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Crohns in the throat

So first of all, hi to everyone. I'm new. My name is Luce... and I've been diagnosed with Crohn's for about 15 years. My weird thing is that my worst symptoms are in my THROAT (though I've had plenty of gut symptoms). My gut is more or less under control though, but my throat is really hard to keep under wraps. It flairs up and it can really run my life.

Anyone else in my boat?
 
Sorry to hear this :(

I have throat problems too. Last colonoscopy/endoscopy showed extreme inflammation in my throat (though I didn't notice anything then) so was put on Nexium. Missed it a few days in a row a few months ago and boy did I have some serious acid reflux! Lol made sure to take it every day since then!

But about half a year ago when my current flare started, the worst thing for me was mouth/throat pain! I had sores everywhere in my mouth, and it even went down my throat. Could barely even drink water, it hurt so much! Got some numbing mouthwash that helped my mouth and top part of my throat (though only lasted like 10 minutes per wash), and prednisone, and it was all gone in a few days. Luckily had no problems since then!

Hope the pain goes away soon for you!
 
Hi Luce,

I have UC, rather than CD, so most of my symptoms are lower down but I did have a hiatus hernia for many years, and took Nexium/Losec/omeprazole so I know how painful the inflammation and acid burn can be and you have my sympathies.

I know it's no cure and doesn't do anything like the omeprazole but Gaviscon liquid was quite soothing for the immediate acid burn. The only other thing that seemed to help was plain water.

Obviously these are different causes and I really hope they can do something for you soon, it sounds dreadful and you may have to be very assertive.
 
I get a really sore throat and tongue on and off every couple of weeks/months ulcers in my mouth, difficulty swallowing etc... I thought I was getting the flu all the time... Then I stared entocort... And it all magically disappeared!! It was only when my dose of entocort was reduced that the symptoms started coming back... When I had my endoscopy the told me they didn't find any inflammation in my throat.... But I do believe I have crohns there as well as my terminal illieum.. What is really annoying is that I'm a singer... so it is really screwing up mu music career!!!
 

David

Co-Founder
Location
Naples, Florida
I get a really sore throat and tongue on and off every couple of weeks/months ulcers in my mouth, difficulty swallowing etc... I thought I was getting the flu all the time... Then I stared entocort... And it all magically disappeared!! It was only when my dose of entocort was reduced that the symptoms started coming back... When I had my endoscopy the told me they didn't find any inflammation in my throat.... But I do believe I have crohns there as well as my terminal illieum.. What is really annoying is that I'm a singer... so it is really screwing up mu music career!!!
I wouldn't expect them to find inflammation in your throat. I'd hypothesize that your issues are due to vitamin deficiency which is due to malabsorption which is due to inflammation in your intestines. When you were on the Entocort, the inflammation in your intestines was reduced enough so sufficient vitamin uptake was happening and the issues in your mouth and throat went away. Cut down on the Entocort and the inflammation in your guts came back and the deficiency started again.
 
I too have this and it is quite painful. I get them mostly right after a gut flare. It is all over my mouth, tongue and down my throat. The only thing I had found to work was drinking cool liquids and hot liquids that aren't super salty or acidic. Mild teas work best. Other than that just ride it out and hope for the best I guess! ;)
 
my very first symptom was mouth ulcers/tongue-gum swelling. what's frustrating is that i can almost get rid of those symptoms completely with high doses of probiotics. however, the probiotics mess up my guts and irritate my fistula!
i'm on a steroid cream for my mouth. i just started remicade a couple weeks ago, and while it's doing wonders for the bottom half, it's not helping the mouth at all.
i was thinking with the remicade that maybe i could try some yogurt, to try to help my mouth and keep away fungal stuff. well, just a few days of it, and yes, my mouth was getting more under control with less steroid cream, but it still messes with my fistula, even on remicade.

so frustrating that it helps one thing and hurts another. maybe it will just take longer to take care of the mouth issues on remicade??
 
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