Shouldering a Burden

Abstract

Non-institutionalized care of the chronically ill and dying is examined from the perspective of the burdens it imposed upon the family and how they received them. Conditions are explicated concerning when and for how long relatives will assume these burdens. Circumstances under which the supporting relative does not question his obligations are scrutinized. Determinants in how long the patient remains at home include the availability of assistance, knowledge about the situation, and the patient's own realm of symbolic meanings. When the supporting relative relinquishes his burden of care, he is apt to face new burdens surrounding the meanings and ambiguities of death.