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

Gluten Free But Not Celiac?


JustCan

Recommended Posts

JustCan Explorer

I just got my biopsy results and there's no evidence of celiac disease. But, after having done a gluten challenge, I know that gluten is poison for me and will definitely maintain a gluten free diet.

That said, while I'm happy the biopsy was negative, I'd still like some kind of proof that I'm gluten intolerant other than the diet itself.

Am I crazy? I'd love to hear from others that live gluten-free but aren't celiacs (wisdom from celiacs is welcome too :D) .


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



Celiac.com Sponsor (A8-M):



Guest j_mommy

It's totally possible that you have results from the diet!!!!

Were you gluten-free before your biopsy???? Did you do a gluten challenge prior to the biopsy if you were gluten-free????

Also remember that you can have false negatives with biopsies if they don't take enough samples!

All that said if the gluten-free diet is working for you, stay with it!!! Do whatever you need to to be healthy.

Have you had testing done for gluten intolerance???

JustCan Explorer
It's totally possible that you have results from the diet!!!!

Were you gluten-free before your biopsy???? Did you do a gluten challenge prior to the biopsy if you were gluten-free????

Also remember that you can have false negatives with biopsies if they don't take enough samples!

All that said if the gluten-free diet is working for you, stay with it!!! Do whatever you need to to be healthy.

Have you had testing done for gluten intolerance???

Thanks for your response! Yes, I was gluten-free before the biopsy and did a month long gluten challenge. I was really sick by the end of the month but there's no way to know if it was long enough. I also had bloodwork that was negative but I was gluten free at that time so it wasn't accurate. But no, I haven't been tested just for gluten intolerance. Is that the Enterolab test or is there another way?

Guest j_mommy

You're right on the part about length of gluten challenge.....there are standards but like celiac...I think it's different for everyone!

I would say your dietary response is enough of proof that you need to be gluten-free.

As for testing...I believe you could get that through entrolab....others will be able to comment on that more! i more knowledgeable about celiac than gluten intolereance!

Good Luck :D

gfpaperdoll Rookie

Dietary trial is the ultimate diagnosis, nothing else is really needed.

A negative biopsy just means that they did not see any abnormality in the tissue samples that they took. You could still have villi damage, it can be patchy & they might not have biopsied that area.

Also, the biopsy is up to the doc's interpretation, did he read it right????

I would not be betting my health on the result of anything as unreliable as a biopsy.

You can test thru Enterolab.com & see if you have a problem with gluten, diary... & get the gene test. I think the gene test is a real clue.

enterolab can just tell you if you have a problem with gluten not whether you are gluten intolerance or celiac, or allergic, well some people use the genes for that gauge, which is really not right either.

Anyway, good for you for figuring out that you are healthier gluten free.!!!

nmw Newbie

I had negative blood tests (had been gluten-free 2 weeks at the time), no biopsy and have been gluten-free for 16 months. Positive dietary response is all I need to confirm that for me, gluten is poison. My doc wrote "non-celiac gluten sensitive" in my chart. I don't feel the need to know anything beyond what I already know.

Dandelion Contributor

My bloodwork came back negative and my biopsy came back with no signs of damage, but my doctor lists me as gluten intolerant based on my dietary response. So I would say that dietary response is proof enough. I too was gluten free before I went to get the blood test and biopsy, but I felt so good that there was not a chance I would eat gluten again just for test results. I went from 9 years of feeling so ill that my general doctor had me tested for lyme disease, lupus, r.a., and cancer of every type to not feeling ill every single day.

If you do want to get other testing done there is also a company called Kimball Genetics that does it(blood and cheek swab). I know they were recently at the Gluten Free Vendor Fair at SUNY Farmingdale. I've never been tested by them, but did contact them for information and they seem very professional. Maybe somebody else on here has used them.


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



Celiac.com Sponsor (A8-M):



Guest Doll

If you feel better gluten free, (and all your tests checked out OK), stay gluten-free. My 2 cents.

andreagrant Apprentice

I had no signs of damage in the 2 (!) samples the GI doc took during my biopsy (and he was a jerk in person too). I went gluten-free anyhow, as my father and grandfather both have celiac and I was having classic symptoms. It's been 5 months and I feel like a new person--totally miraculous change (except the couple glutenings...). When I described my family history, symptom, and dietary response to my new house doctor (the old one got fired for reading my "negative" biopsy to me and suggesting I eat more WHEAT BRAN for my "IBS"), he wrote "celiac" in the chart and we moved on to the next topic. Even without that I would have stuck with it since I feel so good!

  • 2 weeks later...
CMCM Rising Star

I just attended a lecture by Dr. Fine of Enterolab. He discussed all this...so here's the bottom line, which MOST DOCTORS DO NOT UNDERSTAND!!!!

Think of gluten sensitivity as a SPECTRUM of reactions: at one end of the spectrum are those with zero observable symptoms. At the other end of the spectrum are very very sick individuals who OFTEN are diagnosed with celiac disease via biopsy. ONLY those with the celiac gene will end up with celiac disease. However, you do NOT have to have the celiac gene to be sensitive to gluten and to get very sick from it. The symptoms run the gamut of zero to horribly sick. There are some celiacs who have no symptoms. Some celiacs are terribly ill. Some people with gluten sensitivity (but no celiac gene) are just as sick as a sick celiac. And with or without the celiac gene, a gluten sensitive person can eat gluten and cause other auto-immune reactions.

There are a fair number of celiac specialists who are beginning to say it's probable that MOST, if not all Americans are at the very least gluten sensitive, and probably no one should eat gluten. Period.

Ultimately, we have to change the mindset of all this: Lacking a diagnosis of celiac disease (whichis after all, the worst end of the spectrum), you still must look at dietary response: If eating gluten makes you sick, it's probably doing damage to your body and you must stop eating it. If eliminating gluten makes you feel better, there's your answer. You don't need, I repeat, you DO NOT NEED a doctor to say you have celiac disease in order to follow the diet. Eventually, all this will be common medical knowledge, but right now it's not, unfortunately.

gfpaperdoll Rookie

YES, to CMCM's post ....

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. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      25

      Headaches / Migraines and Hypoglycaemia

    2. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      25

      Headaches / Migraines and Hypoglycaemia

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

      KAN-101 Treatment for Coeliac Disease

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

      Body dysmorphia experience

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

      Heat intolerant... Yikes


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,151
    • Most Online (within 30 mins)
      7,748

    Travis25
    Newest Member
    Travis25
    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

    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • 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.      
×
×
  • 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.