My dd had bloodwork to test for Celiac Disease and Thyroid yesterday. I was more nervous than she was I think.... We went in there and they said they took bloodwork just like they do for an adult right out of the arm.... I am looking at this poor little girl's arm thinking you are kidding me.... Well they did it and I was on the verge of tears watching, but Maggie did so good she didn't flinch, she didn't make a peep.... I was so proud of her! I took her out for breakfast afterwards to show her how proud I was.

Then we get home and she takes a 4 hour nap!!!! It must have taken a lot out of her. Then all she wanted to do was eat after she got up.....

Well hopefully we get the results back today or Monday!

Good for Her!!!

My daughter (age 6) was diagnosed with Celiac and now we have to have my son (age 8) tested. I can't tell you how much I dread this. He goes into hysterics whenever he gets his flu shot. I can not imagine what he is going to do for a blood draw.

Anybody got some good suggestions?

Please dont go only by the bloodwork for a 2 year old. My son was 3 when diagnosed and his bloodwork was totally normal, allthough he already had the internal damage. So even if they come back normal, and you think she may still have it go with your gut feeling. Try the diet for a few months and see if there is a change. Just my 2 cents.

Thank You for suggestion...I think no matter what that blood test says i am going to feed her gluten free for awhile and see what happens.....

I can just see so many of the same symptoms i had before i was diagnosed in her.... from the bloated belly all the time, to the horrible gas, to the awful smelling dirty diapers. The days that she is starving to death, and then the days where she is "scared" to eat..... I can just see it all..... and i have a feeling my gut is right on this one.

You might want to get a gold standard biopsy dx before going gluten-free. I made that mistake and regretted it. TO make a child sick again to get a dx was just plain horrific (as well as illogical, but that is the way the system works).

I see no reason that you can not insist on a biopsy, especially if the gene marker is present.