09/24/2026
When you were first diagnosed with PMOS, what do you wish someone had told you? 💗
Maybe it’s something you wish you had known about your symptoms. Maybe you wish someone had explained that PMOS can look completely different from person to person. Or maybe you simply wish someone had told you that you weren’t alone.
Whatever it is, we want to hear from you.
💬 Share your answer in the comments, or head to our Stories to respond there.
Your experience could be exactly what someone newly diagnosed needs to hear today. And your responses can help us shape future O***y Active education, resources, and events around what our community actually needs.
Let’s learn from each other. 💗
***yActive