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 does gluten stay in your system?


1398-Days

Recommended Posts

1398-Days Contributor

I got glutened on November 19th and I'm still not completely better.. For a few days afterwards I felt really sad and anxious, and just not like myself at all. I felt a lot better within a few days, and figured that was that. But I still don't feel like myself. I've been a lot better the past few weeks but will occasionally feel kind of sad for no apparent reason. It still seemed to be gradually getting better though so I wasn't worried.. But now.. the past few days have been rough. I've just been kind of depressed and I have no idea why! Is this still from getting sick almost a month ago? The good news is that I have felt much better today! But is there anything I can do to really get back to feeling completely like myself again?


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Gluten doesn't " stay in your system" .  Food passes through and out the other side in 24-48 hours, usually.  I suppose if you are constipated, it might be another day.  What causes reactions are the antibodies our bodies make while the gluten is passing through the small intestine.  Those antibodies can last for a while. But one isolated glutening shouldn't cause them to be hig a month later.

 

However, I am wondering, after a month, if this might be something not relate to gluten.  Or you are stil getting gluten somewhere?  I am not sure how long you have been gluten-free or if you have Celiac?  If you have Celiac, it can takes months or even a couple of years to heal.

mommida Enthusiast

I can very likely be a vitamin D deficiency from gut damage and season change.  Just think about the added stress of holiday/ family gatherings/ society in general with current issues.  (Just recently my spouse's Christmas party and a few people mentioned the California shooting and were definitely on edge.)

Relax, take care of yourself, and definitely go in to the doctor for a check up.

Positron Newbie
On ‎12‎/‎15‎/‎2015 at 2:08 AM, 1398_Days said:

I got glutened on November 19th and I'm still not completely better.. For a few days afterwards I felt really sad and anxious, and just not like myself at all. I felt a lot better within a few days, and figured that was that. But I still don't feel like myself. I've been a lot better the past few weeks but will occasionally feel kind of sad for no apparent reason. It still seemed to be gradually getting better though so I wasn't worried.. But now.. the past few days have been rough. I've just been kind of depressed and I have no idea why! Is this still from getting sick almost a month ago? The good news is that I have felt much better today! But is there anything I can do to really get back to feeling completely like myself again?

It takes a full 2 years for the damage that a serious gluten issue can cause to heal.  You will still be finding things in them that contain gluten for at least another year on average.  I found lactose in my allergy pills recently.  Remember that maltodextrine  is made from wheat, so always look for corn maltodextrine which is ok.

notme Experienced
7 hours ago, Positron said:

It takes a full 2 years for the damage that a serious gluten issue can cause to heal.  You will still be finding things in them that contain gluten for at least another year on average.  I found lactose in my allergy pills recently.  Remember that maltodextrine  is made from wheat, so always look for corn maltodextrine which is ok.

 

this is alllllllllllllllllllllllllll not true. (except that corn maltodextrine is ok)  i don't even know *what * that second statement even means.  not everybody is lactose intolerant.  once your villi begin to heal, they will produce more of the enzyme your body needs to digest lactose.  and what does maltodextrine have to do with any of this ?  

Positron Newbie
1 hour ago, notme! said:

this is alllllllllllllllllllllllllll not true. (except that corn maltodextrine is ok)  i don't even know *what * that second statement even means.  not everybody is lactose intolerant.  once your villi begin to heal, they will produce more of the enzyme your body needs to digest lactose.  and what does maltodextrine have to do with any of this ?  

Villi do not always heal to the extent that lactose can be tolerated.  Mine never have.  Maltodextrine is a wheat product most of the time, however corn maltodextrine is a corn product and is safe for those who can not consume gluten.

What is maltodextrin?

Maltodextrin is a food additive that is produced from a grain starch. In the United States, it is most commonly produced using corn, but it can also be produced from rice, potatoes and wheat. The starch goes through a process called partial hydrolysis, which uses water, enzymes and acids to create a water-soluble white powder. Interestingly, the partial hydrolysis method leaves maltodextrin with less than 20 percent sugar content. However, full hydrolysis creates corn syrup solids, which have over 20 percent sugar.

ravenwoodglass Mentor
13 hours ago, Positron said:

Villi do not always heal to the extent that lactose can be tolerated.  Mine never have.  Maltodextrine is a wheat product most of the time, however corn maltodextrine is a corn product and is safe for those who can not consume gluten.

What is maltodextrin?

Maltodextrin is a food additive that is produced from a grain starch. In the United States, it is most commonly produced using corn, but it can also be produced from rice, potatoes and wheat. The starch goes through a process called partial hydrolysis, which uses water, enzymes and acids to create a water-soluble white powder. Interestingly, the partial hydrolysis method leaves maltodextrin with less than 20 percent sugar content. However, full hydrolysis creates corn syrup solids, which have over 20 percent sugar.

If the villi took 2 years to recover then folks who had been gluten free for a couple months would not need to do a gluten challenge before a biopsy. The villi actually regrow in a pretty short time but it does take time for us to heal from the effects of the antibodies.  There are folks who just don't tolerate dairy whether celiac or not and you may be one of them. 

As far as maltodextrin is concerned I have been gluten free for over 13 years and have never seen it made from wheat in the US. If it was made from wheat and in a product sold in the US it would have to be labeled as such.

I understand you are new to the diet and still quite angry because it took 3 whole months for you to be diagnosed (sorry if that seems a bit flippant but it took over 40 YEARS for me to get one and I was almost dead) but not all doctors are liars and frauds. Some are just woefully ignorant about celiac but that is getting better. The proof of that is the short time it took for you to diagnosed.  There are folks here trying to help people like yourself with info that has been well researched. Please be sure the info you post is accurate


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



Celiac.com Sponsor (A8-M):



  • 2 years later...
Manijeh Newbie

It will take 8 months for gluten to leave your system and digestive system.

kareng Grand Master
1 hour ago, Manijeh said:

It will take 8 months for gluten to leave your system and digestive system.

What are you basing this very specific  time frame on?  Please post a link to your source.  

Gluten, like any food, will be out of the digestive system within a few days.  That’s how the GI tract works.  

Antibodies can take much longer to leave the body.  There are some studies that show that some people may continiue making antibodies for a few weeks after going gluten-free. 

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
      132,955
    • Most Online (within 30 mins)
      7,748

    JodyBledsoe
    Newest Member
    JodyBledsoe
    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

    • 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.