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The experience of dying is different for each person. It comes in its own time and its own way.
When a person with Alzheimer's disease is in the very late stages of the disease, the focus should be on quality of life and comfort, rather than on lengthening life and giving treatment. Palliative (or comfort) care focuses on the whole person's needs physical, emotional and spiritual.
In this session, a clinical ethicist will help you understand the difficult decisions you may need to make at the end of a family member's life. We will also reflect on what it means to have a "good" death.
Learning Objectives
When you have completed this session, you will be able to:
Work through the various parts of the session at your leisure. Move from one part to another at your own pace and in the order that makes sense to you, based on your own needs and interests.
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Congratulations! You've successfully completed Session 15.
In this session you examined the difficult decisions you may need to make at the end of a family member's life. You also reflected on what it means to have a 'good' death.
The Alzheimer Society in your community can provide educational resources to help you learn more about the disease, referrals to help you access the practical support you need, and one-on-one and group support to help you cope with the emotional impact of the disease. Contact your local Alzheimer Society today.
Note: This online version of the Seeds of Hope Family Learning Series provides guidance but it is not intended to replace the advice of a health care professional. Consult your health care provider about changes in the person's condition, or if you have questions or concerns.
