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

Need Help Please


HSRmom

Recommended Posts

HSRmom Newbie

Hello all, I am new to this group.  I have a 4 year old that we believe has celiacs or at least a gluten sensitivity.  In October she had an endoscopy and blood work.  The blood work was positive, but ther biopsy was negative.  They wanted me to not change her diet and to retest her this month (January).  I did some reading and believe that she may have celiacs and at the very least gluten sensitivity.  I decided in December that prior to retesting I would try a gluten free diet rather than put her through the trauma of a blood draw.  It has only been about 2 1/2 weeks gluten free, but I am not sure if there any changes.  Her pediatrician said that she thought it was ok to try the gluten free diet that she probably has some sort of sensitivity.  Where I need help is, is it safe to assume that she has celiacs or sensitivity based on the one test?  Should I continue with the gluten free diet (I assume it could take some time to see results)?  Her symptoms were/are:  reflux and tummy aches (taking prevacid); exercise induced asthmas (which she uses 2 inhalers); chronic constipation (which she is on miralax), these are the most noticable.  She is an extremely picky eater eating primarily carbs/grains, a few fruits and only tuna fish as a protein (sometimes). 

 

Also, my husband and I went on it with her to make the transition easier.  He has noticed that is IBS is better and so is the arthritis in his left hand.  Do you agree it is ok for us to be on it as well?

 

Thanks to all for your assistance.


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



Celiac.com Sponsor (A8-M):



NoGlutenCooties Contributor

Hi HSRMom and Welcome to the Forum!

 

In my opinion, if her bloodwork was positive for Celiac then she has Celiac.  Many doctors will not confirm the diagnosis without a positive biopsy but from what I understand that can be even trickier in children than it is in adults because they haven't had the disease long enough for there to be enough damage to show up on the tests.  You're also relying on the doctor to happen to biopsy the right spot because the damage is usually spotty.  That said, if you post the bloodtest results with the ranges that the lab uses someone on here may be able to help you confirm what they mean.

 

You're right in that in can take some time to see results from the gluten-free diet, and to see symptom relief you need to make sure she is 100% gluten-free - no cross-contamination, etc.  I did a quick search for Prevacid and Miralax and they are both gluten-free.  Keep in mind that many Celiacs have problems with other grains, especially corn, and sometimes dairy too - especially at first.

 

FWIW... with IBS and arthiritis, your husband may have Celiac too - was he tested prior to going gluten-free?

notme Experienced

celiac is genetic, so if your child has celiac, she had to get it from one of her parents.  if your husband has celiac related problems that are clearing up by eating gluten free, that makes perfect sense. 

 

false negatives are common on the blood test.  false positives are not - your kid has celiac.  you will probably want to read the newbie 101 thread -- it is in the 'coping with' section of this forum -- to get tips on how to keep your daughter gluten free.  there is also a section on here for parents of babies/kids with celiac where other parents share advice :)  welcome to the board and good luck!

brileighlevi Newbie

Yep if her blood work was positive she has celiac. I have the other problem with my daughter... "possibly" positive biopsy, negative on the tests they ran so far. We're waiting on more tests before going gluten-free. I hope she continues to heal and definitely check for cross contamination.

nvsmom Community Regular

Agreed. There are a few other people around here with positive blood work but negative biopsies. It's not as uncommon as you would think.

 

As for going gluten-free, anyone can do it. There is nothing nutritionally needed in gluten. Nothing. Everyone in the world could stop eating wheat, barley and rye and not a single one would be ill because of it... assuming there is are healthy replacement foods that is. Really, the only thing healthy about wheat flours is that they are fortified with added vitamins; taking a multivitamin will give you the same benefits. The only bad thing about the gluten-free diet is having to learn new ways to bake, and the hassle of finding safe places to eat out. That's it.  :)

 

Good luck with the diet. i hope your dd and dh continue to feel better.... You might want dh and yourself, plus any other kids you have, get tested for celiac disease before going gluten-free any longer. Knowing sometimes makes it easier not to cheat.

 

Best wishes.

africanqueen99 Contributor

I'm going to be odd man out here.  We're talking about a kid that will live a long healthy life, but on a crazy, restricted diet.  So I'd run another set of blood work before taking her off gluten.  Yes, it SUCKS doing blood again for kids.  Yes, I did it for my two positive kids.  Yes, I *needed* to know it was positive and not a weird mix-up at the lab.

Cara in Boston Enthusiast

A positive blood test is a positive blood test.  Considering she also has several symptoms (my son had zero symptoms) it is pretty clear.

 

That they didn't find anything on the biopsy just means the didn't FIND anything.  Not that it was not there.  

 

I had a positive blood test and negative biopsy.  All my symptoms cleared up by being gluten free.

 

Both you and your husband should be tested . . . although being gluten free already might make them more inaccurate.  

 

IBS isn't really a disease . . . it is just a term used to describe a collection of symptoms.  The symptoms very well could be caused by Gluten Intolerance or Celiac.


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



Celiac.com Sponsor (A8-M):



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. - trents replied to Paulaannefthimiou's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Bob red mill gluten free oats

    2. - trents replied to jenniber's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      Disaccharide deficient, confusing biopsy results, no blood test

    3. - Paulaannefthimiou posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Bob red mill gluten free oats

    4. - jenniber replied to jenniber's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      10

      Disaccharide deficient, confusing biopsy results, no blood test

    5. - trents replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      High TTG-IgG and Normal TTG-IgA

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,846
    • Most Online (within 30 mins)
      7,748

    Fultonn
    Newest Member
    Fultonn
    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

    • trents
      Not necessarily. The "Gluten Free" label means not more than 20ppm of gluten in the product which is often not enough for super sensitive celiacs. You would need to be looking for "Certified Gluten Free" (GFCO endorsed) which means no more than 10ppm of gluten. Having said that, "Gluten Free" doesn't mean that there will necessarily be more gluten than "Certified Gluten" in any given batch run. It just means there could be. 
    • trents
      I think it is wise to seek a second opinion from a GI doc and to go on a gluten free diet in the meantime. The GI doc may look at all the evidence, including the biopsy report, and conclude you don't need anything else to reach a dx of celiac disease and so, there would be no need for a gluten challenge. But if the GI doc does want to do more testing, you can worry about the gluten challenge at that time. But between now and the time of the appointment, if your symptoms improve on a gluten free diet, that is more evidence. Just keep in mind that if a gluten challenge is called for, the bare minimum challenge length is two weeks of the daily consumption of at least 10g of gluten, which is about the amount found in 4-6 slices of wheat bread. But, I would count on giving it four weeks to be sure.
    • Paulaannefthimiou
      Are Bobresmill gluten free oats ok for sensitive celiacs?
    • jenniber
      thank you both for the insights. i agree, im going to back off on dairy and try sucraid. thanks for the tip about protein powder, i will look for whey protein powder/drinks!   i don’t understand why my doctor refused to order it either. so i’ve decided i’m not going to her again, and i’m going to get a second opinion with a GI recommended to me by someone with celiac. unfortunately my first appointment isn’t until February 17th. do you think i should go gluten free now or wait until after i meet with the new doctor? i’m torn about what i should do, i dont know if she is going to want to repeat the endoscopy, and i know ill have to be eating gluten to have a positive biopsy. i could always do the gluten challenge on the other hand if she does want to repeat the biopsy.    thanks again, i appreciate the support here. i’ve learned a lot from these boards. i dont know anyone in real life with celiac.
    • trents
      Let me suggest an adjustment to your terminology. "Celiac disease" and "gluten intolerance" are the same. The other gluten disorder you refer to is NCGS (Non Celiac Gluten Sensitivity) which is often referred to as being "gluten sensitive". Having said that, the reality is there is still much inconsistency in how people use these terms. Since celiac disease does damage to the small bowel lining it often results in nutritional deficiencies such as anemia. NCGS does not damage the small bowel lining so your history of anemia may suggest you have celiac disease as opposed to NCGS. But either way, a gluten-free diet is in order. NCGS can cause bodily damage in other ways, particularly to neurological systems.
×
×
  • 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.