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?


raen

Recommended Posts

raen Apprentice

corn is generally regarded as OK by celiacs, but i read on celiac.com that it has never been seriously examined, and has some "suspicious" traits, same for rice, millet, teff, etc. "gluten-free" Oats i can say for a fact give me a gluten-reaction, so i am very suspicious.

the past couple of weeks, i have felt just awful, and taking item after item out of my diet until i was down to fruit, veggies, buffalo, and cerial, i was able to pinpoint what i was reacting to.

CORN of all things

this would mean nothing, if i had not been gluten-free for months now.. and able to eat most of what i could not digest before.. and the corn reaction is SUSPICIOUSLY similar to my gluten-reaction.. its exactly like a mild version!

is the reaction just because its been 5 months, and may be better by 8, or is it possible, if your allergic enough to gluten, to have a gluten-reaction to corn?? what about rice? (rice makes my stomach feel strained, similar to gluten)


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



Celiac.com Sponsor (A8-M):



Trust Birth Rookie

Hello there,

My DS had been off gluten for months and also had a strong reaction to corn. I had started putting corn meal in his pancakes and it was fresh corn season so he was having corn on the cob. Each time he had these things, he had the same reaction as he does to gluten (IBS mostly). I'm unsure of exactly why this is but we took him off of it and his symptoms disappeared. Corn is very difficult to avoid, more so then gluten. It is in everything. He seems OK with small amounts here and there (cornstarch in bread) but for the most part I avoid it as it causes him some grief. He doesn't like cereal, so he doesn't get it in that. I try to buy bread without it. I have heard of other celiacs having a problem with corn in the beginning but they are able to eat it after observing a gluten free diet for a year or so.

HTH

Cinthia

YoloGx Rookie

Corn is one of the common allergens. Part of this may be that it often has mold in it due to the high sugar content. However of that I don't really know for certain. I am able to tolerate it better than I used to I think mainly because I almost never have it regularly, i.e., every day or even every week. I also make sure now that its labeled gluten free which does seem to help. Its one of the few things I got right as a child since my brother with Down's was allergic to it too and I sometimes copied what he could or couldn't eat; I thus avoided it for the most part, and saved it for when we'd have corn on the cob or special occasions when we'd have cornbread. Of course the wheat part didn't agree but back then that's what I had regularly anyway...

Bea

mushroom Proficient

Corn was the first thing I cut from my diet when I moved to the US because I didn't know then that I had a problem with gluten. It made a lot of diference but was not the whole answer. Then came lactose, and finally, 15 years later, gluten, followed by soy.

IMHO, it is the genetic modification of corn that has created problems for those of us sensitive to it. The New Zealand corn is mostly GE free, and I can eat it in moderation (due to previous reactions would never consider anything but moderation :P ) without any problem. Also Garden of Eatin' organic corn chips are just fine. My extremelly celiac niece can also eat these corn chips, but no others. Also, I do not have any problems with cornstarch.

YoloGx Rookie
Corn was the first thing I cut from my diet when I moved to the US because I didn't know then that I had a problem with gluten. It made a lot of diference but was not the whole answer. Then came lactose, and finally, 15 years later, gluten, followed by soy.

IMHO, it is the genetic modification of corn that has created problems for those of us sensitive to it. The New Zealand corn is mostly GE free, and I can eat it in moderation (due to previous reactions would never consider anything but moderation :P ) without any problem. Also Garden of Eatin' organic corn chips are just fine. My extremelly celiac niece can also eat these corn chips, but no others. Also, I do not have any problems with cornstarch.

That makes sense! I'll try those corn chips sometime though chips in general are things I avoid these days for the most part.

As far as the gluten-free cornmeal/flour I usually use the blue corn. Its more ancient when you stop and think about it. Less likely to be genetically altered perhaps?

By the way, how can you tell where the cornmeal/flour comes from?? Especially from NZ?

Bea

mushroom Proficient

[quote name='yolo' date='Oct 5 2008,

By the way, how can you tell where the cornmeal/flour comes from?? Especially from NZ?

Bea

ArtGirl Enthusiast
.. and the corn reaction is SUSPICIOUSLY similar to my gluten-reaction.. its exactly like a mild version!

My experience exactly. A milder form of gluten symptoms. It took me a while to discover what the problem was after I went gluten-free. And I was really loving the Bob's Red Mill gluten-free chocolate cake mix - has a lot of corn meal in it.

Until the last few months I have avoided any corn derivative - including citric acid, dextrose, etc. It's been a real challenge being 100% corn-free - MUCH HARDER than just gluten-free. Corn is EVERYWHERE! I just did a corn challenge yesterday to see if I could now, after over a year, tolerate corn - NOPE! I'm mildly ill today. Looks like it's a lifetime allergy for me!

I can, however, eat CC-free oats without any reaction. Millet is okay with me, too.


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



Celiac.com Sponsor (A8-M):



YoloGx Rookie

GM corn is not allowed to be planted here although some has snuck in undetected, later revealed. So there is really not a cross-contamination issue yet. There are however a lot of GM field trials of various crops under way at the Ag colleges (they must be terminated before the plants flower.)

A neighbour thought she was doing me a favour by bringing me a bag of imported stovetop popping corn from the U.S. I thanked her, served her NZ popcorn from my corn popper, and threw hers in the trash after she left. So the answer is "buy New Zealand". Since I already put the labels under a microscope, it is not difficult :P

Incidentally, it could be the problem with soy too?? Most (if not all) of our soy is imported.

Neroli

mushroom Proficient

You guys have so much corn over there, I don't imagine you import any from little ol' New Zealand :rolleyes: . Garden of Eatin' corn chips are produced by the Hain Celestial Group in New York. They do not claim to be GM-free but they are organic.

NZ is a little behind the U.S. in celiac knowledge and food availability, though it is gaining in leaps and bounds. We have a pretty solid British background, lots of Irish and Scots, so celiac is quite prevalent. It sure seems to run in our family. Mother I am sure was undiagnosed (terrible digestive problems), Dad had rheumatoid arthritis, one of my sisters is celiac, as is her daughter; the other sister will not admit to being celiac but I am sure she is. I used to "self-medicate" my gut with scotch, which was the only thing that would shut it up!! Even though I had a celiac sister and niece, I still thought my problem was corn.

I have only eaten out at one restaurant (twice), and without problems. We have a wonderful local gluten free bakery which makes things (besides great bread) like quiches, pizzas, the good ole NZ bacon and egg pie, meat pies (also a Kiwi staple) doughnuts, and other confectionery. I spend a lot of money there!!

That is really funny about you and your ex-boyfriend, dealing with the same issues without knowing it!! (LOL)

Didn't you two ever talk?? :lol:

Neroli

raen Apprentice

CC-free oats give me standard gluten reaction, but corn i feel i may be able to eat in a few more months, because eating things containing Citric Acid and other small amounts of corn seems to leave me feeling un-glutened. it was strait up corn cereal (Gorilla Munch - 100% gluten-free kids cereal with only 3 ingredients) that made me feel sick.

i am so much more concerned about rice now.. rice gives me a full-blown gluten reaction! i get a white coating on my tongue, stomach pains, belching, nausea, lightheaded for days, cant sleep, huge appetite, constipation, tense, etc. it could be a "rice allergy" .. except that i react like gluten. is it just because its so starchy? i thought rice was easy to digest?

it is reassuring to know many celiacs can eat these after a year, though.

----

latley i think im going insane and will either die of lack of edible foods or become the healthiest person alive.

scaled fish, egg yolks/whites/chickens & onions (except green), bananas, chocolate, peanuts/nuts may be an allergy. cellary gives me awful digestive problems. soy, tomatoes, garlic, apple cider vinegar, & low acid gluten-free orange juice may or may not make me sick.

cutting out gluten/milk was an easy adjustment, mentally, but how do you deal with the anxious fear of "what can i even eat?" it seems like i cannot be getting good nutrition with so much cut out of my diet with only red meat, vegetables, and fruits?? they always tell us we need a variety to stay healthy!

bakingbarb Enthusiast

Open Original Shared Linkis highly nutritious, non-glutinous and like buckwheat and quinoa, is not an acid forming food so is soothing and easy to digest. In fact, it is considered to be one of the least allergenic and most digestible grains available and it is a warming grain so will help to heat the body in cold or rainy seasons and climates.

Millet is tasty, with a mildly sweet, nut-like flavor and contains a myriad of beneficial nutrients. It is nearly 15% protein, contains high amounts of fiber, B-complex vitamins including niacin, thiamin, and riboflavin, the essential amino acid methionine, lecithin, and some vitamin E. It is particularly high in the minerals iron, magnesium, phosphorous, and potassium.

The seeds are also rich in phytochemicals, including Phytic acid, which is believed to lower cholesterol, and Phytate, which is associated with reduced cancer risk.

Open Original Shared Link is one of the most nutritious and easily digested of all grains; and it is high in starch, making it a good high energy food. However, like other grains, it is low in calcium, Vitamins A, C, D, and B12, but high in phosphorus, other B vitamins, and iron -- which is higher in millet than any other grain with the exception of amaranth and quinoa (not members of the Grass Family). Millet is very rich in amino acids. The protein content may vary from 5-20%, but generally averages 10-12%. Millet is considered superior to wheat because its proteins are more easily digested, despite remaining low in lysine. Ideally, it can be combined with a legume or a food that is high in lysine (an essential amino acid) to make the dish a complete protein. Millet is also one of two alkaline grains (the other is buckwheat), making it a soothing choice for those with ulcers or colitis.

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. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      5

      Awaiting dermatitis herpetiformis confirmation following biopsy

    2. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    3. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    4. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    5. - catnapt posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

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

    • Total Members
      133,257
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • suek54
      Thank you all for your advice and the dermatitis herpetiformis article. The latter made me realise I had stopped taking my antihistamine, which I will restart today. The Dapsone has cleared the rash entirely but I still get quite a bit itching, absolutely nothing to see though. I know its notoriously hard to clear and its still relatively early days for me.  The iodine issue is very interesting. I do eat quite a bit of salt because I have Addison's disease and sodium retention is an issue. I also have autoimmune hypothyroidism, not sure how a low iodine diet would play into that? Because of my Addison's I am totally steroid dependent, I take steroids 4 x daily and cannot mount any defence against inflammation. I need to increase my meds for that. Now that I know what is wrong I can do just that if Im having a bad day. Life is very sweet, just so damn complicated sometimes! Hey ho, onwards. Thank you again for your advice.  
    • trents
      So, essentially all of the nutrition in the food we eat is absorbed through the villous lining of the small bowel. This is the section of the intestinal track that is damaged by celiac disease. This villous lining is composed of billions of finger-like projections that create a huge amount of surface area for absorbing nutrients. For the celiac person, when gluten is consumed, it triggers an autoimmune reaction in this area which, of course, generates inflammation. The antibodies connected with this inflammation is what the celiac blood tests are designed to detect but this inflammation, over time, wears down the finger-like projections of the villous lining. Of course, when this proceeds for an extended period of time, greatly reduces the absorption efficiency of the villous lining and often results in many and various nutrient deficiency-related health issues. Classic examples would be osteoporosis and iron deficiency. But there are many more. Low D3 levels is a well-known celiac-caused nutritional deficiency. So is low B12. All the B vitamins in fact. Magnesium, zinc, etc.  Celiac disease can also cause liver inflammation. You mention elevated ALP levels. Elevated liver enzymes over a period of 13 years was what led to my celiac diagnosis. Within three months of going gluten free my liver enzymes normalized. I had elevated AST and ALT. The development of sensitivities to other food proteins is very common in the celiac population. Most common cross reactive foods are dairy and oats but eggs, soy and corn are also relatively common offenders. Lactose intolerance is also common in the celiac population because of damage to the SB lining.  Eggs when they are scrambled or fried give me a gut ache. But when I poach them, they do not. The steam and heat of poaching causes a hydrolysis process that alters the protein in the egg. They don't bother me in baked goods either so I assume the same process is at work. I bought a plastic poacher on Amazon to make poaching very easy. All this to say that many of the issues you describe could be caused by celiac disease. 
    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
×
×
  • 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.