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 To Board. Do I Have Celiac? Help Would Be Greatly Appreicated


JT82

Recommended Posts

JT82 Newbie

Hello,

 

I am trying to figure out if I have celiac disease and going in circles. My doctor isn't clear on it as well. I want to travel to other countries but scared to because I don't know what I will eat when there. I have had several tests (see below) but not the biopsy of small intestine. Based on the info does it sound like I have celiac disease if you were to make an educated guess?

Your answers will not change my attempt to find the answers via doctors but I am just curious if anyone has any input. The problem is I should have done the biopsy right away when I ate gluten. Now that I have been gluten free for 6 months they say I need to start eating gluten to have the biopsy. I don't know what to do.

 

Celiac Blood test

IGA - Negative

IGG - Positive - 23.6 on a scale of 1-9 (this was the only test that my doctor was worried about and put celiac in my head)

Gliadin peptide - Negative

 

Gene test

dq2 - negative

dq8 positive - 1 gene (test said I have 1-89 chance of celiac as compared to 1-100 for normal population)

 

Allergy blood test (have a lot of food allergies for some reason)

Gluten - YES 

Diary - YES

Eggs - YES

 

Blood test general health

Everything is pretty good and in range except I have testosterone levels a little low for my age. Going gluten free hasn't helped much with this.

 

 

Symptoms when I ate gluten in the past

Never really had major symptoms from eating gluten. I noticed my nose would get stuffy like other foods I was allergic to. Also it made my thinking foggy. But nothing major and no stomach aches. I had diarrhea often when I ate gluten but overall I was eating a lot of stuff I was allergic to. I would say diarrhea several times a week. I had a couple skin rashes last 3 years but the skin doctor didn't say it was dermetitis hep. He didn't seem to know what it was. My stool was very light and watery in the past and never really solid. I never had stomach aches from eating gluten and could eat a whole pizza without getting a stomach ache. 

 

Symptoms going gluten free.

When I went gluten free it was hard physically/emotionally. I didn't have major symptoms just felt pretty bad and was depressed. Now that I am gluten free I don't have diarrhea ever but my stool is still pretty watery but slightly darker. Still have allergies. The only major improvement I notice is my thinking is way better. My digestion still isn't too great. Had a few colonics that helped a little but now back to normal. My vitamin d levels are in range but could be a little higher. My vitamin b12 levels were tested and actually really high.

 

I am wondering if I should be watching every little thing that I eat and not traveling because of my symptoms/tests. It is really messing up my life. I just want to know if I have it or not. I can get use to either one but I can't get used to not knowing.

 

thanks for your help

 

 

 

 

 

 

 

 


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Well, the next step is a biopsy since you had a positive result, but if you are not up for a gluten challenge (to do the endoscopy) then you can stay off gluten (must be strict) to see of symptoms improve. Six months is not long enough to see improvement for many people with celiac disease. Read our Newbie section under "Coping" for tips especially about cross contamination. You are in a tough spot and have my sympathy.

It is possible to travel internationally and remain on gluten free diet. Lots of us have done it (or are doing it now!). Print of celiac disease language cards as they are helpful and plan!

Oh, there is no known allergy to gluten (wheat, yes). . Not sure how accurate those allergy tests you took were, but they might be helpful in identifying intolerances, so I would continue to avoid eggs and dairy too. Keep a food journal.

I wish you well.

JT82 Newbie

Well, the next step is a biopsy since you had a positive result, but if you are not up for a gluten challenge (to do the endoscopy) then you can stay off gluten (must be strict) to see of symptoms improve. Six months is not long enough to see improvement for many people with celiac disease. Read our Newbie section under "Coping" for tips especially about cross contamination. You are in a tough spot and have my sympathy.

It is possible to travel internationally and remain on gluten free diet. Lots of us have done it (or are doing it now!). Print of celiac disease language cards as they are helpful and plan!

Oh, there is no known allergy to gluten (wheat, yes). . Not sure how accurate those allergy tests you took were, but they might be helpful in identifying intolerances, so I would continue to avoid eggs and dairy too. Keep a food journal.

I wish you well.

 

Thank you for your help. Is the positive IGG test enough to diagnose for celiac? Because I feel like that is what is happening. That is really the only thing that points to celiac besides my gluten allergy. What else could cause high IGG and is it that high?

cyclinglady Grand Master

Like I said, the next step is going to a Gastroentrologist for a consult and possible biopsy. I, myself had only one positive out of the complete celiac panel, yet I had moderate to severe damage per my intestinal biopsies. Again, there is no such thing as a gluten allergy. There is a wheat allergy. Celiac disease is an autoimmune response to gluten from wheat, rye and barley that causes the body to attack the intestinal tract. I have celiac disease but I do not have a wheat allergy.

I would ask for a GI consult.

I can not comment on your "high" result since I am not sure which celiac test you took, but it is obviously out of range.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Rogol72 replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    2. - Scott Adams replied to HAUS's topic in Gluten-Free Foods, Products, Shopping & Medications
      8

      Sainsbury's Free From White Sliced Bread - Now Egg Free - Completely Ruined It

    3. - Scott Adams replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results

    4. - deanna1ynne replied to deanna1ynne's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      13

      Inconclusive results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,441
    • Most Online (within 30 mins)
      7,748

    Linda Boxdorfer
    Newest Member
    Linda Boxdorfer
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Rogol72
      @HAUS, I was at an event in the UK a few years back. I remember ringing the restaurant ahead to inquire about the gluten free options. All I wanted was a few gluten free sandwiches, which they provided and they were delicious. The gluten-free bread they used was Warbutons white bread and I remember mentioning it on this site before. No harm in trying it once. It's fortified with Calcium and Iron. https://www.warburtonsglutenfree.com/warbs_products/white-loaf/ The only other gluten-free bread that I've come across that is fortified is Schar with Iodized salt, nothing else.
    • Scott Adams
      In the U.S., most regular wheat breads are required to be enriched with certain B-vitamins and iron, but gluten-free breads are not required to be. Since many gluten-free products are not enriched, we usually encourage people with celiac disease to consider a multivitamin.  In the early 1900s, refined white flour replaced whole grains, and people began developing serious vitamin-deficiency diseases: Beriberi → caused by a lack of thiamin (vitamin B1) Pellagra → caused by a lack of niacin (vitamin B3) Anemia → linked to low iron and lack of folate By the 1930s–40s, these problems were common in the U.S., especially in poorer regions. Public-health officials responded by requiring wheat flour and the breads made from it to be “enriched” with thiamin, riboflavin, niacin, and iron. Folic acid was added later (1998) to prevent neural-tube birth defects. Why gluten-free bread isn’t required to be enriched? The U.S. enrichment standards were written specifically for wheat flour. Gluten-free breads use rice, tapioca, corn, sorghum, etc.—so they fall outside that rule—but they probably should be for the same reason wheat products are.
    • Scott Adams
      Keep in mind that there are drawbacks to a formal diagnosis, for example more expensive life and private health insurance, as well as possibly needing to disclose it on job applications. Normally I am in favor of the formal diagnosis process, but if you've already figured out that you can't tolerate gluten and will likely stay gluten-free anyway, I wanted to at least mention the possible negative sides of having a formal diagnosis. While I understand wanting a formal diagnosis, it sounds like she will likely remain gluten-free either way, even if she should test negative for celiac disease (Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If her symptoms go away on a gluten-free diet, it would likely signal NCGS).        
    • JoJo0611
    • deanna1ynne
      Thank you all so much for your advice and thoughts. We ended up having another scope and more bloodwork last week. All serological markers continue to increase, and the doc who did the scope said there villous atrophy visible on the scope — but we just got the biopsy pathology report back, and all it says is, “Duodenal mucosa with patchy increased intraepithelial lymphocytes, preserved villous architecture, and patchy foveolar metaplasia,” which we are told is still inconclusive…  We will have her go gluten free again anyway, but how soon would you all test again, if at all? How valuable is an official dx in a situation like this?
×
×
  • 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.