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

My Local Labs Only Run Ttg Iga - What Do I Do Now?


SiandAshs Mom

Recommended Posts

SiandAshs Mom Apprentice

So I asked my doctor for celiac blood tests a few months ago. He sent me for total IgA (1.32 g/L {ref 0.70-4.00}) and the tTG IgA (<1.0 U/mL {ref <7.0}). My total IgA is normal and my tTG IgA is a big fat negative. I then found out that they only run the EMA if there is an elevated tTG IgA so they didn't run that on me. The lab doesn't even do the gliadin tests or the DGP test.

I am almost certain I have an issue with gluten (life long GI issues which previous doc diagnosed as IBS, iron deficiency, depression, fatigue...) and would love to explore all angles so I can care for my kids' health properly. I recently was reading my full bloodwork results and realized that my TSH is high (3.19 mU/L). It wasn't flagged as the labs have a range of 0.20-4.00 but I believe that is high for me. I am going back to my doc next week to have my free T3's, free T4's and antibodies checked. I'm thinking it may be Hashimotos but we'll see. 

I really feel more exploration into celiac is warranted but am not sure how to proceed now. Is there another way to have the gliadin and DGP blood tests run since my local labs won't do it (I'm in Alberta, Canada)? Should I just push for an endoscopy? I appreciate your thoughts! Thanks!

 

ETA: I found this presentation that my lab put out about lab testing for celiac. I find it interesting that the only reason they give for not having the DGP test is that it's expensive :facepalm: 

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Yeah... I'm in Alberta too and couldn't get any more testing either. You might be able to find a mail order lab and have a local lab draw the blood and send it off East or to the States, but I bet it costs a pretty penny.

 

I strongly suspect celiac disease in two of my three boys. They too had negative tTG IgA tests so with no other testing options, I just made them gluten-free. I'm a celiac so I wouldn't be surprised if they are too, but at the very least they are NCGI (non-celiac gluten intolerant) which can result in a host of symptoms and complications if ignored - pretty much the same as celiac disease but minus the villi atrophy.

 

I opted not to do the endoscopy for my kids because I had already determined that they had a gluten intolerance and needed to be gluten-free, so I didn't feel an endoscopy was needed. But that's just my personal view of our own situation. If you feel strongly that an endoscopy should be done, then it should be done. Just be aware that if it is negative, you could still have NCGI as it is 6-10 times more common that celiac disease is. A gluten-free diet of about 6 months is really the only way to diagnose that.

 

Going gluten-free could help your thyroid too. Some find their body meets their thyroid hormone needs better after going gluten-free.  You never know.  

 

Based on my own experiences, you may need to find an "alternative" doctor or naturopath to address your thyroid needs if the lab results continue to be in the normal range. In Calgary, our TSH range is still 0.2-6.0 and I had to fight to get more meds and finally switched doctors.  I hope your doctor is open minded.  Good luck!

SiandAshs Mom Apprentice

Yeah... I'm in Alberta too and couldn't get any more testing either. You might be able to find a mail order lab and have a local lab draw the blood and send it off East or to the States, but I bet it costs a pretty penny.

 

I strongly suspect celiac disease in two of my three boys. They too had negative tTG IgA tests so with no other testing options, I just made them gluten-free. I'm a celiac so I wouldn't be surprised if they are too, but at the very least they are NCGI (non-celiac gluten intolerant) which can result in a host of symptoms and complications if ignored - pretty much the same as celiac disease but minus the villi atrophy.

 

I opted not to do the endoscopy for my kids because I had already determined that they had a gluten intolerance and needed to be gluten-free, so I didn't feel an endoscopy was needed. But that's just my personal view of our own situation. If you feel strongly that an endoscopy should be done, then it should be done. Just be aware that if it is negative, you could still have NCGI as it is 6-10 times more common that celiac disease is. A gluten-free diet of about 6 months is really the only way to diagnose that.

 

Going gluten-free could help your thyroid too. Some find their body meets their thyroid hormone needs better after going gluten-free.  You never know.  

 

Based on my own experiences, you may need to find an "alternative" doctor or naturopath to address your thyroid needs if the lab results continue to be in the normal range. In Calgary, our TSH range is still 0.2-6.0 and I had to fight to get more meds and finally switched doctors.  I hope your doctor is open minded.  Good luck!

Thanks nvsmom. You've given me great feedback in other questions I've posted as well. Yeah, I would be fine just cutting out gluten from my diet completely but the fact that a diagnosis may benefit my kids keeps me from just accepting that. I just ordered the genesure genetic test from glutenpro and even though it wasn't cheap it will maybe help me figure out if I need to push for more testing or if I just need to start the gluten-free diet in earnest (I've done a week or two before but always stopped as I thought I may want more testing). I know the gene test won't tell me if I'm celiac but it will let me know if it's even a possibility. And thanks for the tip on finding a naturopath for thyroid issues. We do have a really good naturopath clinic here so I may end up seeing them if my doctor doesn't think there's any issues. Wow, a range of up to 6.0 is just crazy! There are probably so many people suffering but the lab still says they're fine. So sad! 

nvsmom Community Regular

Good luck with the gensure test.  :)

 

What are you thinking for more testing at this time? I'm not sure if the DGP tests are even available in Alberta. At my last doctor appointment, I discovered that my doctor had never even heard of the DGP tests.   :rolleyes: I know labs can be sent away, because I know one man who had his blood work sent to the Mayo clinic - but this was a different health issue where blood test monitoring is required, and not just helpful like in celiac disease.

 

Naturopaths are often more open to giving T3 than regular docs are. I have actually found a protocol for Calgary (might be Alberta) that says to only give synthetic T4 and that T3 is not needed; it also strongly advises against natural desiccated thyroid... Truly a shame as not everybody feels well on exactly the same meds; it allows for no variation.

 

Sometimes our Alberta Health Care is a blessing, and other times I REALLY wish we could have more control of our health.  :unsure:

SiandAshs Mom Apprentice

Good luck with the gensure test.   :)

 

What are you thinking for more testing at this time? I'm not sure if the DGP tests are even available in Alberta. At my last doctor appointment, I discovered that my doctor had never even heard of the DGP tests.   :rolleyes: I know labs can be sent away, because I know one man who had his blood work sent to the Mayo clinic - but this was a different health issue where blood test monitoring is required, and not just helpful like in celiac disease.

 

Naturopaths are often more open to giving T3 than regular docs are. I have actually found a protocol for Calgary (might be Alberta) that says to only give synthetic T4 and that T3 is not needed; it also strongly advises against natural desiccated thyroid... Truly a shame as not everybody feels well on exactly the same meds; it allows for no variation.

 

Sometimes our Alberta Health Care is a blessing, and other times I REALLY wish we could have more control of our health.  :unsure:

I actually have no idea what testing to do. There really isn't much else here other than the biopsy... my doctor suggested a colonoscopy and I thought that he may send me for an endoscopy as well but I'm not sure he would agree to that - and I'm not sure if it's necessary since the tTG IgA was completely negative.

I know the naturopath here does IgG testing so I could pay for the IgG gliadin test. I've heard conflicting info on its usefulness though. Some seem to think it indicates gluten sensitivity and others think it has no meaning at all so I'm not sure it's worth paying for. Thoughts on that? I guess I will probably see the naturopath for thyroid issues anyway so I can ask her then. I really don't understand why some medical professionals are against T3 and natural thyroid. Does it really make sense medically to only treat with T4 meds? It doesn't make rational sense to me  :huh: Thanks again for your input!

nvsmom Community Regular

The gliadin tests (AGA) don't test for attempted villi damage by autoantibodies like the other tests do, it's thought to work for NGI too but that is not widely accepted yet.  It DOES have a fairly low sensitivity (ability to detect positives) so it's best not to solely rely on it for a diagnosis.

 

I can't remember if I've pointed out this paper (by world gastroenterology organisation) to you yet. On page 10-12 they go through the tests andpoint out how sensitive and specific to celiac disease each test is. All tests discussed are blood tests; fecal testing can be done but they are not generally accepted in the medical community and tend to have a high (false) positive rate.

Open Original Shared Link

 

I don't understand why t3 is down upon either!  I "get" that T4 converts to T3 in parts of our body that need it, but not everyone converts well, or accepts t4 to be converted.... Nope. Not rational. I totally agree that a T3 option should be given to those who need it (and not all do - I just know that i did).

 

Let us know how it goes with the naturopath.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,548
    • Most Online (within 30 mins)
      7,748

    Lunaluv
    Newest Member
    Lunaluv
    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

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.