Systematic review demonstrates severe psychosocial and emotional burdens in lymphatic filariasis, highlighting the need for immediate mental health support and community stigma reduction.
LF significantly impacts the quality of life due to both its physical and emotional consequences. Psychological support for affected individuals is crucial from diagnosis, and the education of transmission and treatment of LF in endemic communities is essential to prevent discrimination and exclusion.
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Vásconez-González et al. (2025) studied this question.
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