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

Different Reactions To Different Foods With Gluten


wsieving

Recommended Posts

wsieving Contributor

I posted this in another forum and never seemed to get any kind of response, so I will post it here in hopes that I can get an answer.

I am wondering if the concentration of gluten is higher in some foods, thus causing a stronger reaction, than in others. Our biggest clue to start looking in the direction of celiac disease was that our DD just cannot tolerate pasta at all. Other foods seem to bother her, but mildly compared to what pastas do to her. Is it because pasta contains more gluten than other things?


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



Celiac.com Sponsor (A8-M):



ksymonds84 Enthusiast
I posted this in another forum and never seemed to get any kind of response, so I will post it here in hopes that I can get an answer.

I am wondering if the concentration of gluten is higher in some foods, thus causing a stronger reaction, than in others. Our biggest clue to start looking in the direction of celiac disease was that our DD just cannot tolerate pasta at all. Other foods seem to bother her, but mildly compared to what pastas do to her. Is it because pasta contains more gluten than other things?

Pasta would be pretty much all gluten, but understand that with celiac it doesn't matter. ANY amount of gluten will cause a reaction if you are celiac. Sometimes you may not have outward symptoms but if you are celiac your intestines are getting damaged all the same. Hope that helps. I would definately have her tested for celiac but keep in mind that sometimes children will get a false negative so if that happens, try the diet and see if that helps. If you start the diet before testing you will probably get a false negative. Welcome, this is a great site to learn about celiac.

MarsupialMama Apprentice

We have just started the gluten-free journey as of about 3 months ago because of my daughter. We put her on the diet before we tested for anything because she was losing weight so fast that I didn't want to wait another day before starting something that might help - and I didn't want to damage her intestines for one more hour. Right now my two daughters (almost 2 and almost 4 y/o) and I have been gluten free for about 3 months. We have all experienced positive results. (My husband still eats wheat bread). I have had digestive issues and other health problems my whole life and I can say for sure that the things that caused me the most indigestion were gluten steaks and whole wheat bread and pasta. Oatmeal was another terrible one, but I guess that might just be my personal thing since the gluten content from cross-contamination is probably not that high.

Gluten steaks are things that I made to replace meat (we are vegetarian) which is 100% gluten. I always got sick after eating them. Bottom line: We are not "diagnosed" celiacs, but have found that in our experience, the more gluten it contained, the worse the bloating and indigestion was. With my daughter though, even a bite of something cross-contaminated will cause her to drop weight and get the dark circles under her eyes and the cranky attitude (and sometimes bloated belly). So I think it depends on the individual, their level of sensitivity, etc.

My friend's son (2 y/o) got a bite of oatmeal and puked immediately from it. When he got ahold of a whole box of oatmeal cookies (and ate 12 of them!) he didn't vomit. But the next few weeks had diarrhea faster than she could clean it up! Maybe the amount of gluten-containing food plays a part as well. If it is complete gluten overload, it seemed with him to by-pass the immediate reaction, but come back full-force after the inital "gluten shock."

Who knows!

Amyleigh0007 Enthusiast

I also had stronger reactions to pasta, especially 100% whole wheat pasta. 100% whole wheat bread bothered me too. I would have to run to the bathroom within 30 minutes of eating. White breads and pastas did not bother me as much but I would still get ill after eating them. I do not have Celiac, but I do have gluten intolerance.

ksymonds84 Enthusiast

Congratulations MarsupialMama on figuring out the gluten intolerance. I wouldn't worry about getting an official diagnoses when your dietary response is so amazing and your little girl is now thriving. As I said in a previous post, a lot of times children are false negative anyway because they haven't produced enough of the antibodies to show positive. Some celiacs can add back oatmeal after their intestines heal but it has to be premium oatmeal from a health food store gauranteed not to have cross contamination. This is what I was told from my local sprue association but I've only been gluten free for 8 months and still don't want to risk it yet. My brother in law was diagnosed 4 years ago and still can't tolerate oatmeal, so like you said, its probably and individual thing, but it does sound like your son loves oatmeal :) 12 cookies! To be a kid again lol!

crunchy-mama Apprentice

I was wondering about this as a newbie. I have suspected gluten for a few years, but always have been confused that sometimes I have a strong reaction to something and sometimes not. I have also noticed the more whole grain something is, the more troublesome it seems.

purple Community Regular

I remember reading somewhere that whole wheat bread has more gluten in it than regular white bread.

I also read that your body reacts the same way.

Think of it likes fleas on a dog...you try to kill them right away. Compared to fleas on the carpet...you smoke bomb the whole house. Both cause harm/trouble. The dogs can get worse, spreads to other animals/carpet.

All gluten causes harm. Some is worse. Eliminate it all to be safe. We don't know about what we can't see...that's the hard part.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,955
    • Most Online (within 30 mins)
      7,748

    AnnaLousGFBakery
    Newest Member
    AnnaLousGFBakery
    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

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.