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

Corn Elimination Diet - How Strict? Derived Ingredients?


sreese68

Recommended Posts

sreese68 Enthusiast

I've been gluten-free almost 4 years.  Never cheat.  I just saw a new functional medicine doctor, and she suggested I eliminate corn.  Sigh.  I already have a very limited diet due to sensitivities to: nightshades, brown rice, fructose, sorbitol, mannitol, carrageenan, guar gum, and flax (seed and oil).  I avoid dairy and soy, but I'm not sure they'd still be a problem at this point.  Oh, and too much alcohol is beginning to be a problem.

 

I do eat a lot of corn - grits, pasta, cereal, etc.  I can figure out a way to replace the foods.  What I'm concerned about is eliminating the supplements that have ingredients derived from corn (like fermented corn dextrose). My B vitamin complex has this for instance.  I have some vitamin B deficiencies (nerve problems, hair loss), so I'm hesitant to stop taking it for a few weeks.

 

So do I need to get rid of ALL traces of corn to find out if it's a problem?  Is some OK to leave in during an elimination diet? (supplements, salt, corn vodka).

 

My main health goals right now are to heal my leaky gut, stop the daily muscle twitches in my legs, grow hair, and get my energy levels back.  My energy is just a bit off.  My ferritin dropped, so that may be it. (Yes, I'm addressing it.  I malabsorb iron.)


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

I was HIGHLY intolerant to corn for a few years. I know a lot of folks here with soy intolerance (I used to have that too) complain that soy is in everything but soy is EASY compared to corn. For one thing, soy is one of the big eight so it will be labeled for, but corn is not so if it is used in processing they don't consider it an ingredient so it won't be mentioned on the label.

 

Here is an example - ready to eat bagged salads and carrots. They are pre-washed in a vegetable wash made with corn. That is never mentioned on the label.

 

Another example: the lining in cans. Used to be most were made with BPA's but because those are bad for people a lot of companies are using a corn based plastic. Same thing with the crystal clear plastic used in individual servings of water. The thing is once again, not all companies will mention it on the label.

 

Yet another example: ascorbic or citric acid. You'd think they were from citrus fruits but they can get it from corn and corn is much cheaper so IS made from corn. I had a particularly bad reaction to that one time and I literally thought I was going to die.

 

Corn starch and corn oil usually don't have corn protein in them. I was even reacting to those at first though. After a while I got them back but the one and only time I got glutened in almost four years, I lost them for a while.

 

Corn dextrose as well as maltodextrin are made from corn starch so there should be no protein in them. The salt, if it is iodized might be a problem because, if I'm not mistaken, it is carried on citric acid. But you can get sea salt instead. Corn vodka is distilled so there should be no protein left in that either, but if you wanted you could buy vodka made from potatoes.

 

So if I were you I would start by only eliminating those things that have corn protein in them. If you don't see improvement within six weeks or so, try eliminating the rest of the corn.

w8in4dave Community Regular

I am corn intolerant, soy intolerant, Lactose intolerant. I can eat cheese now but cannot drink a glass of milk. I am Low on Folic acid wich is a B9 I believe. I just don't eat much Bagged or boxed or canned except for Salads (I wash it 1st) And I also eat Rice but make sure it is Gluten free, other than that I eat fresh meat, and fresh vegetables that I wash. I also buy tea bags. I think I skip the being afraid of being Glutened , or getting Corn in me. Once in a while I will get some Beanito's Or some rice crackers, but not too much.

MycasMommy Enthusiast

I cannot do corn either. I am still reacting to corn starch... I do not know about the protein deal with it, only that it makes me violently ill. Corn Syrup is is just about everything, including corn syrup solids in Udi's products.  It almost tricked me because I thought it just CANNOT BE a gluten issue since it is UDI'S!  It took a bit of work to figure out that corn was off the menu. The only grain I can safely digest seems to be rice. Period.

 

Bartfull...  even now I did not know that about the pre packaged salads!  I was just getting sick from them and NEVER buy them anymore. HA.. Learned something new today, I did!

 

I tried corn a few weeks ago to see if I could handle it after 14 months gluten-free.. nope.. an enormous nope. I will try again in maybe 6 months though.

cahill Collaborator

Most medications use corn/corn starch . To totally eliminate corn is nearly imposable but doable if you are extremely strict .When I eliminated corn I did not eliminate my medications and was lucky enough that I did not have to .

 

 

Bartfull is correct that soy is one of the big 8 allergens so listed on packaging EXCEPT soy oil . There is a loophole in the law that does not require that soy oil be listed as an allergen on packaging

  • 1 month later...
sreese68 Enthusiast

A belated thank you to everyone who posted!!!  I kept meaning to reply, but I've been caught up researching another complex health issue I'm probably going to be diagnosed with soon.  Anyway, it's taken me this long to introduce a couple of other grains (as well as some needed supplements), so that I can cut corn out.  It's only been a few days so far, and at this point, I can only cut out corn as food.  It's in too many supplements that I need for me to cut it out 100%.  I'm going to give it a couple of months and see what happens.

 

Thanks again!!

Archived

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

  • 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. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    2. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    3. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    4. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    5. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,155
    • Most Online (within 30 mins)
      7,748

    lfedas
    Newest Member
    lfedas
    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

    • trents
      This article does not address migraines at all.  Yes, red wine and sulfites are often mentioned in connection with migraine triggers. With me, any kind of alcoholic beverage in very modest amounts will reliably produce a migraine. Nitrous oxide generators, which are vaso dialators, also will give me migraines reliably. So, I think most of my migraines are tied to fluctuations vascular tension and blood flow to the brain. That's why the sumatriptan works so well. It is a vaso constrictor. 
    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
×
×
  • 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.