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

Bloating After 10 Months Of gluten-free Diet?


glutenfreeinminnesota

Recommended Posts

glutenfreeinminnesota Contributor

I was diagnosed Nov of 2009 and have been on a gluten-free diet ever since. I have felt SO much better then I have in years. Well, at first I lost weight, I think because I didn't know what I could eat, so I ate a lot healthier. Now I have discovered more foods, and of course have gained weight right back. I have been glutened here and there, but have done pretty well so far. Well, out of no where I feel like I am bloated all the time. I am pretty skinny...so my lower stomach is pretty obvious when it's sticking out like I'm pregnant. I don't have any effects of being glutened other then the bloating. I was glutened about a month ago while on vacation...that was the last time I believe I consumed gluten. Dairy has not affected me at all along the way...could it suddenly be that? I have been washing things around here like I'm obsessive complusive...thinking maybe I was CCing myself since I live with a gluten eater...but nothing seems to make it go away. Anyone else have this problem without glutening??? Thanks for reading :)


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



Celiac.com Sponsor (A8-M):



i-geek Rookie

I'm having a similar problem after 8.5 months gluten-free, but I'm quite sure it's due to unhealed gut damage from a bad glutening about 3.5 weeks ago and CC events since (trip to Japan where I got really badly glutened the second night there and probably CC'd at least every other day due to the language barrier and lack of known safe foods, then a CC incident last week from candy made on a shared line). I've once again lost the ability to digest dairy (NOT happy about this- last time it took a full five months of gluten-free eating before I healed enough to eat ice cream with lactase pills) and am having mild problems with peppers and cruciferous veggies again.

Long story short: you could be dealing with some gut damage from being glutened. You might want to take it easy with your diet to let your gut rest. I've been off of dairy except for butter for 48 hours now and it has helped my symptoms immensely. Or (and I hope this isn't the case) you could have developed a secondary food intolerance in which case an elimination diet may help you address it.

RiceGuy Collaborator

I agree with what i-geek has said. I would add that I've found digestive enzymes to be very helpful to reduce the balloon belly. I'd suggest the kind derived from microbes. Not only do they tolerate the natural acidity of the stomach, but it'll help avoid possible barley-derived enzymes.

glutenfreeinminnesota Contributor

Thanks so much! I just like to make sure I am not the only one dealing with these stupid "side effects". I will try to keep away from dairy and look into the digestive enzymes. Thanks!!

burdee Enthusiast

I continued to suffer bloating despite abstaining from gluten. After diagnoses of and abstaining from 6 other delayed reaction food allergies, I still had intestinal cramping and bloating. Then I was diagnosed with and treated for 8 successive gut infections (5 bacteria, 2 parasitic and candida). Afterwards I STILL had bloating after meals. I also had been taking a probiotic with FOS during and after treatment for those gut bugs.

When I switched to a higher dose probiotic, which did not contain FOS, my bloating decreased a lot. Then I got a Heidelberg Capsule Test for stomach acid production, which diagnosed hypochloridia or low stomach acid. (Years ago I was misdiagnosed with 'gastritis' and treated with acid blocking drugs when I really had celiac disease.) Once I started HCl supplements (to replace my depleted stomach acid), I finally lost the bloating and no longer feel overly full after eating small amounts. Taking digestive enzymes didn't help me as much as taking HCl, because normal amounts of stomach acid biochemically trigger the release of digestive enzymes.

So I suggest you test for other delayed reaction allergies (ELISA blood test), for gut 'bugs' (stool tests, which can also indicate insufficient good bacteria), and for depleted stomach acid (Heidelberg capsule test). Also avoid probiotics with FOS. All those things can cause chronic bloating after meals.

glutenfreeinminnesota Contributor

I continued to suffer bloating despite abstaining from gluten. After diagnoses of and abstaining from 6 other delayed reaction food allergies, I still had intestinal cramping and bloating. Then I was diagnosed with and treated for 8 successive gut infections (5 bacteria, 2 parasitic and candida). Afterwards I STILL had bloating after meals. I also had been taking a probiotic with FOS during and after treatment for those gut bugs.

When I switched to a higher dose probiotic, which did not contain FOS, my bloating decreased a lot. Then I got a Heidelberg Capsule Test for stomach acid production, which diagnosed hypochloridia or low stomach acid. (Years ago I was misdiagnosed with 'gastritis' and treated with acid blocking drugs when I really had celiac disease.) Once I started HCl supplements (to replace my depleted stomach acid), I finally lost the bloating and no longer feel overly full after eating small amounts. Taking digestive enzymes didn't help me as much as taking HCl, because normal amounts of stomach acid biochemically trigger the release of digestive enzymes.

So I suggest you test for other delayed reaction allergies (ELISA blood test), for gut 'bugs' (stool tests, which can also indicate insufficient good bacteria), and for depleted stomach acid (Heidelberg capsule test). Also avoid probiotics with FOS. All those things can cause chronic bloating after meals.

Thank you for the advice...yeah I was "diagnosed" with GERD years ago before Celiac finally was found as the real culprit...I have never taken probiotics, but I will have to look into it!! Thanks again.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,243
    • Most Online (within 30 mins)
      7,748

    Hurtfeelingz
    Newest Member
    Hurtfeelingz
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.7k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      The positive Anti-deamidated Gliadin IgA result (12 U/ml) suggests possible celiac disease, but it is not definitive on its own, as this marker can also be elevated in other conditions or even in non-coeliac gluten sensitivity (NCGS). Do you know if they also ran a tTg-Iga test? This is the definitive test for celiac disease. The absence of classical symptoms like significant bloating or pain upon gluten reintroduction, along with your history of IBS and sensitivity to legumes, complicates the picture (legumes can be cross-contaminated with wheat). While celiac disease remains a possibility, other conditions like NCGS, leaky gut, or additional food intolerances could also explain your symptoms. A biopsy would provide more conclusive evidence for celiac disease, but for that you need to be eating lots of gluten daily in the weeks leading up to the endoscopy. In the meantime, adopting a gluten-free diet and supporting gut health with supplements (e.g., probiotics, L-glutamine) may help reduce inflammation and symptoms, but it’s important to consult a healthcare professional to tailor your approach and rule out other underlying issues. This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
    • Scott Adams
      You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Liquid lunch
      I don’t think it matters much, there’s another type of cordyceps but I’m not sure if there’s a lot of difference, the one I’m using is cordyceps sinensis from maesyffin in wales, sinensis is the one with a long history of medicinal use in china. I think the alcohol (vodka) in the tincture helps with uptake vs taking capsules. And yes, changing my diet helped but it’s almost impossible to maintain as I can’t eat any lectins or sugar which is almost everything. Low lectin is about the best to hope for, they’re in everything. I can eat teff, millet, hemp seeds, blueberries, strawberries, blackcurrants, yogurt, cheese, walnuts, pistachios, macadamia, Brazil nuts, broccoli, sweet potato, carrots, beetroot, olives, rocket, onions, garlic, avocado, kale, mushrooms, chlorella/spirulina, and fish. That’s about it. I keep quail and make their food myself because lectins get into the commercial pellet fed chickens eggs. It took me years of adding one thing at a time with three weeks of pain every time I got it wrong to figure this out but there’s a finger prick blood test available now that will tell you which foods are triggering your autoimmune system, they test for 200+ different proteins and measure igg and ige antibodies. Good luck, I hope the mushrooms help but best to address the cause of the problem I think and have the igg and ige antibody test. The test won’t work if you’re already taking the mushrooms.
    • trents
      Just a heads up, if your butt sores go away on a gluten free diet, you would need to go back to eating gluten for a period of weeks or months if you want to get formally tested for celiac disease. Otherwise, the testing will be invalidated.
    • trents
      https://www.drugs.com/inactive/sodium-starch-glycolate-128.html https://celiac.org/gluten-free-living/gluten-in-medicine-vitamins-and-supplements/ Santina, are you a super sensitive celiac? If there is gluten in the starch used in this med it would be a very small amount since gluten is the protein component of wheat, not the starchy part. You can never completely separate the two but the starch should have only a trace of gluten I would think. It is also possible that you reacting to the active component of the medication itself.
×
×
  • Create New...