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The Alzheimer's Disease Bill of Rights
Every person diagnosed with Alzheimer's disease or a related disorder deserves the following rights:
- To be informed of one's diagnosis.
- To have appropriate, ongoing medical care.
- To be productive in work and play for as long as possible.
- To be treated like an adult, not like a child.
- To have expressed feelings taken seriously.
- To be free from psychotropic medications, if possible.
- To live in a safe, structured, and predictable environment.
- To enjoy meaningful activities to fill each day.
- To be out-of-doors on a regular basis.
- To have physical contact, including hugging, caressing, and hand-holding.
- To be with individuals who know one's life story, including cultural and religious traditions.
- To be cared for by individuals who are well trained in dementia care.
Source: The Best Friends Approach to Alzheimer’s Care, rev. by Virginia Bell and David Troxel.
Copyright © 2003, by Health Professions Press, Inc. Baltimore. Reprinted by permission from Bell, V.M., & Troxel, D. (1994, September/October). An Alzheimer’s disease bill of rights. American Journal of Alzheimer’s Care and Related Disorders & Research.
© Health Professions Press
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