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.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,980
    • Most Online (within 30 mins)
      7,748

    Susan Upchurch
    Newest Member
    Susan Upchurch
    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

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.