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 Sensitivity in Celiac Temporary or permanent?


tbiz

Recommended Posts

tbiz Newbie

I was diagnosed as having celiac disease in May via biopsy. I went strictly gluten free immediately after diagnosis.  To make a long story short, i'm not feeling better. I was diagnosed a few weeks ago as having Iron Deficiency Anemia (which is causing me to lose a lot of hair), as well as a folic acid and vit D deficiency. All pretty par for the malabsorption/malnutrition course, as I understand it. 

However, I'm starting to suspect corn may be to blame for me not improving. When having a rare "good" day, i ate a few corn chips and it set everything into motion again. ugh. So i'm now wondering if i'm having an issue with corn as well. But my question is more for the future of this suspected new intolerance--is it permanent? Will I always react to corn? Or is it likely this is just a "while your gut is healing" issue? I ask because i'm not a particularly adventurous eater, and to have to eliminate both wheat AND corn is just a bit much to bear. (and not to mention insanely difficult to manage). 

Will corn damage the intestine like gluten does? (ie: if i want to have a corn cheat--IE, i want to go out to dinner with my family and eat a normal gluten-free meal-- and just suck up the indigestion it brings with it, can i do it without seriously wrecking my health?)

Thank you guys! :)


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

I can say that often intolerances are just temporary, but it can months, years or maybe never to overcome.  Best bet is strict avoidance (corn is everywhere).  I know that milk (I think not lactose related) and other things besides celiac disease can cause intestinal damage in some people, but not sure about corn.  Something worth googling.  

We do have members who have corn intolerances.  Let's hope they chime in.  One is Bartful.

bartfull Rising Star

Ah yes, the dreaded corn intolerance. :angry: It took me three and a half years before I could tolerate corn. I'm not 100% sure if it can cause damage but there have been some studies saying it can.

I got corn starch back first. It supposedly has no corn protein in it. Then I got corn oil back. I never did try corn meal or whole corn. I learned over the years to hate the very idea that corn exists, and frankly if there were some kind of blight that killed every single corn plant in the world I think I'd be happy. It is in EVERYTHING! Bagged salads are cleaned in a veggie wash that is made with corn. Citric acid added to most foods is NOT from citrus fruit, it is from corn.

There are a couple of corn allergy forums on the internet that helped me a lot. If you Google corn allergy you'll find them.

One of the worst things about it is medications and supplements. Most of them use corn starch as a filler. If you take something in a capsule you not only have to check the inactive ingredients but the capsule itself. If it is a gelatin capsule you're fine. If it is a vegetable capsule it's corn. I used to have to get all my meds made at a compounding pharmacy - even my Tylenol. VERY expensive.

All I can tell you is to be vigilant, eat plain whole foods that you made yourself. NEVER eat in a restaurant, and check out those corn allergy sites. If corn is used in processing (like those bagged salads), they don't have to list it on the package because corn is not one of the top eight allergens. I kind of laugh when people use the term "hidden gluten". Gluten grains are almost ALWAYS (except for maybe malt sometimes) listed in the ingredients. CORN is the nasty horrible culprit that is truly hidden.

So, I think I'm pretty good at avoiding corn by now and I'll be happy to help you in any way I can. Fire away with questions or PM me and I'll answer the best that I can.

Oh, and one more thing. I DID get corn back after three and a half years. But I got glutened in June and have lost it again. I'm hoping to get it back again someday, not that I actually want to eat the nasty stuff, but just so if I DO accidentally get "corned", I won't react.

bartfull Rising Star

Open Original Shared Link

bartfull Rising Star

Open Original Shared Link

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. - Florence Lillian replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      13

      gluten free cookie recipes

    2. - Russ H replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    3. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

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

    • Total Members
      132,914
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.