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

Corn Problems?


bbdailey

Recommended Posts

bbdailey Explorer

Hey everyone! So Ive been gluten-free for a while now but starting Dec 1 I went on a very strict elimination diet. Around Dec 20 I broke and made some gluten-free cookies and seemed to be fine. Multiple days later I wasnt feeling quite as good(nothing crazy just felt mentally not quite as good. On Dec 26 I reintroduced corn into my diet(honey nut chex) with no reactions. I have been eating it alot since but I feel like mentally Im not feeling quite as well. Im starting to wonder if corn is giving me a slow and almost silent reaction and bringing me down mentally days after. Anyone have similar experiences with corn?


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



Celiac.com Sponsor (A8-M):



Jestgar Rising Star

I don't have mental issues (ok, some might say I do :P ) with corn, but my joint reaction is delayed by three days.

ciamarie Rookie

You might want to try something else that is just corn (like tortillas? or another brand of organic corn cereal), and see if it's any different. I generally react to things within a few hours, or less. I think I've read that the chex cereals are manufactured in the same facility as their gluten-y cereals. I avoid them because I believe the vitamin E they add as a preservative is from soy, though as I recall they don't have soy on the ingredient list. (Most vitamin E is derived from soy, afaict.) I also personally try to stick to organic corn items only, since otherwise there's a possibility that the corn is GMO, and they don't label it so you can tell the difference.

Bubba's Mom Enthusiast

I've been reading the book "Against the Grain". It tells the effect of various grains, including corn. If you think you're having a reaction to corn, reading that book will be a real eye-opener.

Maybe see if your library has a copy?

The Chex cereals are made on equipment that also processes wheat. It's possible to get a batch of sereal with trace CC.

Aly1 Contributor

Interesting the timing of your post, I literally just read an old post that touched on exactly this. Go to and scroll down to Evangeline's post. It was an eye opener for me (I have corn issues too).

domesticactivist Collaborator

My son is allergic to corn in the typical IgE sense but he also gets bad brain fog from it. We are all better off since cutting it and all grains from our diet. We are now on GAPS. There are a couple great sites out there with lists of all the things that contain corn. It doesn't get labeled consistently due to not being a top 8 allergen. Sticking to whole foods is the best way to completely avoid it.

The most surprising source is the citric acid wash used on USDA meat. (citric acid is usually corn derived these days) Fortunately our son doesn't have a severe reaction to such low levels, but when we buy USDA meat for a while it brings back his symptoms. Usually we buy oda meat farm direct and check with the slaughterhouse to make sure they do not use the citric acid on our meat.

bartfull Rising Star

My corn reactions take between eight and twelve hours. But we are all different.

That citric acid wash made from corn is also used on bagged salads and other "pre-washed" veggies. Baby carrots are washed in this stuff, and some brands even dust their frozen vegetables with corn starch to keep them from sticking. Anything that is vitamin fortified, such as milk, most likely has corn in it because corn is the "carrier" of the vitamins. Corn is also the carrier of iodine in iodized salt. (I use only natural sea salt.) If you see something that mentions "flavor", whether it is "natural" or artificial, it is carried (most likely) on corn.

So, yeah, whole foods only is the way to go. Organic if possible, although even THAT doesn't guarantee that there won't be hidden corn somewhere. :angry:


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



Celiac.com Sponsor (A8-M):



Skylark Collaborator

My milk reactions can take a couple days. If you're feeling "iffy" I'd go back to strictly corn-free and see if you get back to feeling well.

bbdailey Explorer

Thanks for the comments! I think I am going to cut corn out until I visit the allergist on Jan 13 and then hopefully I can get some kind of answers. I hope that it isnt corn because corn is in everything:(

bbdailey Explorer

If you have a corn allergy does that mean you cant have anything with corn in it? I thought I heard somewhere that some people can tolerate certain types of corn in certain cases.

bartfull Rising Star

Some people CAN tolerate processed corn but not whole corn. Some are the opposite and have no trouble with whole corn, but can't tolerate the processed stuff. And then there are people like me who are extremely sensitive to corn in any form. (No wonder it takes so long to figure our diets out!)

domesticactivist Collaborator

It depends. For my son, the symptoms from corn look like seasonal allergies. Any tiny amount of corn gives him these symptoms. It also makes him much more reactive to other things he's allergic to. When he had corn as a regular part of his diet he was always really inflamed, and his actual seasonal allergies blew him up like crazy. When he's off corn he can handle some grass pollen, weed pollen, tree pollen, etc. A runny, stuffy nose, puffy, itchy red eyes, dyslexia, and the occasional hives aren't going to harm him the way he'd be harmed by eating gluten. Some people with IgE reactions like my son typically have anaphylactic responses to some of the things they are allergic to. That would call for total avoidance. We try for total avoidance because he gets miserable symptoms, but we aren't completely fanatical about it because it's not a life or death situation.

Aly1 Contributor

Wow there's so much to learn on this forum. I had no idea there was hidden corn everywhere! This makes me rethink things a lot - I regularly find myself with a runny nose at dinner and can't figure out where it might have come from (that's a typical corn reaction for me, as are joint pains). Great posts. :)

Skylark Collaborator

My dairy issues seem dose-related. I got the wrong plate of scrambled eggs by mistake over vacation and they had a little milk. I didn't notice any reaction. That led me to think maybe I could have a nice slice of cheese and there was brie around. I thought I got away with it yesterday, but then the fog hit today. Oops. The brie was almost worth feeling crummy. :lol:

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - PixieSticks replied to PixieSticks's topic in Super Sensitive People
      2

      Working in a kitchen with gluten?

    2. - BoiseNic replied to BoiseNic's topic in Dermatitis Herpetiformis
      11

      Skinesa

    3. - knitty kitty replied to Whyz's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      Feeling ill

    4. - Scott Adams replied to Brianne03's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Advantages vs. Disadvantages of having an official Celiac diagnosis

    5. - Scott Adams replied to Whyz's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      Feeling ill


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,535
    • Most Online (within 30 mins)
      7,748

    Annette Smith
    Newest Member
    Annette Smith
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.5k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • PixieSticks
      Hi yes! I was diagnosed 10 years ago through a biopsy. I’ve been gluten free ever since but no one I’m around is gluten free. I sometimes wore a surgical mask in the kitchen. but I believe particles were still getting through. I’ll definitely look into n95 instead. thanks for the reply. 
    • BoiseNic
      Ya I used to react to iodine, but it doesn't bother me anymore after strict adherence to a gluten-free diet for many years now. I am happy to report that for the first time ever in my life, a probiotic formula is not making me break out, but actually seems to be helping. The strains in this formula have been specifically tested to help with skin issues. It is gluten and dairy free also. 
    • knitty kitty
      @Whyz, I take a combination of Thiamin (Benfotiamin), B12 Cobalamine and Pyridoxine B6 for my pain and headaches.  Really works well without hurting the digestive tract.  Riboflavin B2 also helps with migraines.  Most newly diagnosed people have vitamin and mineral deficiencies.  Check with your doctor and nutritionist.   If you follow the updated gluten challenge guidelines, you can wait until two weeks (minimum) before your appointment, then eat lots of gluten, like six slices of gluten containing bread or "name your poison".   Here's the Updated Gluten Challenge Guidelines: Recommended intake of gluten should be increased to 10 grams of gluten per day for at least two weeks. Or longer. While three grams of gluten will begin the immune response, ten grams of gluten is needed to get antibody levels up to where they can be measured in antibody tests and changes can be seen in the small intestine.   Keep in mind that there are different amounts of gluten in different kinds of bread and gluten containing foods.  Pizza crust and breads that are thick and chewy contain more gluten than things like cake and cookies.   References: https://www.beyondceliac.org/celiac-disease/the-gluten-challenge/ And... Evaluating Responses to Gluten Challenge: A Randomized, Double-Blind, 2-Dose Gluten Challenge Trial https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878429/?report=reader  "In our study, limited changes in Vh:celiac disease (villi height vs crypt depth - aka damage to the small intestine)  following 14-day challenge with 3 g of gluten were observed, in accordance with Sarna et al.  While the 3 g dose was sufficient to initiate an immune response, as detected by several biomarkers such as IL-2, the 10 g dose was required for enteropathy within the study time frame. Based on our data, we would suggest that gluten challenge should be conducted over longer durations and/or using doses of gluten of ≥ 3 g/day to ensure sufficient histological change can be induced." Keep us posted on your progress!
    • Scott Adams
      I don't believe that existing life insurance policies require such notifications--health checks are typically done before such policies are obtained. I believe it would primarily affect any new policy you get, and perhaps any policy renewal.
    • Scott Adams
      You could go gluten-free now, and then start eating lots of gluten for at least 2 weeks before your endoscopy--just be sure to tell your doctor about this beforehand. If your symptoms go away on a gluten-free diet, it is further evidence of celiac disease and/or non-celiac gluten sensitivity.  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.  
×
×
  • Create New...