
IC Awareness Month Series Part 1: Newly Diagnosed With Interstitial Cystitis? Start Here
September is IC Awareness Month, so I’m kicking off a four-part series covering what I want people with interstitial cystitis to know, especially if you’re newly diagnosed. In Part 1, I’m sharing what I’d focus on if I were diagnosed with IC today, including: Understanding that different factors can contribute to IC symptoms Getting evaluated by a pelvic floor physical therapist Hydration and bowel health Approaching food without immediately cutting out everything on an IC diet list Understanding the role of the nervous system Being intentional with supplements Looking for patterns without making your bladder a full-time job I’ve recovered from IC, and I’ve spent years helping others better understand what may be contributing to their symptoms. I want this series to give you more information, more options, and a clearer idea of where to go from here. NEW FREE MASTERCLASS: Want to learn more about my root-cause approach to IC? Watch my free masterclass here! THE IC CONNECTION: The Interstitial Cystitis Association is hosting The IC Connection: Science, Strategies, and Support virtually on Saturday, September 26 from 12:00–4:45 p.m. ET. The conference will cover topics including pain science, sexual health, disability, and more. Click here to register!
