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New Here With 13 Month Old


will'smom

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will'smom Newbie

Hello to all,

Thank you for this board! My name is Julie, and William is my 13 month old. He has been a challenge from day 1. After getting him diagnosed with reflux at 2 months...things were a little better with Prevacid. He was very crabby, colicky, and unhappy most of the time. I always suspected something else going on. Finally, after playing with his diet, I think he may be celiac. My pediatrician is NOW listening FINALLY! We just had the genetic blood test done on him....so I will let you know the results. Until then, I wanted to introduce ourselves and meet other parents that we have something in common with. Also, where do you buy most of your food...what do you make? Any good name brand items that are gluten free....good recipes...ok toothpastes and lotions? Good websites? Anything would be helpful! Are there gluten free fishsticks? or ckn nuggets? Nice to meet all of you,

Thank you,

Julie

William's Mom ( i betcha my mom is right!)

6-26-03


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flagbabyds Collaborator

Wellshire Kids have a gluten free chicken nugget. they say gluten free on the bag and they are really goood.

AmyandSabastian Explorer

Hi welcome to the board. My name is Amy and I have a 7 month old Sabastian who has celiac disease. I am also new but I can offer what I have learned. I am looking for new mommies to chat with, with young babys. There arent many of us. :(

amycopeland@ourbirthclub.com

Amy and Sabastian

Terri-Anne Apprentice

Amy,

I'm just curious how you discovered that Sabastian has celiac at such a young age? My kids were barely onto baby food by that age, and when Logan started having reactions, (terrible rash, diarrhea) he was over two when we finally nailed down whtat the problem was. Sabastian is certainly lucky to have a mommy who was able to figure things out so early, preventing many more months/years of suffering for him!

TrixieMom Rookie

Hi there

My son was diagnosed at 13 months with celiac disease through a biospy. He is also being treated for reflux (Zantac and Prevacid) and severe asthma (Flovent, Serevent and Ventolin). Apparently the reflux is related to the stomach pain etc. of celiac. We've been following the diet for six weeks - and it isn't too bad. It hasn't taken too long to get used to for the most part - and after 4 weeks or so we started to see changes with the bm and that makes to effort worthwhile.

I think it is much easier to start at a young age rather than aquiring a taste for gluten and having to start later.

We are Canadian and I have found the site www.celiac.ca helpful.

Trixie

eternity Explorer

My son is 17 months old and was diagnosed with celiac last week. He had reflux, apnea, asthma, enamel problems, calcium def, cried alot, diarrhea, diarrhea, and more diarrhea.

We are making most of our own food as the convenience foods are so expensive. Betty Haagman has a great book I will have to look at the name. I am using alot of recipes from it. I make fresh homemade bread with her recipes, muffins, and snacks sometimes. I am gluten-free as well since Mason is still nursing. He has been eating homemade stews, soups, etc.

I am trying to learn quickly and have been calling manufactures when I am in doubt about the contents of a product.

The list on this site about safe and forbidden foods has been really helpful.

I have herd to gluten free pantry has some good items. I have their catalog ( you can request a free one on their site) but I haven't ordered anything yet.

The only convience foods we are using are mainly gluten-free pretzels, corn noodles, gluten-free arrowroot cookies.

AmyandSabastian Explorer

Well my story is like most. Sabastian was cranky from day 1 and was labeled colic and never grew out of it. I went from Doc to doc and finally got some answers. He has been gluten-free for (wow) 8 weeks and what a world of difference. He was regressing, had silent reflux, pooping probelms from day 1, on and on and on. My husband and I are waiting for our kit from Enterlab and we are thinking we are postive too. I am 25 and I have had IBS since 4 and I have athritis. Hubby has many probelms too.


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dana-g Newbie

Amy, you have really come a long way in a very short time--you sound like an old pro! It's so good to hear your son is doing well. And how great that you and your hubby are being tested! Good luck with everything. Sebastian is really a lucky boy!

hjkmatthews Apprentice

My daughter was 20 months when she was diagnosed with celiac disease. I have to say though that I have known there was something very wrong since she was nine months old. Around that time she was diagnosed with asthma had to have contiuous breathing treatments with Pulmicort and Xophenex. She also had ear/throat infections non stop, as well as bouts of diahrrea that would last for days at a time. A couple of days after Christmas last year, she had it so bad that as soon as I put a clean diaper on her, she would mess in it again. We took her to the doctor that day, and once a week the next three weeks as she began to vomit after every meal/drink. They told us she just had a stomach virus. And all along her tummy was distended, I look back at all the photos and realize that some doctors are really ignorant. She literally looked like a pregnant baby! Anyways, after three weeks of her just becoming more lethargic, we took her to the ER of a local Children's Hospital, and to make a long story short, she was having intussusseptions in her small intestine. A week into her stay and three bowel surgeries and a biopsy later, they also found that she had Celiac, and that the damage to her intestive was the cause of her intussusseptions and sickness. We were in that hospital for an entire month, and she kept having those 'collapses' in her intestine, and kept having those surgeries. I am thankful for the diagnosis however, and really believe that she is going to be okay now. We are adjusting to her new diet pretty well, but I know we have a long way to go. I just want to wish all of the other parents of little ones and babies the best of luck. They are truly blessings and although things may be a bit harder now, it is not the worst thing that could have happened! :)

Heather

Mother of Kylie

gluten-free for 6 months

AmyandSabastian Explorer

Thank you Dana!! Makes me feel so good. Honestly I am getting pretty good at this!! I havent slipped in 4 weeks now. Not one time. He has been such a happy baby. Life is WONDEFUL. He is super advanced now. He is crawling, talking (mama, nana (grandma), daddy, baba, ouch, hi), trying to WALK, push walking anything he can find, eating with hands like a champ (sweet peas!!!)standing alone for a few seconds, taking two steps. Now mind you he is ONLY 7 months old. Gluten free has saved me from the loney ben!! I wish you all luck, no matter how hard it seems to stick to this diet, take it from me and Sabastian, ITS WORTH IT and you can do it. Oh, and ALWAYS trust your motherly instint!!

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    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
    • knitty kitty
      Food and environmental allergies involve IgE antibodies.  IgE antibodies provoke histamine release from mast cells.   Celiac disease is not always visible to the naked eye during endoscopy.  Much of the damage is microscopic and patchy or out of reach of the scope.  Did they take any biopsies of your small intestine for a pathologist to examine?  Were you given a Marsh score? Why do you say you "don't have intestinal damage to correlate with lifelong undiagnosed celiac disease"?   Just curious.  
    • rei.b
      I was tested for food allergies and environmental allergies about 7 months before I started taking Naltrexone, so I don't think that is the cause for me, but that's interesting!  The main thing with the celiac thing that is throwing me off is these symptoms are lifelong, but I don't have intestinal damage to correlate with lifelong undiagnosed celiac disease.
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