WES

The World Endometriosis Society (WES) is a nonprofit organization working to improve the lives of people affected by endometriosis and adenomyosis. In collaboration with stakeholders and global partners, it advances evidence-based standards and innovation in education, advocacy, clinical care, and research. WES brings together an international community of researchers and clinicians to share scientific knowledge and clinical experience, supporting progress in understanding and managing these conditions.

The Society provides educational resources on endometriosis, including information on symptoms, classification, management, and surgery. Its research and resources program highlights research priorities, publications, and relevant associations and organizations. WES also hosts webinars, known as WESinars, and organizes the World Congress on Endometriosis, creating opportunities for learning and professional exchange.

To support the next generation of specialists, WES offers mentoring for early-career researchers and clinicians, along with research grants, travel grants, and awards recognizing scientific presentations and posters. Membership connects individuals with the Society’s international collaboration.