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Enzymes


SofiEmiMom

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SofiEmiMom Enthusiast

Hello. My children have been diagnosed gluten intolerant through Enterolab and without going into the long story, my pediatrician is very supportive of the diagnosis. However, I know more about celiac/gluten intolerance than she does and I'm pretty much left on my own to how best keep my children healthy. I was wondering if any doctor has recommended Enzymes for your child with celiac? I've been reading up on Enzymes in children with celiac and it seems to be helpful, but then of course, I don't want to give then anything they don't need or spend all the money on something that isn't necessary. Anyone have their child on digestive enzymes and see a benefit? Thanks so much.


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KaitiUSA Enthusiast

Yes, enzymes are excellent. Another thing that is good for them is Probiotics, which give your body healthy bacteria. Make sure they get vitamins too.

I find those 3 things are very essential and they really aided me to get my strength back and build my immune system up.

I take CompleteGest enzymes but Enzymatic Therapy.

Kasey'sMom Enthusiast

SofiEmiMom,

As Katie mentioned these products are very helpful. I have CRC and I've been using the Whole Approach System and my daughter has celiac disease. They recommend Generation+ Digesticol digestive enzymes for both of us. I break open the capsule and only give my daughter about a 1/4 of the powder, which is sprinkled on her food. I take a whole capsule myself. I think the wieght/dose is based on a 150lb. person. You just divided by the childs weight. Her digestion and gas is 100% better with the enzymes. We can both tell if we forget to take them. I give her Country Life, Maxi Baby-dophilus for her probiotic and it comes in a powder form. The EFA I use is from Child Life Essentuals. I called to double check the EFA and they confirmed it was gluten-free.

I hope this helps some,

Kasey's Mom :)

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      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? 
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      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.
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      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.
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