Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 soon do you get symptoms after gluten? Confused


Haveaniceday

Recommended Posts

Haveaniceday Apprentice

I'm really confused trying to track what causes my reactions because it seems that I don't get obvious symptoms for 24-48 hours after ingesting. I will feel some fatigue and allergy type symptoms/head fog for the first 24 hours, but not enough to say definitely glutened. Then I'll get gastro upset (yellow diharrea, stomach pain etc) which lasts for about a week but doesn't start until 48 hours after, get worse over a few days then subsides. It's like it takes a few days for my immune system to really rev up.

It does seem different every time though. Is this possibily related to the amount of gluten? Ie big amount symptoms come on hard and fast, small amount a slow burn?


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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

This can vary greatly from individual to individual. Super sensitive people claim they get severe symptoms only minutes after ingesting gluten, while other may have no symptoms at all. Some people say it takes 24-48 hours, which can make it very hard to identify the source of contamination. How long and severe the symptoms are can also vary greatly. Generally speaking, the more damage your gut has, the worse your reactions can be, and you can even react to other foods that don't contain gluten, like dairy, corn, soy, etc. Once your gut heals some people react less, and can add some of the non-gluten things they react to back into their diets.

Haveaniceday Apprentice
5 hours ago, Scott Adams said:

This can vary greatly from individual to individual. Super sensitive people claim they get severe symptoms only minutes after ingesting gluten, while other may have no symptoms at all. Some people say it takes 24-48 hours, which can make it very hard to identify the source of contamination. How long and severe the symptoms are can also vary greatly. Generally speaking, the more damage your gut has, the worse your reactions can be, and you can even react to other foods that don't contain gluten, like dairy, corn, soy, etc. Once your gut heals some people react less, and can add some of the non-gluten things they react to back into their diets.

Thank you Scott, that's really helpful. I'm curious, could you please elaborate on the reactions to foods like soy etc. I have been already diagnosed as lactose intolerant, my Dr said that may improve in time, but my reactions to diary are just a tiny bit of tummy upset. I react to soy also, but it isn't too extreme. I'm wondering if other food intolerances would cause symptoms similar to the immune response to gluten? Or if they would be markedly different/less severe?

Scott Adams Grand Master

This varies a lot from person to person as well, but I experienced similar gut feelings when I ate corn, chicken eggs, tomatoes and dairy (casein) before and after my diagnosis. This was likely due to the leaky gut situation caused by my flattened villi, and I also had internal bleeding due to the celiac lesions found during my biopsy. I had to also eliminate those foods for a couple of years after my diagnosis, but was able to slowly add them back after my gut healed.

I now plan to take a ALCAT food sensitivity test, and will be writing about my results, as it's possible that I really should still not be eating certain foods. Long before my diagnosis I had to take both food and pollen allergy shots, and scored very high on food allergy testing for various things, including a super high score for wheat. My allergist told me to only eat wheat once or twice a week, and I ignored him (I was 18 or 19). I still wonder what might have happened had I followed his advice. Perhaps the celiac trigger would never have been turned on. 

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,075
    • Most Online (within 30 mins)
      7,748

    Annevt
    Newest Member
    Annevt
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      Just switching to gluten free diet will answer your question without involving anyone else.  Your sister was diagnosed, that puts you at 40% risk of having it also as a first degree relative.  If you improve on a trial gluten free diet, you either have Celiac Disease (autoimmune) or Non Celiac Gluten Sensitivity (not autoimmune).  In any case it is important to address nutritional deficiencies like vitamin D.  Gluten free processed foods are not required to fortify.  The reason gluten foods are fortified is our western diet is deficient in them to the point where the government had to step in and require fortification.   Once you start GFD you'll realize it was the gluten you were afraid of all along, but nobody told you.
    • trents
      Maybe celiac but maybe NCGS that was misdiagnosed as IBS morphing gradually into celiac. Is NCGS a new category to you? It shares many of the same GI symptoms with celiac disease but does not damage the small bowel lining like celiac.
    • knitty kitty
      Thiamine has antifungal properties.  The body uses thiamine to keep bacteria and yeasts from overgrowth in the digestive system.   Fluconazole use can cause thiamine deficiency.   Supplementing with thiamine in the form Benfotiamine would be beneficial as Benfotiamine promotes intestinal healing.   Thiamine and the other B vitamins tend to be low in Celiac due to malabsorption.  Talk to your doctor about supplementing vitamins and minerals.
    • Scott Adams
      Welcome @Natalia Revelo, your experience is profoundly difficult and, sadly, not entirely unique within the celiac community. It's the frustrating reality of "silent" or ongoing damage that isn't captured by the MARSH score alone, which only measures active villous atrophy. Your normal biopsy suggests your diet is preventing the classic autoimmune attack, but it doesn't mean your gut has fully healed or that other issues aren't at play. The inflammation from your newly discovered milk and egg allergies is a huge clue; this constant allergic response can create a low-grade inflammatory environment that severely hampers nutrient absorption, effectively creating a "leaky gut" scenario independent of celiac damage. This is likely why your iron stores deplete so rapidly—your body is both unable to absorb it efficiently and may be losing it through inflammation. While the functional medicine path is expensive, it's clearly providing answers and relief that traditional gastroenterology, focused solely on the gluten-free diet and biopsy results, is missing. To move forward, continue the gut-healing protocols your functional doctor recommends (perhaps exploring alternative options to glutamine that won't irritate your cystitis), maintain your strict avoidance of all allergens and irritants, and know that true healing is a multi-faceted process. You might seek a second opinion from a different gastroenterologist who is more knowledgeable about non-responsive celiac disease and the complex interplay of food allergies and micronutrient absorption, but your current path, while costly, seems to be leading you toward the steady health you need.
    • knitty kitty
      Have you had a DNA test to look for Celiac disease genes?  If she doesn't have any celiac specific genes, look for another explanation.  If she does have Celiac genes, assume they are turned on and active Celiac disease is progressing.  All first degree relatives (mother, father, siblings, children) should be genetically tested as well.   Sometimes blood tests are ambiguous or false negatives if one has anemia, diabetes or thiamine deficiency.  Certain medications like antihistamines and steroids can suppress the immune system and result in false negatives or ambiguous results on antibody tests.  
×
×
  • Create New...