Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Can Celiac Disease Cause Ulcers?


glutefree

Recommended Posts

glutefree Rookie

Hi all, I am wondering if anyone has had a problem with ulcers. I get cankersores regularly, and I know these can be a sign of celiac disease, but I have recurring duodenal ulcers.

All the literature out there says that duodenal ulcers are likely caused by heliobacter pilori bacteria (I have tested negative for this twice) or by NSAID or steroid medication use (I have not used either of those regularly and haven't used them in a loong time).

Anyway, I am wondering if somehow my celiac disease has manifested itself somehow to make me more suseptible to ulcers. I have had painful ulcers at least 3 times in the last few years and it is horrible. I want to find the cause of my ulcers so that I can once again sleep at night and eat a regular diet again.

Thanks!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Welda Johnson Newbie

Hi, I have a long history with Celiac and intolerances to milk & dairy, egg whites, yeast, casein, whey, msg and a couple of other food additives, and for many years I also suffered with duodenal ulcers. As you say, it was truly "horrible." I likened it to a blow torch being turned on in your stomach. However, once I went SERIOUSLY gluten free and stopped all the other foods and additives that I mentioned above, the ulcers went away. That's been about 8 years now, and believe me, it's worth sticking to the diet just for the sake of getting rid of the ulcers, but, fortunately, there are so many other health benefits (less depression, more energy, less asthma, better sleep, a new zest for living, less colitis and digestive upsets, and on and on...) that I will always stick diligently with eating this way. Hope this helps you. Good luck. Welda

glutefree Rookie

Hi, I have a long history with Celiac and intolerances to milk & dairy, egg whites, yeast, casein, whey, msg and a couple of other food additives, and for many years I also suffered with duodenal ulcers. As you say, it was truly "horrible." I likened it to a blow torch being turned on in your stomach. However, once I went SERIOUSLY gluten free and stopped all the other foods and additives that I mentioned above, the ulcers went away. That's been about 8 years now, and believe me, it's worth sticking to the diet just for the sake of getting rid of the ulcers, but, fortunately, there are so many other health benefits (less depression, more energy, less asthma, better sleep, a new zest for living, less colitis and digestive upsets, and on and on...) that I will always stick diligently with eating this way. Hope this helps you. Good luck. Welda

Thank you so much for your reply! I was starting to think I was crazy. I think I have been very good about being gluten free. I have in the last few weeks gone dairy free. I also have a problem eating most nightshades as well (For now I have kept potatoes in my diet, but I am thinking of eliminating those as well). How did you decide to cut out the egg whites, yeast, casein, whey, msg and food additives? Did you know that you were reacting to those items?

My husband tells me not to eliminate random foods. I like to have him onboard as a support system so I like to give him reasons when I can. I think he is afraid that if I cut too many foods that I will waste away. I do have a problem keeping weight on with the wonderful ulcer problem and all.

Thanks again for any advice. Also, how do you stay on such a restrictive diet? Do you have a cookbook that you use or do you just eat lots of veggies, fruits and meat?

ravenwoodglass Mentor

For my daughter ulcers were her primary symptom and I have had them also so it certainly isn't unusual for us.

I used Pepto Bismal for relief from the pain without messing with my normal acid production and for myself and my DD the ulcers were gone soon with the diet. I did have to also stop dairy and soy but I was able to add dairy back in after a couple of months.

I would suggest dropping, of course the gluten but also dairy at first and perhaps also soy. Give it a little while and if you are still having issues then you may need to drop other foods. If you restrict too much at once it is hard to pinpoint what you were reacting to.

Enterolab can do testing for intolerances to casien (protein in dairy), yeast, eggs and soy in addiiton to gluten if you want to be tested for those intolerances. You may find them helpful.

Ivy Rookie

Hi all, I am wondering if anyone has had a problem with ulcers. I get cankersores regularly, and I know these can be a sign of celiac disease, but I have recurring duodenal ulcers.

All the literature out there says that duodenal ulcers are likely caused by heliobacter pilori bacteria (I have tested negative for this twice) or by NSAID or steroid medication use (I have not used either of those regularly and haven't used them in a loong time).

Anyway, I am wondering if somehow my celiac disease has manifested itself somehow to make me more suseptible to ulcers. I have had painful ulcers at least 3 times in the last few years and it is horrible. I want to find the cause of my ulcers so that I can once again sleep at night and eat a regular diet again.

Thanks!

I have a very long history of duodenal ulcers. I have been on proton pump inhibitors for at least 18 years. They check every time I've been scoped about every 4 years, but no pilori. No medicine as cause for explanation. Have always been told that I plain pump too much stomach acid. Have been gluten free about 4 years. Recently removed corn from diet also. With most I've known, it is true that at least one other food intolerance will pop up. Took me a while to figure out it was corn. Think I may finally be ready to try going off proton pump inhibitors again but frankly am not holding my breath. Tried a year and a half ago, didn't go well. I don't think the two (celiac and ulcers) are related in my case.

As for a restricted diet, I have a gluten-free house and I rarely eat out. Have taught my two adult kids to carry their snacks so they can "join in" when friends decide to stop somewhere to grab a bite. There are many good cookbooks out (like Gluten-Free Baking Classics by Annalise Roberts) and a wealth of good recipes on the web.

Good luck.

glutefree Rookie

I have a very long history of duodenal ulcers. I have been on proton pump inhibitors for at least 18 years. They check every time I've been scoped about every 4 years, but no pilori. No medicine as cause for explanation. Have always been told that I plain pump too much stomach acid. Have been gluten free about 4 years. Recently removed corn from diet also. With most I've known, it is true that at least one other food intolerance will pop up. Took me a while to figure out it was corn. Think I may finally be ready to try going off proton pump inhibitors again but frankly am not holding my breath. Tried a year and a half ago, didn't go well. I don't think the two (celiac and ulcers) are related in my case.

As for a restricted diet, I have a gluten-free house and I rarely eat out. Have taught my two adult kids to carry their snacks so they can "join in" when friends decide to stop somewhere to grab a bite. There are many good cookbooks out (like Gluten-Free Baking Classics by Annalise Roberts) and a wealth of good recipes on the web.

Good luck.

Thanks for the reply. I am hoping to get off the proton pump inhibitors soon as I feel that they affect my nutrient absorbption and tend to make me feel a bit icky at times. I have to admit though that they are a Godsend for ulcers because I was not sleeping and barely eating before I went on them. It's good to know I am not the only one out there with mysterious ulcers. If you find out the magic cure, let me know.

glutefree Rookie

For my daughter ulcers were her primary symptom and I have had them also so it certainly isn't unusual for us.

I used Pepto Bismal for relief from the pain without messing with my normal acid production and for myself and my DD the ulcers were gone soon with the diet. I did have to also stop dairy and soy but I was able to add dairy back in after a couple of months.

I would suggest dropping, of course the gluten but also dairy at first and perhaps also soy. Give it a little while and if you are still having issues then you may need to drop other foods. If you restrict too much at once it is hard to pinpoint what you were reacting to.

Enterolab can do testing for intolerances to casien (protein in dairy), yeast, eggs and soy in addiiton to gluten if you want to be tested for those intolerances. You may find them helpful.

Thanks so much for the tips! I may just have to check out the Enterolab tests. Everytime I think I have it figured out, I get rid of something else in my diet. I have been dairy free for a few weeks and I'll see how that goes. It is hard to tell now because I had to go for the proton pump inhibitor medication as the ulcers were too bad.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Thanks so much for the tips! I may just have to check out the Enterolab tests. Everytime I think I have it figured out, I get rid of something else in my diet. I have been dairy free for a few weeks and I'll see how that goes. It is hard to tell now because I had to go for the proton pump inhibitor medication as the ulcers were too bad.

When you decide to go off the PPIs do talk to your doctor about how to taper off. One reason I chose not to take them is that when stopped they often have a 'rebound' effect which can make it difficult to get off them. I hope you get things figured out soon and are feeling better.

glutefree Rookie

When you decide to go off the PPIs do talk to your doctor about how to taper off. One reason I chose not to take them is that when stopped they often have a 'rebound' effect which can make it difficult to get off them. I hope you get things figured out soon and are feeling better.

Thank you so much ravenwoodglass. I am afraid of that rebound effect, so I will discuss tapering off. I really resisted taking them, but after weeks of sleeping sitting up on the couch and not getting sleep and waking in the middle of the night I felt pretty desperate. Since I have been on the PPI's I can at least sleep in a bed now. I am not sure the ulcer is all better yet, but getting more sleep has been nice.

  • 6 months later...
twinkle-toez Apprentice

For my daughter ulcers were her primary symptom and I have had them also so it certainly isn't unusual for us.

I used Pepto Bismal for relief from the pain without messing with my normal acid production and for myself and my DD the ulcers were gone soon with the diet. I did have to also stop dairy and soy but I was able to add dairy back in after a couple of months.

I would suggest dropping, of course the gluten but also dairy at first and perhaps also soy. Give it a little while and if you are still having issues then you may need to drop other foods. If you restrict too much at once it is hard to pinpoint what you were reacting to.

Enterolab can do testing for intolerances to casien (protein in dairy), yeast, eggs and soy in addiiton to gluten if you want to be tested for those intolerances. You may find them helpful.

Not to ask a stupid or naive question, but how long did it take for your (or your daughter's) stomache to stop burning once you went gluten free?

ravenwoodglass Mentor

Not to ask a stupid or naive question, but how long did it take for your (or your daughter's) stomache to stop burning once you went gluten free?

Pretty quickly. Like about a month. I would still have occasional issues until I stopped the soy but now I only have an issue when I accidentally eat something I shouldn't. The pepto liquid stops the pain in minutes when that happens and I usually don't need to take it more than once.

  • 5 years later...
debbie in Oregon Newbie

I have a very long history of duodenal ulcers. I have been on proton pump inhibitors for at least 18 years. They check every time I've been scoped about every 4 years, but no pilori. No medicine as cause for explanation. Have always been told that I plain pump too much stomach acid. Have been gluten free about 4 years. Recently removed corn from diet also. With most I've known, it is true that at least one other food intolerance will pop up. Took me a while to figure out it was corn. Think I may finally be ready to try going off proton pump inhibitors again but frankly am not holding my breath. Tried a year and a half ago, didn't go well. I don't think the two (celiac and ulcers) are related in my case.

As for a restricted diet, I have a gluten-free house and I rarely eat out. Have taught my two adult kids to carry their snacks so they can "join in" when friends decide to stop somewhere to grab a bite. There are many good cookbooks out (like Gluten-Free Baking Classics by Annalise Roberts) and a wealth of good recipes on the web.

Good luck.

Hi, I also have been having recurrent ulcers, and cannot find the cause. I ended up on this website and now I am thinking I may have celiac disease, although I never thought about it before! I was reading that broccoli sprouts are very helpful with curing ulcers, so I am going to start sprouting some! I have read many good hospitals recommend them! Mayo clinic is one of  them. 

debbie in Oregon Newbie

Thank you so much ravenwoodglass. I am afraid of that rebound effect, so I will discuss tapering off. I really resisted taking them, but after weeks of sleeping sitting up on the couch and not getting sleep and waking in the middle of the night I felt pretty desperate. Since I have been on the PPI's I can at least sleep in a bed now. I am not sure the ulcer is all better yet, but getting more sleep has been nice.

I have been taking aloe vera and it is helpful. It is found  in heath food store s. Hope this can help you.

LauraTX Rising Star

Welcome to the forum, Debbie.  Do note this thread is five years old and some of the information may be outdated.  Also, if you have Celiac disease, eating broccoli sprouts and aloe vera is not going to cure it, only a gluten-free diet will.  However, before you trial a gluten-free diet, do head to a gastroenterologist to get properly diagnosed first as you must be consuming gluten for the testing to be accurate.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,317
    • Most Online (within 30 mins)
      7,748

    Arlinda 1987
    Newest Member
    Arlinda 1987
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.2k
    • Total Posts
      71.6k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • lizzie42
      Well, the problem is we kind of did proceed with dietary changes. Until his ASK study test he was eating school lunch 3x a week (high on the gluten) plus occasionally a weekend treat with gluten. Since the test I went to packing his lunch and everything he eats at home is gluten-free due to his sister. I would say 1-2x a week for the last 3 weeks he had a decent serving of gluten like pizza or a cupcake at a party. Will that be enough for an accurate result? I assume a number 12x the limit isn't going to back to zero in 3 weeks of eating *mostly* gluten free. I am kicking myself now because I was so sure he'd be negative I didn't even make an effort to have him keep eating gluten after we drew his blood for the ASK study. Never thought we'd need a confirmation test.  And we probably won't even see the GI so we will have to make our own decision based on the results. The pediatric GI telehealth appointment was almost $500 for a 30 minute appointment and it's just out of our price range to do that again with another kid. 
    • Brown42186
      Hi again! The biopsies from my endoscopy didn't show anything abnormal. The GI said I have EPI like I already said, acid reflux that I didn't know I have, and probably a gluten intolerance since it's showed up on allergy testing.
    • cristiana
      @Scott Adams has done an amazing job at explaining the situation.  Shop at Asda, Morrisons, Tesco's, Sainsbury's, Marks & Spencers and Waitrose which have great gluten free sections and you won't go hungry.  Even small Co-op corner shops tend to have a dedicated gluten free area.  I haven't had much luck with the German store, LIdl.  Can't speak for Aldi but I think they may have a gluten free section..  Food labelling has become very strict here so you should be able to shop anywhere and trust their labels - if the product comes from a shared line, it will say 'May contain traces of gluten'.  If that is the case, avoid those products.  I am not sure how long you are here for but if you are here for a while I second that you join Coeliac UK who produce an app which will help you navigate the supermarket. Personally, I would not eat pasta or pizza out., as in the words of a Food Inspector I know, there is just too much glutenous flour about in these places.   When you order anything, make a big deal about the fact that you are a coeliac.  My line is... "I'm very sorry to be a pain but please can you make sure to tell the chef that I am a coeliac and because I throw up very quickly after being served gluten by mistake!"   That tends to work get the message home!  I find as soon as they hear that they type/write coeliac/or allergy in very big letters on the chit for the kitchen! When the food comes out,  at the point of service, always double check what they are serving IS actually gluten free.  Twice I have narrowly avoided being glutened because my daughter or I double checked the bread was gluten free:  the poor, harried waiting staff had made a mistake and put the wrong bread on the plate. We don't seem to have the medication that you have for glutening episodes, as you do in the US, so if you can I'd bring some with you.    
    • xxnonamexx
      I have cgf oat flour so I should buy potato or tapioca flour mixed together to make "flour" is there a recipe you use to stretch the for. Does it come out to 1:1 when replacing regular flour? Also xanthum gun is that good for you or is there a replacement? There a vegan gluten-free granola bar I purchase locally that I'm trying to replicate I think it's no bake but trying to see if I can copy it bc I can freeze it. Thanks
    • Scott Adams
      While your vigilance is completely understandable, the risk of gluten exposure from those can stains is extremely low. Here’s why: First, gluten proteins can’t penetrate metal cans—any residue would only be on the surface. Second, the amount of potential gluten in a few dried droplets (even if it was a wheat-based drink) would likely be minuscule after drying and exposure to air. For context, research shows most celiacs react to >10mg of gluten daily, and those stains would contain far less—if any gluten at all. That said, if it helps your peace of mind, you can: 1) Wipe the rim with a clean wet cloth before opening, 2) Use a straw to avoid mouth contact with the rim, or 3) Opt for bottled drinks when uncertain. Most celiacs I know (including myself) don’t stress over can stains unless there’s obvious food residue (like dried pasta sauce). The particles you saw were likely dust or manufacturing residue—energy drink facilities rarely handle gluten near filling lines. While it’s great to be cautious, this is one scenario where I’d say you can safely
×
×
  • Create New...