By Konstadina Griva, Aleksandra Luszczynska, Val Morrison Tracey A. Revenson
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Extra resources for Caregiving in the Illness Context
In line with this, one study showed that the percentage of family caregivers who preferred life-preserving treatments was higher than the percentage of patients with terminal cancer who preferred such treatments (Tang, Liu, Lai, Liu, & Chen, 2005). 0006 Caregiving as a Dyadic Process possible, but there may be a limit to the objective burden their caregivers can cope with, perhaps making hospice care necessary. One study examined attitudes toward hospice/palliative care showing that 51 of caregivers preferred such care versus 38 of the patients with terminal cancer (An, Lee, Yun, & Heo, 2014).
Gaugler, Kane, & Newcome, 2005; Salter, Zettler, Foley, & Teasell, 2010). Some studies, however, support the wear and tear hypothesis. 0005 Caregiving in the Illness Context psychosocial resources early in the illness were predictive of depressive symptoms three and five years and eight years later (Kim, Shaffer, Carver, & Cannady, 2014, 2015). Many caregivers who were still actively engaged in cancer caregiving five years after the diagnosis showed a significant increase in distress over those years.
Empathic distress refers to an unpleasant and aversive affective state, which results from observing another person in distress. In this type of response, caregivers experience emotions such as anxiety, nervousness, and distress, which are unpleasant and upsetting. Although empathic distress motivates helping, caregivers offer their help in order to reduce their own distress; helping the person in need is only tangential to this primary outcome. Empathic concern is characterized by positively toned emotions, such as warmth, tenderness, and soft-heartedness, directed at the affected person.
Caregiving in the Illness Context by Konstadina Griva, Aleksandra Luszczynska, Val Morrison Tracey A. Revenson