Endometriose
This study critically analyzed global and local public policies for endometriosis, finding that while some progress exists, consolidated programs addressing health, education, work, and social security are lacking.
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This paper critically analyzes the existence and characteristics of global and local public policies for endometriosis, using a narrative review with documentary analysis focused on whether policies align with patients’ needs for improved access, disease visibility, and implementation of multiprofessional care with a gender perspective. It describes endometriosis as a chronic, systemic condition affecting about 10% of people assigned female at birth during reproductive age, and highlights ongoing problems of underdiagnosis/undertreatment, including a reported 7–9 year diagnostic delay and impacts across physical, emotional, social, and economic domains. The key finding is that, despite some local advances, there is still no consolidated global endometriosis care program covering aspects beyond healthcare, such as education, work, and social security. The paper concludes that integrated, evidence-based, gender-sensitive policies are urgently needed; the analysis is explicitly limited by its narrative/documentary approach rather than systematic evaluation. This paper is centrally about endometriosis — it focuses on reviewing and assessing public policy for diagnosis and multidisciplinary, gender-sensitive care for people affected.
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- Endometriosis in transgender men: recognizing the missing pieces via openalex
- W4408828072 via openalex
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- last seen: 2026-06-10T17:14:06.276822+00:00