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

Frustrated


lopo7883

Recommended Posts

lopo7883 Rookie

Hi everyone,

A week ago I got a call from my endo who tested me for celiac (she thought i might have it cause I have some stomach problems and hashimotos) and she told me that the results indicate I might want to try and avoid gluten and see what happens. She thought one of the values seemed high although it was within the ref range.

I called today because I was wondering what the actual results were. They are all completely normal and I definitely do not have celiac, which is what the nurse practioner there told me.

I had this done at a qwest lab.

IGG- <20 (ref range: <20= negative, 20-30= weak positive, >30 = strong positive)

TTG AB IGG - <3 (ref range: <7 negative, 7-10= equivocal, >10 = positive)

Serum IGA- 162 (ref range 81-463)

IGA- 8 (ref range: <11= negative)

TTG AB IGA- <3 (ref range: <5 = negative)

My serum IGA seems a little low, like clearly in the very very low section of the range, and my IGA seems a little high. That I guess is what my doctor thought seemed suspicious. I have hashi, pretty bad hairloss, low iron stores, low b12 without serious supplementation, my teeth are getting weaker and since I was a child I have a really bizarre set of ridges inside my teeth which my dentist has always made seem were related to a fever, but I didn't have a really high fever when I was developing my permanent teeth apparently- at least according to my parents.

My stomach problems are very much on and off.

I guess I dont have it. Would anything throw that off? I had been avoiding gluten, but definitely not entirely gluten free for a week or so before the test. And after my doc told me a week ago to avoid gluten, I stopped eating it. but should I just start again?

Thanks!


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

I won't be the only one to suggest that the diet is the best way to know for sure. If it were me, I'd go completely gluten-free, no cheating, and see how it goes. I started seeing results after about six months, but I have a lot of damage from what I can tell, so it's gonna be a long time for me.

If you don't have the intestinal damage yet, that's great news, and that may be what the tests are indicating. I am not an expert on that by any means. I never got any tests done, as my experience with doctors has always benn aweful. They never had a clue what was wrong, so I suffered for years, and not even my parents would believe I was really ill. The doctors kept telling my parents I was making it up to get attention.

Don't put it off just because you didn't get an absolutely positive indication. If going on the diet helps you, that's all that matters. Many think the diet is so hard that they don't want to "go through all the trouble for nothing". I can tell you for certain that NOT going gluten-free is far worse if it's what you actually need to do.

Look at it this way: The diet is perfectly safe to try, while waiting for Celiac to develop is not.

tarnalberry Community Regular

Yep, just echoing the "I also didn't have conclusive results, but the dietary challenge certainly demonstrated it was an issue" sentiment.

lopo7883 Rookie

Thanks!

Its just tricky for me, because to some extent I'm not sure what symptoms are related to this at all and I could expect to see alleviated. Then again, I guess that if I tried gluten free and watched to see what happened to my body in general that would be good. I think it's just frustrating, because my stomach problems are very much on and off, and really dont seem as bad as some people's that I read about on the board... I thought I had an ulcer or IBS through college, but never got off my butt to get tested. But when I got my last blood test and saw how low my iron and b12 were and in general started to realize that I think I'm generally undernourished, I started looking for other possibilities that made more sense, and celiac disease happened to fit the bill. I have hashi and stomach problems and other assorted symptoms.

My only real issue, is that I feel borderline phony... since my stomach problems are not as horrible- at least not constantly horrible as other people's that I read about here, I just feel odd telling people I believe I have celiac when my blood test came back overwhelmingly negative. And I'm still really confused as to why my endo would tell me to avoid gluten when she saw such negative results and we didn't really discuss in detail my stomach problems at all.

Very confused.

Rusla Enthusiast
Thanks!

Its just tricky for me, because to some extent I'm not sure what symptoms are related to this at all and I could expect to see alleviated. Then again, I guess that if I tried gluten free and watched to see what happened to my body in general that would be good. I think it's just frustrating, because my stomach problems are very much on and off, and really dont seem as bad as some people's that I read about on the board... I thought I had an ulcer or IBS through college, but never got off my butt to get tested. But when I got my last blood test and saw how low my iron and b12 were and in general started to realize that I think I'm generally undernourished, I started looking for other possibilities that made more sense, and celiac disease happened to fit the bill. I have hashi and stomach problems and other assorted symptoms.

My only real issue, is that I feel borderline phony... since my stomach problems are not as horrible- at least not constantly horrible as other people's that I read about here, I just feel odd telling people I believe I have celiac when my blood test came back overwhelmingly negative. And I'm still really confused as to why my endo would tell me to avoid gluten when she saw such negative results and we didn't really discuss in detail my stomach problems at all.

Very confused.

Well the blood tests can come back negative even if you are celiac, they are not infallable. Now some people have some symptoms and some have none and many don't have the same or severe as anyone else. Thyroid and b12 problems go with this disease also. Try going gluten-free and see if you see a difference. Some take longer to see a difference than others and some see them right away. I see some right away and know when I have been glutened because of my dh, bowels, burning stomach and general lack of energy and malaise. Keep a diary, I do.

We all have gone through something whether we show positive or negative.

Don't worry there is lots of great help here and in here I learned more in one month than I think most doctors know in their whole lives.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,566
    • Most Online (within 30 mins)
      7,748

    Alisha Moose
    Newest Member
    Alisha Moose
    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

    • knitty kitty
      Here's one more that shows Lysine also helps alleviate pain! Exploring the Analgesic Potential of L-Lysine: Molecular Mechanisms, Preclinical Evidence, and Implications for Pharmaceutical Pain Therapy https://pmc.ncbi.nlm.nih.gov/articles/PMC12114920/
    • Flash1970
      Thank you for the links to the articles.  Interesting reading. I'll be telling my brother in law because he has a lot of pain
    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
×
×
  • 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.