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

Doctors And Every One Else Who May Know This Answer, Please Help.


Liveenjoylife

Recommended Posts

Liveenjoylife Apprentice

I had my self tested for celiac disease two days ago, (Friday)through blood work. I think the test was called IgA and have not eaten wheat/gluten for almost a year.(I self diagnosed my self)However, I have recently found out I am allergic to corn, and the day I was to get tested I woke up with a hive on my mouth, a rash on my face, and was having a hard time breathing, my lungs were getting tight. So, my question to you all will my test results have a good chance of showing I have celiac disease now that corn was part of it?


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

I have no idea if the corn will make any difference or not, but the fact that you have not eat gluten for a year certainly will. If you really have not eaten gluten your test will be negative.

T.H. Community Regular

Yeah, afraid the test will be negative if you've been gluten free for a year. Since it's not an allergy, the allergic reaction to corn wouldn't affect the test, though.

Was your doctor aware of your gluten free status when the test was ordered?

If they were, and are still trying to diagnose you this way, they are simply very celiac ignorant. A survey study of GI doctors around the world found that over 50% of them would choose this (incorrect) way of trying to diagnose a celiac who has been gluten free for a long time, so your doc wouldn't be alone in this. <_<

Re: the corn allergy, if you haven't yet, i would really recommend checking out a corn allergy site, because that stuff is in an insane amount of things. Especially if you are having a severe reaction like this, I imagine you need to know.

Iodized salt always has corn, citric acid can be corn contaminated, many tomatoes have a corn based spray on them for ripening, even paper plates sometimes have corn starch between them to prevent sticking - it's all over the place, ya know?

Liveenjoylife Apprentice

Yeah, afraid the test will be negative if you've been gluten free for a year. Since it's not an allergy, the allergic reaction to corn wouldn't affect the test, though.

Was your doctor aware of your gluten free status when the test was ordered?

If they were, and are still trying to diagnose you this way, they are simply very celiac ignorant. A survey study of GI doctors around the world found that over 50% of them would choose this (incorrect) way of trying to diagnose a celiac who has been gluten free for a long time, so your doc wouldn't be alone in this. <_<

Re: the corn allergy, if you haven't yet, i would really recommend checking out a corn allergy site, because that stuff is in an insane amount of things. Especially if you are having a severe reaction like this, I imagine you need to know.

Iodized salt always has corn, citric acid can be corn contaminated, many tomatoes have a corn based spray on them for ripening, even paper plates sometimes have corn starch between them to prevent sticking - it's all over the place, ya know?

But here's the thing. Even if I eat a crumb of wheat, my reaction is severe, even life threatening. This is why she still ordered for the test in hopes it may still show up. Even if I breath in flour my throat will start to close let alone eat any wheat for a test to prove it. I'm basically caught in a hard place. And am hopeful my test may turn out positive. Thanks for the help.

AzizaRivers Apprentice

I am aware that celiac reactions vary greatly from one person to another, and some celiacs have reactions similar to this, but I think it's important to mention that you should consider the possibility of having an wheat allergy rather than celiac, particularly since you were self-diagnosed so I'm assuming that means you never had an endoscopy or anything that would indicate intestinal damage. Since you have a severe corn allergy, consider that it may be a wheat allergy.

If you have been gluten free for a year already and feel better that way, by all means keep doing it. If you've been gluten-free for that long there's a high likelihood that your results will be negative for celiac even if that's what it is. You know gluten/wheat makes you extremely ill, so regardless of your results, don't eat it! And see about getting an Epipen if you haven't already. You don't want to go into anaphylactic shock without one of those nearby, and it seems that's where your reactions could be heading.

psawyer Proficient

The blood tests in the celiac panel will not detect an allergy, no matter how intense. They measure the antibodies produced by the autoimmune reaction to gluten. Those antibodies have a limited life span, and will only be found if you are eating gluten on a regular basis.

An allergic reaction to corn (or anything else) will not affect those antibodies.

GlutenFreeManna Rising Star

But here's the thing. Even if I eat a crumb of wheat, my reaction is severe, even life threatening. This is why she still ordered for the test in hopes it may still show up. Even if I breath in flour my throat will start to close let alone eat any wheat for a test to prove it. I'm basically caught in a hard place. And am hopeful my test may turn out positive. Thanks for the help.

This sounds more like a wheat allergy. Celiac disease or gluten intolerance is not an allergy, it is an autoimmune disease. Have you had IgE testing done for wheat alllergy?

I am currently going through this with milk. I started have anaphylactic reactions to anything with milk. I'm waiting on drs appointments to get offical allergy testing but I have heard it's unreliable. I have one on Monday in which I will ask to get an epipen even though I have not had allergy testing done yet. Other people with life-threatening allergies have told me it is fairly easy to get an epipen after a reaction. If your allergic reactions have been documanted by ER visits or even by your dr you should not have any problem getting some life saving meds. Don't ignore this even if you tests come back negative. You could test yourself with barley to see if your problem is with gluten or with wheat, but don't do that until you have an epipen given your past reactions to wheat. In the end you may have to settle with not knowing if you have celiac or a wheat allergy (some people even have both). The result of having to avoid wheat is pretty much the same no matter what yoru diagnosis is. Only difference is if you are allergic to just wheat you can have the other gluten grains.


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



Celiac.com Sponsor (A8-M):



Liveenjoylife Apprentice

I am aware that celiac reactions vary greatly from one person to another, and some celiacs have reactions similar to this, but I think it's important to mention that you should consider the possibility of having an wheat allergy rather than celiac, particularly since you were self-diagnosed so I'm assuming that means you never had an endoscopy or anything that would indicate intestinal damage. Since you have a severe corn allergy, consider that it may be a wheat allergy.

If you have been gluten free for a year already and feel better that way, by all means keep doing it. If you've been gluten-free for that long there's a high likelihood that your results will be negative for celiac even if that's what it is. You know gluten/wheat makes you extremely ill, so regardless of your results, don't eat it! And see about getting an Epipen if you haven't already. You don't want to go into anaphylactic shock without one of those nearby, and it seems that's where your reactions could be heading.

I know it's celiac disease because my grandmother has it. Our reactions are the same. It is only genetic, and yes she did get tested..I meant to say I have had celiac for 2 years, but prior to that I have also been lactose intolerant. Thanks for your help I will look into an Epipen.

Liveenjoylife Apprentice

The blood tests in the celiac panel will not detect an allergy, no matter how intense. They measure the antibodies produced by the autoimmune reaction to gluten. Those antibodies have a limited life span, and will only be found if you are eating gluten on a regular basis.

An allergic reaction to corn (or anything else) will not affect those antibodies.

Not something I defiantly did not want to hear, but thanks for being so frank.

Liveenjoylife Apprentice

This sounds more like a wheat allergy. Celiac disease or gluten intolerance is not an allergy, it is an autoimmune disease. Have you had IgE testing done for wheat alllergy?

I am currently going through this with milk. I started have anaphylactic reactions to anything with milk. I'm waiting on drs appointments to get offical allergy testing but I have heard it's unreliable. I have one on Monday in which I will ask to get an epipen even though I have not had allergy testing done yet. Other people with life-threatening allergies have told me it is fairly easy to get an epipen after a reaction. If your allergic reactions have been documanted by ER visits or even by your dr you should not have any problem getting some life saving meds. Don't ignore this even if you tests come back negative. You could test yourself with barley to see if your problem is with gluten or with wheat, but don't do that until you have an epipen given your past reactions to wheat. In the end you may have to settle with not knowing if you have celiac or a wheat allergy (some people even have both). The result of having to avoid wheat is pretty much the same no matter what yoru diagnosis is. Only difference is if you are allergic to just wheat you can have the other gluten grains.

My doctor had two tests done one for wheat allergy the other for celiac disease. I can't have any wheat whether it be barley, rye etc. Thanks, even if/when it does come back negative I will find other ways to prove it. Good luck with your dairy testing.

GlutenFreeManna Rising Star

My doctor had two tests done one for wheat allergy the other for celiac disease. I can't have any wheat whether it be barley, rye etc. Thanks, even if/when it does come back negative I will find other ways to prove it. Good luck with your dairy testing.

Thanks. Just curious is there some reason you need to "prove" it? It sounds like your body has given you all the proof you need. You could look into Enterolab if you really need the piece of paper with a positive test result. They do not diagnose celiac, they only tell you if you are gluten intolerant based on stool samples and they do genetic testing too I think. It's expensive however and insurance usually doesn't cover it.

Liveenjoylife Apprentice

Thanks. Just curious is there some reason you need to "prove" it? It sounds like your body has given you all the proof you need. You could look into Enterolab if you really need the piece of paper with a positive test result. They do not diagnose celiac, they only tell you if you are gluten intolerant based on stool samples and they do genetic testing too I think. It's expensive however and insurance usually doesn't cover it.

You're welcome. I am having to prove it for medical reasons that are personal.

frieze Community Regular

You're welcome. I am having to prove it for medical reasons that are personal.

actually, you may have been gluten free too long for enterolab....good luck

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. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    2. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience

    3. - Scott Adams replied to Colleen H's topic in Related Issues & Disorders
      2

      Heat intolerant... Yikes

    4. - Scott Adams replied to Jmartes71's topic in Coping with Celiac Disease
      1

      Related issues

    5. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      23

      Headaches / Migraines and Hypoglycaemia


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,149
    • Most Online (within 30 mins)
      7,748

    dvyoung
    Newest Member
    dvyoung
    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

    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
    • Scott Adams
      The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.      
    • Scott Adams
      I am so sorry you are going through this; it sounds incredibly overwhelming and disheartening to be dismissed by the very medical professionals you're turning to for help. It is completely understandable that you feel lost and exhausted, not just from the relentless physical symptoms like the leg pain, stomach issues, and profound fatigue, but from the psychological toll of being told it's "just IBS" or that you need a therapist when you know your body is signaling that something is wrong. While it's true that a normal tTG test can indicate that celiac disease itself is being managed from a dietary perspective, it is a major oversight for your doctors to ignore your other diagnoses like SIBO, a hernia, and Barrett's esophagus, all of which can contribute significantly to the symptoms you describe. You are absolutely right to be seeking a new Primary Care Physician who will listen to your full history, take your Barrett's diagnosis seriously, and help you coordinate a care plan that looks at the whole picture, because your experience is not just in your head—it's in your entire body, and you deserve a medical team that acknowledges that. I had hernia surgery (laparoscopic), and it's not a big deal, so hopefully you can have your new doctor give you some guidance on that.
    • knitty kitty
      Some people have difficulty processing tyrosine.  Cut out the nuts and cheese and see if there's any difference.  Everyone is different. This study shows that tyrosine can affect our brain with detrimental effects as we age. Neuro-Cognitive Effects of Acute Tyrosine Administration on Reactive and Proactive Response Inhibition in Healthy Older Adults https://pmc.ncbi.nlm.nih.gov/articles/PMC6084775/ "In conclusion, we show age-related effects of tyrosine administration especially on proactive, not reactive, response inhibition, accompanied by signal changes in dopamine-rich fronto-striatal brain regions. Specifically, we observed that tyrosine’s effect on brain and cognition became detrimental with increasing age, questioning the cognitive enhancing potential of tyrosine in healthy aging."
×
×
  • 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.