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The impact of a sibling's life‐limiting genetic condition on adult brothers and sisters

机译:兄弟姐妹终身遗传条件对成年兄弟姐妹的影响

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It is estimated that rare diseases affect the lives of over three million people in the United Kingdom. Of these, a significant proportion are children and young people with genetic life‐limiting or life‐shortening conditions. This study used a qualitative approach with in‐depth semi‐structured interviews to explore the experiences of 10 adult siblings of a baby diagnosed with Trisomy 13 (Patau syndrome) or Trisomy 18 (Edward syndrome). Findings illustrate that parental grief from the time of their child's diagnosis onward is also experienced by siblings. Although young adults may have conflicting feelings as a bereaved sibling, there is evidence that the experience impacts on their world views and their attitudes about prospective and expectant parenthood. The study highlights the importance of providing siblings with short‐term and long‐term support from the time of their brother's or their sister's diagnosis onward and provides new understanding about benefit of professional and peer support in helping young adults develop resilience and coping strategies.
机译:据估计,稀有疾病影响英国超过300万人的生命。其中,大量比例是儿童和青少年遗传生活限制或寿命缩短条件。本研究采用了一种与深入的半结构化访谈进行了定性方法,探讨了患有三术13(Patau综合征)或三术18(Edward综合征)的婴儿的10个成人兄弟姐妹的经验。调查结果说明兄弟姐妹也经历了他们孩子诊断时的父母悲伤。虽然年轻的成年人可能会有冲突的情感,但有证据表明,经验对自己的观点和对前瞻性和预期父母身份的态度影响。该研究强调了向兄弟或其姐姐的诊断时向兄弟姐妹提供短期和长期支持的重要性,并对专业和同行支持的利益提供了新的了解,帮助年轻的成年人发展恢复力和应对策略。

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