Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Canada.
Department of Educational and Counselling Psychology, McGill University, Montreal, Canada.
Disabil Rehabil. 2020 Jun;42(11):1588-1598. doi: 10.1080/09638288.2018.1531151. Epub 2019 Feb 14.
People with rare diseases must cope with many physical and psychological challenges; an endeavor that can be difficult to carry out without external support. The purpose of this study was to understand how patients with scleroderma perceive the social support they need and receive from close relationships to better manage their disease. Four focus groups with patients ( = 19) were conducted. A semi-structured topic guide was used. Discussions were recorded and transcribed, and thematic analysis was performed. Patients reported receiving emotional, informational, and instrumental support, with emotional support being a priority for them. Patients also referred to relational factors (i.e., communication style, active engagement, complementarity) that affected the social support received. More specifically, engaging in honest communication, carefully choosing sources of support, and having close relationships motivated to learn and get involved enhanced support. In contrast, patients who avoided interacting with others or speaking about scleroderma and close relationships with a lack understanding or involvement hindered support. Patients might benefit more from interventions aiming at coping with scleroderma as a collective. Findings from this study help better understand the unique experiences of scleroderma patients while receiving support from close relationships.Implications for RehabilitationPeople with scleroderma may benefit from receiving different types of support from their close social relationships, including emotional, informational, and instrumental support.Professionals working in the area of rehabilitation should encourage patients to identify close social relationships who have specialized knowledge and skills (e.g., comfort looking for resources and information on the Internet) to help them cope better with the challenges associated with scleroderma.As part of the proposed treatment, rehabilitation professionals should encourage patients to actively communicate their social support needs to close social relationships, as well as maintain an open and honest line of communication with them, which will improve their capacity to understand the patient and provide appropriate support.Rehabilitation professionals may support people with scleroderma by encouraging them to seek support from their close social relationships, but also by providing these close relationship with information and supportive services to learn new skills and better cope with their own distress.
患有罕见病的人必须应对许多身体和心理上的挑战;如果没有外部支持,他们很难完成这项任务。本研究的目的是了解硬皮病患者如何感知他们从亲密关系中获得的社会支持,并更好地管理他们的疾病。对 19 名患者进行了 4 次焦点小组讨论。使用半结构化主题指南。记录和转录讨论内容,并进行主题分析。患者报告接受情感、信息和工具支持,情感支持是他们的首要需求。患者还提到了影响社会支持的关系因素(即沟通方式、积极参与、互补性)。具体而言,患者会与他人坦诚交流、谨慎选择支持来源,并与有动力学习和参与的亲密关系,从而增强支持。相反,避免与他人互动或谈论硬皮病、与缺乏理解或参与的亲密关系,会阻碍支持。旨在共同应对硬皮病的干预措施可能会使患者受益更多。本研究的结果有助于更好地了解硬皮病患者在从亲密关系中获得支持时的独特体验。
康复意义
硬皮病患者可能会从亲密的社会关系中获得不同类型的支持,包括情感、信息和工具支持。
从事康复领域工作的专业人员应鼓励患者识别具有专业知识和技能的亲密社会关系(例如,舒适地在互联网上寻找资源和信息),以帮助他们更好地应对与硬皮病相关的挑战。
作为拟议治疗的一部分,康复专业人员应鼓励患者积极向亲密的社会关系表达他们的社会支持需求,并与他们保持开放和诚实的沟通,这将提高他们理解患者并提供适当支持的能力。
康复专业人员可以通过鼓励患者从亲密的社会关系中寻求支持来支持硬皮病患者,还可以为这些亲密关系提供信息和支持服务,以学习新技能并更好地应对自己的困境。