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

Upper Gi Endoscopy Negative, Could I Still Be Celiac?


leethinker

Recommended Posts

leethinker Rookie

Hey all,

I've posted before with my various pains and problems, and have meanwhile gotten an upper GI endoscopy. They found no cancer, nothing else organic. The doctor said she thinks it is definitely a food allergy/intolerance, etc., but doesn't think it is celiac. She supposedly looked the small intestine and said the little villi were all fine.

This is the problem: after having the endoscopy, I decided to just try to find the food culprit myself. So I decided to stop eating gluten for a week. Well,,,,, it is a miracle because only a couple days later, ALL (yes, ALL) of my symptoms disappeared! Then after a week I started eating gluten again. Guess what? My symptoms came back.

So, I'm wondering this: The doctor said she thinks perhaps it could be fructose or lactose intolerance and wants me to do a breath test for each. Now, if my symptoms disappear after eliminating gluten (but NOT eliminating milk products or fruit/fructose), shouldn't I be getting a diagnosis of celiac?

Don't get me wrong, I certainly do not WANT to be celiac. But I really want to know what is wrong with me because I really cannot handle this anymore. I feel like an old lady (aches and pains, bloating, feeling sluggish and tired, depressed, constipation, etc...)... I'm 36. This all started when I was pregnant with my second child, who is now 2!

Can anyone tell me if it is possible to still have celiac even despite negative biopsy?

Thanks!


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

First of all, I think that most of us thought of Celiac as a welcome diagnosis. A simple (well, not so simple in the beginning) dietary change is it's RX.

You most certainly can have Celiac, a gluten intolerance or a gluten allergy. You can rule Celiac in, but testing cannot rule it out. There are no guaranteed diagnosis other than a positive dietary response.

Give the diet a full 100% for about a month and see how you feel. But, I believe you already have found your answer.

ShayFL Enthusiast

Did your doctor just do a "visual"??? Did she take samples to be sent to the lab for analysis? Samples from multiple spots? If she didnt, then she didnt do her job right.

Have you had a complete Celiac panel?

Genetic testing?

You can accept your doctor saying that she doesnt think it is Celiac. Or you can do what you have done. The gluten-free diet.

POS. response to a gluten-free diet is the only accurate way to diagnose.

The scary thing is the people who have "believed" their doctors and went on eating gluten only to develop horrible auto-immune diseases before they FINALLY have enough damage in their intestines to get the "gold standard" diagnosis. Some get dx Celiac when they are being treated for lymphoma (related to untreated Celiac).

You have your answer. If you ever decide you want to eat gluten again, you should at the very least have Genetic testing to see if you have Celiac genes.

KristaleeJane Contributor

WOW

I am shocked that your doctor did an upper GI to check for celiac. That is absolutly not the way to go about testing for celiac unfortuanlty. Before I got diagnosed I was extremly sick, no one could figure out what was wrong with me, and my doc that it could be an ulcer, we did the upper gi and she said no all your results came back normal, your fine its probably IBS.

In order to check the Villa a biopsy needs to be done, because they look at the samples of your villa under a microscope, to the eye my villa looked normal to, but under a microscope I had considerable damage, which confirmed my diagnosis of celiac. I also have very high positive Iga bloodwork.

Now I am no doctor so I may be wrong but going by my experience an Upper Gi cannot diagnose celaic. It is a biopsy which is needed.

Good luck , any more questions, feel free to IM me

Krista

Lisa Mentor
an upper GI endoscopy.

Thanks!

I believe 'leethinker' was refering to an endoscopy exam, rather than an Upper GI Series.

ShayFL Enthusiast

But no biopsies taken????

mymagicalchild Apprentice

The doctor's statement that she didn't think it was Celiac disease but rather a food allergy made me scratch my head. I consulted my "Prescriptions for Nutritional Healing" book and under "Celiac Disease" it says:

"Celiac disease (also called celiac sprue) is a chronic digestive disorder that is caused by a hereditary

intolerance to gluten...."

Is this an incorrect definition?

I have been under the impression that gluten allergy causes the damage to the intestinal lining that then becomes Celiac disease. Which is what the above definition says.

If you are allergic (or intolerant) to gluten and continue to eat it, your doctor will no doubt soon be able to make a Celiac diagnosis. You are incredibly lucky that your symptoms started all at once during your recent pregnancy and that you are old enough to realize the importance of paying attention.

Smart...Lucky...Lady!


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



Celiac.com Sponsor (A8-M):



ShayFL Enthusiast

It is a correct statement, but it isnt complete. Celiac is an auto-immune disease that is triggered by gluten.

It is common for auto-immune diseases to show up after a trauma, major life stress (childbirth, death of a loved one, divorce, etc.) or an infection.

leethinker Rookie

Hi everyone,

First of all, thank you all soooo much for all your thoughtful responses! I really appreciate it a lot. Particularly because it seems the medical world is oblivious to this condition! What's up with that??? :angry:

I *think* I had an endoscopy exam done, but I'm having to translate from German because I live in Germany and everything they've said I've had to hear in German. I'm American but I live here (I was a student abroad and ended up staying...). Anyway, they stick a tube down your throat (I was sedated) and then take pictures. They did take samples and sent it to the lab.

However, the endoscopy was ordered not specifically to check for Celiac, but rather just to see what was going on in there. I mentioned to the specialist that I felt it might be gluten and then she said she'd look at the small intestine too.

Call me paranoid, but I personally think she did NOT do all the tests/biopsies she should have done. She actually said, "You don't want it to be gluten. It's really hard to keep up the diet, it's expensive, etc..." Well, what I want is to know what is wrong with me!!

One of you said the best diagnosis is a positive response to a gluten-free diet. Well, I definitely have that! I would just like to have certainty so that I don't constantly doubt myself! Sometimes I think, "well, maybe it's just because your an anxious person and you're causing your digestive problems". I do have a 4-yr old and a 2-yr. old, I study part-time, and have my own business, so maybe that's why I'm always tired!!

Then the other part of me thinks that is nonsense... I get enough sleep - 8 hours, I am thin, active, I eat healthy, I manage my life just fine. And how could it be just in my head that my symptoms completely go away after eliminating gluten??

Anyway, I don't quite know what to do now... Should I talk frankly with my family doc and force him to do the tests on me??? I like my family doc a lot but even he thinks that my problems are coming from either IBS or anxiety or both.

Having said that,,,, my IgE (I think that's what it is...) was 650 when it should be under 100. EVen he says I definitely have a food allergy, but it is just impossible to test to find out what it is...??

Sorry for rambling, but I'm really frustrated right now!!

Thanks again for your help!

mftnchn Explorer
The doctor's statement that she didn't think it was Celiac disease but rather a food allergy made me scratch my head. I consulted my "Prescriptions for Nutritional Healing" book and under "Celiac Disease" it says:

"Celiac disease (also called celiac sprue) is a chronic digestive disorder that is caused by a hereditary

intolerance to gluten...."

Is this an incorrect definition?

I have been under the impression that gluten allergy causes the damage to the intestinal lining that then becomes Celiac disease. Which is what the above definition says.

If you are allergic (or intolerant) to gluten and continue to eat it, your doctor will no doubt soon be able to make a Celiac diagnosis. You are incredibly lucky that your symptoms started all at once during your recent pregnancy and that you are old enough to realize the importance of paying attention.

Smart...Lucky...Lady!

The body's response to gluten in celiac and in a wheat allergy is quite a different mechanism, so no, they are not the same thing. The treatment is the same though, stay away from it.

mftnchn Explorer

Your experience is a common one. Biopsies can be false negative even when they are done well. Your dietary response is clear however.

Do you need further diagnosis?

You could do an Enterolab test to get some more information, including a gene test. Positive celiac genes and positive dietary response are highly suggestive, especially with elevated ttg.

For many of us, we don't fit into the "gold standard" for many reasons including poor testing. However, ultimately we have researched and experimented and figured it out for ourselves. Its not dependent on a prescription so you don't need your doctor.....

However it is nice to have a practioner take it seriously and moniter for other autoimmune disease, deficiencies, etc.

leethinker Rookie

You're right, really. I don't really need an "official" diagnosis since it is clear to me that my symptoms go on a gluten-free diet, and return after eating gluten.

But you're also right that getting a diagnosis would help ensure someone - besides myself who has no

medical qualifications - could be there to monitor my health, knowing that I have celiac.. Doctors tend to disregard anything a patient says. If I come to a doctor and say, "I have celiac disease", he/she will want to see the documents proving it... Of course I have none.

Also, I have the feeling my family members (not my husband and kids, but my relatives and in-laws, as well as friends, etc.) would be more supportive of this kind of diet if I had a diagnosis. I'd hate to constantly be coming up against resistance just for trying to take care of myself. Does that make sense??

Anyway, I appreciate your help! I am definitely going to continue to eat a gluten-free diet, if for anything, because it makes me feel better!!

:)

mymagicalchild Apprentice

The other side of the coin to not having a medical diagnosis of celiac disease is: you have no preexisting condition diagnosed that must be divulged (so coverage can be excluded) on any future health insurance applications.

You've determined the cause of your problem by the cure you've found. You're your own medical doctor!

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. - SamAlvi replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      High TTG-IgG and Normal TTG-IgA

    2. - knitty kitty replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    3. - lizzie42 replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    4. - knitty kitty replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    5. - lizzie42 replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,873
    • Most Online (within 30 mins)
      7,748

    kellz
    Newest Member
    kellz
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • SamAlvi
      Thanks again for the detailed explanation. Just to clarify, I actually did have my initial tests done while I was still consuming gluten. I stopped eating gluten only after those tests were completed, and it has now been about 70 days since I went gluten-free. I understand the limitations around diagnosing NCGS and the importance of antibody testing and biopsy for celiac disease. Unfortunately, where I live, access to comprehensive testing (including total IgA and endoscopy with biopsy) is limited, which makes things more complicated. Your explanation about small-bowel damage, nutrient absorption, and iron-deficiency anemia still aligns closely with my history, and it’s been very helpful in understanding what may be going on. I don't wanna get Endoscopy and I can't start eating Gluten again because it's hurt really with severe diarrhea.  I appreciate you taking the time to share such detailed and informative guidance. Thank you so much for this detailed and thoughtful response. I really appreciate you pointing out the relationship between anemia and antibody patterns, and how the high DGP IgG still supports celiac disease in my case. A gluten challenge isn’t something I feel safe attempting due to how severe my reactions were, so your suggestion about genetic testing makes a lot of sense. I’ll look into whether HLA testing is available where I live and discuss it with my doctor. I also appreciate you mentioning gastrointestinal beriberi and thiamine deficiency. This isn’t something any of my doctors have discussed with me, and given my symptoms and nutritional history, it’s definitely worth raising with them. I’ll also ask about correcting deficiencies more comprehensively, including B vitamins alongside iron. Thanks again for sharing your knowledge and taking the time to help. I’ll update the forum as I make progress.
    • knitty kitty
      Blood tests for thiamine are unreliable.  The nutrients from your food get absorbed into the bloodstream and travel around the body.  So, a steak dinner can falsely raise thiamine blood levels in the following days.  Besides, thiamine is utilized inside cells where stores of thiamine are impossible to measure. A better test to ask for is the Erythrocyte Transketolace Activity test.  But even that test has been questioned as to accuracy.  It is expensive and takes time to do.   Because of the discrepancies with thiamine tests and urgency with correcting thiamine deficiency, the World Health Organization recommends giving thiamine for several weeks and looking for health improvement.  Thiamine is water soluble, safe and nontoxic even in high doses.   Many doctors are not given sufficient education in nutrition and deficiency symptoms, and may not be familiar with how often they occur in Celiac disease.  B12 and Vitamin D can be stored for as long as a year in the liver, so not having deficiencies in these two vitamins is not a good indicator of the status of the other seven water soluble B vitamins.  It is possible to have deficiency symptoms BEFORE there's changes in the blood levels.   Ask your doctor about Benfotiamine, a form of thiamine that is better absorbed than Thiamine Mononitrate.  Thiamine Mononitrate is used in many vitamins because it is shelf-stable, a form of thiamine that won't break down sitting around on a store shelf.  This form is difficult for the body to turn into a usable form.  Only thirty percent is absorbed in the intestine, and less is actually used.   Thiamine interacts with all of the other B vitamins, so they should all be supplemented together.  Magnesium is needed to make life sustaining enzymes with thiamine, so a magnesium supplement should be added if magnesium levels are low.   Thiamine is water soluble, safe and nontoxic even in high doses.  There's no harm in trying.
    • lizzie42
      Neither of them were anemic 6 months after the Celiac diagnosis. His other vitamin levels (d, B12) were never low. My daughters levels were normal after the first 6 months. Is the thiamine test just called thiamine? 
    • knitty kitty
      Yes, I do think they need a Thiamine supplement at least. Especially since they eat red meat only occasionally. Most fruits and vegetables are not good sources of Thiamine.  Legumes (beans) do contain thiamine.  Fruits and veggies do have some of the other B vitamins, but thiamine B 1 and  Cobalamine B12 are mostly found in meats.  Meat, especially organ meats like liver, are the best sources of Thiamine, B12, and the six other B vitamins and important minerals like iron.   Thiamine has antibacterial and antiviral properties.  Thiamine is important to our immune systems.  We need more thiamine when we're physically ill or injured, when we're under stress emotionally, and when we exercise, especially outside in hot weather.  We need thiamine and other B vitamins like Niacin B 3 to keep our gastrointestinal tract healthy.  We can't store thiamine for very long.  We can get low in thiamine within three days.  Symptoms can appear suddenly when a high carbohydrate diet is consumed.  (Rice and beans are high in carbohydrates.)  A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function, so symptoms can wax and wane depending on what one eats.  The earliest symptoms like fatigue and anxiety are easily contributed to other things or life events and dismissed.   Correcting nutritional deficiencies needs to be done quickly, especially in children, so their growth isn't stunted.  Nutritional deficiencies can affect intelligence.  Vitamin D deficiency can cause short stature and poor bone formation.   Is your son taking anything for the anemia?  Is the anemia caused by B12 or iron deficiency?  
    • lizzie42
      Thank you! That's helpful. My kids eat very little processed food. Tons of fruit, vegetables, cheese, eggs and occasional red meat. We do a lot of rice and bean bowls, stir fry, etc.  Do you think with all the fruits and vegetables they need a vitamin supplement? I feel like their diet is pretty healthy and balanced with very limited processed food. The only processed food they eat regularly is a bowl of Cheerios here and there.  Could shaking legs be a symptom of just a one-time gluten exposure? I guess there's no way to know for sure if they're getting absolutely zero exposure because they do go to school a couple times a week. We do homeschool but my son does a shared school 2x a week and my daughter does a morning Pre-K 3 x a week.  At home our entire house is strictly gluten free and it is extremely rare for us to eat out. If we eat at someone else's house I usually just bring their food. When we have play dates we bring all the snacks, etc. I try to be really careful since they're still growing. They also, of course, catch kids viruses all the time so I  want to make sure I know whether they're just sick or they've had gluten. It can be pretty confusing when they're pretty young to even be explaining their symptoms! 
×
×
  • 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.