic dimensions, investigating the challenges of reframing the dementia experience for all involved.? Part I critiques the stigmas, the negativity, language and fears often associated with a dementia diagnosis, challenging debilitating representations and examining ways to tackle these. Part II examines proactive practices that can support better long-term outcomes for those living with dementia. Part III looks at the relational aspects of dementia care, acknowledging and going beyond the notion of person-centred care. Collectively, these contributions highlight the social and relational change required to enhance life for those with dementia and those who care for them. Engaging in a critical conversation around personhood and social value, this book examines the wider social contexts within which dementia care takes place. It calls for social change, and looks for inspiration to the growing movement for relational care and the caring society. Dementia as Social Experience is important reading for all those people who, in various ways, are living with dementia, as well as for those working in this area as clinicians, researcher and carers. |
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bisacsh |
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(Gaynor Marilyn), |
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1948- |
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Print version: |
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9780815374572 |
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(DLC) 2018018228 |
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Click here to view. |
