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

Testing after Gluten exposure


celichris

Recommended Posts

celichris Rookie

Every time I get exposed to gluten (4 times this year) my Dr wants to test me. I have always been seronegative. I was confirmed celiac through genetics ( I have two genes and considered extremely high risk) plus endoscopy after a three week exposure. 

Do your Dr's have you tested every time you get exposed? I think for me its a waste of time and money since I always come back negative.  I am going in tomorrow because I ate two slices of pizza that was either full gluten or had A LOT of gluten cross contamination one month ago. I am STILL recovering from this. Nobody else was sick during that time I got sick and we have 6 of us in our home. 

I am just curious if that is standard for Drs to test again after exposure? If it takes months to get a positive test while eating a lot of gluten then why would they request this test after someone has be gluten-free for 5-1/2 years and just exposed to it? It just doesn't make sense to me.

 

 


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

I haven't had a doctor do a panel on me since I was diagnosed. IMHO your doctor would be better off checking your vitamin levels and for anemia, liver function etc. If your still having D then stool testing to make sure you didn't get food poisoning or something along those lines would be in order. There really isn't anything they can do to help us get over a severe glutening so maybe he/she is doing the test because he/she thinks you want it done? Have you asked why they are doing it?

cyclinglady Grand Master
2 hours ago, celichris said:

Every time I get exposed to gluten (4 times this year) my Dr wants to test me. I have always been seronegative. I was confirmed celiac through genetics ( I have two genes and considered extremely high risk) plus endoscopy after a three week exposure. 

Do your Dr's have you tested every time you get exposed? I think for me its a waste of time and money since I always come back negative.  I am going in tomorrow because I ate two slices of pizza that was either full gluten or had A LOT of gluten cross contamination one month ago. I am STILL recovering from this. Nobody else was sick during that time I got sick and we have 6 of us in our home. 

I am just curious if that is standard for Drs to test again after exposure? If it takes months to get a positive test while eating a lot of gluten then why would they request this test after someone has be gluten-free for 5-1/2 years and just exposed to it? It just doesn't make sense to me.

 

 

I do not get it either.  While nice to check on follow-up visits,  the jury is still out on the relationship of antibodies and intestinal damage.  

I test positive to only the DGP IgA.  My GI has ordered the the entire panel a few times and now just orders the DGP IgA if I request it.  It saves money for sure.  I confess that I have mostly returned a month or so for testing after what I think was a hidden gluten exposure.  I go, because my post-glutening symptoms change so much.  In five years I have never had a normal DGP IgA.  For piece of mind, I want to be able to figure out what may have glutened me (but I have never definitively been able to identify a source — lots of speculation).  

So, I plan on getting another endoscopy to make sure I have healed over the past five years or at least confirm that my gluten-free diet is working.  

So, what else could elevate my DGP IgA?  Another AI (I already have Hashimoto’s)?  I find very little on the subject.    Celiac disease does not receive much funding and post diagnosis studies are not in abundance.  

Ask your doctor why.  

 

kareng Grand Master
57 minutes ago, celichris said:

Every time I get exposed to gluten (4 times this year) my Dr wants to test me. I have always been seronegative. I was confirmed celiac through genetics ( I have two genes and considered extremely high risk) plus endoscopy after a three week exposure. 

Do your Dr's have you tested every time you get exposed? I think for me its a waste of time and money since I always come back negative.  I am going in tomorrow because I ate two slices of pizza that was either full gluten or had A LOT of gluten cross contamination one month ago. I am STILL recovering from this. Nobody else was sick during that time I got sick and we have 6 of us in our home. 

I am just curious if that is standard for Drs to test again after exposure? If it takes months to get a positive test while eating a lot of gluten then why would they request this test after someone has be gluten-free for 5-1/2 years and just exposed to it? It just doesn't make sense to me.

 

 

Unless its prolonged - like 12 weeks, it probably wouldn't show in a Celiac person's blood test.  Maybe your doctor is trying to convince you you don't have Celiac buy showing you negative tests?  

Actually- how does your doctor even know you were "glutened"?  I don't all my doctor up if it happens.  She can't do anything about it

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,015
    • Most Online (within 30 mins)
      7,748

    Rockette47
    Newest Member
    Rockette47
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
    • trents
      @Martha Mitchell, your reaction to the lens implant with gluten sounds like it could be an allergic reaction rather than a celiac reaction. It is possible for a celiac to be also allergic to gluten as it is a protein component in wheat, barley and rye.
    • JoJo0611
    • Martha Mitchell
      Scott I also have different symptoms than most people. It affects me bad. Stomach ache, headache, nauseous, heart racing, whole body shaking, can't walk then my throat starts to close. It attacks my nervous system. The only thing that saves me is a 1/2 of Xanax...it calms down my nervous system 
    • Martha Mitchell
      Scott Adams. I was dealing with a DR that didn't care about me being celiac. I repeatedly told him that I was celiac and is everything gluten-free. He put an acrylic lens from j&j. I called the company to ask about gluten and was told yes that the acrylic they use has gluten....then they back tracked immediately and stopped talking to me. The Dr didn't care that I was having issues. It took me 6 months and a lot of sickness to get it removed.... which can only happen within 6 months. The Dr that took it out said that it was fused and that's why I lost vision. If they would have removed it right away everything would be fine. He put in a silicone one that was gluten-free and I've had no issues at all in the other eye. Do not do acrylic!
×
×
  • 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.