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

A Week To Feel Glutened?


SanFranGirl

Recommended Posts

SanFranGirl Rookie

I was diagnosed with celiac in June after feeling sick for 2 years with chronic constipation, fevers, bloating, and rashes, and fatigue (and unexplainable hypothyroidism which I am treating and was diagnosed earlier). I was only diagnosed with blood tests (positive for the anitibodies and one of the genes), never had a intestinal biopsy...

Since I combed all the gluten out of my diet I've slowly felt better and better since june, almost feeling like my old self again... So a week ago, I accidentally ate what was definately a significant amount of gluten - pie crust made from wheat (I thought it was gluten free). And I barely reacted. I felt anxious, and had soft stool but it could have been just because I was freaking out (haha). No rash or fever...and now a week later I feel for the first time in months what I associate with gluten. I feel fatigued and anxious and have a fever and very very bloated. still no vomiting ever or stomach aches. And also its really not THAT bad, like half of the severity of what I would experience every other week before going gluten free.

 

So I'm wondering if anyone is similar to me? or if its possible that I dont have celiac's? which just seems ridiculous because of the blood tests and then slowly feeling better on a gluten free diet (though it took a few months before I started feeling better). But if I do have celiac's why didn't I react right away to the gluten? Is it because I have only been gluten free for 6 months?


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Everyone is different. I just had anemia when I was diagnosed. I was a little anxious and crazy, but I was going through menopause at the same time! My antibodies were barely positive yet my endoscopy/biopsy revealed moderate to severe damage.

Your body may take take time to ramp up and produce antibodies. I never had a follow up blood test because my results were so low. It would probably take months for my ferritin levels to drop enough to impact my hemoglobin levels making me anemic again. I also have not been back for a blood test because I know I haven been adhering to my diet since my husband has been gluten free for 13 years! No learning curve for me!

Stay the course and count your blessings that your reaction was not great!

nvsmom Community Regular

My symptoms can be delayed and are worse with repeated glutenings.  I don't feel great if I have gluten but if I accidentally have it again and again, which I did with some fries over a year ago, my symptoms slowly become worse - they creep up on me until they can't be ignored.

 

You do have celiac disease but you either got lucky with your symptoms this time around, or you are like me and you feel worse with repeated exposures.

 

Hope you feel better.

SMRI Collaborator

A week seems like a long time for a delay but maybe.  It could be a virus or something too.  I know we automatically go to gluten when we don't feel well but we still get sick from germs.  Fevers are not a common symptom which makes me wonder if you are just coming down with something.  Flu season is here, and they are saying it's going to be a bad one because there is a new strain out there that was not in the vaccine.

beth01 Enthusiast

I get fevers with glutenings. It was one of my symptoms I complained about for a year, unexplained repeated low grade fevers.

Like the others said, maybe that is how you will react. Sorry dear, but the labs weren't wrong, you have celiac. Hope you get to feeling better soon.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,425
    • Most Online (within 30 mins)
      7,748

    allison calvern
    Newest Member
    allison calvern
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Chronic mildly elevated liver enzymes was what eventually led to my celiac diagnosis but it took thirteen years to ferret that out and by that time I had developed osteopenia.  Yes, you've got a lot going on there in the way of autoimmune disorders and all of them we now know have a connection with celiac disease. It is true that autoimmune disorders tend to cluster. But it sounds like you are getting medical attention and keeping an eye on things. 
    • Lburnett
      Thank you! Yes, I have celiac disease, lupus and Sjögrens. My ALT and AST have been chronically slightly elevated for a couple years and recently had an acute kidney injury (thinking it was from an antibiotic) with increased Lipase. So my primary doctor referred me to a kidney specialist. Other kidney labs are normal. 
    • ChrisSeth
      My test results for TissueTransglutaminase IgA Antibody test came back normal. Like spot on normal. I do not have celiac! My problems are stemming from this H Pylori infection. I think I’ve had it for years. We’ll see if the doctor wants to do an endoscopy to see how extensive the damage is. Otherwise just a regimen of antibiotics will do the trick. The thanks for your guys’s help! 
    • Beck1430
      Thank you both so much for taking the time to reply.    Cristiana - yes the rashes seemed to resolve when he came off gluten too. I haven’t seen those pictures before, thanks for pointing me to them. I’d say his rash isn’t like the more severe photos which are scabbed and very bumpy. His rash is more like lots and lots of patches of eczema than spots. No we have no celiac in the family to my knowledge, though my mum and sister both have autoimmune diseases and wheat sensitivity. I think you’re right and I’ll have to do another trial to confirm if it was the wheat. I’ve been hoping all day that I come down with the bug to rule out the wheat reaction! But the rest of the family are absolutely fine.    Trents - thank you for the info regarding the genes. That’s very interesting and I’d definitely consider doing that as a way to rule it out without putting him back on wheat. I also didn’t know celiacs were commonly intolerant to dairy and soy. I think you’re right and there is definitely enough factors to show something is going on. I think I’ll do a repeat trial of the wheat challenge and if he reacts again I shall look into the genetic testing.    Thank you both so much for your time. Becky          
    • trents
      Welcome to the forum, @Lburnett! Have you been officially diagnosed with celiac disease? I'm just trying to get a handle on the health context from which your question comes.
×
×
  • Create New...