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裘馨兒母親的轉渡經驗

Transitional Experiences among Mothers Becoming the Caregivers of Children with Duchenne Muscular Dystrophy

摘要


研究目的:藉由裘馨氏肌肉萎縮症兒童(裘馨兒)母親的自身敘說來深入了解其成為照顧者的轉渡經驗。研究方法:研究設計採現象學研究法,以立意取樣選取11位「社團法人中華民國肌萎縮症病友協會」之裘馨兒母親。經由一對一的深度訪談以獲取她們的主觀經驗,訪談資料運用Colaizzi(1978)分析法進行訪談資料分析。研究結果:結果呈現出裘馨兒母親的轉渡經驗包含「汩汩苦流中,給自己力量前行」及「滿滿母愛下,竭盡所能給予」。研究結論:本篇研究結果有助於對裘馨兒母親轉渡經驗的初步認識,並能提供政府機關、健康專業機構、教育單位及支持團體聯合照護的參考,讓裘馨兒母親的轉渡經驗能從擺盪中更趨向穩定。

並列摘要


Purpose: This study explored the transitional experiences of mothers as they became caregivers of children with Duchenne Muscular Dystrophy (DMD). The focus of the study was to understand their perspectives. Methods: One-on-one interviews were conducted with 11 mothers of DMD children identified through the Taiwan Muscular Dystrophy Association. Data were analyzed using the Colaizzi phenomenological method. Results: The analysis revealed 2 main themes: ”in a stream of bitterness, finding the strength to move forward”, and ”being in touch with a mother's abundant love to provide the best for a DMD child”. Conclusions: The findings shed light on the transitional experiences of mothers of DMD kids and may serve as an important reference for government, healthcare professionals, educational organizations, and other non-governmental organization support teams to improve their services to this group.

參考文獻


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郭士賢、張思嘉(2004)。華人生活世界中多面向的因果思惟。本土心理學研究。21,233-267。
中華民國內政部(2008):〈重要內政統計指標-人口〉。2008年1月15日,取自http://sowf.moi.gov.tw/stat/indices/list.xls
Abi Daoud, M. S.,Dooley, J. M.,Gordon, K. E.(2004).Depression in parents of children with Duchenne muscular dystrophy.Pediatric Neurology.31(1),16-19.

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