How Palliative Care Must Be Offered For Family Members Of...

Witt Sherman (1998) suggests that palliative care must be offered to family members of patients with terminal illnesses to address the physical, emotional, and social needs associated with being the caregiver of a person with a terminal illness, stating â€Å"the clinician needs to acknowledge the caregivers efforts and assess his or her relationship with the patient and other family members, while encouraging the expression of fears, concerns, loss, and grief. It is important to put the caregiver in touch with respite services before stress, emotional and physical exhaustion, and depression take their toll† (Witt Sherman, 1998). As an intern at a cancer institute, this writer assesses for the mood and needs of patients’ family members by initiating discussions about how they are coping with the patient’s illness. This writer attempts to empower caregivers by asserting the need for self-care at a time when they are devoting most of their time and energy to the family member they are caring for and providing them with the knowledge that the services offered by the Psychosocial Oncology department are available to them, as well as the patient. Prejudice in End-of-Life Care There are many factors that may make it difficult for social workers to be unprejudiced when dealing with patients in End-of life care. These factors include their feelings and beliefs regarding death, bias toward curative or comfort care, and their feelings regarding characteristics of each individual theyShow MoreRelatedPalliative Care : Its Role1503 Words   |  7 PagesPalliative Care: Its Role Importance in Our Lives It’s a fact of life that all people will experience death. A difficult subject for many, yet it’s crucial in modern society that we learn of the available resources for those facing the unavoidable ultimatum. 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