Havermans T, Eiser C
Department of Psychology, Washington Singer Laboratories, University of Exeter, England.
Child Care Health Dev. 1991 Jul-Aug;17(4):259-73. doi: 10.1111/j.1365-2214.1991.tb00696.x.
Mothers of 19 children (mean age = 8.8 years) with spina bifida were interviewed about medical and psychological services available, school placement and restrictions experienced by their children in school and social activities. Mothers also rated their own confidence to care for the child, perceived social support and difficulties experienced by the family. In addition, a measure of the child's disability status was derived. Mothers whose child scored higher in terms of disability reported greater everyday difficulties. In addition, mothers' confidence was related to perceived social support. Mothers reported regular use of medical services but little reliance on specialized nursing or psychological services.
对19名患有脊柱裂儿童(平均年龄8.8岁)的母亲进行了访谈,内容涉及现有的医疗和心理服务、孩子的学校安置情况以及他们在学校和社交活动中所面临的限制。母亲们还对自己照顾孩子的信心、感受到的社会支持以及家庭所经历的困难进行了评分。此外,还得出了一项衡量孩子残疾状况的指标。孩子残疾评分较高的母亲报告说日常困难更多。此外,母亲的信心与感受到的社会支持有关。母亲们报告说经常使用医疗服务,但很少依赖专业护理或心理服务。