ABout Emmi

Emmi is built by PMOS patients who have lived through the pain of navigating multiple providers, painful symptoms, dubious lifestyle advice, and still not getting answers.

We chose the name Emmi to reflect what we believe women with PMOS are truly missing in their care: empathy.

We bridge the gap between provider appointments, provide leading research and physician-backed resources to women with PMOS, and help them address their unique symptoms and needs to navigate this condition for life.

A smiling woman standing by a black fence near a body of water with a city skyline featuring tall buildings in the background.

Meet the Founder

I'm Jenny, the founder of Emmi Health. I was diagnosed with PMOS after dealing with unexplained symptoms for years, and normalized my own PMOS symptoms and clinical markers using systematic, research-driven lifestyle changes.

I built Emmi because I wanted more data, personalization, and support outside of doctor’s appointments, and I saw how powerful it was to finally understand my PMOS.

I’m a biomedical engineer, certified personal trainer, and former pharma strategy consultant — but mostly I'm a PMOS patient who gets it and wants to help.

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