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

Could Some Corn Intolerant People Help Me?


Newtoitall

Recommended Posts

Newtoitall Enthusiast

When you eat corn, what are the reactions to it?

how long does it take to react?

and how long does it last, I am trying desperatly to figure out if I am just still getting small amounts of CC or have corn intolerance.

It just seems like I react to anything with corn in it.


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



Celiac.com Sponsor (A8-M):



BakingQueen Newbie

I'm corn intolerant, and it seems to give similar symptoms as gluten for me. I have heard that it is very common for Celiacs to have trouble with corn

Jestgar Rising Star

Three days for processed corn. My psoriasis flares and my joints hurt. Whole corn takes a couple hours and leaves my body suddenly and painfully. :blink::ph34r: :ph34r:

srall Contributor

My corn reaction is very similar to my wheat reaction, except I get very itchy skin as well. So, extreme abdominal cramping, brain fog, joint pain. I think it passes more quickly than wheat gluten. Also I don't have severe reactions to trace amounts like eating something made with baking powder, although I avoid this. Whereas gluten I would NEVER eat in trace amounts.

RollingAlong Explorer

Can you eat corn on the cob?

cassP Contributor

i am very much like "srall"... as in, it affects me similar to gluten, but goes away quicker- and i dont react to trace amounts like i would with gluten. my symptoms are intestinal cramping, pain, a little tachycardia and hbp, little itchy, a little bit nasal allergies (maybe i also have a little allergy??, but no hives)

domesticactivist Collaborator

My son has a histamine reaction to corn (all stuffed up, "hay fever" symptoms, circles under eyes) as well as brain fog and fatigue. He gets the brain fog and fatigue with gluten but also gets joint pain and stomach aches, etc from it.


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

Jestgar, I too have psoriasis, and I'm on day six of my gluten free diet. By day three I saw a very noticable improvement in my psoriasis. Then I bought some gluten free cornbread mix. Today my P is worse again, so I'm thinking it might be the corn.

But now what should I do? Most of the flour mixtures I have seen here and other places contain corn starch. How can I bake a decent tasting bread without it? I can't imagine living without SOME kind of bread. Giving up the processed foods is easy, but bread was always one of my favorite things to eat. :(

sa1937 Community Regular

But now what should I do? Most of the flour mixtures I have seen here and other places contain corn starch. How can I bake a decent tasting bread without it? I can't imagine living without SOME kind of bread. Giving up the processed foods is easy, but bread was always one of my favorite things to eat. :(

If you bake your own bread from scratch, I'm sure you could substitute arrowroot for the cornstarch.

domesticactivist Collaborator

Watch out for arrowroot. My son and I both react to it dramatically. I don't know if it is cc'd or if it is a problem in itself.

Jestgar Rising Star

I can eat small amounts of corn without noticeable problems. Maybe you'll find a level that works for you as well. You also might react to corn, but not corn starch (not enough protein to bother you). The only way to find out is to experiment. I would avoid corn as much as possible until you get the gluten-free thing figured out, and then start testing.

cahill Collaborator

Fortunately, corn is something that I have been able to add back in to my diet ,,in limited amounts.

I can eat corn(whole corn,corn on the cob ect...) with no problems.

Processed corn(Fritos,corn chips,corn bread ect....) I still get that hole in the gut / brick in the gut feeling if I eat more than a small amount.

Cinderella10 Newbie

I haven't done a lot of experimentation with my corn issues, but here's what I have noticed:

In very small amounts, I can have it, though I do prefer making my own baking powder.

When I get too much corn, I get pain & cramping & D, but like the others said, once it's out of my system, it's out. It also exacerbates my eczema.

Newtoitall Enthusiast

lol..

guess I am the only one who seems to get constipated by it >_>

I had 4 extra strength tylenol (the source of corn I believe) when I nearly broke my ankle, and have been having light stomach issues since.. that was.. tuesday only now starting to get over the constipation...

I suppose everyone can have different reactions to corn?

cahill Collaborator

lol..

guess I am the only one who seems to get constipated by it >_>

Most of my dietary issues have resolved unless I get glutened or CC. , I get D if glutened and C from soy . I still get constipated by large amounts of cheese ( but I think that is a NORMAL :lol: , reaction to large amounts of cheese .

Also if my thyroid is off (hypo) I get constipated .

  • 1 month later...
SkyRed70 Newbie

When you eat corn, what are the reactions to it?

how long does it take to react?

and how long does it last, I am trying desperatly to figure out if I am just still getting small amounts of CC or have corn intolerance.

It just seems like I react to anything with corn in it.

I just had my first reaction to corn at the beginning of May of this year, so I'm still figuring this out.

Here are my reactions:

Corn kernels - esophageal swelling within minutes

Corn syrup - lump in the throat

Cornstarch - tickly scratchy throat

Citric acid - hives and itchy/scaley skin, scratchy throat like post nasal drip and a migraine, usually next day

White vinegar - hives and itchy/scaley skin

Xanthan gum - hives and itchy/scaley skin

I still accidentally get corned but I have been keeping a food diary since my corn reaction so I've been figuring most of it out thanks to this list I found on the net: Open Original Shared Link HTH!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,861
    • Most Online (within 30 mins)
      7,748

    Priscilla Buxton
    Newest Member
    Priscilla Buxton
    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

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.