ABSTRACT
People with cognitive changes caused by Mild Cognitive Impairment have an increased risk of developing Alzheimer’s or dementia. The issue of dementia from an ethics point of view is to understand the needs of both the provider and the caregiver. Physicians need to explain to the family the stages of dementia and what will happen to the patient in each of them. During the late stages of dementia, the role of the caregiver is focused on preserving the quality of life and dignity of the patient. The health care provider needs to educate the family with a common goal; the decision is about making sure the person receives the care needed. The underlying philosophy of the hospice focuses on quality of life and dignity by providing comfort, care, and support services for people with terminal illnesses and their families. The health care providers need to have the personnel to help to cope with Alzheimer’s patients for the family members.
