被收养的孩子被诊断患有智力障碍后,母亲们的经历

Louise Camm-Crosbie
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摘要

与亲生父母和无智障儿童的收养父母相比,收养父母和智障儿童的父母都存在额外的压力源。然而,尽管在被收养的儿童中患有ID的儿童比例过高,但人们对收养后被诊断患有ID的孩子的父母经历知之甚少。本研究采用解释现象学分析对8位养母的访谈进行分析,了解她们的孩子在被收养后被诊断为本我。三个主要的主题是:“智力残疾的创伤”,与背叛、失去和在意外诊断的背景下寻找答案的经历有关;"孤立和边缘化"说明了与朋友、家人和专业人士隔绝的经历;“成长和韧性”强调了母亲们如何面对挑战,重新协商对未来的希望。调查结果突出表明,服务机构缺乏适当定制的收养后和诊断后支持。养母们要求在诊断过程中增加包容性和透明度。研究结果表明,收养母亲“找到自己的部落”很重要,这表明收养后和身份服务可以做得更多,以促进有共同经历的人的支持网络。
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Mothers’ experiences of their adopted child being diagnosed with an intellectual disability post-adoption
Adoptive-parenting and parenting a child with intellectual disabilities (ID) both present additional stressors relative to birth parenting and adoptive parenting of children without an ID. However, despite children with ID being overrepresented among adopted children populations, very little is known about the parental experiences of having a child diagnosed with an ID post adoption. Interpretative Phenomenological Analysis was used to analyse interviews from eight adoptive mothers regarding their experiences of their child being diagnosed with an ID post-adoption. Three superordinate themes were developed: ‘Trauma of intellectual disability’ related to experiences of betrayal, loss and searching for answers in the context an unexpected diagnosis; ‘isolation and marginalisation’ illustrated experiences of isolation from friends, family and professionals alike; and ‘growth and resilience’ highlighted how mothers leant into challenges and renegotiated their hopes for the future. The findings highlighted a lack of appropriately tailored post-adoption and post-diagnostic support from services. Adoptive mothers requested greater inclusion and transparency during the diagnostic process. The findings indicated the importance of adoptive mothers ‘finding their tribe’ suggesting that post-adoption and ID services could do more to facilitate support networks of people with shared experiences.
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