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

Toddler With Symptoms, Blood Tests Negative...help


CN808

Recommended Posts

CN808 Newbie

I am new to this, so please excuse my use of terminology. My daughter (16 months) has had chronic diarhhea / then consitpation, severe bloating & cramping, among other symptoms since she was 8 months old. She has had all of the blood tests for food allergies, celiac, etc. and her condition is still undiagnosed. I am almost at the end of my rope with the doctors. My daughter is suffering and they are only treating the symptoms of her severe constipation (unscuccessfully) b/c her Celiac screen came back negative. We have had 3 x-rays of her stomach taken over the past few months, each showing a back up of stool through her entire digestive tract. I have noticed a bad smell on her breath, which the DR says is not related...but how can I ignore this??? I am not sure whether to demand an endoscopy at this point. Is it possible to have the blood work come back negative, but still have the diease? Everything I have read says that villi testing is the "gold standard" for diagnosis, but I though I would ask the ppl who know best -those who are suffering with the disease. Help! I am interested in knowing if it is possible to have negative blood test results but still have the disease. One other important fact -my dad was diangosed w/ Celiacs as a child....not sure how reliable the testing was back then, so who knows if he actually had it.


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

Yes, it is not only possible to have Celiac disease and/or gluten intolerance and get a false negative on the tests, but that seems to be a very common experience.

Your child is fortunate not to have suffered for years before you began tracking it down. Basically, Celiac disease is very difficult to accurately diagnose, especially in small children. I would not rely on any tests to determine this at all, except the diet test. You haven't mentioned putting your child on a gluten-free diet, so I'm guessing you haven't tried that. I'd highly recommend doing so immediately. It doesn't require anything from any doctor, it's perfectly safe, and you will have the best diagnosis known to exist.

Your daughter also has not had years of eating gluten-containing foods, so changing the diet will be easier now. Probably much easier for her than for you, since you will need to get yourself informed as quickly as possible. Thankfully, you've found this site and forum, which will give you practically everything you need to get a good start in the right direction. Feel free to ask anytime you have questions, as we are always here to help - day or night.

tyr6 Newbie

Does anyone know anywhere in the world where the Gluten Rectal challenge

test is performed at this time ?

(this test was mentioned in Dangerous grains, and elsewhere on the forum, but noone knows where it's done !!)

At Dr.Marsch's previous clinic in Manchester they don't do it anymore.

Thankyou very much !

DonnaD Apprentice

" Help! I am interested in knowing if it is possible to have negative blood test results but still have the disease. "

Yes my daughter's blood was negative although they only ran IgA Tissue transglutaminase and serum Iga and did some RAST tests for wheat, milk, eggs which were also negative. We were a wheat free household because of my IBS. She could not tolerate milk at all when she was smaller.

She had one scope and biopsy which did not show 'enough' damage so had to eat wheat again then have it repeated 6 weeks ago this time more damage showed up , and the Consultant said he would issue the diagnosis based on the positive reaction to the gluten-free diet and the biopsy.

My daughter had a GA for the scope rather than be awake and it wasn't so bad.

Please insist that you get the endoscopy & biopsy before going to gluten-free to avoid a false negative. also ask for several samples to be taken, out of 3 only 1 had damaged villi so it would have been easy to miss.

Guest nini

It is not necessary to get a biopsy. It can easily be missed in children. There is no harm in trying the diet first. IF IT WORKS YOU HAVE YOUR ANSWER. If you are still unsure after a while, administer the gluten challenge (feed her lots of gluten after she's been gluten-free for a while) and watch how her body reacts.

She does not have to have full blown celiac to have a problem with gluten. TRY THE DIET. You do not need a Dr.s permission for this.

The biopsy is NOT the gold standard of diagnosis anymore. This is outdated information. The Dr.s that are clinging to this notion need an education in Gluten Intolerance...

The blood tests can be very inconclusive and inaccurate in children (and even adults)... the gluten free diet is a very effective easy way of finding out if this is the problem.

nettiebeads Apprentice

I agree with those who recommend the diet challenge for your child. Non-invasive, and with children you usually get noticiable results fairly quickly. I haven't ever had any of the blood work or biopsies or anything like that. My gp dx'd me via the diet. No gluten = no D. Voila! Dx!! And believe me, I know I have celiac disease. Give me gluten and my body and mind are messed up for a week. The only test I'm interested in for myself and my dd is the gene testing. Anyhow, another mother here tried the diet for her toddler son and was impressed within two or three days! Her post was about two days ago. I can't remember her name, but you could search the site for her posts.

  • 3 weeks later...
celiackid? Newbie

I am also fairly new to this...

After my daughter turned 1 she developed stomach cramping, severe constipation and a small rash around her mouth. She was treating for 6 months for constipation - until March 2005 she had blood in her stool and not eating. Finally blood work was done which showed her being borderline Celiac. Went on gluten-free diet for 6 months then re-tested. Well blood work came back showing no sign of celiac disease. She seemed to be doing well on the gluten-free diet until recently when she developed severe constipation again and blood iin stool which dr states is a fissue.

Went to see ped GI who said the only way to tell if she is Celiac is to have a biopsy. We are VERY concerned to put our 2 1/2 yr old "under" in order to perform test.

Are there any other tests to take? Want to find a dr who specializes in celiac disease in Palm Beach County FL. -- anyone have any suggestions for concerned parents?


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



Celiac.com Sponsor (A8-M):



  • 2 years later...
xaecies Newbie
I am new to this, so please excuse my use of terminology. My daughter (16 months) has had chronic diarhhea / then consitpation, severe bloating & cramping, among other symptoms since she was 8 months old. She has had all of the blood tests for food allergies, celiac, etc. and her condition is still undiagnosed. I am almost at the end of my rope with the doctors. My daughter is suffering and they are only treating the symptoms of her severe constipation (unscuccessfully) b/c her Celiac screen came back negative. We have had 3 x-rays of her stomach taken over the past few months, each showing a back up of stool through her entire digestive tract. I have noticed a bad smell on her breath, which the DR says is not related...but how can I ignore this??? I am not sure whether to demand an endoscopy at this point. Is it possible to have the blood work come back negative, but still have the diease? Everything I have read says that villi testing is the "gold standard" for diagnosis, but I though I would ask the ppl who know best -those who are suffering with the disease. Help! I am interested in knowing if it is possible to have negative blood test results but still have the disease. One other important fact -my dad was diangosed w/ Celiacs as a child....not sure how reliable the testing was back then, so who knows if he actually had it.

4% of people with celiac don't have the antibodies that they test for. i would make them do a biopsy. if they wont just take her off wheat. they couldn't find anything wrong with me either and i had the same symptoms your daughter has. two weeks after i went off wheat my symptoms cleared up. also yogurt everyday helps tremendously!

now my identical twin boys (18 months) are getting tested one has the antibodies for celiac and the other doesn't

  • 2 weeks later...
BBadgero Newbie

Don't forget to avoid barley and rye as well - this site addresses it all, but since you said you are new to this, realize that gluten comes in many forms.... I too never had blood tests, but with elimination have seen a night and day type improvement, even though I didn't always seem to get the symptoms before I found out....

There could be other food intol. as well, but from what I have read and know, gluten seems to cause the most common GI symptoms....

Good luck!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,015
    • Most Online (within 30 mins)
      7,748

    Rockette47
    Newest Member
    Rockette47
    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

    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
    • trents
      @Martha Mitchell, your reaction to the lens implant with gluten sounds like it could be an allergic reaction rather than a celiac reaction. It is possible for a celiac to be also allergic to gluten as it is a protein component in wheat, barley and rye.
    • JoJo0611
    • Martha Mitchell
      Scott I also have different symptoms than most people. It affects me bad. Stomach ache, headache, nauseous, heart racing, whole body shaking, can't walk then my throat starts to close. It attacks my nervous system. The only thing that saves me is a 1/2 of Xanax...it calms down my nervous system 
    • Martha Mitchell
      Scott Adams. I was dealing with a DR that didn't care about me being celiac. I repeatedly told him that I was celiac and is everything gluten-free. He put an acrylic lens from j&j. I called the company to ask about gluten and was told yes that the acrylic they use has gluten....then they back tracked immediately and stopped talking to me. The Dr didn't care that I was having issues. It took me 6 months and a lot of sickness to get it removed.... which can only happen within 6 months. The Dr that took it out said that it was fused and that's why I lost vision. If they would have removed it right away everything would be fine. He put in a silicone one that was gluten-free and I've had no issues at all in the other eye. Do not do acrylic!
×
×
  • 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.