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
      128,073
    • Most Online (within 30 mins)
      7,748

    David Croft
    Newest Member
    David Croft
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.6k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      @KRipple, thank you for the lab results from your husband's celiac disease blood antibody testing. The lab result you share would seem to be the tTG-IGA (Tissue Transglutaminase IGA) and the test result is in excess of 10x normal. This is significant as there is an increasing tendency for physicians to grant a celiac disease diagnosis on the basis of antibody testing alone when the scores on that particular test exceed 10x normal. This trend started in the UK during the COVID pandemic when there was tremendous pressure on the medical system over there and it has spread to the USA. The tTG-IGA is the centerpiece of celiac disease blood antibody testing. All this to say that some doctors would grant a celiac disease diagnosis on your husband's bloodwork alone and not feel a need to go forward with an endoscopy with biopsy. This is something you and your husband might wish to take up with his physicians. In view of his many health issues it might be wise to avoid any further damage to his small bowel lining by the continuing consumption of gluten and also to allow healing of such to progress. The lining of the small bowel is the place where essentially all of our nutrition is absorbed. This is why celiac disease when it is not addressed with a gluten free diet for many years typically results in additional health problems that are tied to nutritional deficiencies. The millions and millions of tiny finger-like projections that make up the nutrient absorbing surface of the small bowel lining are worn down by the constant inflammation from gluten consumption. In celiac disease, the immune system has been tricked into labeling gluten as an invader. As these finger-like projections are worn down, the efficiency of nutrient absorption becomes more and more compromised. We call this villous atrophy.   
    • KRipple
      Thank you so much! And sorry for not responding sooner. I've been scouring the hospital records and can find nothing other than the following results (no lab info provided): Component Transglutaminase IgA   Normal Range: 0 - 15.0 U/mL >250.0 U/mL High   We live in Olympia, WA and I will be calling University of Washington Hospital - Roosevelt in Seattle first thing tomorrow. They seem to be the most knowledgeable about complex endocrine issues like APS 2 (and perhaps the dynamics of how APS 2 and Celiacs can affect each other). His diarrhea has not abated even without eating gluten, but that could be a presentation of either Celiac's or Addison's. So complicated. We don't have a date for endoscopy yet. I will let my husband know about resuming gluten.    Again, thank you so much for sharing your knowledge with me!
    • Jmartes71
      Ginger is my best friend, it helps alot with tummy issues..
    • aattana
      Hi Phosphone, did you ever figure out what elevated your DGP?  I am in the same boat. 
    • trents
      Scott makes a good point about the prednisone. It has a general suppressing effect on the immune system. Don't misunderstand me. In view of your husband's several autoimmune afflictions, it would seem to be an appropriate medication therapy but it will likely invalidate endoscopy/biopsy test results for celiac disease.
×
×
  • Create New...