PCOS · now also called PMOS

You're not imagining it. And you're not alone.

PCOS/PMOS affects 1 in 8 women and girls worldwide, and most don't know they have it. We help you understand it, find care that takes you seriously, and connect with a community of more than a million people who get it.

501(c)(3) nonprofit · Serving the PCOS/PMOS community since 2012
Five smiling women in PCOS Awareness Association shirts and lanyards at PCOS CON 2019
Together at PCOS CON 2019.
PCOS → PMOS

Same condition. A more accurate name.

In 2026, PCOS was renamed PMOS: polyendocrine metabolic ovarian syndrome. The new name reflects what our community has always known: it affects hormones and metabolism across the whole body, not just the ovaries. You'll see both names here while the world catches up.

What the new name means for you → Source: The Lancet, May 2026.
1 in 8women and girls worldwide live with PCOS/PMOS
70%may be undiagnosed, per the WHO
1M+people in our community worldwide
15years of advocacy, celebrated in 2027
Together, we can…

…close the diagnosis gap. …change how PMOS is treated. …make sure no one faces it alone.

Advocacy in action

PCOSAA at the White House.

On December 11, 2024, the PCOS Awareness Association was invited to the White House Conference on Women's Health Research in Washington, DC. We brought the voice of the PCOS/PMOS community into a national conversation about the future of women's health research.

White House Conference on Women's Health Research · Wednesday, December 11, 2024

PCOSAA's invitation to the White House Conference on Women's Health Research, December 11, 2024
Guests seated in the East Room during the session The Business Case for Investing in Women's Health
In the East Room for "The Business Case for Investing in Women's Health."
Guests arriving through the White House East Colonnade, decorated for the holidays
Arriving through the East Colonnade.
Take action

Two easy ways to make a difference today.

Advocate

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Our State Advocacy Letter Generator creates an official letter on PCOSAA letterhead, addressed to your Governor, asking for PCOS programs, funding and awareness.

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Wear your support.

Teal is the color of PCOS awareness. Shop PCOSAA apparel and gear and start conversations wherever you go.

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PCOS CON 2027 · 15 years · In honor of Cryssy

PCOS CON is hitting the road.

It's an odd year, and you know what that means: our annual conference goes in person. Three cities, one community.

SEATTLESeptember 2027
CHICAGOSeptember 2027
RALEIGHSeptember 2027
Teal Talk podcast cover art
Teal Talk Podcast

Teal Talk is coming back. We want your voice on it.

Honest conversations, expert insight and lived experience. We're relaunching the podcast and booking three kinds of guests: patient voices, expert insights and resource spotlights.

For donors

Give monthly. Change what's possible.

Monthly gifts give us steady support for Teal Talk, PCOS CON, and programs for teens, partners and allies.

For sponsors & partners

Reach a community of 1M+ that trusts us.

Sponsor PCOS CON 2027, underwrite Teal Talk or fund a program, during our 15th anniversary year.

Campaign: Help us build the PCOS Specialist Search
Fund the search
With gratitude to our partners
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Shades of Teal Network Find your people

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Our online community for people living with PCOS/PMOS and the people who love them. Ask questions, share wins and connect with people who get it.

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