EP3: Who to See if You Have NCS

Welcome back to the NCS Podcast!As many of you might already know, navigating the world of vascular compressions can feel like a joke—especially if you've been diagnosed with Nutcracker Syndrome. Out of my five-doctor team, only two even knew what NCS was. That’s exactly why I hope this podcast can provide some insight into the steps you can take to move from point A to point B on this journey.My own path began with my beloved GYN, Dr. Olga Muldoon, who referred me to an interventional radiologist. That’s where I was diagnosed with both May-Thurner Syndrome (MTS) and NCS. But please remember—there’s no single way to reach a diagnosis and then embark on the journey. Some of you listening may have discovered your condition through a completely different route, and I love that.My hope is that by sharing my journey, I can help you find a possible next step and offer guidance on what you can do in the meantime to make the process as smooth and efficient as possible.Enjoy the episode!