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Dementia, Healthcare Decision Making, and Disability Law
1Megan S. Wright, J.D., Ph.D., is an Assistant Professor at Penn State Law and an Assistant Professor in the Departments of Humanities and Public Health Sciences at Penn State College of Medicine. She is Affiliate Faculty in the Department of Sociology and Criminology and the Rock Ethics Institute at Pennsylvania State University. She is also an Adjunct Assistant Professor of Medical Ethics in Medicine at Weill Cornell Medical College.
Abstract:
Persons with dementia often prefer to participate in decisions about their health care, but may be prevented from doing so because healthcare decision-making law facilitates use of advance directives or surrogate decision makers for persons with decisional impairments such as dementia. Federal and state disability law provide alternative decision-making models that do not prevent persons with mild to moderate dementia from making their own healthcare decisions at the time the decision needs to be made. In order to better promote autonomy and wellbeing, persons with dementia should be accommodated and supported so they can make their own healthcare decisions.
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