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. - JoJo0611 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Awaiting Biopsy results

    2. - cristiana replied to emzie's topic in Related Issues & Disorders
      1

      Stomach hurts with movement

    3. - emzie posted a topic in Related Issues & Disorders
      1

      Stomach hurts with movement

    4. - Flash1970 replied to Ginger38's topic in Related Issues & Disorders
      3

      Shingles - Could It Be Related to Gluten/ Celiac


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,455
    • Most Online (within 30 mins)
      7,748

    jscal6
    Newest Member
    jscal6
    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

    • JoJo0611
      I have had my endoscopy this morning with biopsies. My consultant said that it looked like I did have coeliac disease from what he could see. I now have to wait 3 weeks for the biopsy results. Do I continue eating gluten till my follow appointment in three weeks.  
    • cristiana
      Hi @emzie and welcome to the forum. Perhaps could be residual inflammation and bloating that is causing sensitivity in that area.  I was diagnosed with coeliac disease in 2013 and I remember some years ago my sister telling me around that time that she had a lady in her church, also a coeliac, who  had real pain when she turned her torso in a certain direction whilst doing exercises, but otherwise was responding well to the gluten-free diet. As far as I know is still the picture of health. I often end up with pain in various parts of my gut if I eat too much rich food or certain types of fibre (for some reasons walnuts make my gut hurt, and rice cakes!) and and as a rule, the pain usually hangs around for a number of days, maybe up to a week.   When I bend over or turn, I can feel it.  I think this is actually due to my other diagnosis of IBS, for years I thought I had a rumbling appendix but I think it must have just been IBS.  Reading the experiences of other sufferers, it seems quite typical.  Sensitized gut, build up of gas - it stands to reason that the extra pressure of turning can increase the pain. When I am glutened I get a burning, gnawing pain in my stomach on and off for some days - it isn't constant, but it can take up a few hours of the day.  I believe this to be gastritis, but it seems to hurt irrespective of movement.   Anyway, you are doing the right thing to seek a professional opinion, though, so do let us know how you get on.   Meanwhile, might I suggest you drink peppermint tea, or try slices of fresh ginger in hot water? A lot of IBS sufferers say the former is very helpful in relieving cramps, etc, and the latter is very soothing on the stomach. Cristiana
    • emzie
      Hi! One of the usual symptoms I have with a gluten flare up has deviated a bit and I thought I'd search for advice/opinions here. Also to see if anyone goes through similar stuff. Monday all of a sudden I got really bad pain in my stomach (centre, right under the chest, where the duodenum would be located). I ended up having to throw up for 2 hours, my body was trying to get rid of something from all sides and it was just horrible. Since then I havent been nauseous anymore at all, but the pain has stayed and it always worsens the moment i start moving. The more I move the more it hurts, and when i rest longer it seems to dissapear (no movement). I've had this before, but years ago I think around when I first got diagnosed with coeliac, where each time I moved, my stomach would hurt, to the point where I went to the ER because doctors got freaked out. That only lasted 1 night though, and Now it's already wednesday, so 3 days since then, but the pain persists and remains leveled. it doesn't get crazy intense, but it's still uncomfortable to the point I cant really go out because Im afraid itll turn into a giant flare up again. I couldn't think of where I could possibly have been glutened at this bad of a level and why it hasn't passed yet. I went to the GP, and as long as I have no fever and the pain isnt insane then its fine which I havent had yet. Tomorrow im also seeing a gastroenterologist specialized in IBS and coeliac for the first time finally in years, but I thought I'd ask on here anyway because it still hasnt dissapeared. It also hurts when someone presses on it. Maybe it's just really inflamed/irritated. I'm just frustrated because I'm missing out on my uni lectures and I do a sports bachelor, so I can't get behind on stuff & next to that i'm also going to go to the beach with my boyfriend's family this weekend: ( 
    • Flash1970
      Hi. So sorry to hear about your shingles. There is a lidocaine cream that you can get at Walmart that will help numb the pain.  That's what I used for mine. It can't be put near your eyes or in your ears. I hope your doctor gave you valacyclovir which is an antiviral.  It does lessen the symptoms. If it is in your eyes,  see an ophthalmologist.  They have an antiviral eye drop that can be prescribed.  Shingles in the eye could cause blindness.  I was unsure whether you have celiac or not.  If you do,  follow the diet.  I believe that extra stress on your body does affect everything. Shingles can recur. If you start getting the warning signs of nerves tingling,  see the dr and start taking the valacyclovir to prevent a breakout. If I sound technical,  I am a retired pharmacist. 
    • Scott Adams
      You are right to be proactive, as research does indicate that individuals with celiac disease can have a higher predisposition to enamel defects, cavities, and periodontal issues, even with excellent oral hygiene. While many people with celiac successfully undergo orthodontic treatment without complication, your caution is valid. It may be beneficial to seek a consultation with an orthodontist who is familiar with managing patients with autoimmune conditions or who is willing to collaborate with your daughter's gastroenterologist or a periodontist. They can perform a thorough assessment of her current oral health, discuss your specific concerns about recession and decay, and create a tailored hygiene plan. This second opinion could provide a clearer risk-benefit analysis, helping you decide if addressing the cosmetic concern of the lower teeth is worth the potential risks for your daughter, especially if they are not currently affecting function or her confidence. 
×
×
  • 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.