The Best Friends™ Dementia Bill of Rights

Dementia can deeply affect how individuals experience the world, but it should never strip them of their dignity, autonomy, or humanity. The Dementia Bill of Rights is a powerful reminder that people living with dementia still have fundamental rights—rights to be respected, included, and supported. This guiding document outlines our key principles that ensure compassionate care, meaningful relationships, and person-centered support for those navigating life with dementia.

The Best Friends™ Dementia Bill of Rights
Every person diagnosed with Alzheimer’s disease or other dementia deserves:

To be informed of one’s diagnosis.

To have appropriate, ongoing medical care.

To be treated as an adult, listened to, and afforded respect for one’s feelings and point of view.

To be with individuals who know one’s life story, including cultural and spiritual traditions.

To experience meaningful engagement throughout the day.

To live in a safe and stimulating environment.

To be outdoors on a regular basis.

To be free from psychotropic medications whenever possible.

To have welcomed physical contact, including hugging, caressing, and handholding.

To be an advocate for oneself and others.

To be part of a local, global, or online community.

To have care partners well trained in dementia care.