Hospice palliative care provides physical, psychological, social, spiritual and practical support to people with a life-limiting illness and to their loved ones. Care teams include physicians, volunteers, nurses, spiritual counselors, friends, and family. It can be provided at home, in hospitals, nursing homes, or freestanding hospice facilities. Hospice palliative care helps make a very difficult life passage both manageable and meaningful for people facing death, as well as for their loved ones. In light of Canada’s aging population and ongoing health care reform, hospice palliative care is becoming an increasingly essential service to cope with the growing demand for compassionate, high quality, and cost-effective end-of-life care. The Canadian hospice palliative movement is still in its formative stages and requires significant help to meet this enormous need.


Palliation (or palliative care) is defined as health care that focuses on the control of pain and suffering in a patient with a life-threatening illness. The goal of palliation is to maximize a patient’s quality of life at the end of life rather than to cure the disease or prolong the patient’s life. It is based on:


Highly-developed medical expertise in pain and symptom management.


Timely and responsive patient-centered communications.


Interdisciplinary team work.



Advance Care Directives are a patient’s formal or informal instructions concerning expectations of care and choice of treatment options in response to potential illnesses or conditions (legal connotations vary by jurisdiction; includes a living will).



Alternate or complementary integrative therapies are terms often used to describe independent healing systems outside the realm of conventional medical theory and practice.



A caregiver can be broadly defined as anyone who provides care. This definition can be further broken into two categories of caregivers, formal and informal. Formal caregivers are members of an organization and accountable to defined norms of conduct and practice. They may be professionals, support workers, or volunteers. They are sometimes called ‘providers’. Informal caregivers are not members of an organization. They have no formal training and are not accountable to standards of conduct or practice. They may be family members or friends.



The term family refers to those closest to the patient in knowledge, care, and affection and may include:


The biological family.


The family of acquisitions (related by marriage/contract).


The family of choice and friends (including pets).


The patient defines who will be involved in his/her care and/or present at the bedside.



Illness is an absence of wellness due to disease, another condition, or aging. Illness can be further categorized as acute, chronic, advanced, and life-threatening. An acute illness is one that is recent in onset and likely to be time-limited. If severe, it could be life threatening. A chronic illness is likely to persist for months to years. With progression, it may become life threatening. An advanced illness is likely to be progressive and life threatening. A life-threatening illness is likely to lead to death in the near future.



A provider is a formal caregiver who is a member of an organization and accountable to defined norms of conduct and practice. They may be professionals, support workers, or volunteers.



A volunteer is a person who freely gives of his/her time, talent, and energy. Volunteers are members of an organization and accountable to that organization’s standards of conduct and practice.

Charitable Registration # : 10751 6320 RR0001

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