We are No Longer Invisible

Poroi Pub Date : 2020-01-07 DOI:10.13008/2151-2957.1296
Raquel M. Robvais
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引用次数: 3

Abstract

: Sickle cell discourses are not merely descriptions of medical matters but contentious sites that invoke rhetorical arguments to support racialized medical borders, human difference, and ontological essentialism. In this essay, I examine the way that those stricken by Sickle Cell Anemia appropriate the disease to advocate for their voice and visibility. I disclose how the construction of SCA as a black disease becomes a contested terrain which is often a “cultural centering on identity and dignity.” At odds is how the body is inscribed with a set of meanings in its association with blackness, the woeful ignorance that’s pervasive in the medical community of those who treat sickle cell patients and the indomitable will of the warrior to survive regardless. I c onsider the “warring ideals in one dark body,” urgings to be seen and heard. These manifest as performances of resistance, acts of resilience, and ways of asserting agency to maintain a semblance of humanity in the midst of situations that are anything but.
我们不再是隐形人
:镰状细胞话语不仅是对医学问题的描述,而且是有争议的场所,它们援引修辞论点来支持种族化的医学边界、人类差异和本体论本质主义。在这篇文章中,我研究了那些患有镰状细胞性贫血的人如何利用这种疾病来宣传他们的声音和可见性。我披露了SCA作为一种黑人疾病的构建是如何成为一个有争议的领域的,这通常是一种“以身份和尊严为中心的文化”。不一致的是,身体如何在与黑人的联系中被赋予一系列意义,治疗镰状细胞病患者的医学界普遍存在着可悲的无知,战士们不顾一切地顽强求生。我认为“在一个黑暗的身体里交战的理想”,渴望被看到和听到。这些表现为抵抗的表现、恢复力的行为,以及在完全不同的情况下维护人性外表的方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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