About PCOS Awareness Association
We turned a diagnosis into a movement.
PCOS Awareness Association exists to make PCOS easier to understand, faster to diagnose, and less lonely to live with—through education, advocacy, and community.
How it started
PCOSAA was founded in 2012 by Megan M Stewart after experiencing the confusion, dismissal, and lack of clear resources that so many people with PCOS face.
What began as a commitment to share accurate, accessible information grew into a community-driven organization focused on awareness, education, advocacy, and connection.
Milestones
A quick look at how the movement has grown—update the milestones to match your history.
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2012
PCOSAA is founded
Built to close the gap between PCOS symptoms and clear, compassionate information.
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2015
Community + content expansion
More stories, more resources, and a stronger network of advocates.
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2019
First PCOS CON Event + Programs scale
Support pathways evolve to meet the emotional and metabolic realities of PCOS.
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2023
PCOS CON + national momentum
Education and connection in-person—bringing evidence-based care closer to the community.
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Today
Tools + advocacy
Building resources that help people find care faster and advocate with confidence.
Impact, so far
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What we believe
People first
Everyone deserves to be heard, respected, and supported—especially when navigating chronic health.
Evidence + empathy
We translate research into plain language—without judgment, shame, or one-size-fits-all advice.
Advocacy that moves
We push for better awareness, better policies, and better pathways to diagnosis and care.