If you’ve had Crohn’s long enough, you know the ER all too well. And if you’re lucky enough to have avoided it—hold onto that golden ticket.
For the rest of us, ER visits are a necessary evil. Here’s the thing, though: walking into an ER with Crohn’s can be frustrating. Some doctors understand. Others hear “stomach pain” and assume you’re just there for pain meds. (Pro tip: Always use the words “Crohn’s flare” and “obstruction risk” so they take you seriously.)
So, here’s my ER survival guide:
- Bring a list of your meds – Trust me, you won’t remember them all when you’re in agony.
- Advocate for yourself – If a doctor brushes you off, ask for a GI consult.
- Know your triggers – If you’re in unbearable pain, don’t wait until it’s a full-blown crisis.
- Pack a small ER bag – A phone charger, warm socks, and a little comfort item go a long way.
Most importantly, don’t feel guilty for seeking help. You deserve care. And if a doctor ever makes you feel otherwise, find a new one.
Stay Strong!

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