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Christine E

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  1. My son was diagnosed at age one. He had digestive problems since birth. Gas, cramping, constipation, spitting up. We went through formulas up through Neocate, reflux medicines. By one year old he was eating rice cereal and baby food pears and losing weight. He was diagnosed by positive gene test, and an endoscopy that showed slight changes in the lining...
  2. My son hasn't had any problems with Pebbles cereals, but FYI the new Marshmallow Pebbles has gluten in it. Also, keep in mind the top 8 allergens do not include barley, rye, or oats. Watch for behavioral changes in your kids too. Melt downs, long tantrums, excessive whining seem to be symptoms of glutening in my child.
  3. Oh, and neither of my kids will eat peanut butter or drink shakes, smooties.
  4. My 6 year old son was diagnosed Celiac at 13 months. He is about the size of your 6 year old now, small. He also will not drink milk. I always assumed he was sensitive and knew to avoid it. He drinks OJ with Calcium added, and doesn't have a problem with cheese, pudding, ice cream or yogurt. His nutritionist suggested adding a tablespoon of olive oil...
  5. This is for restaurant food. The chef indicated They cannot heat up or prepare outside food. If they buy bread, cake mix, cookies, they'll apparently charge for the product plus 10 percent (service charge?). If this is actually the case I will look into other options. I'm.quite disappointed since we've generally been well accommodated, even being charged...
  6. I've emailed ahead of a trip to a large chain, high end hotel about gluten-free meals for my 6- year-old son, and have been informed I will be charged extra for any gluten-free products they purchase to feed my son. Has anyone else ever encountered this? I think it's crazy!
  7. The pediatrician diagnosed him. He has celiac. You can ask for a genetic test if you want. My son was age one when his endoscopy showed " changes". He's now 6 and has never had a positive blood test (annual). His genetic test was positive. He was severely constipated and also was supposed to have had reflux. All resolved on gluten-free diet. I strongly...
  8. My son was diagnosed at age 1 and is now 6. He has never had a positive blood test. His endoscopy showed slight changes, and his genetic test was positive. With those and his gaining weight once on the gluten-free diet, he was dx with celiac. You can now get a less expensive cheek swab test to see if your son has the genetic marker. I'm not complaining...
  9. My son was diagnosed at age 1. His blood screens have always been negative. The doctor diagnosed him based on a positive genetic test and a successful gluten-free diet. He did have an endoscopy that showed slight "changes" but now at the age of almost 6 he has never tested positive on the blood screens.
  10. My son supposedly had GERD his whole first year, on meds, Neocate formula. When he started losing weight at a year, a different ped GI did the biopsy and blood work, both of which were negative. The biopsy showed slight changes, but he did test positive for the gene marker. The diet worked. He has never had a positive blood test. I would assume the gluten...
  11. My son has eaten the Honey Rice version with no problems. Wheat free does not mean gluten free, and sometimes gluten free doesn't even mean gluten free. I've noticed a few products that state they are gluten free, but when you read the ingredients, they have malt, or oats, or another gluten-containing product. Not all companies fully understand the definition...
  12. My son had a biopsy at 13 months. It showed "changes" in the mucosa lining. The slides were read by pathologists at Children's Memorial in Chicago and University of Chicago Hospital, and the pathologists agreed there were slight changes, but not difinitive for Celiac. His blood tests were negative and have remained so. He is now 4. The GI's confirmed...
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