Abstract
Patient empowerment in lupus is a process wherein patients actively participate in decision-making with healthcare professionals and take responsibility for their own condition. In order to effectively be involved in their medical care and achieve the best treatment outcomes, patients have to be equipped with a sufficient body of knowledge and understanding of lupus and its intricacies. Furthermore, the significant roles of families and caregivers, other healthcare professionals and support systems, and policymakers in each country have an immense impact on health outcomes and the overall quality of life.
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