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

Did I Get Glutened Or...?


CNV2855

Recommended Posts

CNV2855 Contributor

A couple months ago, I made some cornbread, which isn't something I usually eat, and roughly around that time I started feeling poorly. I really wasn't sure what was going on because I didn't notice any GI symptoms so I figured it was just an autoimmune flare. It took me a week to eat the cornbread and I stayed sick for about a week and then over the next couple weeks I bounced back to normal.

Then last week I decided to make some more cornbread. I slowly got sick the first day I ate it, then the second, and I stopped eating it and immediately felt better. This time I did notice very slight GI symptoms and my rash reappeared, something that only happens when I'm glutened. I waited a day or two then ate one more piece of cornbread just to be sure...(and because it was delicious :) and immediately felt horrible for about two days.

Now I've had partial resolution of my symptoms gluten free but not total. I'm not sure what is going on though, the corn flour I used was BRM from a local health food store, and there's very little risk of CC on my kitchenware because I cook my own food. Bob's Red Mill is supposed to be good with contamination, aren't they?

These symptoms I experienced were exactly the same everytime I get glutened, It just seemed like I recovered from it much quicker - and with much less GI symptoms.

Even the rash which was completely gone (suspected DH) reappeared and started flaring again.

Stopped eating corn since this incident and I'm just now about getting back to normal. Even if corn is completely safe for us, which science tells us it is - and I believe them - then if a specialized corn product that I bought in a health food store is giving me a reaction due to CC, then how do I know the corn used in the manufacture of any generic processed food isn't contaminated? If we're to avoid oats because of possible cross contamination, then what about corn?

Thinking back, I typically remember having some sort of reaction almost every time that I've tried corn chips, and I always put it down with me just being super sensitive or being unlucky with cross contamination. Frito Lay does put out the disclaimer that equipment is shared.

Could I be having a reaction to the corn though? Like oats?

I'm having an endoscopy done monday and I'm pretty anxious to see the results.


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



Celiac.com Sponsor (A8-M):



Roda Rising Star

Are you sensitive to oats? If so Bob's Red Mill may not be safe for you. They process gluten free oats on shared lines so there is the potential for cross contamination from them. I don't tolerate any of their products anymore. You could have an issue with corn also. I'm not very helpful on the corn aspect though.

cait Apprentice

BRM makes a gluten-free corn flour and a non-gluten-free (presumably the same thing but manufactured in different plants). If you accidentally grabbed the wrong bag, it could be CC from that. But corn affects some people in ways similar to gluten, so it could also be that. Sorry it made you feel lousy. Discovering new problems sucks.

CNV2855 Contributor

BRM makes a gluten-free corn flour and a non-gluten-free (presumably the same thing but manufactured in different plants). If you accidentally grabbed the wrong bag, it could be CC from that. But corn affects some people in ways similar to gluten, so it could also be that. Sorry it made you feel lousy. Discovering new problems sucks.

Well I'd rather discover what's making me ill, than stay ill.

If I'm sensitive enough to react to CC in corn, assuming that's the problem, is HFCS an ingredient I can count on being gluten free or not? If I react to corn CC, I'd assume that I'd have very, very minor reactions to HFCS and other corn byproducts, right?

cait Apprentice

Well I'd rather discover what's making me ill, than stay ill.

If I'm sensitive enough to react to CC in corn, assuming that's the problem, is HFCS an ingredient I can count on being gluten free or not? If I react to corn CC, I'd assume that I'd have very, very minor reactions to HFCS and other corn byproducts, right?

I think it's less likely that you're reacting to inherent CC in corn and more likely that either the corn flour was processed in a factory that also deals with wheat, or that you're reacting to corn in general for reasons other than CC. BRM marks things pretty clearly. If the corn flour says gluten free, then it's probably a problem with corn and you should avoid corn products for a while and then test them to see if you get the same reaction. If the bag does not say gluten free, then maybe that flour was processed in a BRM factory that also processes gluten grains and therefore WAS contaminated. In that case, corn in general might not be a problem. Just corn processed in a plant with wheat, etc.

CNV2855 Contributor

I think it's less likely that you're reacting to inherent CC in corn and more likely that either the corn flour was processed in a factory that also deals with wheat, or that you're reacting to corn in general for reasons other than CC. BRM marks things pretty clearly. If the corn flour says gluten free, then it's probably a problem with corn and you should avoid corn products for a while and then test them to see if you get the same reaction. If the bag does not say gluten free, then maybe that flour was processed in a BRM factory that also processes gluten grains and therefore WAS contaminated. In that case, corn in general might not be a problem. Just corn processed in a plant with wheat, etc.

Yeah, but what guarantees are there than generic corn byproducts like "HFCS" aren't also produced in a facility with wheat?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,584
    • Most Online (within 30 mins)
      7,748

    MaMa Donna
    Newest Member
    MaMa Donna
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Ben98! If you have been consciously or unconsciously avoiding gluten because of the discomfort it produces then it is likely that your blood antibody testing for celiac disease has been rendered invalid. Valid testing requires regular consumption of generous amounts of gluten. The other strong possibility is that you have NCGS (Non Celiac Gluten Sensitivity) which shares many of the same symptoms with celiac disease but does not have the autoimmune component and thus does not damage the small bowel lining. It is 10x mor common than celiac disease. There is currently no test for NCGS. Celiac disease must first be ruled out. Some experts in the field believe it can be a precursor to the development of celiac disease. Having one or both of the primary genes for developing celiac disease does not imply that you will develop active celiac disease. It simply establishes the potential for it. About 40% of the population has the genetic potential but only about 1% develop active celiac disease. 
    • Ben98
      TTG blood test and total IGA tested on many occasions which have always remained normal, upper GI pain under my ribs since 2022. I had an endoscopy in 2023 which showed moderate gastritis. no biopsy’s were taken unfortunately. genetic test was positive for HLADQ2. extreme bloating after eating gluten, it’ll feel like I’ve got bricks in my stomach so uncomfortably full. the pain is like a dull ache under the upper left almost like a stitch feeling after a long walk. I am just wanting some advice has anyone here experienced gastritis with a gluten issue before? thank you  
    • Wheatwacked
      "Conclusions: The urinary iodine level was significantly lower in women with postmenopausal osteoporosis, and iodine replacement may be important in preventing osteoporosis"  Body iodine status in women with postmenopausal osteoporosis Low iodine can cause thyroid problems, but Iodine deficiency will not show up in thyroid tests.  Iodine is important for healing, its job is to kill off defective and aging cells (Apoptosis). Skin, brain fog, nails, muscle tone all inproved when I started taking 600 mcg (RDA 150 - 1000 mcg) of Liquid Iodine drops. Some with dermatitis herpetiformis, Iodine exacerbates the rash.  I started at 1 drop (50 mcg) and worked up to 12 drops, but I don't have dermatitis herpetiformis.
    • cristiana
      That's great news, you can do this.  Let us know how things go and don't hesitate to ask if you have any more questions. Cristiana 😊
    • petitojou
      Thank you so much for sharing your experience and I found myself giggling with happiness as I read how your body reached such spring! And I hope that your current journey is also successful!! Definitely starting the food diary! So many amazing advices. And it’s very scary. It really hits all our soft spots as well as our confidence system. Most doctors I went thought I was underage despite being in my late 20s. Right now I look like am I twelve, but is also this body that’s taking so much, so I might as well love it too! Going to make the necessary changes and stay in this path. Thank you again! 🫶
×
×
  • 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.