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 next I feel like I’m on a rollercoaster.
🦵 Joint pain that makes me feel ancient – Crohn’s arthritis? Didn’t see that coming.
🥵 Night sweats – Waking up soaked for no reason? Love that for me.
🥴 Random nausea (even when I haven’t eaten anything weird)Explain yourself, intestines.
💨 Gas pain that feels like a heart attack – No, I’m not dying. Yes, I might explode.

Crohn’s is so much more than a “bathroom disease.” And honestly? I’d like a refund.

Stay Strong.

Leave a comment

I’m Kelly

Welcome to My Crohnstipated Life, a space where I share the raw, real, and often humorous journey of living with Crohn’s disease. From unpredictable flares to parenting while managing a chronic illness, this blog is a mix of personal stories, practical tips, and a whole lot of laughter—because sometimes, humor is the best medicine. Whether you’re living with Crohn’s, love someone who is, or just want a peek into the rollercoaster of chronic illness, I’m glad you’re here. 💜 Stay Strong.

Let’s connect