The Polyendocrine Metabolic Ovarian Syndrome Association, Inc. PMOS, (formerly known as the PCOS Association) is a 501(c)(3) nonprofit organization dedicated to empowering women with PMOS through evidence-based education, expert partnerships, and comprehensive resources that address the root causes of this complex condition. Founded in 1995, the PMOS Association has been a pioneering force in PMOS education, patient advocacy, and professional collaboration. At a time when public awareness of PCOS was virtually nonexistent — and even many physicians were unfamiliar with its diagnosis and management — the PMOS Association emerged as a crucial voice for women seeking answers, support, and a better future. Our mission is to equip every woman with the tools and partnerships necessary to achieve personal ownership of her healthcare journey, grounded in evidence-based discovery and expert guidance. Our vision is a future where women with PMOS/ PCOS have equitable access to education, clinical partnerships, and individualized resources that allow them to identify and address the fundamental causes of their condition — achieving lifelong health, autonomy, and wellbeing. What We Do: * Provide clear, well-vetted educational resources on PMOS management and treatment. * Foster connections between patients and expert practitioners specializing in PMOS care. * Advocate for better PMOS diagnosis, awareness, and support within the medical community. * Stay at the forefront of scientific research, communicating timely updates to our community. Through our efforts, we aim to ensure that no woman faces PMOS alone — and that each individual has the opportunity to thrive with confidence, hope, and empowerment.
The mission of the PMOS Association, founded by women for women, is to empower every individual with Polyendocrine Metabolic Ovarian Syndrome to confidently take ownership of her healthcare journey — grounded in evidence-based discovery, supported by expert guidance, and strengthened through community.
Our vision is to create a future where women with PMOS have equitable access to the education, clinical partnerships, and individualized resources necessary to identify and address the fundamental causes of their condition — achieving lifelong health, autonomy, and wellbeing.
