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

Walk-In Clinic Doctor


Coinkey

Recommended Posts

Coinkey Apprentice

Alright. I finally went to the walk-in clinic doctor about my gluten free discovery, hoping he'd do a test to formally diagnose Celiac. He just said, "so there are no more symptoms now that you don't eat gluten? Great, keep doing that." He gave me a sheet to go get tested at a lab for a whole list of things but never explained why he was testing for those things. I was hoping someone here could try and enlighten me on why these tests would be done:

CBC, routine urine analysis, electrolytes (Na, K, Cl, CO2), Albumin, alkaline Phosphatase, Alanine Aminotransferase, Bilirubin- total only, calcium, creatine kinase, creatinine, ferritin, glucose-random, GGT, Hemoglobin A1c, Lipase, Magnesium, Phosphate, Protein- Total, Thyroid (TSH and Free thyroxine), B12 and Vitamin D, E5R and something in doctor writing that starts with tissue tromglutaSCRIBBLE.

I am guessing they are all something to do with nutrition. I really wish that doctor would have been easier to talk to and explain stuff to me.


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



Celiac.com Sponsor (A8-M):



burdee Enthusiast

Alright. I finally went to the walk-in clinic doctor about my gluten free discovery, hoping he'd do a test to formally diagnose Celiac. He just said, "so there are no more symptoms now that you don't eat gluten? Great, keep doing that." He gave me a sheet to go get tested at a lab for a whole list of things but never explained why he was testing for those things. I was hoping someone here could try and enlighten me on why these tests would be done:

CBC, routine urine analysis, electrolytes (Na, K, Cl, CO2), Albumin, alkaline Phosphatase, Alanine Aminotransferase, Bilirubin- total only, calcium, creatine kinase, creatinine, ferritin, glucose-random, GGT, Hemoglobin A1c, Lipase, Magnesium, Phosphate, Protein- Total, Thyroid (TSH and Free thyroxine), B12 and Vitamin D, E5R and something in doctor writing that starts with tissue tromglutaSCRIBBLE.

I am guessing they are all something to do with nutrition. I really wish that doctor would have been easier to talk to and explain stuff to me.

That last item is tissue transglutaminase (antibodies) which is a test for intestinal inflammation from gluten reactions. The rest are various indices for malabsorption of fats, protein, blood sugar, calcium, B12, etc. which can all occur with celiac damage to the intestines. Yes, those all are related to nutritional deficiencies which can occur with undiagnosed celiac disease.

However, his comment about gluten and 'keep doing that (avoiding gluten)' makes me wonder whether he's looking for other problems to diagnose or he's really well informed about celiac disease and the nutritional deficiencies that can occur with undiagnosed celiac. You could 'google' any of those tests for more info, to understand how those might relate to nutritional deficiencies or even celiac disease. Then you could 'explain stuff' to that doctor when you return very well informed about everything he didn't bother to explain to you.

SUE

T.H. Community Regular

First - this is an awesome doctor, IMO. :) If you can get him again, I'd go for it. I know regular doctors who don't do these tests, and they SHOULD.

I don't recognize all of them, but the ones I do recognize are for vitamin deficiencies, and I believe a couple check certain levels of 'something' that checks how certain organs are functioning. I recognize the thyroid test, for example - many celiacs have hypothyroidism.

Adult discovered celiacs often have vitamin deficiencies and can have some of their organs malfunctioning as well, so this guy is awesome!

Also, re: the celiac test? Are you still gluten free? The numbers I hear most are that you need to be eating a good amount of gluten for 6 weeks prior to the test or it can test negative, so if you are still gluten free, or have been until recently, a knowledgeable doctor wouldn't do the test.

Also, some doctors recommend you go back on gluten so they can do the test. Many people here, and some doctors, question that, since it means you have to deliberately hurt yourself (eat gluten) to the point that it affects your body so badly that they can see it in a test.

Some of us think that's seems counterproductive to being healthy, ya know?

You CAN get a genetic test done to see if you have the Celiac Gene. Many doctors will give you a celiac diagnosis if you have the gluten challenge - which you have - and the gene.

Alright. I finally went to the walk-in clinic doctor about my gluten free discovery, hoping he'd do a test to formally diagnose Celiac. He just said, "so there are no more symptoms now that you don't eat gluten? Great, keep doing that." He gave me a sheet to go get tested at a lab for a whole list of things but never explained why he was testing for those things. I was hoping someone here could try and enlighten me on why these tests would be done:

CBC, routine urine analysis, electrolytes (Na, K, Cl, CO2), Albumin, alkaline Phosphatase, Alanine Aminotransferase, Bilirubin- total only, calcium, creatine kinase, creatinine, ferritin, glucose-random, GGT, Hemoglobin A1c, Lipase, Magnesium, Phosphate, Protein- Total, Thyroid (TSH and Free thyroxine), B12 and Vitamin D, E5R and something in doctor writing that starts with tissue tromglutaSCRIBBLE.

I am guessing they are all something to do with nutrition. I really wish that doctor would have been easier to talk to and explain stuff to me.

Coinkey Apprentice

So if that last item, the tissue transglutaminase test is to do with gluten antibodies- shouldn't I be eating gluten before I do the test? It's only been 6 weeks and I've accidently glutened myself at least once a week since doing it (and once on purpose- food courts and dizzy hungry BAD combo). I get to make an appointment with the lab to get them done, so do you guys think it would be better to gluten myself for a week and then do the tests just to get a more accurate result? I don't really want to put myself through that but I don't want to get a false negative either.

burdee Enthusiast

So if that last item, the tissue transglutaminase test is to do with gluten antibodies- shouldn't I be eating gluten before I do the test? It's only been 6 weeks and I've accidently glutened myself at least once a week since doing it (and once on purpose- food courts and dizzy hungry BAD combo). I get to make an appointment with the lab to get them done, so do you guys think it would be better to gluten myself for a week and then do the tests just to get a more accurate result? I don't really want to put myself through that but I don't want to get a false negative either.

I don't know how long TtG (tissue transglutaminase) antibodies survive in the blood (assuming you get a blood test for Ttg. However I took an Enterolab stool test over 2 months after I mostly stopped eating gluten, though I still was taking a digestive supplement which I didn't realize contained barley. My Ttg test was still positive enough to diagnose gut inflammation consistent with celiac disease. If you have had some accidents, even though you're trying to follow a gluten free diet, you may still have enough gut inflammation to produce enough TtG antibodies, even though you won't produce enough gluten antibodies to leak from your gut into your blood.

Nevertheless, that's just my guess, because I got a stool test for TtG, not a blood test. Maybe someone who's had a TtG blood test could share their experience/expertise ...

SUE

summerteeth Enthusiast

You CAN get a genetic test done to see if you have the Celiac Gene. Many doctors will give you a celiac diagnosis if you have the gluten challenge - which you have - and the gene.

My doctor diagnosed me based on dietary response, medical history, and family history (history of bowel cancers). From what I gather, more and more doctors are doing this.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    2. - Colleen H replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    3. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    4. - AlwaysLearning replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,090
    • Most Online (within 30 mins)
      7,748

    Jamie B
    Newest Member
    Jamie B
    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

    • AlwaysLearning
      Get tested for vitamin deficiencies.  Though neuropathy can be a symptom of celiac, it can also be caused by deficiencies due to poor digestion caused by celiac and could be easier to treat.
    • Colleen H
      Thank you so much for your response  Yes it seems as though things get very painful as time goes on.  I'm not eating gluten as far as I know.  However, I'm not sure of cross contamination.  My system seems to weaken to hidden spices and other possibilities. ???  if cross contamination is possible...I am in a super sensitive mode of celiac disease.. Neuropathy from head to toes
    • Jmartes71
      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
×
×
  • 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.