Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

celiac disease In 9 Month Old?


asdoodle

Recommended Posts

asdoodle Newbie

I"m posting on here as a whim that someone might have some experiences like mine. My pediatrician is sending my 9 month old daughter to a GI doctor to rule out celiac disease. We have no one in our family with this... never even heard of it until her symptoms began.

At 5 months - we tried her on oatmeal for a week. She broke out in this mysterious rash two days later.(later identified and confirmed as hives). During this week her reflux was at it's worse. Finally realized the oat coincidence and stopped feeding it to her. At that point she started breaking out in these hives to any contact with oat after 24 hours of contact (Aveeno, etc). We were told to stay away from oat and did. However in December (at 7 mths) , we fed her Gerber puffs (again for a week before realizing symptoms). Her hives appeared and she broke out in eczema rash all over her body (before she had eczema it was very mild on her face only). After eading the gerber label realized the puffs have oat in them (reason for hives) and became suspicious about wheat. I waited a week or two to let her skin calm down some and them tried feeding her wheat cereal for the first time. Again her eczema all over her body flared up. THe eczema is extremely hard to treat even though we are off all oat and wheat. So at this point we are thinking allergies/intolerances to oat and wheat. Our ped wants us to be tested for celiac disease.

Is he jumping the gun? Her only symptoms is skin rash and vomiting with oatmeal. However, she's never consumed either grain more than 5 days and at small quantities, so if she had any GI upset we wouldn't know. I'm nervous. She's so young and don't want her having to under go unnecessary testing.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



nmlove Contributor

I'd lean towards allergies myself. Interesting her doc jumped to celiac. Of course she could have it. But you also said she's not consuming that much so I'm wondering if the tests will even be accurate. Also, has she reacted to wheat in other things? Sounds to me, based on your post, she's reacting to oatmeal (as a cereal) and in a product (the puffs). Good luck figuring it all out!

Link to comment
Share on other sites
asdoodle Newbie

I'd lean towards allergies myself. Interesting her doc jumped to celiac. Of course she could have it. But you also said she's not consuming that much so I'm wondering if the tests will even be accurate. Also, has she reacted to wheat in other things? Sounds to me, based on your post, she's reacting to oatmeal (as a cereal) and in a product (the puffs). Good luck figuring it all out!

She's definitely reacting to oatmeal as a whole. She's had hives for the oatmeal cereal, Gerber puffs and the Aveeno lotion/wash, which we've tried numerous times. Each time same thing happens. As for wheat, her first encounter was the puffs, which she had the 'eczema reaction.' I tried her again on wheat cereal a few weeks later with same reaction. I haven't tried her again on wheat but am thinking I might soon as her skin is pretty clear right now. If she begins breaking out on wheat cereal, I'll know for sure it was the wheat and not a coincidence. I also wondered how they would diagnos her if she's not consuming gluten. She wouldn't have the intestinal damage,etc b/c I haven't allowed her to have it in her diet. Poor thing is living off of rice cereal, four vegetables and two fruits. I did read that you can have a gluten intolerance/sensitivty but not celiacs. I'm keeping my fingers crossed for that if anything.

Link to comment
Share on other sites
nmlove Contributor

That sounds like a good plan to me. And the good thing is, if it is allergies/intolerances, she has a good chance of outgrowing them if you keep them away from her for the first few years. I still question the celiac testing (as far as accuracy) but that's something to go through with the doc.

By the way, do you breastfeed? I know it seems hard to believe - especially in today's world where everyone compares babies - but a baby can do just fine on breast milk (or formula) alone for the first year of life. It's something I keep telling myself. My 7 month old likes sweet potatoes and kind of likes peas and apples. But she doesn't like anything else and has had two bad reactions so far (horrible constipation from just a bit of bananas and throwing up after rice cereal). Oh, plus I have to eliminate dairy/soy from my diet because she reacts to it.

Link to comment
Share on other sites
  • 3 weeks later...
laurensmommy Newbie

I'm new here this is my first post and I could have written this topic myself. My daughter is 8 months. She has a dairy intolerance of some form so early on she was put on soy formula. She was also had colic and was diagnosed with reflux which was treated with prilosec. Things seemed to be going fine until we introduced finger foods and combination baby foods recently. We started giving her gerber puffs and cheerios. Additionally some of the combination foods we gave her were peach, pear, barley or other cereal and fruit mixes that has wheat in the ingredients. Since she started having finger foods we began noticing she'd eat then would end up spitting up a slimey almost vomit type mucus. Her skin is a mess she has patches of exczema on her legs, arms, and around her mouth. Her mood has been awful very cranky, whiney, and at times nothing would please her. She wouldn't eat much of her food at all. And she was growing but only gained a pound over 4 months...doctor said her weight gain had slowed increase calories. I started to think with all these spitups something was wrong as we'd never seen these before until recently and it was always after we had been feeding her but this hadn't happened prior to the introductions of finger foods. Over the past 2 days I have eliminated all finger foods, stop using any baby food that had grains and went basic again. Her skin has already cleared up alot, she is barely spitting up at all and if she does it's like her old milk spitups that we have seen since she was born, and my mom who watches her daily said she was in a better mood today then she has been in for awhile. And the child that never slept through the night always had frequent night wakings recently things became worse with us having to go in and pick her up and she'd burp slept through the night with no night wakings.

Am I crazy or could this be a wheat / gluten intolerance???

Link to comment
Share on other sites
lovegrov Collaborator

From everything I've read, there's just no way to determine celiac at this age.

Link to comment
Share on other sites
nmlove Contributor

Correct me if I'm wrong, you had not introduced any grains prior to finger foods/mixed baby foods? I can't answer if it's celiac or not but obviously she's reacting to something - at least an intolerance or even an allergy. It's been awhile since I looked at the ingredient list of puffs or cheerios but is there any chance it's something else altogether (outside of the wheat)? If you want to know for sure, take her back to where she was at before when she was well. After her symptoms go away, give her just baby cereal with known items (i.e., barley cereal or a mixed cereal if she's already had rice/barley/oats). Just try to keep everything else status quo or you'll be questioning any reactions.

Going through this with my 7 month old. Except it's rice and gluten-free oats. Stinks.

Link to comment
Share on other sites

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
      121,094
    • Most Online (within 30 mins)
      7,748

    Tracym
    Newest Member
    Tracym
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Oh, okay. The lower case "b" in boots in your first post didn't lead me in the direction of a proper name. I thought maybe it was a specialty apothecary for people with pedal diseases or something.
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! There are other things that may cause elevated tTg-IgA levels, but in general a reaction to gluten is the culprit:    
    • cristiana
      Hi @trents Just seen this - Boot's is a chain of pharmacies in the UK, originally founded in the 19th Century by a chap with the surname, Boot.  It's a household name here in the UK and if you say you are going to Boot's everyone knows you are off to the pharmacist! Cristiana
    • Denise I
      I am looking to find a Celiac Dietician who is affiliated with the Celiac Disease Foundation who I can set up an appointment with.  Can you possibly give some guidance on this?  Thank you!
    • Posterboy
      Nacina, Knitty Kitty has given you good advice. But I would say/add find a Fat Soluble B-1 like Benfotiamine for best results.  The kind found in most Multivitamins have a very low absorption rate. This article shows how taking a Fat Soluble B-1 can effectively help absorption by 6x to7x times. https://www.naturalmedicinejournal.com/journal/thiamine-deficiency-and-diabetic-polyneuropathy quoting from the article.... "The group ingesting benfotiamine had maximum plasma thiamine levels that were 6.7 times higher than the group ingesting thiamine mononitrate.32" Also, frequency is much more important than amount when it comes to B-Vitamin. These are best taken with meals because they provide the fat for better absorption. You will know your B-Vitamin is working properly when your urine becomes bright yellow all the time. This may take two or three months to achieve this.......maybe even longer depending on how low he/you are. The Yellow color is from excess Riboflavin bypassing the Kidneys....... Don't stop them until when 2x a day with meals they start producing a bright yellow urine with in 2 or 3 hours after the ingesting the B-Complex...... You will be able to see the color of your urine change as the hours go by and bounce back up after you take them in the evening. When this happens quickly......you are now bypassing all the Riboflavin that is in the supplement. The body won't absorb more than it needs! This can be taken as a "proxy" for your other B-Vitamin levels (if taken a B-Complex) ...... at least at a quick and dirty level......this will only be so for the B-1 Thiamine levels if you are taking the Fat Soluble forms with the Magnesium as Knitty Kitty mentioned. Magnesium is a Co-Factor is a Co-factor for both Thiamine and Vitamin D and your sons levels won't improve unless he also takes Magnesium with his Thiamine and B-Complex. You will notice his energy levels really pick up.  His sleeping will improve and his muscle cramps will get better from the Magnesium! Here is nice blog post that can help you Thiamine and it's many benefits. I hope this is helpful but it is not medical advice God speed on your son's continued journey I used to be him. There is hope! 2 Tim 2:7 “Consider what I say; and the Lord give thee understanding in all things” this included. Posterboy by the grace of God,  
×
×
  • Create New...