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

Anyones Advice. Input From Celiacs, Intolerants, People With My Issues..anyone!


runningcrazy

Recommended Posts

runningcrazy Contributor

Hi, im new here!

for the record I AM eating gluten now, I have been since April

I've been having many problems with my stomach. Constipation,stomach ache after each time i eat, bloating , and I lost some weight.

I am a 13 year old girl, 5'4 and right now I weigh about 94lbs.

In around February I weighed 81lbs, which means I lost about 12 lbs in the last 6 months. I was also experiencing pretty bad constipation despite my daily running and vegetarian/high fiber diet and loads of water. Me and my mom figured we would give a gluten free diet a try.

I went gluten free for 20 days. In that time I gained about 8lbs. I was feeling better at first, but my stomach aches were still there. I ended up going to a pediatrician to get a blood test to ensure it was celiacs. She said that even thoigh I hadnt eaten gluten, the blood test would still be accurate. It came back negative. I was given a prescription for Miralax and at my follow up appointment I was told to eat gluten again and was prescribed dulcolax along with miralax.

I've been eating gluten since half way through april and I have gained about 6 lbs still, so that might mean its not gluten problem? And since i had been eating it two months i got another blood test which came back negative again.

My first blood test from April is a bit confusing to us. I had a CBC in April and just a celiac test in June. Here are my celiac results in comparison from not eating to eating it:

April(no gluten): Tissue Transglutaminade AB IGA: 0.8 (ref range: 0.0-3.9)

IgA: 236 (ref range 80-450)

Other things to note were low iron, high lymphocytes(about 5 above the highest for "normal") Low White blood count, and low glucose.

June result: Tissue Transglutaminase Ab IGA: 0.9 (ref range-0.0-3.9)

IgA: 189 (ref range- 80-450)

So from no gluten to eating it my Transglutaminase went up SLIGHTLY and my IgA went down a bit. They still all were in the range of normal.

Still have stomach aches, still am severely constipated(according to multiple xrays) still am bloated all the time, and as prescribed by my pediatrician I take 2 doses of miralax, 2 colace, and 2 dulcolax daily. For about 2 months now. Miralax longer.

I will see a gastroenteroligist sometime hopefully this month but i just want some input from celiacs or intolerants. Does this sound like a celiac/intolerant case?

Im very confused. My pediatrician said i may get an endoscopy and if all is normal possibly IBS, but ive heard over half the time IBS is really celiacs!

Any iput would be great, sorry for such a long story!!


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



Celiac.com Sponsor (A8-M):



Becci Enthusiast

If you have already cut out gluten, have you thought about trying to cut out something else to see if that is a problem as well?

I had to cut out both gluten and dairy. Since then, I am fine...

Another problem you could be having is accidentally getting into gluten without knowing it.

Have you checked your soaps, shampoos, makeup, etc?

And do you check ingredients in foods before eating them? You could be getting glutened and not know it.

And as for not eating gluten and your test still being accurate as to you having Celiac, that is not true. As far as I know, once you stop eating gluten, your tests will come back negative, because it is no longer in your system. Once you go Gluten-Free, your tests will most likely be negative as there is no gluten in your system.

Have you checked the ingredients in the meds they are giving you?

debmidge Rising Star
Hi, im new here!

I've been having many problems with my stomach. Constipation,stomach ache after each time i eat, bloating , and I lost some weight.

I am a 13 year old girl, 5'4 and right now I weigh about 94lbs.

In around February I weighed 81lbs, which means I lost about 12 lbs in the last 6 months. I was also experiencing pretty bad constipation despite my daily running and vegetarian/high fiber diet and loads of water. Me and my mom figured we would give a gluten free diet a try.

I went gluten free for 20 days. In that time I gained about 8lbs. I was feeling better at first, but my stomach aches were still there. I ended up going to a pediatrician to get a blood test to ensure it was celiacs. She said that even thoigh I hadnt eaten gluten, the blood test would still be accurate. It came back negative. I was given a prescription for Miralax and at my follow up appointment I was told to eat gluten again and was prescribed dulcolax along with miralax.

I've been eating gluten since half way through april and I have gained about 6 lbs still, so that might mean its not gluten problem? And since i had been eating it two months i got another blood test which came back negative again.

My first blood test from April is a bit confusing to us. I had a CBC in April and just a celiac test in June. Here are my celiac results in comparison from not eating to eating it:

April(no gluten): Tissue Transglutaminade AB IGA: 0.8 (ref range: 0.0-3.9)

IgA: 236 (ref range 80-450)

Other things to note were low iron, high lymphocytes(about 5 above the highest for "normal") Low White blood count, and low glucose.

June result: Tissue Transglutaminase Ab IGA: 0.9 (ref range-0.0-3.9)

IgA: 189 (ref range- 80-450)

So from no gluten to eating it my Transglutaminase went up SLIGHTLY and my IgA went down a bit. They still all were in the range of normal.

Still have stomach aches, still am severely constipated(according to multiple xrays) still am bloated all the time, and as prescribed by my pediatrician I take 2 doses of miralax, 2 colace, and 2 dulcolax daily. For about 2 months now. Miralax longer.

I will see a gastroenteroligist sometime hopefully this month but i just want some input from celiacs or intolerants. Does this sound like a celiac/intolerant case?

Im very confused. My pediatrician said i may get an endoscopy and if all is normal possibly IBS, but ive heard over half the time IBS is really celiacs!

Any iput would be great, sorry for such a long story!!

Hi Glad to see a new face ;)

Were you tested for lactose intolerance?

DM

runningcrazy Contributor

I have been eating gluten for almost 3 months. I haven't been gluten free since April. My doctor said since I don't have diarhea or other lactose intolerant symptoms that it's not dairy.

Becci Enthusiast

If your eating gluten after going gluten-free, then that is probably your problem with the pains.

I went gluten free and then ate some on accident, and now I am having horrible stomach pains that have to do with eating gluten.

Stop eating it and see if it goes away. It may take a few days.

nora-n Rookie

It could be early celiac. Also, your numbers are not 0.

My weight used to go UP and up, and after a while off gluten by accident (Went low-carb) and then noticing I got sick from gluten, and a gluten challenge for five weeks (too short) my weight started to drop all by itself.

If you read around here on celiac.com, in the articles, about obesity, it looks like many obese people are celiac, but only partially. The tests are very inaccurate in partial villi damage.

And in partial villi damage, there is a huge problem with absorbing fatty acids and the whole metabolism goes to starvation mode and grabs as much energy from food as possible. Thence the weight gain.

It is hard to get a diagnosis in early celiac, or with partial villous damage.

maybe an endoscopy with biopties will show increased intraepitelial lymphocytes, if they bother to count them. They did not count mine.

See www.thefooddoc.com and look for his blog there and he explains about the IEL's.

nora

Lawspike Rookie
Hi Glad to see a new face ;)

Were you tested for lactose intolerance?

DM

Sorry to hijack this thread.. LOL

Deb, I am a new member and do not yet have enough posts to message you. I noticed that your husband can't tolerate many of the additional things I can't. The dietitians in my state we currently live in (TN) are almost completely UNFAMILIAR with Celiac, and I can't consume (besides wheat), casein, (lactose as well) soy, eggs, honey and coconut (discovered due to a really bad reaction I just had during my elimination process).

I would LOVE to chat with you about what exactly your husband DOES and can eat... I was JUST diagnosed on 7/13/09 and am overwhelmed, frustrated and feel like a sinking ship... I too have been misdiagnosed for almost all of my 35 years on earth, and I too, have suffered every other imaginable condition and ailment, which I believe could have been avoided with a proper diagnosis.

THANKS a MILLION!

As to Nora,

There may be other issues going on as well, I would - if it were me - go through with the biopsy. They test for additional disorders, in addition to Celiac, and this may be the puzzle piece that solves what you are going through! Whatever your decision, I sincerely hope you start feeling better and get to the bottom of this!


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.

  • 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. - trents replied to GlorietaKaro's topic in Super Sensitive People
      2

      Am I nuts?

    2. - Russ H posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Anti-endomysial Antibody (EMA) Testing

    3. - Scott Adams replied to JoJo0611's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Just diagnosed today

    4. - Scott Adams replied to GlorietaKaro's topic in Super Sensitive People
      2

      Am I nuts?

    5. - Scott Adams replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      28

      My journey is it gluten or fiber?

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

    • Total Members
      132,805
    • Most Online (within 30 mins)
      7,748

    lalan45
    Newest Member
    lalan45
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Welcome to the celiac.com community, @GlorietaKaro! As Scott indicated, without formal testing for celiac disease, which would require you to have been consuming generous amounts of gluten daily for weeks, it would be not be possible to distinguish whether you have celiac disease or NCGS (Non Celiac Gluten Sensitivity). Their symptoms overlap. The difference being that celiac disease is an autoimmune disorder that damages the lining of the small bowel. We actually no more about celiac disease than we do about NCGS, the mechanism of the latter being more difficult to classify. There are specific antibody tests for celiac disease diagnosis and there is also the endoscopy/biopsy of the small bowel lining. Currently, there are no tests to diagnose NCGS. Celiac disease must first ruled out. Researchers are working on developing testing methods to diagnose celiac disease that do not require a "gluten challenge" which is just out of the question for so many because it poses serious, even life-threatening, health risks. But we aren't there yet.
    • Russ H
      I thought this might be of interest regarding anti-EMA testing. Some labs use donated umbilical cord instead of monkey oesophagus. Some labs just provide a +ve/-ve test result but others provide a grade by testing progressively diluted blood sample. https://www.aesku.com/index.php/ifu-download/1367-ema-instruction-manual-en-1/file Fluorescence-labelled anti-tTG2 autoantibodies bind to endomysium (the thin layer around muscle fibres) forming a characteristic honeycomb pattern under the microscope - this is highly specific to coeliac disease. The binding site is extracellular tTG2 bound to fibronectin and collagen. Human or monkey derived endomysium is necessary because tTG2 from other mammals does not provide the right binding epitope. https://www.mdpi.com/1422-0067/26/3/1012
    • Scott Adams
      First, please know that receiving two diagnoses at once, especially one you've never heard of, is undoubtedly overwhelming. You are not alone in this. Your understanding is correct: both celiac disease and Mesenteric Panniculitis (MP) are considered to have autoimmune components. While having both is not extremely common, they can co-occur, as chronic inflammation from one autoimmune condition can sometimes be linked to or trigger other inflammatory responses in the body. MP, which involves inflammation of the fat tissue in the mesentery (the membrane that holds your intestines in place), is often discovered incidentally on scans, exactly as in your case. The fact that your medical team is already planning follow-up with a DEXA scan (to check bone density, common after a celiac diagnosis) and a repeat CT is a very proactive and prudent approach to monitoring your health. Many find that adhering strictly to the gluten-free diet for celiac disease helps manage overall inflammation, which may positively impact MP over time. It's completely normal to feel uncertain right now. Your next steps are to take this one day at a time, focus on the gluten-free diet as your primary treatment for celiac, and use your upcoming appointments to ask all your questions about MP and what the monitoring plan entails. This dual diagnosis is a lot to process, but it is also the starting point for a managed path forward to better health. This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    
    • Scott Adams
      Your experience is absolutely valid, and you are not "nuts" or a "complete weirdo." What you are describing aligns with severe neurological manifestations of gluten sensitivity, which is a recognized, though less common, presentation. Conditions like gluten ataxia and peripheral neuropathy are documented in medical literature, where gluten triggers an autoimmune response that attacks the nervous system, leading to symptoms precisely like yours—loss of coordination, muscle weakness, fasciculations, and even numbness. The reaction you had from inhaling flour is a powerful testament to your extreme sensitivity. While celiac disease is commonly tested, non-celiac gluten sensitivity with neurological involvement is harder to diagnose, especially since many standard tests require ongoing gluten consumption, which you rightly fear could be dangerous. Seeking out a neurologist or gastroenterologist familiar with gluten-related disorders, or consulting a specialist at a major celiac research center, could provide more validation and possibly explore diagnostic options like specific antibody tests (e.g., anti-gliadin or transglutaminase 6 antibodies) that don't always require a gluten challenge. You are not alone; many individuals with severe reactivity navigate a world of invisible illness where their strict avoidance is a medical necessity, not a choice. Trust your body's signals—it has given you the most important diagnosis already.
    • Scott Adams
      Some members here take GliadinX (a sponsor here) if they eat out in restaurants or outside their homes. It has been shown in numerous studies to break down small amounts of gluten in the stomach, before it reaches your intestines. This would be for small amounts of cross-contamination, and it would not allow any celiac to eat gluten again.
×
×
  • 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.