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

Food Journaling to Find the Gas Culprit


chrissy-b

Recommended Posts

chrissy-b Apprentice

Hi All!

I have been having the worst gas for the last two weeks and need to find out what is causing it.

I have bloating and gas pretty much all day, but it is worst at night. I stopped eating dairy and soy weeks ago (last time was in July), and I thought that avocado and hummus were causing it (although I have never had a problem with these foods before) so I cut those out too about two weeks ago, but the gas persists. Now I'm thinking maybe it's cauliflower or brussels sprouts or onions (which again I've never had a problem with) but since I'm gassy mostly all day I can't really tell which is the offender. 

What is the timeline for gas to appear after you've eaten a particular food item? Does it happen right away, or is it hours later? The next day? How should I go about an elimination diet to find which foods aren't agreeing with me? 

I have been gluten-free since March 19th, 2018. And the last time I was knowingly glutened was June 3rd. 

A typical day looks like this:

Breakfast: My paleo "cereal" of ground flaxseed, cacao nibs, shredded coconut, raisins and fresh berries with almond/coconut milk. Somedays I make a smoothie with frozen berries, almond milk, and raw spinach. 

Lunch: Stir fry of a slice of bacon or a sausage with yam, onion, mushrooms, squash, kale & spinach cooked with avocado oil. (I mix up the vegetables too and include bell peppers, brussels sprouts, sweet potatoes -- basically any vegetable when I get bored.)

Dinner: A small portion of steak, chicken or pork with steamed veggies (broccoli, cauliflower, green beans, or brussels sprouts) OR with a mixed green salad with vinaigrette. 

Snacks: Raw carrots, or fruit (usually a peach or orange, sometimes a banana), sometimes a handful of nuts, and usually an almond milk protein smoothie before bed. The protein is whey so maybe that is now the issue? 

None of these items have ever given me a problem before, but maybe you all see something I should cut out for a while? Any advice is much appreciated. Thank you!!!


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



Celiac.com Sponsor (A8-M):



chrissy-b Apprentice

Also, I don't know if this matters, but I am also on an iron supplement and Vit D sublingual as both of those are low.  The iron does constipate me somewhat but has never given me gas but thought I should mention it just in case. 

Ennis-TX Grand Master

Starches and Carbs are common issues on a gluten free diet as we are prone to SIBO and Cadida with our damaged celiac intestines. I see a good amount of fiber in there and some things that cause issues for some. As you noted Brussels, Onions, Hummus,  are common gas culprits. Some have issues with Coniferous vegetables like cauliflower, cabbage, kale and broccoli. If it is SIBO or Candida you will have to give up the potatoes, berries, fruit, and any other carb or sugar. Several other foods your eating can kill the bad bacteria, and fungus and be causing die off and bloat/gas.
Keep a food diary and try a SIBO or Candida Diet, or a Keto Diet to lower carb intake and stuff the bad bacteria and or fungus might be feasting on. The lower carb diet will less to ferment so 2 birds one stone.

Awol cast iron stomach Experienced

Hi Chrissy,

I bloat within 30-45 min of CC from gluten. I of course avoid gluten and cc. Ironically the slightest CC now I get a flood of symptoms including DH which ironically no DH appeared during my challenge while under a Dr. care. :(

  I have additional intolerances as well. After my Gluten challenge I had 13 intolerances while I was healing over the course of two years. They had me go off everything -gluten and the top 8  allergens.  I had a very boring diet. After my Dr. gave me testing to determine I did not have IgE mediated allergies she left me sitting there (as I had told her I reacted to things, but had never reacted to allergy testing i.e. no food allergies, but that I reacted to foods within 30 minutes described my symptoms.) She came in checked to confirm I had no IgE mediated allergies, but asked me how I was feeling  I explained I was having symptoms and she asked me to describe them. After I described them she stated those symptoms you just described to me those are the ones you need to be aware of during your food journaling and diet. Listen and look for those symptoms to guide you when eating. They guided me then and even today. I was told as I introduced each new food to start with 1/2 c of the new food, then raise to 1 c, then 2 c etc. I did 3 days of a new food (graduating the levels) if it was not a problem (no symptoms) I could add it  back to diet. Then try next food. Is that similar to your food elimination diet.Once uou find the offenders you can perhaps try whole 30. I found that helpful then as I incorporated more foods staying low inflammatory AIP and Paleo.

As I healed I was able to add more into the diet. I am now down to 3 intolerances (the obvious gluten), corn, and milk. The corn is tricky as my body can react to things preservatives/additives derived from corn although in theory  people say I should not react as the proteins have been removed.  My body knows I don't know how it does so I just listen to the body. When damaged my highly reactive immune system/body knew something was foreign and  let me know. During those initial stages of healing I had to be very plain and boring food wise just to uncover the intolerances even spices etc could be troublesome.

 

Good luck

chrissy-b Apprentice

Thank you Ennis_TX & Awol! Very helpful info.

I actually started the Keto diet a few weeks after going gluten-free and only recently went off it. I did not have these issues while Keto, but I also didn't have these issues prior to going gluten-free. Possibly I just introduced too many gas-inducing veggies all at once. Last night I ate two hot dogs with Udi's buns and no veggies. I barely had any gas and no bloating. 

It could also be from CC though I don't know from what. I don't eat out anymore at all, and have already ridded my house of all potential CC items (bought a new cutting board and pans and wooden spoons), and cleaned my house.

I will definitely be more consistent with logging my food to see if I can pinpoint what it is and after I eat all the gas inducing foods that are still in my house (can't let them go to waste!) I will move back to the Keto to see if there is improvement. 

Thanks again both of you for taking the time to offer some advice. Much appreciated! 

pikakegirl Enthusiast

I had terrible gas which was sharp because of all my endometriosis scar tissue. Going on the FODMAP diet eliminating specific fruits, vegetables and legumes was like magic. Wish probiotics helped more but they only take the edge off. I still have to limit portion size and amount daily of leafy greens or the gas is back.

chrissy-b Apprentice

Thank you for your input, pikakegirl. I have looked at the FODMAP list and I'm eating almost all of the fruits and veggies that are banned. Aha. I'll have to make a list of safe foods for shopping this week and see how it goes. Thanks again!


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



Celiac.com Sponsor (A8-M):



Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Jordan Carlson posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Fruits & Veggies

    2. - wellthatsfun posted a topic in Gluten-Free Recipes & Cooking Tips
      0

      heaps of hope!

    3. - knitty kitty replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      6

      Help understand results

    4. - knitty kitty replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      10

      Insomnia help

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,994
    • Most Online (within 30 mins)
      7,748

    KimberlyS
    Newest Member
    KimberlyS
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Jordan Carlson
      Hello everyone! Been a while since I posted. The past few moths have been the best by for recovery for myself. I have been the least bloated I have ever been, my constant throat clearing is almost gone, I have stopped almost all medication I was prevously taking (was taking vyvanse for adhd, pristiq for anxiety,fomotadine/blexten for histamine blockers and singulair). Only thing I take now is Tecta. I also no longer get any rashes after eating. Things are going very well. Most success came actually once I upped my B12 daily dose to 5,000 mcg. I do have one thing I am un able to figure out and want to see if anyone else has this issue or has experience working around it. Ever since I was born I have always had a issue getting fruits and veggies down. No matter how hard I tried, it would always result in gagging or throwing up. Always just thought I was a picky eater. Now that my stomach and system has healed enough that I can feel when something is off almost istantly, I notice that after eating most fruits (sometimes I am ok with bananas) and veggies, my stomach instantly starts burning and my heart starts to pound and I get really anxious as if my body doesnt know what to do with what just enetered it. So I am thinking now that this is what probably was going on when I was born and my body started rejecting it before which caused this weird sensory issue with it causing the gagging. Hoping someone has some exprience with this as well because I would love to be able to enjoy a nice fruit smoothie once in a while haha. Thanks everyone!
    • wellthatsfun
      i know i've been rather cynical and sad about being fully diagnosed in june 2025, but my boyfriend has been consistently showing me the wonderful world that is gluten free cooking and baking. in the past couple of days he's made me a gluten free rice paper-wrapped spanakopita "pastry", plus a wonderful mac and cheese bechamel-ish sauce with gluten free pasta (san remo brand if you're in australia/if you can get your hands on it wherever you are).  those meals are notably gluten free, but mainly he's been making me easy gluten free meals - chili mince with white rice and sour cream, chicken soup with homemade stock from the chicken remains, and roast chickens with rice flour gravy and roast veggies. i'm a bit too thankful and grateful lol. how lucky could i possibly be? and, of course, for those who don't have someone to cook for them, it's quite easy to learn to cook for yourself. i've been making a lot of meals for us too. honestly, cooking is pretty darn fun! knowing basic knife skills and sanitary practices are all you really need. experimenting with spices will help you get on track to creating some really flavourful and yummy dishes. coeliac is a pain, but you can use it to your advantage. healthier eating and having fun in the kitchen are major upsides. much luck to all of you! let's be healthy!
    • knitty kitty
      That test is saying that your daughter is not making normal amounts of any IGA antibodies.  She's not making normal amounts of antibodies against gliadin, not against bacteria, not against viruses.  She is deficient in total IGA, so the test for antigliadin antibodies is not valid.  The test was a failure.  The test only works if all different kinds of antibodies were being made.  Your daughter is not making all different kinds of antibodies, so the test results are moot.  Your daughter should have the DGP IgG and TTG IgG tests done.   The tests should be performed while she is still consuming gluten.  Stopping and restarting a gluten containing diet can make her more sick, just like you refuse to eat gluten for testing.  Call the doctor's office, request both the IGG tests. Request to be put on the cancellation list for an appointment sooner.  Ask for genetic testing.   Celiac disease is passed on from parents to children.  You and all seven children should be tested for genes for Celiac disease.  Your parents, your siblings and their children should be tested as well.  Eating gluten is not required for genetic testing because your genes don't change.  Genetic testing is not a diagnosis of Celiac disease.  Just having the genes means there is the potential of developing Celiac disease if the Celiac genes are activated.  Genetic testing helps us decide if the Celiac genes are activated when coupled with physical symptoms, antibody testing, and biopsy examination. It's frustrating when doctors get it wrong and we suffer for it.  Hang in there.  You're a good mom for pursuing this!  
    • knitty kitty
      @hjayne19, So glad you found the information helpful.  I know how difficult my struggle with anxiety has been.  I've been finding things that helped me and sharing that with others makes my journey worthwhile. I like Life Extension Bioactive Complete B Complex.  It contains the easily activated forms of B vitamins needed by people with the MTHFR genetic variation often found with Celiac disease.   Avoid B Complex vitamins if they contain Thiamine Mononitrate if possible.  (Read the ingredients listing.)  Thiamine Mononitrate is the "shelf-stable" form of B 1 that the body can't utilize.  B vitamins breakdown when exposed to heat and light, and over time.  So "shelf-stable" forms won't breakdown sitting on a shelf in a bright store waiting to be bought.  (It's also very cheap.)  Thiamine Mononitrate is so shelf-stable that the body only absorbs about thirty percent of it, and less than that is utilized.  It takes thiamine already in the body to turn Thiamine Mononitrate into an active form.   I take MegaBenfotiamine by Life Extension.  Benfotiamine has been shown to promote intestinal healing, neuropathy, brain function, glycemic control, and athletic performance.   I take TTFD-B1 Max by Maxlife Naturals, Ecological Formulas Allthiamine (TTFD), or Thiamax by EO Nutrition.  Thiamine Tetrahydrofurfuryl Disulfide (TTFD for short) gets into the brain and makes a huge difference with the anxiety and getting the brain off the hamster wheel.  Especially when taken with Magnesium Threonate.   Any form of Thiamine needs Magnesium to make life sustaining enzymes and energy.  I like NeuroMag by Life Extension.  It contains Magnesium Threonate, a form of magnesium that easily crosses the blood brain barrier.  My brain felt like it gave a huge sigh of relief and relaxed when I started taking this and still makes a difference daily.   Other brands of supplements i like are Now Foods, Amazing Formulas, Doctor's Best, Nature's Way, Best Naturals, Thorne, EO Nutrition. Naturewise.  But I do read the ingredients labels all the time just to be sure they are gluten and dairy free. Glad to help with further questions.  
    • trents
      Welcome to the celiac.com community @pothosqueen!   Can you be more specific about which IGA test was run that resulted in 114 score and said to be "normal" and could you please include the reference range for what would be normal? By the size of that number it looks like it may have been what we call "total IGA" but that test is not usually run without also running a TTG-IGA. Total IGA tests for IGA deficiency. If someone is IGA deficient, then the celiac-specific IGA tests like the TTG-IGA will be inaccurate. Was this the only IGA test that was run? To answer, your question, yes, a positive biopsy is normally definitive for celiac disease but there are some other medical conditions, some medications and even some food proteins in rare cases that can cause positive biopsies. But it is pretty unlikely that it is due to anything other than celiac disease.
×
×
  • 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.