Jump to content
  • 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

Is It Normal/okay To Have Stomach Pain After 1 Year?


raisin

Recommended Posts

raisin Enthusiast

Okay, I'm at 10 months gluten-free, 3 months CC-free.. But I still have significant dyspepsia (stomach pain, bloating, heartburn, belching), even when not glutened.

It's definitely calmer than when I was on gluten. It revs up if I'm contaminated somehow.. But it also acts up on its own, it seems. I couldn't say for sure if the recent "rev" was caused by my newly-found coconut allergy, or just total random. If I don't eat at a regulated schedule, or eat eggs, broccoli, or have strong coffee, without other foods, my stomach gets upset and I start belching. My stomach won't let me skip a meal, and won't let me go to bed without eating before (opposite of acid reflux - where you shouldn't eat before bed - but I occasionally get "hot/burning" burps, a sign of heartburn? acid reflux? I am pretty confused).

Does anyone else experience this? Will it probably diminish as I continue to heal?

I goggled "dyspepsia" and "celiac" only to find they coexist commonly. Dyspepsia is a sign of Celiac, or Celiac causes it, I don't really know.


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



Celiac.com Sponsor (A8-M):



cat3883 Explorer

My GI told me it will take 2 years for my gut to completely heal. Maybe thats your case too.

MaryJones2 Enthusiast

I would agree that it can take quite a while to fully heal. It took 2 years for a lot of my symptoms to disappear and another year before I could tolerate a lot of foods. Pepto Bismol is your friend. Tagment HB also works well for me.

raisin Enthusiast

Wow, really?

I never had an endoscopy, sense I was diagnosed young, and had no signs of complications. But had a small number of TTG antibodies which would imply some gut damage had been done. (the TTGs are the ones that do it right?)

For some reason I thought it was supposed to take me 1 year, but 2 years is much more believable. Oh wow, that means there is a chance I can eat corn and potatoes again. Citrus fruit, and other spicy/acid things too. :D Fatty things like eggs, without salad on the side. Not having to worry about calming my stomach would certainly help me gain weight ..and sleep.

For some reason, I also thought celiacs were not supposed to take antacids like peptobismol, because it's more common to have heartburn from low stomach acid for us? - Even if that's true, Peppermint tea seems to cure my dyspepsia, but it would be nice for pepto to be an option.

ravenwoodglass Mentor

I really like the pepto because for me it stops the pain very quickly and many times the pain doesn't return. That said you may want to check with your doctor as celiac is not the only reason for stomach pain. Other conditions independant of the celiac may be responsible.

MaryJones2 Enthusiast

As ravenswood said you should be checked out by a doctor to make sure it's not something more serious.

I observed something odd in my body and will share. I had major issues with lots of foods. I discussed with my doctor and he suggested taking Tagment HB daily and Pepto twice daily for 3 weeks. I did this 3 months ago I've seen dramatic improvement in my overall heath and absorbtion since then and I can now tolerate fresh corn, very small amounts of dairy and soy sauce occasionally. One could also argue that I was finally fully healed and I wouldn't disagree with that either but I do wonder why I improved so much. (I am getting tested for H. Pylori the next time I go back in.) I think there is something to the Pepto helping to coat the intestinal tract and helping it heal.

So this might be worth asking your doctor about. The combo of Pepto and acid reducers is part of the treatment for ulcers (research triple therapy).

Open Original Shared Link

raisin Enthusiast

It does the same for me, which is why I'd love to add it back to my list of "takeable medicines" :D

I was worried about it being a second stomach condition when I posted this, but after thinking it over.. I don't know what I could be tested for. Certainly not the right symptoms for a hiatal hernia, stomach ulcer, cancers, or anything else I can think of. Acid reflux also runs in my family, with two of my siblings and one parent having it. This would imply the dyspepsia is related to (or caused by) a combo of acid reflux and dyspepsia.

I don't know if there is enough reason to see a gastro doctor, but I will at least get a lab done for H. Pylori, as Janet mentioned. If that comes back negative, or I develop new symptoms (had these sense childhood and doctors keep claiming its "normal") that would be reason enough.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor
I don't know what I could be tested for. Certainly not the right symptoms for a hiatal hernia, stomach ulcer, cancers, or anything else I can think of.

Your doctor would be the person who would know better what your symptoms fit and what tests should be done. If the pain doesn't resolve with selfhelp measures soon please go ahead and book an appointment. It is better to be safe than sorry.

raisin Enthusiast
Your doctor would be the person who would know better what your symptoms fit and what tests should be done. If the pain doesn't resolve with selfhelp measures soon please go ahead and book an appointment. It is better to be safe than sorry.

Sadly, I have no choice.

I called about having a lab done for H. pylori, and a local hospital offers it, but they won't do it without a doctors referral and they won't proscribe medicine if it comes back positive.

My best bet is a family health care facility that has labs on-site. Probably cheaper and faster.

ang1e0251 Contributor

I didn't notice whether you are still having dairy. If you are you might stop that for awhile and see if it helps. Lots of us cannot tolerate dairy. Some can add it back in later.

Also you mentioned coconut. Do you drink water from a filter? Many water filters have coconut fibers in them and can kick in your allergic response. I read a poster who once said they were having problems with coffee filters but didn't say what substance was the offending one. You could take a second look at these items. Drink spring water instead of filtered. Even refridgerator water goes through a filter.

Hope this helps.

raisin Enthusiast

Oh, I never ate dairy. Allergic all my life. ;) I used to drink filtered water, but it didn't give me a problem. I do drink bottled now. That is very interesting though, I guess I'd better call the company before buying filters in the future.

I actually found.. my stomach problems do not seem to be ulcer related, but food related, just not in a way I would ever have expected.

I recently added Kiwi Fruit and Almond-butter back into my diet. Now initially I removed almond butter and felt a great deal better, added it back and felt worse. But I was still having symptoms in between, and remembered not liking kiwis as a child. I decided to look for a connection.

Kiwis and almonds are allergen-related in only one way : Birch Pollen.

Here is a combo of two lists I found :

o Root vegetables: potato, carrot, celery, parsnip

o Fruit and other vegetables: apple, pear, peach, kiwi fruit, plum, mango, tomato, sweet pepper, oranges, limes, kumquats, Melons, cherries.

o Spices: mustard, caraway, turmeric, ginger, cinnamon

o Others: walnut, almond, fennel, wheat, peanuts, and hazelnuts

Here is Wikipedia's list :
Open Original Shared Link

Birch pollen: almonds, apples, apricots, avocados, carrots, celery, cherries, chicory, coriander, fennel, fig, hazelnuts, kiwifruit, nectarines, parsley, parsnips, peaches, pears, peppers, plums, potatoes, prunes, soy, strawberries, wheat;
Potential:
walnuts

Everything on that list I have actually eaten before, at least sparks a mild reaction in me. A number of them spark harsh reactions. Soy is an especially severe allergy for me. Birch also causes seasonal allergies, which I've had sense I was a child and run in one side of my family, but never found which plant (or plants) caused it.

--

I'm actually ecstatic.. I only cut almonds and kiwis out of my diet last night, and my symptoms are already improving! I feel better (especially related to my stomach) than I have in weeks. :D It also explains why I'm so sensitive to so many foods, and opens the door for me to openly try new foods again without fret! I'm getting an allergy test done next week, and the H. Pylori test done, as a precaution, later.

dilettantesteph Collaborator

Just because your blood test is clear doesn't mean that you aren't getting any gluten. There are lots of celiacs diagnosed with negative blood tests and positive biopsies (who are eating gluten). Just wanted to put that out there.

After I got a negative blood test, I found gluten in my diet, eliminated it and felt better.

Hope you feel better soon.

raisin Enthusiast
Just because your blood test is clear doesn't mean that you aren't getting any gluten. There are lots of celiacs diagnosed with negative blood tests and positive biopsies (who are eating gluten). Just wanted to put that out there.

After I got a negative blood test, I found gluten in my diet, eliminated it and felt better.

Hope you feel better soon.

I am a super sensitive. When I get glutened.. I definitely know. The only prepackaged food I even eat is Lundberg rice, and I don't bake with anything "gluten-free" either. Can't get much safer than "all raws + rice".. + gluten-free home, + no eating out, + dedicated soaps, toothpaste, etc.

But thank you for the heads up. :)

dilettantesteph Collaborator

Good for you having such a good diet. I'm almost there myself, but still eat a few processed things. Sorry you are having pain still.

  • 5 weeks later...
bibbity Newbie
Oh, I never ate dairy. Allergic all my life. ;) I used to drink filtered water, but it didn't give me a problem. I do drink bottled now. That is very interesting though, I guess I'd better call the company before buying filters in the future.

I actually found.. my stomach problems do not seem to be ulcer related, but food related, just not in a way I would ever have expected.

I recently added Kiwi Fruit and Almond-butter back into my diet. Now initially I removed almond butter and felt a great deal better, added it back and felt worse. But I was still having symptoms in between, and remembered not liking kiwis as a child. I decided to look for a connection.

Kiwis and almonds are allergen-related in only one way : Birch Pollen.

Here is a combo of two lists I found :

o Root vegetables: potato, carrot, celery, parsnip

o Fruit and other vegetables: apple, pear, peach, kiwi fruit, plum, mango, tomato, sweet pepper, oranges, limes, kumquats, Melons, cherries.

o Spices: mustard, caraway, turmeric, ginger, cinnamon

o Others: walnut, almond, fennel, wheat, peanuts, and hazelnuts

Here is Wikipedia's list :
Open Original Shared Link

Birch pollen: almonds, apples, apricots, avocados, carrots, celery, cherries, chicory, coriander, fennel, fig, hazelnuts, kiwifruit, nectarines, parsley, parsnips, peaches, pears, peppers, plums, potatoes, prunes, soy, strawberries, wheat;
Potential:
walnuts

Everything on that list I have actually eaten before, at least sparks a mild reaction in me. A number of them spark harsh reactions. Soy is an especially severe allergy for me. Birch also causes seasonal allergies, which I've had sense I was a child and run in one side of my family, but never found which plant (or plants) caused it.

--

I'm actually ecstatic.. I only cut almonds and kiwis out of my diet last night, and my symptoms are already improving! I feel better (especially related to my stomach) than I have in weeks. :D It also explains why I'm so sensitive to so many foods, and opens the door for me to openly try new foods again without fret! I'm getting an allergy test done next week, and the H. Pylori test done, as a precaution, later.

Hello Raisin,

I wanted to let you know that you are not alone. I have been gluten free now for 7 months and at first felt much better. Then after 3 months I was still having stomach problems and decided to go off dairy (I have several family members who are gluten and casein intolerant), felt great for about 2 weeks and then started to have what I thought was ulcer pain. My Doctor perscribed pepcid antacid which helped a bit but the h-pylori test was negative and the pain was still there.

Finally last week I went back to the Doctor with more strange symptoms like a stuffed and runny nose, itchy ears, throat, mouth and eyes as well as an itchy rash around my mouth, across my face and stomach. She took a look and said it was most likely oral allergy syndrome caused by an allergy to birch pollen and told me to take an antihistamine. Low and behold my stomach pain, rash and itching are gone although will flare up a bit if I'm not careful to avoid most of the foods on the birch pollen list. The next step is to see an allergist in a few weeks and try and determine which foods are okay and which are not.

I am also thrilled to have the list of foods to avoid. I'd been baking with almond flour for months - who knew?!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,961
    • Most Online (within 30 mins)
      7,748

    Noa
    Newest Member
    Noa
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.