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

Protien Allergy In Infants And Celiac Disease


cgilsing

Recommended Posts

cgilsing Enthusiast

Both my children (now 3yo and 5yo) were diagnosed with severe protien allergy as infants. They were on nutramigen AA for the first year, and elecare until they were 2. Other than their formula they were on a strict meat free, milk free, egg free, soy free, bean free diet. At about two they were each given a clean bill of health. However, we have some lingering problems. They are both very thin, prone to diarreah and skin problems. I have celiac disease as do several other people in my extended family. Because of all this my sons went in this morning for the celiac blood test. Because it has been so long since i have been diagnosed, I went home to do some searching in hopes that the test is now accurate enough that they wont be subjected to the endoscope. I didn't find anything conclusive on that (and if anybody knows please tell me!), but I did find an artical that said that a biopsy of a child with a milk protien allergy is indestinguishable from that of someone with celiac disease. It got me wondering if there is a relationship between children with milk protien allergies and the development of celiac disease later. Does anyone know?


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



Celiac.com Sponsor (A8-M):



Metoo Enthusiast

Both my children (now 3yo and 5yo) were diagnosed with severe protien allergy as infants. They were on nutramigen AA for the first year, and elecare until they were 2. Other than their formula they were on a strict meat free, milk free, egg free, soy free, bean free diet. At about two they were each given a clean bill of health. However, we have some lingering problems. They are both very thin, prone to diarreah and skin problems. I have celiac disease as do several other people in my extended family. Because of all this my sons went in this morning for the celiac blood test. Because it has been so long since i have been diagnosed, I went home to do some searching in hopes that the test is now accurate enough that they wont be subjected to the endoscope. I didn't find anything conclusive on that (and if anybody knows please tell me!), but I did find an artical that said that a biopsy of a child with a milk protien allergy is indestinguishable from that of someone with celiac disease. It got me wondering if there is a relationship between children with milk protien allergies and the development of celiac disease later. Does anyone know?

I am no expert. But Celiac is genetic. It is very likely your children have it. The blood test has a 30% failure rate, it will negatively report someone as not having celiac, when they actually do. Its even more inaccurate in children. You don't need an actual diagnose to have them eat gluten free if the tests are negative and you don't want to go through the scope.

Milk allergies/food allergies in general can be a secondary symptom of celiac, because the auto immune system is so over active from gluten.

pricklypear1971 Community Regular

My son was assumed to be milk protein intolerant. I thought soy, too. He was on breastmilk (I was milk, soy free - I hated life) and Nutrimiagen. So far he tests - for Celiac, but does have some low vitamin levels. We will trial gluten-free/df next month.

Hubby was milk protein intolerant, too, as a newborn.

Stepson has a milk allergy he has not outgrown. And judging by his health when he was here last he needs to get off the milk and pronto. And he said he doesn't like eating wheat because it makes him feel bad. Geez.

cgilsing Enthusiast

I do know that at least in the beginning there was more going on than just celiac disease or a gluten intolerence because i was gluten free during my pregnancies and neither of the boys had ever been exposed to gluten until they were well over two. However, gluten would have fallen squarely in the do not eat list for them because it is a protien.

You both mentioned trying the gluten-free diet before getting a conclusive diagnosis. It is so tempting to do, and my husband and i have talked about it. My fear is that if it is celiac and we cure it, they will never get a diagnosis. The thought of ever intentionally eating gluten to me is horrible, and my doctor has said a person would have to do it for months for it to show up on a scope. If a cure was ever developed the kids wouldnt be eligable for it without a diagnosis....

pricklypear1971 Community Regular

My son had a full Celiac panel done and had vitamin deficiencies. Sometimes in kids that's all you get.

Its a trial. If there's a difference we'll go from there.

Sometimes you just can't sit there and watch, wondering. I can't ignore his behavior and keep grounding him if he's having a neuro reaction. It just isn't right or fair.

That said, he's grounded today...

cgilsing Enthusiast

I hear you, Its not an easy decision. We should get back our boys' results in a week or so. Im probably jumping the gun even worrying about it before then. I hope your son doesn't have too bad of a day!

pricklypear1971 Community Regular

Oh he deserves it. I think of a brain on gluten like a drunk... You can try to reason with them but you're better off waiting til theyre sober.

It's hard waiting for results. Harder to figure out what to do with them if they are inconclusive.


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



Celiac.com Sponsor (A8-M):



StephanieL Enthusiast

Many Dr.s are willing to say yes if you a) have a genetic link to someone with celiac disease (parent or sib), B) test + on blood work and c) respond to the diet. I would ask your ped about this.

Skylark Collaborator

Do you have the link to the effect of milk allergy on biopsy? I'd really like to see it.

If your kids have positive blood tests it's very reasonable to ask that they not undergo endoscopy. Some Drs will diagnose with a celiac parent, bloodwork that falls on the gluten-free diet, and a big response to the diet.

cgilsing Enthusiast

Thanks fo the info about the scope! If it comes down to it, I will push to skip it. Here is the link I ws reading. Particularly the second paragraph under small bowel biopsy.

Open Original Shared Link

Skylark Collaborator

Thanks fo the info about the scope! If it comes down to it, I will push to skip it. Here is the link I ws reading. Particularly the second paragraph under small bowel biopsy.

Open Original Shared Link

Interesting, thanks!

I hope you get your kids doing better.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      10

      Ibuprofen

    2. - Colleen H replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      10

      Ibuprofen

    3. - Colleen H posted a topic in Coping with Celiac Disease
      0

      Oh my goodness medication causing pain !!!!

    4. - Colleen H replied to Colleen H's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Stomach burning and neuropathy


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,847
    • Most Online (within 30 mins)
      7,748

    rossick11
    Newest Member
    rossick11
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Yes, some people do get withdrawal from gluten but gluten withdrawal doesn't usually cause gut pain. Maybe more like general body aches and discomfort. We have articles on gluten withdrawal on this forum. You might do a search for them. Applesauce is very acidic and some brands have added vitamin C (ascorbic acid) which makes them more acidic. This can damage the stomach lining if you eat it too often. Especially if your stomach lining is already compromised. Ibuprofen inhibits the body's ability to rebuild the stomach's protective mucosal lining. That's why it can cause peptic ulcers. As strange as it may sound, low level irritation/inflammation stimulates the body to rebuild the stomach lining. There are two steps in this rebuilding process known as COX 1 and COX 2. Ibuprofen represses both COX 1 and COX 2. Celecoxcib, a prescription anti inflammatory, inhibits only COX 2, making it less likely to cause damage to the gut lining.
    • Colleen H
      Do you or anyone know alot about ibuprofen  I wasn't sure if I was eating too much apple sauce.   Something is making my pain so much worse  I'm referring to the intense pins and needles in my feet and lower legs.  Jaw actually has tardive dystonia and muscle spasms throughout my back Almost like an opposite effect that a pain reliever would do. I'm fairly new to this. Whatever is going on seems to be worsening  Do people get a withdrawal effect from gluten?  It's extremely painful 😖  I'll post that question or research on the site  Thank you everyone for responding 
    • Colleen H
    • Colleen H
      I think I found a huge culprit for severe reactions to create worsening of my c symptoms. Do people with celiac have sensitivity and /or have opposite reaction to certain medications Where can I find a list ?  I'm new here I'm.wondering why I am getting worse when I take certain medicine...the burning feet.  Rebound muscle pain so intense  How many people get opposite effects or have a horrible attack after these meds
    • Colleen H
      Does anyone know if that includes scrambled eggs and healthy smart butter (,gluten free) I add a very tiny amount of margarine less than a teaspoon.  I did no't have any bread    It just seems like no matter what I eat my stomach and nerves over fire and here comes a host of horrible symptoms. My lower abdomen feels horrible, my right leg thigh muscle.. very odd. Jaw pain. Burning feet , joint pain , you name it  The anxiety just creeps up into brain fog. I don't think I could explain this to anyone who is unfamiliar.  Also,  I most likely will not remember posting this until I check it.  This is highly unusual for me because I have an excellent memory.  One weekend before I knew anything about celiac I lost an entire weekend from severe brain fog, confusion, pain, etc.  I honestly thought I was losing my mind. When I think back I recall eating a lot of PBJ sandwiches and turkey sandwiches.  Once again did not know about gluten.  I was just too sick to cook. Do people fast during attacks ?? It seems horrible to keep going through this. I hope I'm not causing my own problems... I wonder if I should fast because I'm not eating gluten .  Chicken ,  scrambled eggs no milk , canned carrots,  gluten free low sugar low fat Greek yogurt which I already posted about 😞 Any suggestions I am open... I am bedridden when this happens to me.  Thank you Celiac community. 🙏🏻❤️      
×
×
  • 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.