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

So Confused!


runnerjen

Recommended Posts

runnerjen Apprentice

Hello,

So I'm very confused about this. I've been sick for as long as I can remember with various stomach issues. I've always been told it's just IBS, but it's increasingly gotten worse over the years. I went to a new gastroenterologist who did the blood tests for Celiac and they came back positive. So he had me do an endoscopy back in December. I started the gluten-free diet the day after, and have been on it since. I haven't really notices the IBS like symptoms getting any better (mostly diarrhea), but I have noticed that I haven't had any migraines (which I would get weekly), my face has cleared up, I'm sleeping better and I'm not having the night sweats like I used to.

So this weekend I finally got a call back from the Dr. with the results from the endoscopy and it's normal. No flattening of the villi or any damage. So he told me that doesn't necessarily mean anything, as it could be a false negative and that I should remain on the gluten-free diet for another 2 months and then go back again for blood tests.

I'm so confused! I have an appt with a nutritionist next week, she specializes in people with gluten intolerances/celiac. But I just don't know if I should stay on the diet or not. It's so frustrating since my IBS symptoms haven't gone away!

Thanks for letting me rant a bit. Anyone else go through this?

Jen


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



Celiac.com Sponsor (A8-M):



lovegrov Collaborator

If you hve celiac, you haven't been gluten-free long enough to heal. Some people continue with some symptoms for months and months. The things that have improved indicate the gluten-free diet is having a positive effect.

Your doctor is giving you the best advice. Your blood tests were positive and false positives for celiac are very rare. You most likely have it. Your doctor is also correct in that the biopsy could be wrong. Celiac damage can be patchy and they might have taken samples from healthy looking areas. Or the samples could have been read wrong. At this point, I would absolutely follow his advice. I'd also be grateful you have a dcotor who seems to know his stuff. Many doctors would come back and tell you you don't have it when in fact you very might.

richard

RiceGuy Collaborator

I saw little or no change in digestive issues for about the first six months. Then surprise! What a difference it began to make. Therefore, as has already been noted, you should stay on the gluten-free diet longer. Besides, you already know it helps you with other things, so that in itself should help encourage you to keep moving forward, not back-step to where you began. Also watch for other food allergies or intolerances, as they can tend to show up after you go gluten-free.

GlutenWrangler Contributor

You should definitely stay on the diet. It takes a long time to heal and restore normalcy. It is great that you are seeing a nutritionist. She may help speed your recovery. If you had positive blood tests, you have celiac disease. Fortunately, you were diagnosed before your villi flattened. It time, the villi would have flattened, and you would be in much worse condition. So stay patient and you will see more improvement as time goes by. Good luck.

-Brian

sonja69 Rookie
Hello,

So I'm very confused about this. I've been sick for as long as I can remember with various stomach issues. I've always been told it's just IBS, but it's increasingly gotten worse over the years. I went to a new gastroenterologist who did the blood tests for Celiac and they came back positive. So he had me do an endoscopy back in December. I started the gluten-free diet the day after, and have been on it since. I haven't really notices the IBS like symptoms getting any better (mostly diarrhea), but I have noticed that I haven't had any migraines (which I would get weekly), my face has cleared up, I'm sleeping better and I'm not having the night sweats like I used to.

So this weekend I finally got a call back from the Dr. with the results from the endoscopy and it's normal. No flattening of the villi or any damage. So he told me that doesn't necessarily mean anything, as it could be a false negative and that I should remain on the gluten-free diet for another 2 months and then go back again for blood tests.

I'm so confused! I have an appt with a nutritionist next week, she specializes in people with gluten intolerances/celiac. But I just don't know if I should stay on the diet or not. It's so frustrating since my IBS symptoms haven't gone away!

Thanks for letting me rant a bit. Anyone else go through this?

Jen

Hi Jen,

I have also a negative diagnosis. I have bowel troubles since two decades and they turned into real problems a few years ago. now I am on a glutenfree diet,since doctors seems to unable to help me,I took things in my own hands. you already have some positive effects, so I recommend you to keep on eating glutenfree and try an elimination diet to rule out diary and soy and also fructose. I also have somepositive effects through the glutenfree diet, so I hope the problems will eventually disappear.

the problem with the endoscopy is that results are dependent on the location where the sample was taken, the damage in the intestine can be patchy and how expereienced the analyst is.

I had/have some serious drwbacks this week, since it is very difficult to maintain a normal life and being gluten- and lactosefree, you have to check every label and being careful and alert all the time, at least in the beginning. and, in the healing process, the body might be more sensitive to disturbers, since now the body can really take care about the real prblem. at least, that's what I believe and now, when you're feeling better you might be more sensitive, since mistakes, or other culprit foods will be like s sledgehammer. that's my experience: I had never stomach pain and nausea, could eat what I want, drink what I want (alcohol), and did not notice because I always already felt crappy anyway, so I did not notice 'outliers'. but now I feel them very hard with stomach pain and other issues.

keep on being glutenfree, be patient (I have to learn this too). a trial can't hurt!

good luck,

Sonja

Nancym Enthusiast

Unfortunately food intolerances seem to come in multiples a lot of times. You might also be having problems with dairy, soy, nuts, eggs... long list of things. Best thing to do is try an elimination diet and keep a log of how you feel. Diary and gluten seem to be my issues, with soy kind of trailing along. Also, I have to really be careful how many seeds I eat (sunflower, pumpkin).

I really think this IBS thing is usually food intolerances. It sure is in my case!

Electra Enthusiast
Hello,

So I'm very confused about this. I've been sick for as long as I can remember with various stomach issues. I've always been told it's just IBS, but it's increasingly gotten worse over the years. I went to a new gastroenterologist who did the blood tests for Celiac and they came back positive. So he had me do an endoscopy back in December. I started the gluten-free diet the day after, and have been on it since. I haven't really notices the IBS like symptoms getting any better (mostly diarrhea), but I have noticed that I haven't had any migraines (which I would get weekly), my face has cleared up, I'm sleeping better and I'm not having the night sweats like I used to.

So this weekend I finally got a call back from the Dr. with the results from the endoscopy and it's normal. No flattening of the villi or any damage. So he told me that doesn't necessarily mean anything, as it could be a false negative and that I should remain on the gluten-free diet for another 2 months and then go back again for blood tests.

I'm so confused! I have an appt with a nutritionist next week, she specializes in people with gluten intolerances/celiac. But I just don't know if I should stay on the diet or not. It's so frustrating since my IBS symptoms haven't gone away!

Thanks for letting me rant a bit. Anyone else go through this?

Jen

It seems to me that you have a very knowledgeable dr. From what I hear a lot of dr's will say you don't have celiac if your biopsy alone is negative, so when your dr. tells you it could be a false negative he/she is right and I would definitely stay on the diet. I know it's not fun, but you might only have to be on it for a bit longer and if it's determined that you don't have celiac then you know you did your best to feel better while you were waiting ;)

I also had a positive blood test and had been sent to the hospital a few times due to severe pain and "altheimers" like behavior, and since going gluten free most of the pain and altheimers symptoms have vanished. I still have the stool problems though, but from what I hear it has taken some people over a year to get their bowels straightened out!!

Good Luck and I hope you feel better soon!!


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



Celiac.com Sponsor (A8-M):



NewB Newbie
Hello,

So I'm very confused about this. I've been sick for as long as I can remember with various stomach issues. I've always been told it's just IBS, but it's increasingly gotten worse over the years. I went to a new gastroenterologist who did the blood tests for Celiac and they came back positive. So he had me do an endoscopy back in December. I started the gluten-free diet the day after, and have been on it since. I haven't really notices the IBS like symptoms getting any better (mostly diarrhea), but I have noticed that I haven't had any migraines (which I would get weekly), my face has cleared up, I'm sleeping better and I'm not having the night sweats like I used to.

So this weekend I finally got a call back from the Dr. with the results from the endoscopy and it's normal. No flattening of the villi or any damage. So he told me that doesn't necessarily mean anything, as it could be a false negative and that I should remain on the gluten-free diet for another 2 months and then go back again for blood tests.

I'm so confused! I have an appt with a nutritionist next week, she specializes in people with gluten intolerances/celiac. But I just don't know if I should stay on the diet or not. It's so frustrating since my IBS symptoms haven't gone away!

Thanks for letting me rant a bit. Anyone else go through this?

Jen

NewB Newbie

The best advice is as everyone says: Stick with it...it took a while for me to just slightly improve with all the multiple symptoms and I sometimes wonder if I'll ever be completely normal again...but things got better...but now I am worrying about soy (since reading this forum). You have to be vigilant. Good luck!

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. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

    2. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    3. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

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

      Newly diagnosed mam to coeliac 11 year old

    5. - tiffanygosci posted a topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

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

    • Total Members
      132,956
    • Most Online (within 30 mins)
      7,748

    Srowton
    Newest Member
    Srowton
    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

    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
    • Dizzyma
      Hi Trent and Cristiana, thank you so much for taking the time out to reply to me.  My daughters GP requested bloods, they came back as showing a possibility of celiac disease, she advised me to continue feeding gluten as normal and wait on a hospital appointment. When we got that the doctor was quite annoyed that the gp hadn’t advised to go gluten free immediately as she explained that her numbers were so high that celiac disease was fairly evident. That doctor advised to switch to a gluten-free diet immediately which we did but she also got her bloods taken again that day as it made sense to double check considering she was maintaining a normal diet and they came back with a result of 128. The hospital doctor was so confident of celiac disease that she didn’t bother with any further testing. Cristiana, thank you for the information on the coeliac UK site however I am in the Rrpublic of Ireland so I’ll have to try to link in with supports there. I appreciate your replies I guess I’ll figure things as we go I just feel so bad for her, her skin is so sore around her mouth  and it looks bad at an age when looks are becoming important. Also her anxiety is affecting her sleep so I may have to look into some kind of therapy to help as I don’t think I am enough to help. thanks once again, it’s great to be able to reach out xx   
    • tiffanygosci
      I have been feeling so lonely in this celiac disease journey (which I've only been on for over 4 months). I have one friend who is celiac, and she has been a great help to me. I got diagnosed at the beginning of October 2025, so I got hit with all the major food holidays. I think I navigated them well, but I did make a couple mistakes along the way regarding CC. I have been Googling "celiac support groups" for the last couple days and there is nothing in the Northern Illinois area. I might reach out to my GI and dietician, who are through NW Medicine, to see if there are any groups near me. I cannot join any social media groups because I deleted my FB and IG last year and I have no desire to have them back (although I almost made a FB because I'm desperate to connect with more celiacs). I'm glad I have this forum. I am praying God will lead me to more people to relate to. In my opinion, celiac disease is like the only food- related autoimmune disease and it's so isolating. Thanks for walking alongside of me! I'm glad I know how to help my body but it's still not easy to deal with.
×
×
  • 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.