I'm concerned a month of gluten isn't enough, as I've read it takes longer. I hope you find answers, too. Let us know how she does.
KNOWLEDGE = POWER. BODY = TEMPLE. FOOD = MEDICINE. PREVENTION IS THE CURE. YOU ARE WHAT YOU ABSORB! One person's food is another person's poison. __________ Celiac Disease: An autoimmune reaction from eating gluten grains: wheat, rye, barley and contaminated oats=nutrient deficiency=cancer. Have 1 of 300 symptoms? bit.ly/cdsymptoms CD stories: bit.ly/cdstories Nutrition/Cancer: bit.ly/Quillinnutrition
I will be praying for your DD and your family. This has got to be hard. I watched my oldest have problems for her first 3.5 years of her life before we had a Dr. who found out what was wrong with her. It is so good to finally find answers.
oh! I'm so sorry for what you're dealing with! I'm the only one in my family w/ Celiac, so I never had to go that route with my kids. I'm sure it's hard. I'll be thinking of you both and hope all is well!
My 20 month old is getting a biopsy on Tuesday; please keep her in your thoughts. Has anyone else had a young child get a biopsy? How did the experience go? I really think this is the key that is going to help her out. We did have her gluten free most of the time, but she has been eating gluten for the last month for the biopsy. And it has been rough. Regardless of the results, we are definitely going back to gluten free for her. But it will be nice to know for sure when it comes to her starting preschool, school, others watching her, etc.
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