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A Unique Case of COVID Pneumonia, Tuberculosis, and Silicosis COVID - 19肺炎、肺结核和矽肺病的独特案例
Pub Date : 2021-05-01 DOI: 10.1164/AJRCCM-CONFERENCE.2021.203.1_MEETINGABSTRACTS.A4087
B. Jakubowski, R. Mehta
A 72-year-old man presented to our emergency room for evaluation of fevers, chills, and myalgias for twelve weeks. He also reported a history of chronic productive cough and chest tightness. Two weeks prior to presentation, he was working at the local international airport in March of 2020 when he noticed increasing dyspnea with exertion whilst performing routine tasks at his job. At the time of our interview, he denied sick contacts and no known history of tuberculosis exposure. He also reported a remote history of working as a stone cutter in concrete mines in Honduras. A chest x-ray was performed and demonstrated bilateral mass-like upper lobe opacities that were present on imaging two years prior. Computed tomography of the chest (figure 1) revealed volume loss and mass-like perihilar upper lobe predominant opacities with fibro-retractile architectural distortion, peribronchovascular and centrilobular nodules, and scattered areas of patchy ground-glass opacification with bibasilar predominance. His fibrotic changes were thought to be consistent with silicosis with progressive massive fibrosis secondary to prior inorganic dust inhalation. A superimposed process underpinning his acute presentation was suspected given the findings of patchy ground-glass opacities. A SARS-CoV-2 PCR test was obtained and was positive. Given several months of symptoms preceding this acute presentation, a third process was suspected, especially in light of his immigration history and centrilobular nodular pattern on imaging. An interferon gamma release assay for tuberculosis, mycobacterium tuberculosis PCR and mycobacterial cultures from expectorated sputum were obtained, all with positive results. He was discharged with a standard regimen of Rifampin, Isoniazid, Pyrazinamide, and Ethambutol with follow-up with the health department at which point he had recovered from his acute illness. He did remarkably well in regards to his COVID-19 diagnosis. He did not receive any COVID specific therapies given his active diagnosis of TB and was discharged home on room air. Silicosis is a well-known predisposing factor to development of tuberculosis, thought to arise from silica particulate macrophage dysfunction. A combination of immune dysfunction related to silicosis and occupational exposure likely led to development of viral pneumonia in this patient. His occupation at a large international airport in March 2020 prior to the institution of quarantine and travel restrictions uniquely put him at risk for both TB and COVID-19 pneumonia, which is nicely demonstrated with these classic CT findings.
一名72岁男性因发烧、寒战和肌痛12周来到我们的急诊室。他还报告有慢性生产性咳嗽和胸闷史。在演讲前两周,他于2020年3月在当地国际机场工作,当时他注意到在工作中执行日常任务时用力呼吸困难。在我们采访时,他否认有患病接触,也没有已知的结核病接触史。他还报告说,他曾在洪都拉斯的混凝土矿里当过切石工。胸部x光片显示双侧肿块样上肺叶混浊,两年前影像学表现。胸部计算机断层扫描(图1)显示体积损失和肿块样肺门周围上肺叶混浊为主,伴纤维收缩性结构扭曲,支气管血管周围和小叶中心结节,散在区片状磨玻璃混浊,以双基底动脉为主。他的纤维化改变被认为与矽肺病一致,并伴有进行性大规模纤维化,继发于先前的无机粉尘吸入。他的急性表现被怀疑是叠加过程造成的,因为他发现了斑驳的毛玻璃不透明。进行了SARS-CoV-2 PCR检测,结果呈阳性。考虑到急性表现前几个月的症状,特别是考虑到他的移民史和小叶中心结节的影像学表现,我们怀疑有第三种疾病。对结核、结核分枝杆菌PCR和痰液分枝杆菌培养进行干扰素γ释放试验,结果均为阳性。出院时给予利福平、异烟肼、吡嗪酰胺和乙胺丁醇标准治疗方案,并与卫生部门进行随访,此时他已从急性疾病中康复。他在COVID-19诊断方面做得非常好。鉴于他对结核病的积极诊断,他没有接受任何针对COVID的治疗,并在室内空气中出院。矽肺是众所周知的诱发结核的因素,被认为是由二氧化硅颗粒巨噬细胞功能障碍引起的。与矽肺相关的免疫功能障碍和职业暴露的结合可能导致了该患者病毒性肺炎的发展。在隔离和旅行限制制度实施之前,他于2020年3月在一个大型国际机场工作,这使他面临结核病和COVID-19肺炎的独特风险,这些经典的CT结果很好地证明了这一点。
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引用次数: 0
Hemothorax as Rare Complication from COVID-19 Infection 新冠肺炎感染罕见并发症血胸
Pub Date : 2021-05-01 DOI: 10.1164/AJRCCM-CONFERENCE.2021.203.1_MEETINGABSTRACTS.A4094
Z. Muzaffarr
Introduction The novel coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 has been linked with many sequelae not typical of other respiratory viruses. One of the unique features of this virus, known as COVID coagulopathy, has been associated with bleeding and/or clotting diathesis in the setting of a prothrombotic state. This has put patients at risk for hemorrhagic complications such as frank disseminated intravascular coagulation, and antiphospholipid syndrome activation. This is a case of hemothorax as a rare complication of COVID-19 infection. Case Presentation This is the case of a 48 year old male with a history of ESRD requiring dialysis, who presented to our facility with shortness of breath. He was recently admitted a month prior to an outside facility for a dialysis catheter infection and was found to be COVID-19 positive. He received IV antibiotics and supplemental oxygen. He was discharged home with plans for IV antibiotics. He presented to our facility with five days of shortness of breath. In the ED he was afebrile, tachypneic and tested negative for COVID-19. Computed Tomography of the chest was significant for a moderate to large right pleural effusion with loculated components. The next day he underwent a thoracentesis and 600 cc of bloody pleural fluid was aspirated. He then underwent a VATS, decortication, pleurodesis a few days later as the effusion failed to resolve. Cytology of the initial thoracentesis was negative for malignant cells and pathology from the VATS was positive for fibrosis, hemorrhage with fibrin deposition and acute and chronic inflammation. Discussion Hemothorax as a complication of COVID -19 has yet to be described in the literature. Altered markers such as D-dimer and fibrinogen were associated with increased coagulation and thrombotic complications respectively. Furthermore, studies have reported intra-alveolar hemorrhages and GI bleeding in post-mortem analysis of COVID patients. This case highlights the uniqueness of this novel virus and the vast array of complications that can result from infection.
由严重急性呼吸综合征冠状病毒2引起的新型冠状病毒病2019 (COVID-19)与许多其他呼吸道病毒不典型的后遗症有关。这种病毒的一个独特特征是COVID - 19凝血功能障碍,它与血栓形成前状态下的出血和/或凝血能力有关。这使患者面临出血性并发症的风险,如弥散性血管内凝血和抗磷脂综合征激活。血胸是COVID-19感染的罕见并发症。这是一个48岁的男性,有ESRD病史,需要透析,以呼吸短促就诊。他最近在一个月前因透析导管感染被送往外部设施,并被发现是COVID-19阳性。他接受了静脉注射抗生素和补充氧气。他出院回家时,计划给他静脉注射抗生素。他到我们这里来的时候有五天的呼吸急促。在急诊室里,他发烧、呼吸急促,COVID-19检测呈阴性。胸部计算机断层扫描对于中度至大量的右侧胸腔积液具有定位成分具有重要意义。第二天,他接受了胸腔穿刺,并抽吸了600毫升带血的胸腔积液。几天后,由于积液未能消除,他接受了VATS、脱屑和胸膜切除术。最初胸腔穿刺的细胞学检查为恶性细胞阴性,VATS病理检查为纤维化、纤维蛋白沉积出血和急慢性炎症阳性。血胸作为COVID -19的并发症尚未在文献中描述。改变标记物如d -二聚体和纤维蛋白原分别与凝血和血栓并发症增加有关。此外,研究报告了COVID患者死后分析中的肺泡内出血和胃肠道出血。该病例突出了这种新型病毒的独特性以及感染可能导致的大量并发症。
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引用次数: 0
Bilateral Adrenal Gland Infarction in the Setting of COVID-19 Infection COVID-19感染背景下双侧肾上腺梗死
Pub Date : 2021-05-01 DOI: 10.1164/AJRCCM-CONFERENCE.2021.203.1_MEETINGABSTRACTS.A4075
S. Haider, F. Shaikh, V. Rayasam, Dilpat Kumar, N. Helmstetter
A 71-year-old man with past medical history pertinent for chronic kidney disease stage III, hypertension, hyperlipidemia, atrial fibrillation (AF) on oral anticoagulation, and hypothyroidism presented with acute on chronic kidney disease (AoCKD), elevated transaminases and failure to thrive. COVID-19 polymerase chain reaction (PCR) was positive. Chest x-ray showed patchy bilateral airspace disease. Computed tomography (CT) of chest, abdomen, pelvis and magnetic resonance imaging (MRI) abdomen were unremarkable apart from Bilateral patchy infiltrates in the lungs. The patient did not require steroids and/or remdesivir as he was not hypoxic. He was discharged five days later on rivaroxaban. A week after discharge, he presented with worsening generalized weakness, worse in the lower extremities, culminating in a fall. On readmission, laboratory studies revealed rhabdomyolysis, AoCKD, and elevated transaminases. Additionally, a leukocytosis was present without symptoms concerning for infection. COVID-19 testing was repeated and was positive, with the remainder of the infectious workup including blood cultures being unremarkable. A repeat CT scan of chest, abdomen, pelvis with contrast demonstrated fat stranding around both adrenals concerning for infarction in the setting of COVID-19 infection (image 1). Subsequently, a morning cortisol was obtained, which was low concerning for adrenal insufficiency. This suspicion was confirmed with cosyntropin stimulation testing, which demonstrated adrenal insufficiency. He was started on hydrocortisone and fludrocortisone with improvement in symptoms over the next three days. Common causes of adrenal infarction and hemorrhage include thromboembolic disease, hypercoagulable states, HIT, physical trauma, the postoperative state, sepsis, and any cause of severe physiologic stress. We are still gaining insight into the multisystem disease manifestations of COVID-19 and its prothrombotic effects despite chronic oral anticoagulation therapy at prophylactic doses for other maladies like AF. Adrenal insufficiency due to infarction should be considered in patients who present with non-specific symptoms such as weakness, hypotension, electrolyte abnormalities, abdominal pain, nausea and/or vomiting in the setting of COVID-19 infection when other causes have been ruled out. Adrenal infarction has been reported in patients with COVID-19 infection, such as our patient. The adrenal glands are susceptible to infarction and hemorrhage due to their vascularity. It has been hypothesized that the hypercoagulable state wrought by SARS-CoV-2 viremia poses a particular risk to the adrenal microvasculature. In turn, reperfusion injury and hemorrhage can ensue due to anticoagulant therapy and secondary adrenal necrosis.
1例71岁男性,既往有慢性肾脏疾病III期、高血压、高脂血症、口服抗凝治疗心房颤动(AF)和甲状腺功能减退,表现为急慢性肾脏疾病(AoCKD)、转氨酶升高和发育不良。新型冠状病毒聚合酶链反应(PCR)阳性。胸部x线显示双侧空域斑片状病变。胸部、腹部、骨盆CT及腹部磁共振成像(MRI)除双侧肺片状浸润外,未见明显病变。患者不需要类固醇和/或瑞德西韦,因为他没有缺氧。五天后,他服用利伐沙班出院。出院一周后,患者出现全身无力加重,下肢加重,最后摔倒。再入院时,实验室研究显示横纹肌溶解、AoCKD和转氨酶升高。此外,白细胞增多,无感染症状。重复进行COVID-19检测,结果呈阳性,其余的感染性检查包括血培养均无显著差异。胸部、腹部、骨盆的重复CT扫描显示,在COVID-19感染的情况下,脂肪滞留在双肾上腺周围,与梗死有关(图1)。随后,获得早晨皮质醇,与肾上腺功能不全有关。这一怀疑被共syntropin刺激试验证实,结果显示肾上腺功能不全。他开始使用氢化可的松和氟化可的松,在接下来的三天里症状有所改善。肾上腺梗死和出血的常见原因包括血栓栓塞性疾病、高凝状态、HIT、物理创伤、术后状态、败血症和任何严重生理应激的原因。我们仍在深入了解COVID-19的多系统疾病表现及其对房颤等其他疾病的预防性剂量慢性口服抗凝治疗。在排除其他原因的情况下,在COVID-19感染背景下出现非特异性症状(如虚弱、低血压、电解质异常、腹痛、恶心和/或呕吐)的患者,应考虑梗死引起的肾上腺功能不全。在COVID-19感染患者中有肾上腺梗死的报道,例如我们的患者。由于肾上腺血管丰富,容易发生梗塞和出血。据推测,SARS-CoV-2病毒血症造成的高凝状态对肾上腺微血管有特殊的风险。抗凝治疗和继发性肾上腺坏死可导致再灌注损伤和出血。
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引用次数: 2
Coccidioidomycosis in an Immunocompetent Host During the COVID-19 Era COVID-19时代免疫活性宿主的球孢子菌病
Pub Date : 2021-05-01 DOI: 10.1164/AJRCCM-CONFERENCE.2021.203.1_MEETINGABSTRACTS.A4085
A. Arjuna, M. Olson, C. Rogers, B. Buddhdev
Introduction: Coccidioides immitis and posadasii are dimorphic fungi endemic to the southwestern United States. Most immunocompetent hosts who contract coccidioidomycosis will clear the infection without symptoms. We detail the case of an immunocompetent, 56-year-old female who presented with symptoms of lower respiratory tract infection and concern for COVID-19 infection given significant exposure history. Case Description: The patient was referred to our advanced lung disease center (located in the southwestern United States) for subacute, productive cough associated with clear-yellow phlegm, dyspnea on exertion, infrequent night sweats, and abnormal chest x-ray (Figure A). The patient denied any history of fever, chills, hemoptysis, unintentional weight loss, or chest pain. Six-weeks prior to admission, the patient had significant exposure to multiple symptomatic persons with COVID-19. Two RT-PCR tests for COVID-19 to date were ruled negative, and a third test performed on admission was also negative. Computed tomography of the chest revealed right upper lobe cavitary consolidation with surrounding nodules bilaterally (Figure B). Sputum smear was negative for acid-fast bacillus or other bacterial organisms, prompting a bronchoscopy with bronchoalveolar lavage. Results demonstrated fungal cultures of Coccidioides immitis/posadasii. The patient also had significant IgG antibodies against Coccidioides species. She was started on therapeutic doses of fluconazole with a gradual improvement in symptoms. Discussion: History of significant exposure to COVID-19 warrants prompt and thorough investigation for disease status. Nonetheless, clinicians should still maintain a high suspicion and vigilance for excluding other, potentially treatable infectious etiologies, even regional endemic fungal infections that tend to manifest without symptoms.
简介:球孢子虫和球孢子虫是美国西南部特有的二态真菌。大多数感染球孢子菌病的免疫能力强的宿主会在没有症状的情况下清除感染。我们详细介绍了一名免疫功能正常的56岁女性病例,她表现出下呼吸道感染症状,并考虑到严重的暴露史,担心感染COVID-19。病例描述:患者因亚急性咳伴明黄色痰、用力时呼吸困难、罕见盗汗和胸部x线异常(图A)被转介至我们的晚期肺部疾病中心。患者否认有发热、寒战、咯血、意外体重减轻或胸痛史。入院前6周,患者与多名有症状的COVID-19患者有明显接触。迄今为止,两次COVID-19 RT-PCR检测均为阴性,入院时进行的第三次检测也为阴性。胸部计算机断层扫描显示右上肺叶空腔实变,双侧周围有结节(图B)。痰涂片抗酸杆菌或其他细菌阴性,提示支气管镜检查并支气管肺泡灌洗。结果证实了球虫/波萨达斯的真菌培养。患者对球虫种类也有明显的IgG抗体。她开始服用治疗剂量的氟康唑,症状逐渐改善。讨论:对COVID-19的重大暴露史进行及时和彻底的疾病状态调查是必要的。尽管如此,临床医生仍应保持高度的怀疑和警惕,以排除其他潜在的可治疗的感染性病因,甚至是倾向于无症状表现的区域性地方性真菌感染。
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引用次数: 0
“I Wouldn’t Change You If I Could” “如果可以,我不会改变你”
Pub Date : 2021-02-23 DOI: 10.18574/nyu/9781479816637.003.0001
Alison Piepmeier, George Estreich, R. Adams
When Alison Piepmeier finds out that her intentional pregnancy might result in a child with Down syndrome, she shares her anxiety with readers of her blog. With many of them assuring her that she’ll probably not have a baby with a disability, Alison looks elsewhere for reassurance. Three activists, who are also parents of children with Down syndrome, embody the evolution in popular thought about Down syndrome and other conditions. Emily Perl Kingsley, Cindi May, and Stephanie Meredith experienced society’s evolving view of disability with their children. Each woman has worked toward presenting disability as part of the diversity of human beings. With time, Alison learns that her daughter, Maybelle, need not attain cultural definitions of normal and that Maybelle’s valued personhood demands broader societal recognition.
当Alison Piepmeier发现她故意怀孕可能会导致一个患有唐氏综合症的孩子时,她与她博客的读者分享了她的焦虑。他们中的许多人都向她保证,她可能不会生一个有残疾的孩子,艾莉森向其他地方寻求安慰。三名活动家也是唐氏综合症儿童的父母,他们体现了唐氏综合症和其他疾病的流行思想的演变。艾米丽·珀尔·金斯利、辛迪·梅和斯蒂芬妮·梅雷迪思和她们的孩子一起经历了社会对残疾的不断演变的看法。每一位女性都致力于将残疾视为人类多样性的一部分。随着时间的推移,艾莉森了解到她的女儿梅贝尔不需要达到正常的文化定义,梅贝尔有价值的人格需要更广泛的社会认可。
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引用次数: 0
Six Questions on the Special, the Inclusive, and the Universal 关于特殊、包容和普遍的六个问题
Pub Date : 2021-02-23 DOI: 10.18574/nyu/9781479816637.003.0006
R. Adams
Rachel Adams uses a question-and-answer format to extend the conversations she has had with her friend and colleague Alison Piepmeier and to imagine which issues Alison might have tackled, had her friend lived beyond 2016. Rachel believes that Alison would have been wary of such developments in genomics as the commercialization of prenatal genetic tests, direct-to-consumer genetic services, and the gene-editing technology CRISPR-Cas9. She discusses Alison’s likely concerns about how genetic technology can influence society’s perception of disability, identity, and social justice. Rachel considers Alison’s response to conservatives’ continued use of disability to curtail women’s reproductive freedom today. The chapter also describes Alison’s likely concern that the #MeToo movement has overlooked people with disabilities. Rachel assumes that as Maybelle, Alison’s daughter, grows older, Alison’s own experience with a teenager and then an adult would have propelled her toward further examining such issues as sexuality, employment, and independence for people with intellectual disabilities. Finally, Rachel asks whether Alison would have had more to say about the differences between disability and illness and how much Down syndrome can represent other disabilities and how much it is simply one unique characteristic of some people.
雷切尔·亚当斯(Rachel Adams)用问答的形式扩展了她与朋友兼同事艾莉森·皮埃普迈尔(Alison Piepmeier)的对话,并想象如果她的朋友活过2016年,艾莉森可能会解决哪些问题。瑞秋认为,艾莉森会对基因组学的发展持谨慎态度,比如产前基因检测的商业化、直接面向消费者的基因服务以及基因编辑技术CRISPR-Cas9。她讨论了艾莉森可能关心的基因技术如何影响社会对残疾、身份和社会正义的看法。瑞秋认为艾莉森对保守派继续利用残疾来限制女性生育自由的反应。这一章还描述了艾莉森可能担心的#MeToo运动忽视了残疾人。瑞秋认为,随着艾莉森的女儿梅贝尔长大,艾莉森自己与青少年和成年人的经历将推动她进一步研究性、就业和智障人士的独立性等问题。最后,雷切尔问艾莉森是否会更多地谈论残疾和疾病之间的区别,以及唐氏综合症在多大程度上代表了其他残疾,又在多大程度上只是某些人的一种独特特征。
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引用次数: 0
Accessible Words 可以的话
Pub Date : 2021-02-23 DOI: 10.18574/nyu/9781479816637.003.0005
George Estreich
Though Alison Piepmeier was best known as a feminist literary critic with a strong focus on disability, academic writing was insufficient to her range, creativity, and questing mind. Her informal writing—op-eds, articles, blogs—displayed something else, an essayist’s skill with metaphor and narrative, a taste for stylistic experiment, and a drive to connect with readers outside the academy. This writing reached its peak in Alison’s blog Every Little Thing, which ran from 2013 to 2016 and in which she dealt with the core topics of this book: disability, illness, and motherhood. In this chapter, George Estreich looks at the blog and follows its transformation as Alison herself is transformed by her evolving serious health issues.
虽然Alison Piepmeier是一位女权主义文学评论家,她非常关注残疾人,但学术写作对她的视野、创造力和探索精神来说是不够的。她的非正式写作——专栏、文章、博客——展示了另一种东西,一个散文家运用隐喻和叙事的技巧,对风格实验的品味,以及与学院以外的读者建立联系的动力。从2013年到2016年,艾莉森的博客《每一件小事》(Every Little Thing)达到了她写作的顶峰,她在博客中讨论了本书的核心主题:残疾、疾病和母亲。在这一章中,乔治·埃斯特赖希(George Estreich)审视了这个博客,并跟随它的转变,就像艾莉森自己被不断发展的严重健康问题所改变一样。
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引用次数: 0
The Welcome Table 欢迎桌
Pub Date : 2021-02-23 DOI: 10.18574/nyu/9781479816637.003.0003
Alison Piepmeier, George Estreich, R. Adams
In this chapter, Alison Piepmeier describes how eating at a table can figuratively and literally show the barriers people with disability face in trying to connect with a larger community. She interviews adults with Down syndrome and parents of children with Down syndrome to learn how some people are included in, or excluded from, social gatherings like family meals, children’s parties, school activities, and organizational meetings. Alison recalls disability rights activist Harriet McBryde Johnson’s fight for accommodation and Johnson’s interaction with a professor whose views on euthanasia are criticized as being ableist. Being invited to sit at a table—be it a dinner party among friends or an organization’s luncheon—means accepting a person’s value as fully human. Alison points out that even some well-intentioned groups forget the importance of inclusion. She quotes disability advocacy leader Nancy Brown’s observation “We segregate those we don’t value.”
在这一章中,Alison Piepmeier描述了在餐桌上吃饭是如何形象地和字面地展示了残疾人在试图与更大的社区联系时所面临的障碍。她采访了患有唐氏综合症的成年人和唐氏综合症儿童的父母,以了解有些人是如何被包括在或被排除在家庭聚餐、儿童聚会、学校活动和组织会议等社交聚会之外的。艾莉森回忆起残疾人权利活动家哈里特·麦克布赖德·约翰逊争取住宿的斗争,以及约翰逊与一位教授的互动,这位教授对安乐死的看法被批评为残疾主义者。被邀请坐在一张桌子旁——无论是朋友之间的晚宴还是一个组织的午宴——意味着接受一个人作为一个完整的人的价值。艾莉森指出,即使是一些善意的团体也忘记了包容的重要性。她引用了残疾人权益倡导领袖南希·布朗的话:“我们把那些我们不重视的人隔离开来。”
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引用次数: 0
Saints, Sages, and Victims 圣人、圣人和受害者
Pub Date : 2021-02-23 DOI: 10.18574/nyu/9781479816637.003.0004
Alison Piepmeier, George Estreich, R. Adams
This chapter examines a complicated genre: the memoir written by a parent of a child with a disability. Despite the formulaic presentation of these narratives as a triumph over adversity, Alison Piepmeier describes many of them as sites of dehumanization. Parental memoirs often overly focus on grief or a medicalized picture of disability. They can reinforce familiar, deeply troubling attitudes about people with disabilities as tragic, burdensome, and unworthy. At the same time, Alison shows that parental memoirs can serve an activist function, acting as sites of resistance, challenging misinformation, and reworking prevailing perceptions of disability.
本章考察了一种复杂的类型:残疾儿童的父母所写的回忆录。尽管这些故事被公式化地描述为战胜逆境的胜利,但艾莉森·皮普迈尔(Alison Piepmeier)将其中许多描述为非人性化的场所。父母的回忆录往往过度关注悲伤或残疾的医学图景。它们可以强化人们熟悉的、令人深感不安的态度,认为残疾人是悲惨的、负担沉重的、不值得的。与此同时,艾莉森表明,父母回忆录可以起到积极的作用,作为抵抗的场所,挑战错误的信息,重塑对残疾的普遍看法。
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引用次数: 0
The Inadequacy of “Choice” “选择”的不足
Pub Date : 2021-02-23 DOI: 10.18574/nyu/9781479816637.003.0002
Alison Piepmeier, George Estreich, R. Adams
This chapter examines the limitations of feminist discussions about disability and reproduction. Feminism and disability rights often hold different places in reproductive justice discussions. Feminism often oversimplifies the idea of reproductive choice, focusing on individual women and endorsing cultural stereotypes of disability. As a counterpoint to the scholarly literature of these issues, Alison Piepmeier interviewed twenty-nine parents of children with Down syndrome, asking them about their pregnancy, prenatal testing, and their families. The responses of these parents illustrate how families need more support than just individual rights to raise a child with a disability. Although reproductive decisions may rest on an individual woman, she must also consider community support and health services in her decision to raise a child, particularly one with a disability.
本章考察了女性主义关于残疾和生殖的讨论的局限性。女权主义和残疾人权利在生殖正义的讨论中往往占据不同的位置。女权主义往往过分简化了生育选择的概念,把重点放在女性个人身上,支持对残疾的文化刻板印象。作为对这些问题的学术文献的对照,Alison Piepmeier采访了29位唐氏综合症儿童的父母,询问他们的怀孕、产前检查和家庭情况。这些父母的回应说明,抚养残疾儿童,家庭需要的不仅仅是个人权利,还有更多的支持。虽然生育决定可能取决于妇女个人,但她在决定抚养孩子,特别是残疾孩子时,也必须考虑到社区的支持和保健服务。
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TP100. TP100 UNEXPECTED COVID-19 CASE REPORTS
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