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

Understanding my lab results.


BFristoe03

Recommended Posts

BFristoe03 Newbie

I just received my lab results and I'm more than confused.  :(  I asked my doctor to test me for celiac because I just have been feeling like crap lately and it's random but constant, if that makes any sense.  I was told when I was younger that I had IBS and was told to avoid red meat, dairy and fried foods.  The problem was/is, I could eat a salad with none of the above ingredients and still get a flare up.  In the last few months it seems as if my symptoms have been getting worse and new symptoms have appeared.  My skin gets really itchy, but no rash.  Sometimes I'm constipated but mostly loose stools, headaches are a norm lately.  My back is always hurting, my foot hurts (maybe planters fasciitis), but if I avoid foods with gluten I noticed that the inflammation was almost nil.  Anyway...this is why I asked the doctor to give me the test.  She called me last week and the conversation went like this.  "Hi Brandie, I have your test results, looks like you have celiac, do you have any questions?"  Unfortunately she called while I was sitting with my grandmother in hospice, so no, my brain wasn't thinking of questions at the time and she didn't offer any advice either.  I've called and left my doctor two messages now and I still haven't heard back.  (Disclaimer:  We did just have a MAJOR hurricane hit, so I know that I'm not a high priority and that's okay, but I still want some answers.)  Here are my lab results:

Immunoglobulin A, Qn, Serum:  298 Normal (Reference Range: 87-352 mg/dL)

Deamidated Gliadin Abs, IgA:  11 Normal (Reference Range: 0-19 units)

t-Transglutaminase (tTG) IgA:  46 High  (Reference Range: 0-3 U/mL) (Negative 0-3, Weak Positive 4-10, Positive >10)

Endomysial Antibody IgA:  Negative

Someone, please help!

 


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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

Your doctor does appear to be correct, if these are your blood test results, so be sure to discuss them in more detail with her. Before starting a gluten-free diet it is possible that she may want you to undergo an endoscopy to confirm the diagnosis, so be sure not to go gluten-free until directed by your doctor. 

On a positive note, if this is the source of your various health issues you should see a big improvement of your symptoms once you do go gluten-free.

drkelli Rookie

The gold standard is still an endoscopy to confirm. She should refer you to a gastro. Good luck. 

squirmingitch Veteran

I agree. Make sure you keep eating gluten until after the endoscopy. 

Yes, I'm sure she's probably swamped but do try to get clarification on whether she's going to refer you to a GI. If your insurance does not require a referral then you could go ahead & make an appt. yourself. 

I hope you & your home are okay. If you're talking about Michael, I'm about 200 mi east of that area & will be eternally thankful it did not track this way. 

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
      132,524
    • Most Online (within 30 mins)
      7,748

    Wlseamans
    Newest Member
    Wlseamans
    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

    • cristiana
      More great tips, and a good excuse to shop at M&S and also buy more iced buns!   I wish we had an ASDA near us, as the few times we've been to one their gluten-free pasta range seemed very reasonably priced compared to other shops.  Thanks so much, @Russ H.
    • Russ H
      I hope you are on the mend soon. About 1 in 5 people who contracted chicken pox as a child go on to develop shingles in later life - it is not uncommon. There are 5 known members of the herpes virus family including chicken pox that commonly infect humans, and they all cause lifelong infections. The exact cause of viral reactivation as in the case of shingles or cold sores is not well understood, but stress, sunburn and radiotherapy treatment are known triggers. Some of the herpes viruses are implicated in triggering autoimmune diseases: Epstein-Barr virus is suspected of triggering multiple sclerosis and lupus, and there is a case where it is suspected of triggering coeliac disease. As to whether coeliac disease can increase the likelihood of viral reactivation, there have been several cohort studies including a large one in Sweden suggesting that coeliac disease is associated with a moderate increase in the likelihood of developing shingles in people over the age of 50. US 2024 - Increased Risk of Herpes Zoster Infection in Patients with Celiac Disease 50 Years Old and Older Sweden 2018 - Increased risk of herpes zoster in patients with coeliac disease - nationwide cohort study
    • Russ H
      BFree bread is fortified with vitamins and minerals as is ASDA own-brand gluten-free bread. All the M&S bread seems to be fortified also.
    • Flash1970
      You might try Heallix.  It's a silver solution with fulvic acid. I just put the solution on with a cotton ball.  It seemed to stop the nerve pain. Again,  not in your eyes or ears.   Go to heallix.com to read more about it and decide for yourself Also,  I do think nerve and celiac combined have a lot to do with your susceptibility to shingles breaking out. 
    • trents
      Celiac disease requires both genetic potential and a triggering stress event to activate the genes. Otherwise it remains dormant and only a potential problem. So having the genetic potential is not deterministic for celiac disease. Many more people have the genes than actually develop the disease. But if you don't have the genes, the symptoms are likely being caused by something else.
×
×
  • 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.