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

Blood Tests, Diagnosis, And Dithering


hannely

Recommended Posts

hannely Newbie

Hello! This week marks a year since I got blood results suggesting I have celiac disease. I got the results just a couple days after discovering I was pregnant (hooray!!). I didn't want to stay on gluten for even a second longer, given my concerns about my baby's health, so I didn't bother with a biopsy, figuring I could always do a gluten challenge later.

My initial blood test showed a TTG-IGA result of 110. We repeated the test about six months later, and it was down to only 8. To me that suggests that gluten was the cause.

BUT BUT BUT now I'm dithering. Before getting these results, I never really considered that I could have celiac disease. My doctor only ordered the test because I have/had thyroid issues, which she says often go along with celiac. And then I went gluten free while pregnant, so it was hard to evaluate any improvement because my body wasn't feeling normal anyway.

So now I'm in this spot where I am carefully gluten-free, but psychologically I kind of still don't think I have celiac disease because I didn't do a biopsy.

Do I do a gluten challenge and go through with a biopsy, or should I just get over my denial and accept that I absolutely do have celiac disease? Should I just go out and eat a doughnut one day to see what happens? That last question is only mostly a joke.

Sorry this is so long. Thanks for any insight you can offer. I really appreciatr the amazing resource that is this community.


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



Celiac.com Sponsor (A8-M):



beth01 Enthusiast

You know the answer, read your post.  It's all there in black and white.  Your tTg IgA was 110 on gluten and then dropped to 8 after a gluten free diet. Not everyone needs a biopsy for a diagnosis.  I am not saying this to be b%$@#y, just reading between the lines of your own words. I am pretty sure you know you are a celiac.  Pregnancy only last nine months and it's been a year since your diagnosis.  You could have cheated before now, but you haven't.

 

My advise, and I will probably get yelled at for saying this, have the donut!  If it makes you sicker than a dog, you have another piece of evidence.  If it doesn't make you sick, see your doctor and ask for a endoscopy and biopsy - you have to do a gluten challenge for that anyway which is why I said eat the donut.

hannely Newbie

Thanks! You're right; it does seem pretty obvious with those kinds of numbers, doesn't it? I appreciate the straight talk :).

I'm not trying to sound whiny about this or anything. I have really no desire to "cheat," and I don't think, after a year of gluten free, that I'm suffering by living this way. I just feel like I don't KNOW know, and it's kind of crazy-making. I don't even really know how I actually react to gluten because it's not something I paid attention to at all before going gluten free, so it's been tough over the last year to pinpoint if I've been glutened or if I was just feeling pregnant, for example.

I also recognize that you guys can't necessarily interpret test results for me. But my doctor seems uninformed, too, and I'm having trouble wading through the info to understand just how reliable the ttg-iga positive is as a diagnostic.

beth01 Enthusiast

Some people on here are really good about the tests results.  Amazingly after being a Med Lab Tech for 16 years I know nothing about these tests.  I am a relatively new celiac also, so no help there. From what I understand, it's more likely to have a false negative than a false positive. 

 

My daughter was just diagnosed and her tTg IgA was >100. She hasn't had an endoscopy yet and I am not sure if she will.  She sees the Ped's GI on the 18th. It says Celiac on her chart.

 

I am assuming your doctor had to have other reasons to test you for celiac besides just a thyroid problem. Did you have any other health problems?  Otherwise, I want to go back 11 years and see your doctor lol.  That was when my thyroid problems started and I just got diagnosed two months ago after 30 years of health problems.

 

You said it seems your doctor is misinformed also?  Are you at least having your health monitored?  There is a whole work up you need every year to see how you are doing.  More intense than you would need if you weren't celiac.  Maybe you need to see someone that specializes in celiac if there is one in your area, or at least see a GI.

hannely Newbie

Really, it was just that my doctor thought it would be worth checking because of my thyroid. She's very thorough with things like that! However, in retrospect it might explain some things, like my chronically abysmal iron levels and (maybe?) recurring migraines.

So my doctor is good in that proactive way, but I don't know about the follow-up stuff. Like yearly work-ups. Do you know what extra stuff I should be looking into? I'm in Canada, and it's a bit tough here to get in to see specialists, but maybe I'll ask my doc for a referral...

How old is your daughter? What made you decide to look into celiac testing for her?

beth01 Enthusiast

Yearly you should be tested for B12, Folate, Vitamin D, Iron, a Complete Blood Count, a Comprehensive Metabolic Panel ( which needs to include calcium and magnesium), and you should also have your thyroid checked every year.

 

I can tell you that a lot of people with celiac also get migraines.  I have had them my whole life except for the last two months, I was diagnosed two months ago and haven't had a true migraine since going gluten free.  I was getting 4 a week on bad weeks.

 

I had my children tested when I was diagnosed with celiac.  It's hereditary so family members should get tested.  She was positive and my son was not. You will want to get your children tested.  My doctor didn't want to test them even though my daughter was having unexplained fainting episodes but I pushed for it. Sure am glad I did.

 

I know Canada is different for health care but I know that there are people on here that are also from Canada and more knowledgeable than I am.  Hopefully one of them comments.  You definitely need follow up care for this disease though.

RMJ Mentor

Here's how I think about it. I was tested because of migraines. No GI issues. I didn't have a biopsy due to an unrelated medical reason. But my feeling is - I had a positive blood test that said my body was attacking itself (TTG IgA is an antibody against a normal protein). I was willing to go on a gluten free diet to keep my body from attacking itself. My antibody levels went way down, which tells me that the gluten free diet is working. And I have far fewer migraines!


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



Celiac.com Sponsor (A8-M):



hannely Newbie

Thanks for the info. I was so focused on pregnancy and the crazy newborn period that I honestly haven't done anything beyond "okay, now I'm living without gluten." Now that my baby is four months old and I've got a bit of mental space for something past the basics, it's time I got some stuff figured out! And I'm driving my husband nuts with the should I or shouldn't I waffling re: endoscopy.

I'm glad to hear your stories about migraines! Gives me hope.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    Carol Zimmer
    Newest Member
    Carol Zimmer
    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

    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
×
×
  • 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.