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

Biopsies Negative For Celiac Disease


TRB

Recommended Posts

TRB Rookie

I am actually really surprised that my biopsies were negative because the problems I was having totally cleared up by cutting out gluten. Except if I accidentally get glutened and then I have a horrible reaction ... 10x worse then when I was eating gluten regularly (is that normal?).

Doc is saying biopsies came back with mild gastritis ... but every reference I check says nothing about a gluten free diet as treatment for that.

So I'm wondering why I feel better without gluten when I don't seem to have any reason to be reacting badly to it in the first place. This is all very confusing. :blink:


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



Celiac.com Sponsor (A8-M):



gfpaperdoll Rookie

i would get a second opinion on the biopsies...

Fiddle-Faddle Community Regular

Biopsies are totally hit or miss. You have 22 feet of intestine, and they biopsy 4 to 6 (if you are lucky) quarter-inch (or less) sections. That leaves, um, 21.9 feet left that they haven't biopsied--and celiac damage is often patchy and not visible to the naked eye.

Seems to me your doctor is being unusually intelligent in noticing that yes, gluten IS causing you a major problem.

Sure, he could tell you, "well, our biopsy didn't turn up any signs of celiac so you can safely eat gluten again," but WHY? So you can do more obvious damage?

The more damage one does by continuing to eat gluten when the body is already making antibodies against it, the more irreversible the damage is, and that includes neuro damage AND cancer.

I'm assuming that the doctor ordered the biopsy in the first place because your bloodwork showed elevated antibodies to gluten. That, coupled with your dietary response, is practically irrefutable proof that you should be on a gluten-free diet.

TRB Rookie
Biopsies are totally hit or miss. You have 22 feet of intestine, and they biopsy 4 to 6 (if you are lucky) quarter-inch (or less) sections. That leaves, um, 21.9 feet left that they haven't biopsied--and celiac damage is often patchy and not visible to the naked eye.

Seems to me your doctor is being unusually intelligent in noticing that yes, gluten IS causing you a major problem.

Sure, he could tell you, "well, our biopsy didn't turn up any signs of celiac so you can safely eat gluten again," but WHY? So you can do more obvious damage?

The more damage one does by continuing to eat gluten when the body is already making antibodies against it, the more irreversible the damage is, and that includes neuro damage AND cancer.

I'm assuming that the doctor ordered the biopsy in the first place because your bloodwork showed elevated antibodies to gluten. That, coupled with your dietary response, is practically irrefutable proof that you should be on a gluten-free diet.

My bloodwork did show elevated antibodies to gluten which is why I had the biopsy.

That explanation makes a lot of sense and I greatly appreciate you taking the time and explaining it to me. It would have been nice if the doctor had done so. I hadn't even considered the fact that the damage might not be throughout the intestine.

Fiddle-Faddle Community Regular

What the doctors keep forgetting is that the damage doesn't HAVE to be in your intestine.

There is a condition called dermatitis herpetiformis that is considered an automatic diagnosis of celiac. It is a skin rash. This means that the immune system is attacking the skin instead of the intestinal villi.

It's not such a stretch to figure that the immune system might be triggered by gluten to attack all kinds of things: the thyroid (Hashimoto's, Grave's disease), the pancreas (diabetes), the stomach (GERD, bloating, intestinal pain), the liver (autoimmune hepatitis), the joints (rheumatoid arthritis), the neurological system (fibromyalgia, and all kinds of other neuro issues), the brain (bipolar syndrome, depression, brain fog, autism, who knows what else).

All of those conditions have a higher concurrence rate among celiacs than amongst the "normal" population. And all are supposedly "treated" with medications that mask the symptoms but do nothing to address the cause.

marie06 Rookie
Biopsies are totally hit or miss. You have 22 feet of intestine, and they biopsy 4 to 6 (if you are lucky) quarter-inch (or less) sections. That leaves, um, 21.9 feet left that they haven't biopsied--and celiac damage is often patchy and not visible to the naked eye.

Seems to me your doctor is being unusually intelligent in noticing that yes, gluten IS causing you a major problem.

Sure, he could tell you, "well, our biopsy didn't turn up any signs of celiac so you can safely eat gluten again," but WHY? So you can do more obvious damage?

The more damage one does by continuing to eat gluten when the body is already making antibodies against it, the more irreversible the damage is, and that includes neuro damage AND cancer.

I'm assuming that the doctor ordered the biopsy in the first place because your bloodwork showed elevated antibodies to gluten. That, coupled with your dietary response, is practically irrefutable proof that you should be on a gluten-free diet.

THANK You for your post. My biopsy (altho singular - not even 4-6) came back negative but so many of my symptoms have disappeared on a gluten free diet that I was confused. My doc (not a deliac doc) said my nausea was due to 'chronic pain'. However, after just 1 week on the gluten-free diet the neausea (that I had for almost 2 years) was gone and has not returned. I went to see a food allergist on Sat and he is doing bloodwork for celiac (even tho I have been Gluten-free Casein-free since 6/5/08). HE seems to think that I DO have Celiac.

Fiddle-Faddle Community Regular

Why is he doing celiac bloodwork if you've been gluten-free for a month? You shouldn't BE producing antibodies against gluten if you're not being exposed to it. Or is he doing genetic testing???


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



Celiac.com Sponsor (A8-M):



marie06 Rookie
Why is he doing celiac bloodwork if you've been gluten-free for a month? You shouldn't BE producing antibodies against gluten if you're not being exposed to it. Or is he doing genetic testing???

I was there for food allergy testing. He asked me if I wanted to do the bloodwork for Celiac. He said it may come back negative because Ive been gluten-free...but he said if it came back + I knew for sure it was Celiac, vs just an assumption.

gabby Enthusiast

Sounds like you've got a great doctor!

:)

IMWalt Contributor
So I'm wondering why I feel better without gluten when I don't seem to have any reason to be reacting badly to it in the first place. This is all very confusing. :blink:

Yep. Very confusing. Same thing with me. Doc said biopsy showed mild gastritis. They only grabbed one spot of my duodenum, and it looked normal. However, after being gluten-free for a few months (during which time all of my symptoms went away), I have a much bigger reaction than I used to have. Now, it seems like a couple crumbs and I have horrible cramps and gas, sometimes D.

Grrrrrrr.

amg2389 Newbie
I am actually really surprised that my biopsies were negative because the problems I was having totally cleared up by cutting out gluten. Except if I accidentally get glutened and then I have a horrible reaction ... 10x worse then when I was eating gluten regularly (is that normal?).

Doc is saying biopsies came back with mild gastritis ... but every reference I check says nothing about a gluten free diet as treatment for that.

So I'm wondering why I feel better without gluten when I don't seem to have any reason to be reacting badly to it in the first place. This is all very confusing. :blink:

I had two tests for Celiac...a biopsy and blood test. And both came back negative. But my doctor also said to go gluten-free. Supposedly the testing for Celiac can be really flaky and inaccurate (especially in children and teens, like me)--I have several friends who have Celiac but tested negative. After going gluten-free, I have felt much better. It's still sort of a mystery to me too though!

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.