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  • 1
    UID:
    edoccha_BV049321452
    Format: 1 Online-Ressource.
    ISBN: 978-3-031-27223-3
    Series Statement: Palgrave pivot
    Additional Edition: Erscheint auch als Druck-Ausgabe, Hardcover ISBN 978-3-031-27222-6
    Language: English
    URL: Volltext  (kostenfrei)
    URL: Volltext  (kostenfrei)
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  • 2
    UID:
    almafu_BV049321452
    Format: 1 Online-Ressource.
    ISBN: 978-3-031-27223-3
    Series Statement: Palgrave pivot
    Additional Edition: Erscheint auch als Druck-Ausgabe, Hardcover ISBN 978-3-031-27222-6
    Language: English
    URL: Volltext  (kostenfrei)
    URL: Volltext  (kostenfrei)
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  • 3
    UID:
    edocfu_BV049321452
    Format: 1 Online-Ressource.
    ISBN: 978-3-031-27223-3
    Series Statement: Palgrave pivot
    Additional Edition: Erscheint auch als Druck-Ausgabe, Hardcover ISBN 978-3-031-27222-6
    Language: English
    URL: Volltext  (kostenfrei)
    URL: Volltext  (kostenfrei)
    Library Location Call Number Volume/Issue/Year Availability
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  • 4
    UID:
    b3kat_BV049321452
    Format: 1 Online-Ressource
    ISBN: 9783031272233
    Series Statement: Palgrave pivot
    Additional Edition: Erscheint auch als Druck-Ausgabe, Hardcover ISBN 978-3-031-27222-6
    Language: English
    URL: Volltext  (kostenfrei)
    URL: Volltext  (kostenfrei)
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  • 5
    UID:
    almahu_9949568765402882
    Format: 1 online resource (154 pages)
    Edition: 1st ed.
    ISBN: 9783031272233
    Note: Intro -- About the Book -- Contents -- List of Figures -- Chapter 1: Introduction -- Meet the Co-authors -- Let's Write a Book -- Writing Sessions -- Missing Voices -- Emotional Content -- Dementia Statistics Overview -- Chris's Story -- Useful Resources: -- LGBTQ+ Community -- Useful Resources: -- Alzheimer's Society -- Alyson, Sheila, and David's Story -- Useful Resource: -- References -- Chapter 2: 'You Don't Look Like You Have Dementia' -- What Does Dementia at the Different Stages Look Like? -- Fighting for Financial Aid -- Raising Awareness Through a 'dementia card' -- Does It Help if People Know? -- Educating People About Dementia -- MAQ's Story -- MAQ -- Useful Resources: -- Winnie and Wullie's Story -- Winnie -- Useful Resources: -- Willy's Story -- Willy -- Useful Resources: -- References -- Chapter 3: 'How Does Your Dementia Affect You?' -- Understanding the Brain -- Myths About the Brain -- Areas of the Brain -- Myths About Dementia -- Myth 1: 'Dementia Only Affects Older Adults' -- Myth 2: 'There Is Nothing You Can Do to Change Your Risk of Dementia' -- Myth 3: 'Alzheimer's Disease and Dementia Are the Same Thing' -- Alzheimer's Disease -- Lived Experience -- Vascular Dementia -- Lived Experience -- Posterior Cortical Atrophy -- Lived Experience -- Frontotemporal Dementia -- Lived Experience -- Semantic Dementia -- Lived Experience -- Lewy Body Dementia -- Lived Experience -- Diagnosis Experience -- Martin's Story -- Myra and Archie's Story -- Agnes' Story -- Useful Resources: -- References -- Chapter 4: 'I Didn't Know I Was a Carer' -- Working with Paid Carers -- Being Recognised as Experts by Experience -- Sharing Home Space -- Examples of Best Practice in Care -- Planning Ahead -- Jenny and Her Mum's Story -- Useful Resources: -- Fred's Story -- Useful Resources: -- David and Anne's Story -- References. , Chapter 5: What Research Means to Us: NRS Neuroprogressive and Dementia Network -- Getting to Know the Neuroprogressive and Dementia Network -- What Got You into Researching Dementia and Neuroprogressive Conditions? -- Could You Share Your Experiences of Dementia Research Over the Past 10-15 Years? -- Why Is Research Important? -- What Do You Wish People Knew about Research? -- Approaches to Clinical Trials in Dementia -- Lessons from COVID-19 Clinical Trials -- Hear from Research Participants from the Neuroprogressive and Dementia Network -- Spectrum of Research -- Understandings of Research -- Building a Partnership -- Examples of Best Practice in Co-produced Research -- Meet The Smarties -- Dementia Alumni -- Dementia Enquirers -- What We Would Like to See from Research Going Forward -- Stuart & -- Eileen's Story -- Sue's Story -- Rosie's Story -- References -- Chapter 6: Final Thoughts -- Question 1 -- Question 2 -- Question 3 -- For People Living with Dementia -- Family Members -- Professionals -- Members of the Public -- Get in Touch -- Embedded Links -- Index.
    Additional Edition: Print version: Ashworth, Rosalie Challenging Assumptions Around Dementia Cham : Springer International Publishing AG,c2023 ISBN 9783031272226
    Language: English
    Keywords: Electronic books.
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  • 6
    UID:
    almahu_9949561334902882
    Format: 1 online resource (154 pages)
    Edition: 1st ed. 2023.
    ISBN: 3-031-27223-4
    Content: This open access book explores the expectations surrounding dementia, what it ‘looks like’ and how people have been treated by others. It aims to raise awareness of the different types of dementia, and how they impact the brain, body, and lived experience, including experience of Alzheimer’s disease, Vascular Dementia, Posterior Cortical Atrophy, Frontotemporal Dementia, Semantic Dementia, and Lewy Body Dementia. The co-authors reflect on their experience with informal and formal care, before finishing with a focus on the spectrum of dementia research from clinical trials to user-led research. Throughout the book, co-authors have shared personal stories of how dementia has affected them and people with lived experience of dementia share what they wish people knew about living with the disease. Co-produced by people with lived experience of dementia, academics and health care professionals, this book is an accessible resource about dementia from the perspective of people actively involved in the field and essential reading for healthcare professionals wishing to learn more about the experience of this neuroprogressive condition, as well as policymakers, and members of the public. Dr Rosie Ashworth leads Partners in Research for NRS Neuroprogressive and Dementia Network, UK. As a research psychologist, Rosie is passionate about co-production, ethics, and actively involving people with lived experience in research. She is also the co-lead for ENRICH Scotlands ‘Patient and Public Involvement’ group RICH (Research in Care Homes) Voices, a Fellow with Advanced Higher Education, an advisor to the Dementia Enquirers, and a volunteer for About Dementia. Partners in Research co-authors including Agnes Houston, Chris Maddocks, David Ross, Fred S. Wilson, Masood Qureshi, Martin Robertson, Myra Lamont, Stuart Hay, Sue Fyvel, Willy Gilder, Winnie Henry, and Alyson Hill.
    Note: 1. Coproducing a book on dementia research -- 2. Taking part in Alzheimer’s disease research -- 3. Taking part in Vascular dementia research -- 4. Taking part in Fronto-Temporal dementia research -- 5. Taking part in Parkinson’s dementia research -- 6. Taking part in dementia with lewy bodies research -- 7. Taking part in PCA dementia research -- 8. Lessons for future research in dementia.
    Additional Edition: ISBN 3-031-27222-6
    Language: English
    Keywords: Llibres electrònics ; Llibres electrònics
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  • 7
    UID:
    almahu_9949552710002882
    Format: XIII, 146 p. 18 illus. , online resource.
    Edition: 1st ed. 2023.
    ISBN: 9783031272233
    Content: This open access book explores the expectations surrounding dementia, what it 'looks like' and how people have been treated by others. It aims to raise awareness of the different types of dementia, and how they impact the brain, body, and lived experience, including experience of Alzheimer's disease, Vascular Dementia, Posterior Cortical Atrophy, Frontotemporal Dementia, Semantic Dementia, and Lewy Body Dementia. The co-authors reflect on their experience with informal and formal care, before finishing with a focus on the spectrum of dementia research from clinical trials to user-led research. Throughout the book, co-authors have shared personal stories of how dementia has affected them and people with lived experience of dementia share what they wish people knew about living with the disease. Co-produced by people with lived experience of dementia, academics and health care professionals, this book is an accessible resource about dementia from the perspective of people actively involved in the field and essential reading for healthcare professionals wishing to learn more about the experience of this neuroprogressive condition, as well as policymakers, and members of the public. Dr Rosie Ashworth leads Partners in Research for NRS Neuroprogressive and Dementia Network, UK. As a research psychologist, Rosie is passionate about co-production, ethics, and actively involving people with lived experience in research. She is also the co-lead for ENRICH Scotlands 'Patient and Public Involvement' group RICH (Research in Care Homes) Voices, a Fellow with Advanced Higher Education, an advisor to the Dementia Enquirers, and a volunteer for About Dementia. Partners in Research co-authors including Agnes Houston, Chris Maddocks, David Ross, Fred S. Wilson, Masood Qureshi, Martin Robertson, Myra Lamont, Stuart Hay, Sue Fyvel, Willy Gilder, Winnie Henry, and Alyson Hill.
    Note: 1. Coproducing a book on dementia research -- 2. Taking part in Alzheimer's disease research -- 3. Taking part in Vascular dementia research -- 4. Taking part in Fronto-Temporal dementia research -- 5. Taking part in Parkinson's dementia research -- 6. Taking part in dementia with lewy bodies research -- 7. Taking part in PCA dementia research -- 8. Lessons for future research in dementia.
    In: Springer Nature eBook
    Additional Edition: Printed edition: ISBN 9783031272226
    Additional Edition: Printed edition: ISBN 9783031272240
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 8
    UID:
    edoccha_9961235409202883
    Format: 1 online resource (154 pages)
    Edition: 1st ed. 2023.
    ISBN: 3-031-27223-4
    Content: This open access book explores the expectations surrounding dementia, what it ‘looks like’ and how people have been treated by others. It aims to raise awareness of the different types of dementia, and how they impact the brain, body, and lived experience, including experience of Alzheimer’s disease, Vascular Dementia, Posterior Cortical Atrophy, Frontotemporal Dementia, Semantic Dementia, and Lewy Body Dementia. The co-authors reflect on their experience with informal and formal care, before finishing with a focus on the spectrum of dementia research from clinical trials to user-led research. Throughout the book, co-authors have shared personal stories of how dementia has affected them and people with lived experience of dementia share what they wish people knew about living with the disease. Co-produced by people with lived experience of dementia, academics and health care professionals, this book is an accessible resource about dementia from the perspective of people actively involved in the field and essential reading for healthcare professionals wishing to learn more about the experience of this neuroprogressive condition, as well as policymakers, and members of the public. Dr Rosie Ashworth leads Partners in Research for NRS Neuroprogressive and Dementia Network, UK. As a research psychologist, Rosie is passionate about co-production, ethics, and actively involving people with lived experience in research. She is also the co-lead for ENRICH Scotlands ‘Patient and Public Involvement’ group RICH (Research in Care Homes) Voices, a Fellow with Advanced Higher Education, an advisor to the Dementia Enquirers, and a volunteer for About Dementia. Partners in Research co-authors including Agnes Houston, Chris Maddocks, David Ross, Fred S. Wilson, Masood Qureshi, Martin Robertson, Myra Lamont, Stuart Hay, Sue Fyvel, Willy Gilder, Winnie Henry, and Alyson Hill.
    Note: 1. Coproducing a book on dementia research -- 2. Taking part in Alzheimer’s disease research -- 3. Taking part in Vascular dementia research -- 4. Taking part in Fronto-Temporal dementia research -- 5. Taking part in Parkinson’s dementia research -- 6. Taking part in dementia with lewy bodies research -- 7. Taking part in PCA dementia research -- 8. Lessons for future research in dementia.
    Additional Edition: ISBN 3-031-27222-6
    Language: English
    Keywords: Llibres electrònics
    Library Location Call Number Volume/Issue/Year Availability
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  • 9
    UID:
    edocfu_9961235409202883
    Format: 1 online resource (154 pages)
    Edition: 1st ed. 2023.
    ISBN: 3-031-27223-4
    Content: This open access book explores the expectations surrounding dementia, what it ‘looks like’ and how people have been treated by others. It aims to raise awareness of the different types of dementia, and how they impact the brain, body, and lived experience, including experience of Alzheimer’s disease, Vascular Dementia, Posterior Cortical Atrophy, Frontotemporal Dementia, Semantic Dementia, and Lewy Body Dementia. The co-authors reflect on their experience with informal and formal care, before finishing with a focus on the spectrum of dementia research from clinical trials to user-led research. Throughout the book, co-authors have shared personal stories of how dementia has affected them and people with lived experience of dementia share what they wish people knew about living with the disease. Co-produced by people with lived experience of dementia, academics and health care professionals, this book is an accessible resource about dementia from the perspective of people actively involved in the field and essential reading for healthcare professionals wishing to learn more about the experience of this neuroprogressive condition, as well as policymakers, and members of the public. Dr Rosie Ashworth leads Partners in Research for NRS Neuroprogressive and Dementia Network, UK. As a research psychologist, Rosie is passionate about co-production, ethics, and actively involving people with lived experience in research. She is also the co-lead for ENRICH Scotlands ‘Patient and Public Involvement’ group RICH (Research in Care Homes) Voices, a Fellow with Advanced Higher Education, an advisor to the Dementia Enquirers, and a volunteer for About Dementia. Partners in Research co-authors including Agnes Houston, Chris Maddocks, David Ross, Fred S. Wilson, Masood Qureshi, Martin Robertson, Myra Lamont, Stuart Hay, Sue Fyvel, Willy Gilder, Winnie Henry, and Alyson Hill.
    Note: 1. Coproducing a book on dementia research -- 2. Taking part in Alzheimer’s disease research -- 3. Taking part in Vascular dementia research -- 4. Taking part in Fronto-Temporal dementia research -- 5. Taking part in Parkinson’s dementia research -- 6. Taking part in dementia with lewy bodies research -- 7. Taking part in PCA dementia research -- 8. Lessons for future research in dementia.
    Additional Edition: ISBN 3-031-27222-6
    Language: English
    Keywords: Llibres electrònics
    Library Location Call Number Volume/Issue/Year Availability
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  • 10
    UID:
    kobvindex_HPB1397331480
    Format: 1 online resource (170 pages)
    ISBN: 9783031272233 , 3031272234
    Content: This open access book explores the expectations surrounding dementia, what it looks like and how people have been treated by others. It aims to raise awareness of the different types of dementia, and how they impact the brain, body, and lived experience, including experience of Alzheimers disease, Vascular Dementia, Posterior Cortical Atrophy, Frontotemporal Dementia, Semantic Dementia, and Lewy Body Dementia. The co-authors reflect on their experience with informal and formal care, before finishing with a focus on the spectrum of dementia research from clinical trials to user-led research. Throughout the book, co-authors have shared personal stories of how dementia has affected them and people with lived experience of dementia share what they wish people knew about living with the disease. Co-produced by people with lived experience of dementia, academics and health care professionals, this book is an accessible resource about dementia from the perspective of people actively involved in the field and essential reading for healthcare professionals wishing to learn more about the experience of this neuroprogressive condition, as well as policymakers, and members of the public. Dr Rosie Ashworth leads Partners in Research for NRS Neuroprogressive and Dementia Network, UK. As a research psychologist, Rosie is passionate about co-production, ethics, and actively involving people with lived experience in research. She is also the co-lead for ENRICH Scotlands Patient and Public Involvement group RICH (Research in Care Homes) Voices, a Fellow with Advanced Higher Education, an advisor to the Dementia Enquirers, and a volunteer for About Dementia. Partners in Research co-authors including Agnes Houston, Chris Maddocks, David Ross, Fred S. Wilson, Masood Qureshi, Martin Robertson, Myra Lamont, Stuart Hay, Sue Fyvel, Willy Gilder, Winnie Henry, and Alyson Hill.
    Note: 1. Coproducing a book on dementia research -- 2. Taking part in Alzheimers disease research -- 3. Taking part in Vascular dementia research -- 4. Taking part in Fronto-Temporal dementia research -- 5. Taking part in Parkinsons dementia research -- 6. Taking part in dementia with lewy bodies research -- 7. Taking part in PCA dementia research -- 8. Lessons for future research in dementia.
    Additional Edition: Print version: ASHWORTH, ROSALIE. CHALLENGING ASSUMPTIONS AROUND DEMENTIA. [Place of publication not identified] : PALGRAVE MACMILLAN, 2023 ISBN 3031272226
    Language: English
    Keywords: Electronic books.
    Library Location Call Number Volume/Issue/Year Availability
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