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

How Long After Starting A Gluten Free Diet Will Symptoms Recede?


Omiak

Recommended Posts

Omiak Newbie

Went to my doctor originally thinking I have a stomach parasite. I've had some recurring digestion issues that started just after I returned from a bicycle tour in central america (I drank the water a lot of places I probably shouldn't have).

 

The doctor did a blood test and told me I have Celiacs disease. My tissue transgutimase results were abnormal (a 21 with normal range being 0-19). He refused to write a referral to get a biopsy by a gastroenterologist (no idea why). I'd read that the biopsy is necessary to diagnose celiacs disease so I went to another doctor and asked for a referral. He told me that I probably didn't have celiacs disease and wrote me the referral to speak to the gastroenterologist but they couldn't get me in for over a month and a half. In the meantime I've been gluten free for a little over two weeks and my symptoms haven't changed. I did accidentally eat falafel once in the middle there.

 

I'm aware that I need to be on a gluten diet for an extended period before I have the biopsy.

 

Just wondering if anyone knows if two weeks of eating gluten free is normally enough time to see some change or reduction in symptoms. Any insight would be appreciated.

 

Thanks.


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

No, it can takes months to YEARS to have symptoms resolve! Some people do not have any symptoms at all!

I would strongly do some research. The University of Chicago has a great celiac website and discusses testing. Doctors, even GI doc get it wrong all the time. Just read all the threads in this forum.

You do have to be eating gluten to get tested. Since you are just mildly positive, I would take the blood test over in a few weeks after consuming gluten and ask for biopsies (up to six).

I was barely positive and my biopsy showed a moderate to severe damage. My only symptom was anemia at the time of my diagnosis. ,

You could also still have a parasite issue on top of celiac disease. Was that eliminated?

Here is a list of the tests:

-tTG IgA and tTG IgG

-DGP IgA and DGP IgG

-EMA IgA

-total serum IgA and IgG (control test)

-AGA IGA and AGA IgG - older and less reliable tests largely replace by the DGP tests

-endoscopic biopsy - make sure at least 6 samples are taken

Welcome to the forum and let us know how it goes!

Omiak Newbie

Thanks. It seems much more reasonable to me to get the biopsy right away rather than to try and spend months or years trying to diagnose myself by trial and error with the diet. I'm not sure why the first doctor I saw refused to write the reference. I asked both doctors this question about how long it would take to see improvement by changing my diet and both of them said they didn't know.

 

DGP IgA and IgG were both negative (9 and 4 respectively).

 

I was given metronidazole for possible parasite issues but it did not resolve my symptoms. I know that some stomach parasites are treated with other drugs such as praziquantel, but I'm not sure if those parasites are immune to treatment with metronidazole. Things to ask the GI specialist I suppose.

cyclinglady Grand Master

Obtaining a biopsy is still considered the "gold standard" by leading experts in diagnosing celiac disease. It is nice to know or have a benchmark of damage and to check for cancer.

My husband went gluten-free 14 years ago per the advice of my allergist and his GP. It worked. He feels great. But he would be the first to tell you that I get a ton of support from family, friends and medical staff having a firm celiac disease diagnosis two years ago. Plus, our doctor did not blink an eye when we asked (and will continue to ask) for testing for our kid even though she is symptom free!

There is no way for my husband to do a gluten challenge. He knows and we know that gluten makes him sick, but it took a lot of trial and error and that constant wondering if he really has celiac disease (though we are pretty sure since autoimmune disease runs very strongly in our families -- kid is doomed!)

I wish you well!

Oh, and a biking adventure! Maybe when I retire!

ravenwoodglass Mentor

Did your doctor do stool testing to check for parasites? If not that should be done. The medication that you were given does have D as a side effect so even if the diet was helping (if you are in fact celiac) the side effects of the med may be masking any improvement. 

 Meanwhile get back on gluten and get full panels done along with the biopsy. How soon it takes to improve on the diet varies. For some folks it takes a long time to see symptom resolution but for others it can happen pretty quickly. In my own case the digestive issues cleared up within days (although mistakes on the diet brought them back full force until I eliminated all sources of CC) but other problems took much longer to resolve. 

Hope this gets figured out and you are feeling better soon. 

nvsmom Community Regular

Just wondering if anyone knows if two weeks of eating gluten free is normally enough time to see some change or reduction in symptoms. Any insight would be appreciated.

 

 

In some people, two weeks on the gluten-free diet is enough to see improvements in some symptoms, although not all.  I had less bloating and fewer stomach aches within days of going gluten-free.  Headaches and a few other symptoms were getting better at about a month gluten-free.  After a year gluten-free, my arthritis improved.  It really depends on the person and the symptoms.

 

Also, some people get worse before they get better.  I had withdrawal for about 10 days - I still remember that headache.  after 2-3 months gluten-free, my arthritis and fatigue became much worse.  I really started to feel like I was getting well after being gluten-free for 6 months.  2 weeks is really nothing.  :(

 

I am somewhere between both of those doctors; I think your weak positive tTG IgA probably points to celiac disease because 95% of positive tTG IgA tests are from celiac disease.  Those weak positives are usually the ones caused by other issues (like crohn's, colitis, thyroiditis, liver disease, diabetes, or a serious infection) when it is not caused by celiac disease (which it usually is).  My guess is that you probably have celiac disease, but can't state it with 100% certainty.  

 

The biopsy requires a gluten challenge of 2-4 weeks of eating about 1/2 to 4 (1-2 is average) slices of bread per day.  If a biopsy is ordered you will need to resume gluten.  If your Gastro wants to retest, you should go back on gluten immediately because 2-3 months of gluten is needed for accurate blood tests. You may not want to go gluten-free yet.

 

If you retest your tTG IgA after some months gluten-free, and your result is down, that could also be confirmation of a celiac disease diagnosis.

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. - GlorietaKaro replied to GlorietaKaro's topic in Super Sensitive People
      3

      Am I nuts?

    2. - trents replied to GlorietaKaro's topic in Super Sensitive People
      3

      Am I nuts?

    3. - lalan45 replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      29

      My journey is it gluten or fiber?

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

      Anti-endomysial Antibody (EMA) Testing

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

      Just diagnosed today

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

    • Total Members
      132,806
    • Most Online (within 30 mins)
      7,748

    IleneG
    Newest Member
    IleneG
    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

    • GlorietaKaro
      Thanks to both of you for your responses!  Sadly, even after several years of very strict gluten avoidance, I remember the symptoms well enough that I am too frightened to risk a gluten challenge— heartbeat and breathing problems are scary— Scott, thank you for the specific information— I will call around in the new year to see if I can find anyone. In the meantime, I will carry on has I have been— it’s working! Thanks also for the validation— sometimes I just feel crushed by disbelief. Not enough to make me eat gluten though—
    • 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.
    • lalan45
      That’s really frustrating, I’m sorry you went through that. High fiber can definitely cause sudden stomach issues, especially if your body isn’t used to it yet, but accidental gluten exposure can feel similar. Keeping a simple food/symptom journal and introducing new foods one at a time can really help you spot patterns. You’re already doing the right things with cleaning and separating baking—also watch shared toasters, cutting boards, and labels like “may contain.”
    • 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.):    
×
×
  • 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.