No woman with PMOS should have to face her diagnosis alone and afraid. Ever again.

That is the world we are building toward. Josie is a comprehensive digital health platform for the 1 in 8 women living with PMOS, giving them the tools to understand their condition, advocate for themselves in medical settings, and navigate a care system that was not built for them.

Why Josie exists

PMOS care is broken. We are here to fix what we can.

“Josie exists because we lived this. And because we believe it can be better.”
Laure & Manon

1 in 8

PMOS affects around 1 in 8 women of reproductive age, making it one of the most common hormonal conditions in the world.

Once diagnosed, care is fragmented. Gynaecologists, endocrinologists, dermatologists, nutritionists, and mental health professionals all play a role, but no system connects them. Women are left to coordinate their own care, track their own symptoms, and advocate for themselves in a system that routinely underestimates the complexity of their condition.

Existing digital tools do not solve this. Period trackers assume regular cycles. Nutrition apps push one-size-fits-all diets. None of them address the full metabolic, reproductive, and psychological picture of PMOS, and none of them help women prepare for the medical appointments that actually determine their care.

A gynaecologist, endocrinologist, dermatologist, nutritionist and mental health professional around Josie, with no lines connecting them

What we stand for

Our values

Four promises we hold ourselves to, and that you can check us on.

  • Evidence before opinion

    Every article in the app is reviewed by a clinician before it is published, and reviewed again when the guidelines change.

  • Your data stays yours

    Stored in the EU, encrypted in transit and at rest, exportable or deletable at any time. We never sell it.

  • Built from lived experience

    Both founders live with PMOS. Every feature starts from something we needed ourselves and could not find.

  • Honest about our limits

    Josie is a tracking and preparation tool, not a diagnosis. We say that plainly, everywhere it matters.

Built by two women who understand PMOS from the inside.

Lived experience, clinical rigour, and a shared conviction that PMOS care has to get better.

Laure Santolini

Co-Founder

Laure was diagnosed with PMOS after years of dismissed symptoms and fragmented care. That experience, combined with her background in strategy consulting at EY, an MBA from UCLouvain, and an Advanced Master in Biotech and Medtech Ventures from Solvay Business School, drove her to build the tool she wished she had.

At Josie, Laure leads technical development, strategy, regulatory affairs, and fundraising.

  • Technology
  • Strategy
  • Regulatory
  • Fundraising

Manon Vervaeke

Co-Founder

Manon knows firsthand how isolating a PMOS diagnosis can feel. That experience, combined with her background in international sales at La Collection, an MBA in Business Administration and Management from Vrije Universiteit Brussel, and a passion for design, drove her to build an app that makes women with PMOS feel seen, prepared, and in control.

At Josie, Manon leads design, UX, business development, and content creation.

  • Design
  • UX
  • Business development
  • Content

Our scientific board

Guided by experts.

Our scientific advisory board reviews Josie's health content for clinical accuracy, dosing guidance and alignment with current PMOS research and clinical guidelines. Each article on this site shows its review status.

Board composition includes specialists in gynaecology, endocrinology, and nutrition with PMOS expertise. Board members are listed here as they are formally announced.

Our mission

Give women the right tools and the right words.

Our mission is to give women with PMOS the tools to understand their condition, the data to advocate in medical settings, and the support to navigate fragmented care.

  • Two steps are in the app today
  • Three are what we are working toward

In the app today

  1. Give women the right words and tools.

    Intelligent symptom tracking, pattern recognition, doctor-specific appointment preparation, and evidence-based education that closes the information gap between women and the system that is supposed to serve them.

  2. Bring doctors into the conversation.

    Structured appointment prep reports, longitudinal data exports, and interoperability-ready data make it easy for healthcare providers to see the full picture of a patient's PMOS experience across specialists.

What we are working toward

  1. Open the dialogue with insurers.

    Clinical evidence demonstrating measurable health outcomes positions Josie for reimbursement conversations with public and private insurers across Europe.

  2. Make reimbursement a right, not a privilege.

    We are pursuing structured reimbursement pathways in Belgium, France, and Germany so that access to PMOS management tools is covered by public health insurance, not just available to those who can afford a subscription.

  3. Integrate the whole ecosystem.

    Hospital partnerships, healthcare system connectivity, and longitudinal data create a PMOS management ecosystem where women, doctors, and insurers are aligned.

Supported by

  • We Are Founders
  • Bryo, StartUp Advanced by Voka
  • Start it @KBC

We are here to help

Using the app.

Answers to common questions about tracking, reports and sharing.

Read the FAQ

Your data.

Export your record or delete your account at any time from Privacy and data in the app.

How we protect your data

Contact us.

Questions, feedback or partnership ideas:

Josie's Instagram profile on a phone

Instagram

Behind the scenes on @josie.app

Product updates, research notes, and the people building Josie.

Follow @josie.app

Start your own PMOS record today

Josie is the tool Laure and Manon wished they had, and it is out now. Log what you notice in about a minute a day and bring a clear story to your next appointment.

Hands holding a phone with the Josie app