Voluntary Registries to Support Improved Interaction Between Police and People Living with Dementia

Journal of Law, Medicine and Ethics 50 (2):348-363 (2022)
  Copy   BIBTEX

Abstract

This paper provides an overview of the societal impact of a rising dementia population and examines the legal and ethical implications posed by voluntary registries as a community-oriented solution to improve interactions between law enforcement and individuals with dementia. It provides a survey of active voluntary registries across the United States, with a focus on Arizona, which has the highest projected growth for individuals living with dementia in the country.

Other Versions

No versions found

Links

PhilArchive

    This entry is not archived by us. If you are the author and have permission from the publisher, we recommend that you archive it. Many publishers automatically grant permission to authors to archive pre-prints. By uploading a copy of your work, you will enable us to better index it, making it easier to find.

    Upload a copy of this work     Papers currently archived: 103,566

External links

Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

Similar books and articles

Deception in Dementia: Adding Caregivers to the Equation.Jalayne J. Arias - 2021 - Journal of Law, Medicine and Ethics 49 (2):263-265.
Dementia : an ethical overview.Michael Dunn - 2014 - In Charles Foster, Jonathan Herring & Israel Doron, The law and ethics of dementia. Portland, Oregon: Hart Publishing.
Advance Directives and Alzheimer's Disease.Deena S. Davis - 2018 - Journal of Law, Medicine and Ethics 46 (3):744-748.

Analytics

Added to PP
2022-07-29

Downloads
20 (#1,111,046)

6 months
4 (#957,314)

Historical graph of downloads
How can I increase my downloads?

References found in this work

Add more references