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

Testing Kids - How Far To Push When It's Negative?


T.H.

Recommended Posts

T.H. Community Regular

This is my first post here, so sorry if it's a bit scattered!

My father has celiac disease, and I was just diagnosed with it 9 days ago - eek, big changes! But since that made 2 in our family, I immediately requested the celiac blood panel for my kids. My 11 year old daughter came back positive for celiac, and my 8 year old son came back negative.

I don't know if the doctor is going to suggest biopsy for my daughter to confirm or not, and I would welcome anyone's experience in having the biopsy done for their children, or avoided for their children.

Also, I am worried about my son. He already has issues with consuming dairy, and has all his life. And he's tiny - at least a head shorter than the average kid his age. He's active, but often has these mood issues, like he's tired and cranky and can't 'cope.' In the past, we've noticed him like this when he accidentally has dairy, but recently, I'm starting to notice it when I can't think of anything that might be causing it, not even simply being tired and cranky. Or maybe I should say, there's this subtle difference when he really IS just tired and cranky, and it's not the same as what I'm seeing now periodically.

So I very much worry about whether we are getting a false negative with him, but I don't really want to subject him to unnecessary tests. Has anyone else run into this with their own children? What did you do?

As an added note, he is likely going to be going on a gluten free diet, in any case, because I'm the cook, and with two of us to cook for who are gluten free...the whole family is going to get to enjoy that diet too. :-) But I would hate to miss something important about his health by not testing, and I know if he's going gluten free, the tests would be useless later...

So, again...any words of advice, experience with this? Any help you could give would be much appreciated!

Thanks,

T.H.


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



Celiac.com Sponsor (A8-M):



runningcrazy Contributor

Hi, Im fairly new to this too so im sorry if this isnt a huge help.

I would say be strict with him being gluten free as well, see if you notice any changes. I have had 3 negative blood tests, but we ordered an enterolab test to see what it says, and ive been gluten free nearly 2 weeks now and i feel great. So i think even with the negative tests i react to gluten.

The blood tests can check for celiac, not intolerance, there is the possibility of that.

If you want some answers, i would consider looking into enterolab tests if you can pay for it. I got the gene testing and the stool test to check for antibodies. You may or may not want to do the gene test because you know you must have the gene since you have celiac.

It can tell you if your son is reacting to gluten. It is much more sensitve than the blood test. Type in enterolab in the thread searcfh box on this website and youll see a lot more info. It takes about 3 days to recieve your kit and 2-3 weeks for results. Myh results should be here soon!

good luck~

Rondar2001 Apprentice

Hi, my daughter had an endoscopy to confirm her diagnosis when she was 7. We felt that having a definitive diagnosis would be important as she gets older. There is no questioning a positive biopsy and hopefully this will be a tool to keep her gluten free as she gets into her teens and may want to cheat on the diet. A confirmed diagnosis also gives us a little more credibility when dealing with teachers and family in our effort to keep her gluten free.

The biopsy itself was quick and painless. She was at the hospital at 7 am and home by noon with no lasting effects.

For you son, I would discuss his symptoms with his doctor and see if they would biopsy him as well. In addition to checking for celiac, they may see another issue that could be causing his symptoms.

The choice to biopsy is of course yours, these are just the reasons that we decided to go ahead with it.

Good luck!

momxyz Contributor
Hi, my daughter had an endoscopy to confirm her diagnosis when she was 7. We felt that having a definitive diagnosis would be important as she gets older. There is no questioning a positive biopsy and hopefully this will be a tool to keep her gluten free as she gets into her teens and may want to cheat on the diet. A confirmed diagnosis also gives us a little more credibility when dealing with teachers and family in our effort to keep her gluten free.

The biopsy itself was quick and painless. She was at the hospital at 7 am and home by noon with no lasting effects.

For you son, I would discuss his symptoms with his doctor and see if they would biopsy him as well. In addition to checking for celiac, they may see another issue that could be causing his symptoms.

The choice to biopsy is of course yours, these are just the reasons that we decided to go ahead with it.

Good luck!

if the biopsy comes back positive, I agree, then you have a confirmed diagnosis.

But since his antibodies were negative, the biopsy could very well come back negative. Some people with celiacs don't present with GI symptoms as their first or main problem......

I think the gene testing would be very useful.

DanAbimytwomiracles Newbie

An elimination diet is just as accurate as a biopsy. And I don't ever see a need to put a child under general anesthesia when there is a perfectly acceptable non-surgical method to determine an answer. With my daughter, who had more mild, atypical celiac symptoms and a negative blood panel, we knew within 3 days that things were better, and after 4 weeks it was amazing the difference. Giving her a gluten challenge after those 4 weeks made all the symptoms return. Our final proof was that after 1.5 years of barely growing (from 2-3.5 she gained 8 ounces), she then gained 5 lbs in one year.

T.H. Community Regular

Thanks for all the replies! I'm thinking I may avoid testing any further for the little guy and simply keep good track of how he's reacting to the gluten-free diet. Thanks!

T.H.

balmerhon Rookie

My 3 yo son's blood work came back negative. He had an endoscopic biopsy and that also came back negative for celiac. BUT they did find allergy cells (eosinophilic colitis). This is despite his RAST tests coming back negative as well.

We did 2 weeks of gluten free with no change in his symptoms (diarrhea). This was prior to the endoscopy. We're now doing dairy-free. We know he now has an allergy, but we don't know yet what it is. We may have to revisit a gluten elimination if dairy does not seem to be the problem.

So, bear in mind, it's not always celiac. But blood tests for younger kids are often incorrect.


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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,983
    • Most Online (within 30 mins)
      7,748

    Bryan s
    Newest Member
    Bryan s
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch--thanks for the tip about Dupixent, and I've added it to the article:  
    • Scott Adams
      I just want to clarify that what I posted is a category of research summaries we've done over the years, and nearly each one shows that there is definitely a connection to celiac disease and migraine headaches. The latest study said: "the study did indicate some potential causal associations between celiac disease and migraine with or without aura, as well as between migraine without aura and ulcerative colitis...this study did not find evidence of a shared genetic basis..." Anyway, there is definitely a connection, and you can go through more of the articles here if you're interested: https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/migraine-headaches-and-celiac-disease/
    • SusanJ
      Two months ago, I started taking Dupixent for dermatitis herpetiformis and it has completely cleared it up. I can't believe it! I have had a terrible painful, intensely itchy rash for over a year despite going fully gluten-free. See if your doctor will prescribe Dupixent. It can be expensive but I am getting it free. When the dermatitis herpetiformis was bad I could not do anything. I just lay in bed covered in ice packs to ease the pain/itching and using way too Clobetasol. Dapsone is also very good for dermatitis herpetiformis (and it is generic). It helped me and the results were immediate but it gave me severe anemia so the Dupixent is better for me. Not sure if it works for everyone. I cannot help with the cause of your stress but from experience I am sure the severe stress is making the celiac and dermatitis herpetiformis worse. Very difficult for you with having children to care for and you being so sick. Would this man be willing to see a family therapist with you? He may be angry at you or imagine that your illness is a psychosomatic excuse not to take care of him. A therapist might help even if he won't go with you. Also do you have any family that you could move in with (with the kids) for a short time to get away? A break may be good for you both.
    • knitty kitty
      @tiffanygosci, Thiamine deficiency is a thing in pregnancy for "normal" people, so it's exponentially more important for those with celiac disease and malabsorption issues. I studied nutrition before earning a degree in Microbiology because I was curious what the vitamins were doing inside the body.  See my blog.  Click on my name to go to my page, scroll to drop down menu "activities" and select blog.   So glad you're motivated to see the dietician!  We're always happy to help with questions.  Keep us posted on your progress! 
    • tiffanygosci
      Thank you for sharing all of this, Knitty Kitty! I did just want someone to share some commonality with. I did not know This one Deficiency was a thing and that it's common for Celiac Disease. It makes sense since this is a disorder that causes malabsorption. I will have to keep this in mind for my next appointments. You also just spurred me on to make that Dietician appointment. There's a lot of information online but I do need to see a professional. There is too much to juggle on my own with this condition.<3
×
×
  • 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.