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 Celiac - Seeing Gi On Tuesday Need Help


ccooper

Recommended Posts

ccooper Newbie

My 11 year old son seen his pediatrician for his sixth grade physical. He was born with Hirschsprung's disease and has always had "intestinal issues". We always assumed it was the Hirschsprung's disease. At the appointment for his physical the Pediatrician recommended testing for thyroid and celiac because of his short stature (5th percentile). The lab completed a celiac panel and the results are positive for celiac. We have an appointment with a GI specialist at Norton Hospital Louisville KY on Tuesday. I have driven myself crazy reading everything everywhere. I would like to know how accurate is the celiac panel, and what I need to ask or be prepared for when meeting the specialist. Any information would be helpful, because I don't want to be worrying myself if the celiac panel is not very accurate, but I don't want to be under educated if it is accurate. Thanks


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



Celiac.com Sponsor (A8-M):



CeliacMom2008 Enthusiast

The blood test is about 98% accurate. Many/most doctors will recommend a biopsy to confirm the diagnosis, as the biopsy is considered the "gold standard test" for Celiac. You'll find controversy on the biopsy. Some feel that with the high reliability of the blood test the biopsy is costly and unnecessary. Others will tell you that the biopsy is necessary and in addition to confirming the diagnosis for Celiac, they will tell you it can show other issues/problems as well. You and your doctor will have to determine if it is right for you.

If you end up with a biopsy, don't fret over it. It is a pretty simple procedure and doesn't cause your child much discomfort (most of the discomfort is just the worry!). It's really not anything to get worked up over. You do need to keep your son eating gluten until after all the testing is done. Taking him off gluten before the tests will decrease their accuracy because once the gluten is gone the body stops reacting to it.

Since there is such a high chance that he has Celiac, I give you the advice to take a few calming breaths and relax. Having Celiac is not the end of the world - not by a long shot. The first few months are overwhelming as you learn a new the diet, but once you're through the learning curve it truly is not that big of a deal if you don't make it a big deal. Find a support group (online (here) is good, but a real live group to visit with in person is even better). If you can afford it or if your insurance covers it, visit with a dietician (preferably one who is very familiar with Celiac). And strap on a good attitude and a smile.

Treat this as an adventure that can bring you and your family closer together and not some tragedy. You can get a lot of information from this forum, but do remember that most of us are just normal people (not specialists of any kind) and so you may get conflicting opinions on some issues. As you travel through the next couple of months consider all of us your new best friends. We've all been where you're most likely headed and we make good listeners and advice givers. :)

Welcome!

ccooper Newbie

Thank you for the information. I am actually excited about the diet thinking that it will benefit my whole family. I am just worried because I am a mom and this is very serious to me and not so serious with my husband (yet, he'll get there eventually). I live in a very rural area and nobody has ever heard of celiac, so resources are slim. I am a teacher and work very closely with my special education director, so I know the school will work with me on the needs of my child. I am so glad to have found this site, it's a wealth of information for a me.

As far as the biopsy goes, if the GI request it we will do it. My son has had so many problems with the other disease that I would rather be safe than sorry no matter the cost. He's been through several operations before and even had a colostomy for a while, so this procedure seems minor.

Thanks again for responding, I felt like I was alone in the world of celiac until now!

LDJofDenver Apprentice

If you end up going gluten free, there are resources out there that make every day shopping less difficult. Many mainstream products (Kraft, Heinz, Kroger, Hormel, etc.) are gluten free, more than you think.

There are grocery shopping guides you can buy that will make your life WAY easier at the store. Lists items by category (soups, chips, dressings, spaghetti sauce, etc.)

Gluten-Free Grocery Shopping Guides:

Open Original Shared Link

Open Original Shared Link

There

ang1e0251 Contributor

Don't worry because you are rural, I am too and there are alternatives. You can buy all kinds of specialty items on the internet, if you choose. But regular mainstream whole foods are in every market and very good food for the person with celiac disease. Do you have access to a large chain grocery or a Walmart you could shop at maybe once a month? They will have many gluten-free products like pasta and frozen foods.

If you meet with a nutritionist, take your husband along. Can't hurt for him to hear the recommendations first hand.

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.