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
Where are you starting from?
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.For everyone PCOS/PMOS touches
Online communityShades of TealOur online community, a place to connect with people who get it.
For teensTeens of TealEducation and confidence-building for the most formative years.
For partnersPartners in TealGuidance and communication tools for spouses and significant others.
For male alliesMan of TealTurning the men in our lives into informed advocates.
WorldwideGlobal PCOSVoices and experiences from every corner of the world.
Blog & podcastTeal TalkHonest conversations, expert insight and lived experience.
…close the diagnosis gap. …change how PMOS is treated. …make sure no one faces it alone.
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
Two easy ways to make a difference today.
Write to your Governor in minutes.
Our State Advocacy Letter Generator creates an official letter on PCOSAA letterhead, addressed to your Governor, asking for PCOS programs, funding and awareness.
Write your letterWear your support.
Teal is the color of PCOS awareness. Shop PCOSAA apparel and gear and start conversations wherever you go.
Shop TealPCOS 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.
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.
Give monthly. Change what's possible.
Monthly gifts give us steady support for Teal Talk, PCOS CON, and programs for teens, partners and allies.
Reach a community of 1M+ that trusts us.
Sponsor PCOS CON 2027, underwrite Teal Talk or fund a program, during our 15th anniversary year.
Find your people
Join Shades of Teal
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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