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 Opinion On My Daughter


scaredparent

Recommended Posts

scaredparent Apprentice

Hi I have a son who is 23 mo old and has been gluten-free since Febuary and is do well. We have not seen much weight gain but he doesn't have diahrea any more :D . My son had a postiive dietary change and negeitive test results on blood and biopsy. ( I think because he was to young for postitive result).

Here is my problem. I have 5 children and child number 2 and 5 are sick all the time. Number 5 is Braunson the 23 mo old and Brittani is number 2 and she is 7. She has a lot of medical problems like constipated all the time she can be on laxitive 3 times a day with no results. She gets sinus imfections all the time. She was dx with a immudificency problem at the age of 2. She has had 14 surgeries and close to 50 iv's for medications 3 picc line and 2 portacathiders. And to make a long story short she has had Igg panels ran at the age of 2 and I got a hold of them the other day and found out that she had an abnormal IgA level. It was not realllly bad but a bit abnormal.

Is one of the test for celiac disease the IgA test? If so what number indicates celiac disease? Did any one else of trouble with sinus infections and constipation and then get dx with celiac disease? I am debating on putting her through the biopsy and the rest of the blood work. She often looks bloated and pregant. She has never been under wieght. She weight 83 lbs and is 54 in tall and will be 8 in August. But she was anemic at age 1. Can celiac disease run from one extreme to the other in the same family? Any opinion on what I should do? Any ones opinion is welcomed and appeciated? Sorry for the long questions ? Thanks for the help in advance


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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

I sent you a PM in regards to your question you had for me. I tried to respond to the email but it said something about your email address being down and sent it right back so I used the PM..hope you got it

Anyways, yes it sure can be in families like that.

The full panel of celiac disease is the following:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Total Serum IgA

The tTG and EMA are very specific for celiac. If she did not have these done then she should. A false reading on these are very slim to none chance. She should be continuing a gluten filled diet until after testing though.

When you have antibodies on the regular IgA this means your body is having some reaction to gluten so in my opinion it should be investigated further.

Constipation is a very common symptom in celiac actually. I had it before diagnosis. Some doctors seem to think if you don't have diarrhea or certain symptoms then you don't have it but that is completely false.

Also, her being anemic is another big sign. Anemia is also a symptom of celiac.

Hope this helps a bit and let me know if I can help you out.

Boojca Apprentice

My son is 3, he was diagnosed a year ago exactly (endoscopy anniversary was yesterday, actually) at age 2 1/2. Definitely have your other children tested. It sounds like celiac disease to me, and I have yet to hear anyone who has the exact same symptoms...and some don't ever have ANY symptoms.

It can't hurt to get them tested, but it sure could hurt not to!

Bridget

VydorScope Proficient

The way I see it, since this is a gentic thing, If anyone one person inyour direct blood line has celiac disease, you all should be tested.

lbsteenwyk Explorer

Your older child's symptoms sound exactly like celiac disease to me. One of my daughter's symptoms was SEVERE constipation. I would instist that your pediatrician to a complete celiac panel on her.

Regarding your younger child, be aware that the weight gain can come slowly. My daughter started on a gluten-free diet at 26 months and it took about 6 months to see significant weight gain.

Guest Lucy

My son had NO symptoms. He was diagnosed at 2.5. The only reason he was screened was because his Endocronologist ran it as standered procedure for all type 1 diabetics.

One thing I have found is that some people with celiac also have intestinal yeast. This can act like gluten. For your son, maybe see if you can get him and the rest of your kids on acidophylos. I don't know if I spelled that right. It will clear up a yeast problem, and then you should see improvement on the gluten free diet.

pwalasik Newbie

My 2nd child, as well as other people who have Celiac Disease, present with constipation versus diarehea. My 1st child had diarehea, so yes the symptoms can be very different from child to child. Good luck, my thought is that all family members should be tested and genetic testing is a good option too.


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. - lizzie42 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Son's legs shaking

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

      Bob red mill gluten free oats

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

      Disaccharide deficient, confusing biopsy results, no blood test

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

      Bob red mill gluten free oats

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

      Disaccharide deficient, confusing biopsy results, no blood test

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

    • Total Members
      132,850
    • Most Online (within 30 mins)
      7,748

    Cindy Shreve
    Newest Member
    Cindy Shreve
    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

    • lizzie42
      My 5yo was diagnosed with celiac last year by being tested after his sister was diagnosed. We are very strict on the gluten-free diet, but unsure what his reactions are as he was diagnosed without many symptoms other than low ferritin.  He had a school party where his teacher made gluten-free gingerbread men. I almost said no because she made it in her kitchen but I thought it would be ok.  Next day and for a few after his behavior is awful. Hitting, rude, disrespectful. Mainly he kept saying his legs were shaking. Is this a gluten exposure symptom that anyone else gets? Also the bad behavior? 
    • 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.
×
×
  • 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.