School of Social Policy and Practice, University of Pennsylvania, Philadelphia, PA, USA; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA.
Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA.
Soc Sci Med. 2022 May;301:114905. doi: 10.1016/j.socscimed.2022.114905. Epub 2022 Mar 17.
Experiences of illness change the physical body and embodiments, or the ways in which the world and the self are known through the body. When illness is anticipated, such as with inherited cancer predisposition syndromes, risk becomes embodied and shared in family groups. Embodied risk is experienced whether or not symptoms have manifested. To examine how individuals and families with genetic risk experience the world and understand their disease through their bodies, we employ Li-Fraumeni syndrome (LFS) as an exemplar. LFS is a rare, genetic, cancer predisposition syndrome with nearly 100% lifetime cancer risk starting from birth, limited opportunities for prevention, rigorous screening protocols, and early mortality.
Forty-five families, including 117 individuals aged 13-81 years, enrolled in the National Cancer Insitute's LFS study (NCT01443468) completed 66 open-ended interviews regarding LFS experiences. An interdisciplinary team used modified grounded theory to explore physical aspects of living with LFS in psychosocial contexts.
The physicality of living with LFS included constant monitoring of LFS bodies across the family to identify physical change that might indicate carcinogenesis. Cancer screening, risk reduction, and treatment acted as dually protective and invasive, and as an unavoidable features of LFS. Connections between family members with similar embodiments normalized aesthetic changes and supported coping with visible markers of difference. In some circumstances, participants objectified the body to preserve the self and important relationships. In others, intense pain or loss created thresholds beyond which the self could no longer be separated from the body to support coping.
This paper focuses on Li-Fraumeni syndrome, a familial condition with a well-established genetic identity in which the body-self is experienced in relation to important others, to medical imaging, and to historical experiences with cancer. We expand on theories of embodied risk and inter-embodiment to describe experiences across disease trajectories, with attention to division and union between body, self, and other.
疾病体验会改变身体和体现,或者通过身体来认识世界和自我的方式。当预期到疾病时,例如遗传性癌症倾向综合征,风险就会在家族群体中体现和共享。无论是否出现症状,都会体验到体现的风险。为了研究具有遗传风险的个体和家庭如何通过身体体验世界并理解他们的疾病,我们以李-佛美尼综合征(Li-Fraumeni syndrome,LFS)为例。LFS 是一种罕见的遗传性癌症倾向综合征,从出生起就有近 100%的终生癌症风险,预防机会有限,筛查方案严格,早期死亡率高。
45 个家庭,包括 117 名年龄在 13-81 岁的个体,参加了美国国立癌症研究所的 LFS 研究(NCT01443468),完成了 66 次关于 LFS 体验的开放性访谈。一个跨学科团队使用改良的扎根理论来探索在社会心理背景下与 LFS 一起生活的身体方面。
与 LFS 一起生活的身体方面包括对 LFS 身体进行持续监测,以识别可能预示癌变的身体变化。癌症筛查、降低风险和治疗既是保护性的,也是侵入性的,是 LFS 的一个不可避免的特征。具有相似体现的家庭成员之间的联系使美学变化正常化,并支持应对可见的差异标志。在某些情况下,参与者使身体客观化以保护自我和重要关系。在其他情况下,强烈的疼痛或损失会造成无法承受的阈值,以至于自我无法与身体分离来应对。
本文主要关注李-佛美尼综合征,这是一种家族性疾病,其身体-自我的体验与重要他人、医学影像和癌症的历史经历有关。我们扩展了体现风险和相互体现的理论,以描述跨越疾病轨迹的体验,同时注意身体、自我和他人之间的分裂和统一。