My Crohnstipated Life

Crohn’s has taken a lot from me. But weirdly? It’s also made me stronger in ways I never expected. 💜 I can handle discomfort better than most people. (I mean, if I can survive Crohn’s cramps, I can survive anything.)💜 I’ve learned how to advocate for myself. Doctors, workplaces, relationships—if…

For years, I tried to get certain people to understand my Crohn’s. I explained the symptoms, the exhaustion, the unpredictability. But some people? They just don’t get it. And they don’t want to. So, I stopped trying. 💜 If someone brushes off my pain, I don’t waste my energy convincing…

I used to pack for trips like a normal person. Now? It’s a strategic mission. Before I go anywhere, I: ✔ Map out every restroom within a 50-mile radius.✔ Pack an emergency kit (meds, wipes, snacks, spare clothes—because you never know).✔ Mentally prepare for the worst-case scenario.✔ Pray to the…

When I was first diagnosed, I thought Crohn’s was just a stomach disease. Oh, how wrong I was. Here are some weird symptoms no one warned me about: 😬 Mouth ulcers – Because apparently, my gut wasn’t enough of a battleground.😵‍💫 Random dizzy spells – One minute I’m fine, the…

For years, I fought against the need to rest. Society tells us that busy = productive = valuable, and when I couldn’t keep up, I felt guilty. But here’s what I’ve learned: Resting isn’t lazy—it’s survival. 💜 Crohn’s drains energy in ways people can’t see. It’s not just “feeling tired.”…