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

19 Month Old Being Tested For Celiacs Disease


sparklette

Recommended Posts

sparklette Rookie

These are my DD's symptoms:

Becomes constipated when she consumes full cream cows milk (large bulky, slime covered poos),

Very windy and unsettled after weetbix,

Windy and colicky in general - she often wakes up at night and cries until she belches up wind.

When she is on NanHA formula her poos and really soft (almost like diahorrea) and full of mucous, and seem to cause her discomfort for 10 minuted prior to passing them.

I suspected a cows milk protein intollerance, but the GP suggested celiacs or gluten intolerance.

Do these symptoms sound like celiac / gluten sensitivity symptoms?

We had a blood test yesterday (RAST allergies and celiacs) and will get the results on Friday. I was just wondering whether these symptoms seemed to indicate possible celiacs to you? Can celiac disease sometimes show as a cows milk protein problem?


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

Celiac Disease is developed through an autoimmune reaction to the proteins found in wheat, barley, malt and rye.

Due to the damage caused by this autoimmune reaction, dairy often can be problematic. It may resolve with the removal of gluten from your daughters diet after some time, if in fact she has Celiac Disease.

How much wheat and/or gluten is in her diet currently?

Mother of Jibril Enthusiast

Welcome to the group!

I found this website to be helpful:

Open Original Shared Link

It has lots of links to other articles... very thorough and scientific. My son is intolerant to casein (the protein in cow's milk), not just lactose. It's possible that your daughter could have celiac disease... or cow's milk intolerance... or both! You'll figure it out eventually. Hopefully the RAST testing will point you in the right direction.

ps - If your GP suspects celiac then it would be good to run those tests. RAST is not the same thing. However... testing is unreliable in small children, so even if the test comes back negative, don't be afraid to experiment with the gluten-free diet.

sparklette Rookie

My DD does have some grains in her diet. She nearly always has porridge and toast with vegemite for breakfast, approx. 1 slice of white bread a day and occassionally a savoy or teddy bear biscuit. Would this put enough gluten in her system for the blood test to be accurate?

It is very reassuring to know that the dairy problems may cure themselves if she is celiac and has a gluten free diet.

Thanks also for the weblink - I will check it out.

B'sgirl Explorer

If you are doing a blood test or a biopsy there is no guarantee that the test will come up positive no matter how much gluten in in the diet. My son's tests came up negative but he is most definitely sensitive to gluten as well as casein and soy. We eventually had him tested through Enterolab and although he had not had milk or gluten for almost a year his test still showed a very high count of antibodies against casein and gluten--their tests are much more sensitive. Insurance doesn't cover them though.

I guess what I should really say is don't rely too much on the blood tests, especially if they come up negative. Just try removing gluten from the diet and see what happens. Who cares what the test says if your child improves with a removal of gluten from the diet? It's the child's health that is important, not on official diagnosis.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,037
    • Most Online (within 30 mins)
      7,748

    cbattiato
    Newest Member
    cbattiato
    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
      This is an older article, but may be helpful.  
    • gfmom06
      I have had orthodontic work done. The 3M invisalign material was no problem. BUT my retainers are another matter. They seemed okay for a few months. Now, however, they cause a burning sensation on my tongue, gums and insides of my lips. The burning sensation is now spreading to my throat. I notice it when I breathe. This is annoying and interferes with my enjoyment of eating. I am visiting with my provider tomorrow. We'll see where this goes from here.
    • Beverage
      Exactly which blood tests were done? There are a few different ones and some docs don't do them all. Also, your results and reference ranges for each?
    • Jmartes71
      Thankyou so much for your words.Its a hard battle when a supposed well known hospital whose celiac " specialist " has down played me because my colon looks fine and put it in my medical and so pcp doesn't take seriously. In their eyes we all carry that gene.Im having alot of bad days trying to be positive because of it.
    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
×
×
  • 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.