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



    Upload a copy of this work     Papers currently archived: 101,130

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 (eds.), 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.
“The heart still beat, but the brain doesn't answer”.Mary C. Olson - 1999 - Theoretical Medicine and Bioethics 20 (1):85-95.

Analytics

Added to PP
2022-07-29

Downloads
17 (#1,146,966)

6 months
5 (#1,035,390)

Historical graph of downloads
How can I increase my downloads?

References found in this work

Add more references