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

New Member With Questions


LoriG

Recommended Posts

LoriG Contributor

Hello,

In May I went to an applied kinesiologist who muscle tested me and said I have a gluten intolerance with malabsorption. This sort of made sense because I am hypothyroid with hashimotos disease and have for years felt fatigued and depressed and insomnia.

He told me my thyroid meds weren't working well because of the malabsorption. So I began a gluten-free diet and after one month ate some gluten with no reaction. I began to think I don't have it. I tried for the most part to keep gluten-free, but not 100% since then. It has been hard sticking to the diet when I am not getting well doing it.

I recently went back to the AK and he said again that I have this and I need to stick with the diet. Ugh!

I asked my family doc to run some blood work and she said it is highly inaccurate and refused. Not sure what to do at this point.... should I do enterolab? should I find a doc to do blood work and if so, why do I say I want it? It sounds weird to say I suspect malabsorption issues with my thyroid. Also I have constipation which I have attributed to my thyroid all of this time. Do I trust the muscle testing?

I do believe I have family that has this but never got tested. I just need some direction right now. Thank you.


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



Celiac.com Sponsor (A8-M):



mftnchn Explorer

Hi, and welcome to the forum.

Your symptoms of thyroid issues, fatigue, depression and insomnia, plus constipation all paint a picture that could be celiac. I am not very sure about the alternate approach to diagnosis though.

Since you have been gluten free or gluten lite for awhile, the blood tests and biopsy could be negative, and you could still have celiac. There is another good thread here about celiac versus gluten intolerance, you might find that helpful. What I understand from this forum is that there is a blood test very specific for celiac, and that false positives are unlikely, but false negatives are common. False positive biopsy is also very unlikely as long as it is reliable person doing the examination.

I think that given your situation, enterolab would be a good option if you can afford the testing. It would not diagnose celiac, but could give you more information about the gluten sensitivity aspect. If it confirms the malabsorption and gluten sensitivity, plus shows that you have celiac genes, that would mean that you need to carefully consider whether you should be eating gluten.

The other option is to eat gluten normally for 6-8 months (equivalent to 3-4 slices of bread a day) and then do blood testing and biopsy. This only picks up celiac when there is enough intestinal damage present. So when you go gluten free/lite, the intestine heals enough that the testing is negative.

If you do have celiac, you can be asymptomatic, but still have damage accumulating in your body and be more susceptible to other autoimmune diseases. The longer you eat gluten the more damage occurs.

This forum is a good place to get input and information.

LoriG Contributor
Hi, and welcome to the forum.

Your symptoms of thyroid issues, fatigue, depression and insomnia, plus constipation all paint a picture that could be celiac. I am not very sure about the alternate approach to diagnosis though.

Since you have been gluten free or gluten lite for awhile, the blood tests and biopsy could be negative, and you could still have celiac. There is another good thread here about celiac versus gluten intolerance, you might find that helpful. What I understand from this forum is that there is a blood test very specific for celiac, and that false positives are unlikely, but false negatives are common. False positive biopsy is also very unlikely as long as it is reliable person doing the examination.

I think that given your situation, enterolab would be a good option if you can afford the testing. It would not diagnose celiac, but could give you more information about the gluten sensitivity aspect. If it confirms the malabsorption and gluten sensitivity, plus shows that you have celiac genes, that would mean that you need to carefully consider whether you should be eating gluten.

The other option is to eat gluten normally for 6-8 months (equivalent to 3-4 slices of bread a day) and then do blood testing and biopsy. This only picks up celiac when there is enough intestinal damage present. So when you go gluten free/lite, the intestine heals enough that the testing is negative.

If you do have celiac, you can be asymptomatic, but still have damage accumulating in your body and be more susceptible to other autoimmune diseases. The longer you eat gluten the more damage occurs.

This forum is a good place to get input and information.

Thank you for your help and information. You sure explained the blood tests and biopsy well for me. I may just pay for enterlab. Thanks.

mftnchn Explorer

You are welcome, and hope you let us know how things go.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,534
    • Most Online (within 30 mins)
      7,748

    RUKen
    Newest Member
    RUKen
    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

    • lmemsm
      I've used magnesium taurinate and magnesium taurate vitamins.  Didn't notice much of a difference when I used them.
    • Scatterbrain
      Anyone experimented with Taurine supplementation either via electrolyte powders or otherwise? Thanks
    • Jmartes71
      Yarrow Pom works really well with the skin issues I found out.I had to stop so my doterra because dealing with medical celiac circus. I had shingles in Feb 2023. Prayers for healing 
    • 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
×
×
  • 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.