Holding Ashley (X): Bestowing Identity Through Caregiving in Profound Intellectual Disability.

Q3 Medicine Journal of Clinical Ethics Pub Date : 2017-01-01
Lisa Freitag, Joan Liaschenko
{"title":"Holding Ashley (X): Bestowing Identity Through Caregiving in Profound Intellectual Disability.","authors":"Lisa Freitag,&nbsp;Joan Liaschenko","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The controversy over the so-called Ashley Treatment (AT), a series of medical procedures that inhibited both growth and sexual development in the body of a profoundly intellectually impaired girl, usually centers either on Ashley's rights, including a right to an intact, unaltered body, or on Ashley's parents' rights to make decisions for her. The claim made by her parents, that the procedure would improve their ability to care for her, is often dismissed as inappropriate or, at best, irrelevant. We argue, however, that caregiving is a central issue in the controversy, as Ashley's need for caregiving is a defining characteristic of her life. In this article, we analyze the ethics of the Ashley Treatment within the context of family caregiving. Through the physical and emotional work of caregiving, families participate in the formation and maintenance of personal identity, a process that Hilde Lindemann recently called \"holding.\" We argue that, in an intellectually disabled person such as Ashley, who depends on her family for every aspect of her care, the family's contribution to identity is an essential source of personhood. We believe that the treatment can be justified if it is indeed an instance of appropriate family \"holding\" for Ashley.</p>","PeriodicalId":39646,"journal":{"name":"Journal of Clinical Ethics","volume":" ","pages":"189-196"},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Ethics","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

The controversy over the so-called Ashley Treatment (AT), a series of medical procedures that inhibited both growth and sexual development in the body of a profoundly intellectually impaired girl, usually centers either on Ashley's rights, including a right to an intact, unaltered body, or on Ashley's parents' rights to make decisions for her. The claim made by her parents, that the procedure would improve their ability to care for her, is often dismissed as inappropriate or, at best, irrelevant. We argue, however, that caregiving is a central issue in the controversy, as Ashley's need for caregiving is a defining characteristic of her life. In this article, we analyze the ethics of the Ashley Treatment within the context of family caregiving. Through the physical and emotional work of caregiving, families participate in the formation and maintenance of personal identity, a process that Hilde Lindemann recently called "holding." We argue that, in an intellectually disabled person such as Ashley, who depends on her family for every aspect of her care, the family's contribution to identity is an essential source of personhood. We believe that the treatment can be justified if it is indeed an instance of appropriate family "holding" for Ashley.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
抱着阿什利(X):深度智障患者通过看护赋予身份。
所谓的阿什利治疗(AT)是一系列抑制智力严重受损女孩身体生长和性发育的医疗程序,争议通常集中在阿什利的权利上,包括拥有完整、未改变的身体的权利,或者集中在阿什利父母为她做决定的权利上。她的父母声称,手术可以提高他们照顾她的能力,但这种说法经常被认为是不合适的,或者充其量是无关紧要的。然而,我们认为,照顾是争议的中心问题,因为阿什利需要照顾是她生活的一个决定性特征。在本文中,我们分析了在家庭护理的背景下阿什利治疗的伦理。通过身体和情感上的照顾,家庭参与了个人身份的形成和维护,希尔德·林德曼(Hilde Lindemann)最近称之为“持有”的过程。我们认为,对于像阿什利这样的智障人士来说,她的每一方面都依赖于家庭的照顾,家庭对身份的贡献是人格的重要来源。我们认为,如果阿什利确实是一个适当的家庭“控制”,那么这种治疗是合理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Clinical Ethics
Journal of Clinical Ethics Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
31
期刊介绍: The Journal of Clinical Ethics is written for and by physicians, nurses, attorneys, clergy, ethicists, and others whose decisions directly affect patients. More than 70 percent of the articles are authored or co-authored by physicians. JCE is a double-blinded, peer-reviewed journal indexed in PubMed, Current Contents/Social & Behavioral Sciences, the Cumulative Index to Nursing & Allied Health Literature, and other indexes.
期刊最新文献
Dual Advocates in Deceased Organ Donation: The Potential for Moral Distress in Organ Procurement Organization Staff. Duty to Family: Ethical Considerations in the Resuscitation Bay. Home Birth in the United States: An Evidence-Based Ethical Analysis. How Should We Allocate Divisible Resources? An Overlooked Question. New Ways to Help Patients Worst Off.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1