PART I: MEDICAL FUNDAMENTALS
1. What is Dementia?
Elissa L Ash
2. The Demographics of Dementia
Israel (Issi) Doron
3. The Genetics of Dementia
Sophie Behrman, Klaus P Ebmeier and Charlotte L Allan
4. Can Dementia be Prevented?
Amos D Korczyn and Veronika Vakhapova
5. Clinical Management of Dementia: An Overview (1)
Noa Bregman and Orna Moore
6. Clinical Management of Dementia: An Overview (2)
Chris Fox, Carolyn Chew-Graham, Emma Wolverson, Ian Maidment and
Andrea Hilton
7. Best Interests Determination: A Medical Perspective
Hugh Series
8. Advance Decisions and Proxy Decision-Making in the Elderly: A
Medical Perspective
Gary Sinoff and Natalia Blaja-Lisnic
9. The Happy Dementia Patient
Hugh Series
10. Dementia: A Perspective from Primary Care
Daniel Lasserson
PART II: ETHICAL PERSPECTIVES
11. Dementia: An Ethical Overview
Michael Dunn
12. Best Interests Determinations and Substituted Judgement:
Personhood and Precedent Autonomy
Andrew McGee
13. Proxy Decision-Making
José Miola
14. Telling the Truth: The Ethics of Deception and White Lies in
Dementia Care
Maartje Schermer
15. Research on Patients with Dementia
Adrian Treloar and Claudia Dunlop
16. Genetics and Dementia: Ethical Concerns
Caroline J Huang, Michael Parker and Matthew L Baum
17. Common Perceptions of Dementia
Perla Werner
18. Ethical Perspectives on End-of-Life Care: Euthanasia, Assisted
Suicide and the Refusal of or Withdrawal of Life-Sustaining
Treatments in those Living with Dementia
Michael Gordon
19. Resource Allocation Issues in Dementia
Leah Rand and Mark Sheehan
20. Sexuality in Dementia
Julian C Hughes, Aileen Beatty and Jeanette Shippen
21. The Use of New Technologies in Managing Dementia Patients
Julian C Hughes
22. Abuse, Safeguarding and Dementia
Bridget Penhale
PART III: LEGAL PERSPECTIVES
23. A Legal Overview
Mary Donnelly
24. Assessing Capacity
Lesley King and Hugh Series
25. Best Interests and Dementia
Jonathan Herring
26. Proxy Decision-Making: A Legal Perspective
Winsor C Schmidt
27. Being and Being Lost: Personal Identity and Dementia
Jesse Wall
28. Dementia, Autonomy and Guardianship for the Old
Margaret Isabel Hall
29. Restriction of Liberty
Michael Schindler and Yael Waksman
30. Research on Patients with Dementia
Phil Bielby
31. Dementia and Carers: Relationality and Informal
Carers’ Experiences
Rosie Harding
32. End-of-Life Care
Ofra G Golan
33. Health Care Resource Allocation Issues in Dementia
Keith Syrett
34. The Use of New Technologies in the Management of Dementia
Patients
Karen Eltis
PART IV: SOCIAL ASPECTS OF DEMENTIA
35. Discrimination
Doug Surtees
36. Physical, Financial and other Abuse
Ruijia Chen, E-Shien Chang, Melissa Simon and XinQi Dong
37. Driving and Dementia
Desmond O’Neill
38. Voting and Political Participation
Nina A Kohn
PART V: PATIENT AND CARER PERSPECTIVES
39. This is My Life
Peter JS Ashley
40. Dad’s Dementia
Andrew Billen
41. Lewy Body Disease: A Carer’s Perspective
Sue Berkeley and Rob Berkeley
42. Our Journey
Shirley Nurock
43. The Power of Imagination
Peter Richards
44. Dementia Care: Workpoints
U Hla Htay
Charles Foster is a Fellow of Green Templeton College,
University of Oxford and a practising barrister.
Jonathan Herring is Professor of Law at the University of
Oxford.
Israel Doron is Head of the Department of Gerontology, University
of Haifa.
The Law and Ethics of Dementia is a very big book - in every sense
of the word. It has sat on my bedside table for a few months, where
I have eyed it guiltily - put off by its size and weighty subject
matter. I wish I hadn't. I picked it up one Sunday morning a few
weeks ago, intending to read one or two articles, and found I could
not put it down. The chapters I read (and I have, by now, read most
of them) were well written, and the perfect length to convey an
idea well and clearly. The chapters are accessible enough for
somebody who is new to this field to read and understand, whilst
still exploring cutting edge questions that will interest people
who are familiar with these issues.
In short, this book is a real chocolate box of well written and
interesting articles. Although most of the articles consider UK
law, several chapters offer a more international perspective, and
the ethical and medical chapters will be of interest to readers
around the world.
The book could be of interest for those with personal experiences
of dementia, not merely philosophers and lawyers. As I was going
through, I used up an entire packet of sticky index tabs to flag up
passages that I wanted to return. I suspect this is a book I will
be re-reading and thinking about for years to come.
*The Small Places Blog, December 2014*
The Law and Ethics of Dementia is the sort of academic book that
you can read from start to finish, or whose chapters you can dip
into individually ... its relevance will endure, and the great
effort and energy that have evidently been expended by the editors
and contributors will be repaid many times over. I could not
recommend it more highly.
*European Journal of Health Law*
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