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      Frequently Asked Questions About Celiac Disease   09/30/2015

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to Celiac.com's FREE weekly eNewsletter   What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease? - list blood tests, endo with biopsy, genetic test and enterolab (not diagnostic) Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet What if my doctor won't listen to me? An Open Letter to Skeptical Health Care Practitioners Gluten-Free recipes: Gluten-Free Recipes

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I just received the call that we expected. The endoscopy biopsies revealed Celiac, but also Eosinophilic Esophagitis. I was expecting the first diagnosis, but the second was not expected. We have been referred back to the allergist for more testing due to the EoE. So, I'm a little confused???? If they find that he is allergic to other things, what will I be able to give my child? We are also still waiting on results for the lactose and sucrose tests to see if we need to restrict those things as well. Does anyone have experience with the EoE diagnosis???

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I don't know a lot about EoE but I do know there's a great group of parents at Kids With Food Allergies forums that are pros at it! Maybe check it out!

Hugs and good luck!

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A lot of EoE children are on some sort of elemental formula whether that is by mouth or via g-tube. Neocate and Elecare are the two most elemental formulas and what the majority of EoE children use.

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My daughter has both Celiac and EoE. Celiac was diagnosed when she was 17 months old, EoE was diagnosed when she was 6. All of her allergy testing was NEGATIVE, and that is normal for EoE cases. (because an eosinophil reaction is not a truely "allergic" reaction) We did an elimination diet that included all top 8 allergens and peas free. (YES, it is possible) We narrowed it down for her to be gluten free (never ate gluten since she was 17 months) egg, fish, shellfish, and pea free diet. Identifing the "triggers" and she has never needed to be on a feeding tube.

There is now a proven connection between Celiac and EoE.

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My daughter had the same thing! On their way down for the biopsy they found EE. Her back test showed all beans, peas, rice, pork, mustard, cantaloupe, tree nuts, and apples. I have no idea if she is really allergic to any of that. My friend's son showed nothing on the back prick. I had 2 doctors tell me 2 different things.

1) flovent and food trials. Put her to sleep every 3 months to go look.

2) until she has symptoms don't worry about it. I am not putting her to sleep to just go look. If it gets bad, she will have symptoms. She said that GI doctors do food trials to check if the symptoms go away so if she doesn't have any...then there is no need to do it.

Not sure which one was right. What did they tell you to do?

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My daughter had the same thing! On their way down for the biopsy they found EE. Her back test showed all beans, peas, rice, pork, mustard, cantaloupe, tree nuts, and apples. I have no idea if she is really allergic to any of that. My friend's son showed nothing on the back prick. I had 2 doctors tell me 2 different things.

1) flovent and food trials. Put her to sleep every 3 months to go look.

2) until she has symptoms don't worry about it. I am not putting her to sleep to just go look. If it gets bad, she will have symptoms. She said that GI doctors do food trials to check if the symptoms go away so if she doesn't have any...then there is no need to do it.

Not sure which one was right. What did they tell you to do?

So far we were told to consult our allergist for more food testing. So I called our allergist to see where we need to start. We have started the Flovent and also Previcid. I'm not sure I know what symptoms in him look like? The nurse didn't describe it well and the internet is a little confusing. I'm like you I certainly don't want to put him to sleep that often. What are her symptoms?

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Symptoms (as explained to me by my child who has has EoE for over 3 years)

headaches

dark circles under the eyes

pain when she was younger it was her whole belly area (circled above hip bones, including sides of belly, and up to the lower ribs (solar plexus)~ now that she is older she complains about her throat down into her neck

vommitting ~ GERD like vommitting small amounts of vommit that can come up at any time. especially a sudden stop in the car. But before diagnoses she was all out vommitting about 5 times a day.

she was always a slow eater

was diagnosed with anemia, in younger kids they will chew food and spit it out. as part of the craving non-food items.

the pain does seem worse when the lay down to sleep. so that does leave them overtired and irritable.

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Symptoms (as explained to me by my child who has has EoE for over 3 years)

headaches

dark circles under the eyes

pain when she was younger it was her whole belly area (circled above hip bones, including sides of belly, and up to the lower ribs (solar plexus)~ now that she is older she complains about her throat down into her neck

vommitting ~ GERD like vommitting small amounts of vommit that can come up at any time. especially a sudden stop in the car. But before diagnoses she was all out vommitting about 5 times a day.

she was always a slow eater

was diagnosed with anemia, in younger kids they will chew food and spit it out. as part of the craving non-food items.

the pain does seem worse when the lay down to sleep. so that does leave them overtired and irritable.

Thanks - those seem to be close to Celiac. Those are all the symptoms (except throwing up) that lead drs. to think Celiac. Thanks for all the support.

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Yes, they were nearly all the symptoms of Celiac. My daughter was diagnosed with Celiac when she was a toddler. Had been gluten free for about 4 years. I thought there was cross contamination coming from school or something. Everything was just getting worse and then all the vommitting started.

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So far we were told to consult our allergist for more food testing. So I called our allergist to see where we need to start. We have started the Flovent and also Previcid. I'm not sure I know what symptoms in him look like? The nurse didn't describe it well and the internet is a little confusing. I'm like you I certainly don't want to put him to sleep that often. What are her symptoms?

My daughter has no symptoms. That doesn't mean they couldn't start but she doesn't have any right now.

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