Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Had Negative Biopsy Yesterday And


hungryforlife

Recommended Posts

hungryforlife Apprentice

I had my biopsy and a colonoscopy yesterday. When I had originally went to the gastro, I met with his PA, I met the doctor only two minutes before the procedure. As we were talking he was confirming my symptoms, and I told him about eating oatmeal and changing my diet to whole grains and getting progressively worse over the past three years. He just said hummmm. Then I said I had found out that my bother had celiac and felt that I should be tested since I had been having the same symptoms; and that after I took oats out of my diet alot of the symptoms lessened or disappeared.

He stated: "Well, I've only had one case where siblings have both had celiacs." Then standing over me he said, "The blood panel that your doctor took is usually pretty accurate."??? I felt dread at that point! My PCP only did the Aga IgA/IgG tests, not the whole panel. I knew I was not going to be getting any gluten (anything) diagnosis from him!!!! I told him that my brother tested negative and that his body didn't even produce IgG antibodies. He said, "Hummm...."

My test all came back normal. He only did two biopsies. Said my small intestines were normal.

I have just been stunned silent ... I still plan on going gluten free - but I sure was hoping for some concrete news. (I am assuming they can tell if the villi are flattened by looking?)

Thanks guys!


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



Celiac.com Sponsor (A8-M):



Guest nini

he didn't take enough samples for an accurate biopsy... even still if the is any damage, it can be sporadic and easily missed especially if they are only doing BLIND samples, by not using a scope to see what they are doing and looking carefully at the areas they are sampling... most GI's are still just looking in until they get right into the upper part of the intestines and just taking one or two samples and not looking around or probing further to look for any inflammation or scalloping or anything.

I think even though you wanted some kind of concrete proof, you may have to self diagnose. Do the gluten-free diet, keep a food journal, after at least 3-6 months, then if you want to test it by trying to reintroduce gluten you can, but keep in mind, not everyone gets symptoms all the time. So, you may want to just see how you feel gluten-free. And go from there. Good luck.

hungryforlife Apprentice

Yes, I know he looked around, Ive got the pictures :)...lol I just think he doesn't think I have celiac and did the obligitory two biopsies and called it a day.

I know for myself, just by giving up OATS, I already feel better and have only had "D" one time and that was the day I ate oats after going to the gastro. ALso the pressure in my head and the "drugged feeling" went away as well. So, maybe I do not have celiac, but I know that I do have a strong reaction to oats.

I still plan on going gluten free, just because I know the seven days I spent gluten free I felt fabulous! Now, my problem is - is when I give up wheat products my blood sugar drops quickly. This morning I felt the dizziness and lightheadedness so I had an egg and cheese on corn tortilla and an orange. I still go dizzy and lightheaded about twenty minutes later. A glucose tablet stablized it??

Anyway, as you say, It is not a crime to give up gluten and if you feel better giving it up then you have your diagnosis! No Gluten!

Carriefaith Enthusiast

Maybe you could get a celiac gene test. If your doctor won't order one, you could order one from enterolab.

Open Original Shared Link

num1habsfan Rising Star

any biopsies I had from an endoscopy and colonoscopy were negative. a lot of GIs seem to believe that it dont matter how long you are gluten-free before getting the biopsies, the tests should still be positive and he should still be able to see damage. So according to them if the test is negative, you dont have it.

Thats what happened with me. But I just say I am gluten-free because I know myself it's Celiac.

I guess this is just so you know you're not alone

~lisa~

moonunit Apprentice

Hi there! Your story is very similar to mine -- I'm on day 3 of a gluten-free diet after positive bloodwork but a negative diagnosis. My doc also only took two samples to biopsy, though the recommended from Columbia University is 4 to 6. The UCSD medical research center suggests at least 6.

Here are a couple links telling us without a doubt that the partial blood panel we both got is outdated and no longer recommended as a diagnostic tool:

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

I'd think NIH would be a pretty reliable source... :) I may give these links to my doctor when I explain why I'm firing her and going somewhere else for my medical treatment -- I tried to tell her this during my visit with her and she blew me off like I was a gnat.

We may never know "officially" whether we have celiac disease, but what happens on the diet is the important thing. As my husband pointed out, at least we don't need to rely on these doctors for medicine or operations or anything! The power is with us! (Or with you, anyway -- until I've been on the diet for a while, I won't know for sure that this is what I actually have!)

Good luck to you!

SeaTwo Newbie

I can top all that:

My GI orders the Celiac Sprue Panel and then schedules me for a colonoscopy (only). How is that for a good testing combination!?

At my follow up visit he told me that it's way too extensive to test for celiac, but, if I feel better from being gluten-free for 12 days now, then it's pretty sure that I have it.


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
      127,685
    • Most Online (within 30 mins)
      7,748

    Janahawk
    Newest Member
    Janahawk
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.3k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Thanks for the additional information. I was thinking of asking you if your daughter was taking methylated vitamins since she has the MTHFR gene but you beat me to it. To answer the question you posed in your original post, as I explained, celiac disease does not damage the colon but the lining of the small bowel. If the damage is pronounced enough and the doc doing it is experienced, yes, the damage done to the lining of the small bowel can be spotted with the naked eye.
    • cameo674
      I could not locate the correct Gary Brecka video where he explains the methylation process and specifically states things about how people with the MTRR homozygous gene mutation are known to suffer from heartburn due to a weakened valve/sphincter where the esophagus and the stomach connect.  My brother had the youtube video sent to him from 10x health which is probably why I cannot locate it.     I will have read up on mast cell activation.  I do not know anything about it.  Tums is my preferred gerd treatment.  I always figured a little extra calcium could not hurt me.  
    • cameo674
      Trents: Due to a genetic mutation, my daughter has inherited from both parents she cannot process the Folic Acid provided in the fortified American grains.   An MD told her to avoid eating fortified grains.   My daughter makes the assumption that unless she makes the food item, that the baker used a fortified grain so she has been limiting her gluten intake since 2020.   Her Psychiatrist was who tested her for MTHFR gene issue because she suffers from depression and severe anxiety. The Psychatrist also instructed my daughter to supplement with a methylated version of folate once she knew my daughter was homozygous, because the methylated version bypasses the mutated gene step so her body can absorb it.  Low folate absorption impacts serotonin and dopamine production.  My husband and I also both have two other homozygous gene mutations that interfere with vitamin absorption: MTRR and VDR taq.  The first interferes with B-12 absorption which requires us to take a methylated B-12 vitamin and the second with Vitamin D absorption so we have to take higher doses to stay within normal levels.   My brother, who has the exact same gene mutations, went through 10x health genetic testing for vitamin supplements (paid by his employer) and received a huge report saying the same things about which types of supplements had to be taken.  Gary Brecka does videos on how these gene mutations impact the vitamin absorption pathways.       If my brother had not gotten his testing through work, he would never would have started his supplement journey.  His testing is what triggered my getting functional health testing that tested similar biomarkers to his.  Again the celiac testing was an add-on test that I did off the cuff.  
    • trents
      Welcome to the forum, @growlinhard1! If eliminating gluten from your diet makes significant improvement in your symptoms then there are two possibilities. Either you have celiac disease (aka, gluten intolerance) or NCGS (Non Celiac Gluten Sensitivity, aka, gluten sensitivity). The difference is that celiac disease is an autoimmune disorder that creates inflammation and, over time, damages the lining of the small bowel which inhibits nutrient absorption whereas NCGS does not damage the lining of the small bowel. They share many of the same symptoms. At the end of the day, the antidote for both is to abstain from foods that contain wheat, barley or rye, the three gluten-containing grains. Some countries supply stipends and healthcare benefits for those with an official celiac diagnosis. If you live in the USA that does not apply. The main reasons for seeking an official celiac diagnosis are psychological and social. Many people have a hard time not falling off the gluten free bandwagon without an official diagnosis. They find it easy to rationalize it all away as being temporary or due to something else. When you have an official diagnosis, you tend to take gluten-free eating more seriously. Socially, family and friends are more likely to respect and attempt to comply with your need to eat gluten free if you have an official diagnosis of celiac disease. Your physician is more likely to take you seriously as well if you have an official diagnosis because there are typically other health problems that are spinoffs which develop from celiac disease in time. One autoimmune disease invites others. There are no tests for NCGS. Celiac disease must first be ruled out. We do have specific tests for celiac disease. By the way, some experts believe that NCGS can transition into celiac disease. If your endoscopy/biopsy is only a month away, I would encourage you to stick it out and go back on gluten to get an official diagnosis. You still have time to get a valid test result if you start back on gluten now, 10g of gluten daily which is about the amount found in 4-6 slices of wheat bread.
    • BoiseNic
      I have the same problem. No matter what I eat, I seem to get a break out every 1 to 2 months. I do not do oats, citrus fruits, apples, onions and other foods also, as those cause reactions. The only time I have zero problems is when I fast. The only staple grain I have is quinoa, as that doesn't seem to cause me issues. I have linked mine to a microbiome imbalance. I am currently on month 3 of Skinesa. It's supposed to take 3 months before seeing results. I guess we'll see.
×
×
  • Create New...