The impact of fibromyalgia on society

Camilo Silva-Sánchez
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Abstract

Fibromyalgia is a disease characterized by intense generalized chronic musculoskeletal pain. Its etiology is not known and there is no curative treatment but only symptomatic and focused on pain management. The lack of empathy on the part of family, work, friends and health professionals increases the psychosocial discomfort. Educating the population and health professionals on the behavior of the disease could be an opportunity to improve social ties, including friendships, family, health and work. The development of the community approach in the study of fibromyalgia is of significant importance in the understanding and management of this complex chronic disease. Fibromyalgia not only affects the individual sufferer, but also has a profound impact on their social and family environment. By adopting a community approach, it is recognized that community support and understanding is crucial to improving the quality of life for those living with fibromyalgia. This approach involves building support networks and promoting public awareness of fibromyalgia, which in turn reduces the stigma associated with the disease. In addition, the development of community education programs and support groups can help empower people with fibromyalgia to better manage their symptoms and find effective coping strategies.
纤维肌痛对社会的影响
纤维肌痛是一种以强烈的全身慢性肌肉骨骼疼痛为特征的疾病。其病因尚不清楚,没有治愈治疗,但只有症状和重点疼痛管理。家庭、工作、朋友和卫生专业人员缺乏同理心会增加心理上的不适。对民众和卫生专业人员进行有关该病行为的教育,可能是改善社会关系(包括友谊、家庭、健康和工作)的机会。社区方法在纤维肌痛研究中的发展对于理解和管理这种复杂的慢性疾病具有重要意义。纤维肌痛不仅影响患者个人,而且对其社会和家庭环境产生深远影响。通过采用社区方法,人们认识到社区的支持和理解对于改善纤维肌痛患者的生活质量至关重要。这种方法包括建立支持网络和提高公众对纤维肌痛的认识,从而减少与该疾病相关的耻辱。此外,社区教育项目和支持团体的发展可以帮助纤维肌痛患者更好地控制他们的症状,找到有效的应对策略。
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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