Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 Children are often glutened at school - pasta pay, math games with food items, play dough, stickers, licking stamps, etc. Could that be happening? > > Hello! My 6 yr. old has had celiac diagnosed for 3 months. Our whole > house is gf and we are very careful!!! Her first level at diagnosis > was 22. Now, her level is 17. The doctor didn't seem too concerned and > said that she was " moving in the right direction " . He said that 6 > months from now, he wants her to be under 12. 17 did not seem like it > had come down too much. Is that the norm? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 Children are often glutened at school - pasta pay, math games with food items, play dough, stickers, licking stamps, etc. Could that be happening? > > Hello! My 6 yr. old has had celiac diagnosed for 3 months. Our whole > house is gf and we are very careful!!! Her first level at diagnosis > was 22. Now, her level is 17. The doctor didn't seem too concerned and > said that she was " moving in the right direction " . He said that 6 > months from now, he wants her to be under 12. 17 did not seem like it > had come down too much. Is that the norm? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 Is she taking a medication with a hidden gluten? Does she eat at others' homes? Are the grandparents on the same page w/ respect to " gluten free " ? I'd have them check again in another month or 3 and then worry if it still hadn't gone back down. But perhaps that's just me. I was totally (and joyfully) shocked when my numbers had gone to zero in only 3 months' time. I don't think that's the norm. Esther in RI > > > > Hello! My 6 yr. old has had celiac diagnosed for 3 months. Our whole > > house is gf and we are very careful!!! Her first level at diagnosis > > was 22. Now, her level is 17. The doctor didn't seem too concerned > and > > said that she was " moving in the right direction " . He said that 6 > > months from now, he wants her to be under 12. 17 did not seem like > it > > had come down too much. Is that the norm? > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 Is she taking a medication with a hidden gluten? Does she eat at others' homes? Are the grandparents on the same page w/ respect to " gluten free " ? I'd have them check again in another month or 3 and then worry if it still hadn't gone back down. But perhaps that's just me. I was totally (and joyfully) shocked when my numbers had gone to zero in only 3 months' time. I don't think that's the norm. Esther in RI > > > > Hello! My 6 yr. old has had celiac diagnosed for 3 months. Our whole > > house is gf and we are very careful!!! Her first level at diagnosis > > was 22. Now, her level is 17. The doctor didn't seem too concerned > and > > said that she was " moving in the right direction " . He said that 6 > > months from now, he wants her to be under 12. 17 did not seem like > it > > had come down too much. Is that the norm? > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 Is she taking a medication with a hidden gluten? Does she eat at others' homes? Are the grandparents on the same page w/ respect to " gluten free " ? I'd have them check again in another month or 3 and then worry if it still hadn't gone back down. But perhaps that's just me. I was totally (and joyfully) shocked when my numbers had gone to zero in only 3 months' time. I don't think that's the norm. Esther in RI > > > > Hello! My 6 yr. old has had celiac diagnosed for 3 months. Our whole > > house is gf and we are very careful!!! Her first level at diagnosis > > was 22. Now, her level is 17. The doctor didn't seem too concerned > and > > said that she was " moving in the right direction " . He said that 6 > > months from now, he wants her to be under 12. 17 did not seem like > it > > had come down too much. Is that the norm? > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 > > > > Hello! My 6 yr. old has had celiac diagnosed for 3 months. Our whole > > house is gf and we are very careful!!! Her first level at diagnosis > > was 22. Now, her level is 17. The doctor didn't seem too concerned > and > > said that she was " moving in the right direction " . He said that 6 > > months from now, he wants her to be under 12. 17 did not seem like > it > > had come down too much. Is that the norm? Sorry for tagging a response on the back of someone elses message. We are learning more about celiac disease and what we are learning complicates the understanding of the disease. It is clear that T-cell recognition and gluten-tTTG interaction is important to the disease, therefore removal of the gluten does not remove tTG since tTG is endogenous protein of the GI tract, and its covelant linkage to other allergenic or antigenic dietary proteins could continue the response. In an Ideal world one has to consider what the normal response to tTG is in humans, let us say its a 3 and lets say that the starting state is 22, the half life of antibodies in circulation is 120 days. And let us also argue that the accuracy of the test is +/-20%. 120 days is four calender months, at that time if the testing were perfect one would expect the tTG antibodies to fall to 3(non specific binding) + (22-3)/2 or 9.5 = 12.5 a guess would be that the levels would be at 15 or 16 after only 3 months. The confidence range of that would be +/-20% or 3.0 pts and the confidence range on the initial score would also be about 4.5 pts so 'statistically' speaking the result of 17 is not yet deviating from the ideal. As I said in may not be ideal half-life decay curve from the moment on removes gluten. If you are like most of here it probably took you a few weeks to find all the little traces of gluten sneaking into your childs diet. I have a Ph.D. in biochemistry and it took me 4 months, even though removing the biggies certainly helped (of course I am more set in my ways than a child who has parents who decide what he eats). There were issues, like flour added to soups, and the wheat in soy sauce I was unaware of. No one is perfect. Even so had you been perfect, tTG likes to bind certain motifs, and the gluten/food-protein interaction causes a great many food reactions, and these foods can also bind tTG, so you have a certain lag time before antibodies subside to consumed foods, elimination most of the food allergans, and the time when the peak stimulation of tTG response begins to subside to less than 1/2. The half-life of antibodies are not the same, some are more stable and some are less stable. B-lyphocytes continue to express antibodies even after the T- lymphocyte stimulation disappears, they eventually die off, some are retained as memory cells and go quiescent. So cheer up! really! anyway because the declining of numbers is consistent with the expectations under a gluten free diet and is close to ideal. The peak stimulation of the celiac disease is on the decline and so the search should be on dietary allergens that result in secondary symptoms. In terms of GF 'accidents', if common experience here is an indicator, chances are they will show up in the 'I don't feel so good [pitter patter to the bathroom]' catagory first before you will see a marked alteration of the antibody response. The only thing I would say is that early onset CD is the most severe and gluten synsitivity is very high, I cannot say whether a milligram per week of gluten will cause a rise in antibody titer, but it certainly causes a persistence of disease in some individuals. At least during the first year complete gluten abstinence should be maintained. My impression is that sensitivity at this level as the GI heals it will immediately recognize gluten contamination with a more immediate (i.e. chowder time at the ole toilet bowl) versus longterm response. BTW, if the expected level is 15 +/-3 or 12 to 18 and the previous level is 22 +/-4 or 18 to 26 the current value of 17 is within the 96% CI of the previous value, but also the expected value is in the same limits. A test at 3 months only indicates a probable trend, even under ideal circumstances. That sounds scarey but alas thats the nature of the clinical examination versus natural variation. The doctor wants to see your child in 6 more months, this is relevant because the ideal level would be 2 half lives or 1/4 the original nonspecific component value 19.5 or about 4.75 + 3 or between 7 and 8, around 7.5. The error is about 1 pt so the standard range is 6 to 9 and this is signficantly different from 18 to 26 score and the standard error ranges do not overlap, therefore at this time if his score is closer to the upper relative to the lower range then one has a basis for concern. The best you can do is keep your cool and follow the rules and bide your time till the next test, you'll be ok. Another alternative is to go over to my group " Gliadin Science " and read up on all the fascinating science being done on CD, it wont get rid of your worries but you'll probably fall asleep trying to understand all the sciency jargon. :^). Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 4, 2006 Report Share Posted May 4, 2006 We had some issues at school ourselves. It took me a while to figure it out, because our daughter didn't have blatent symptoms (her normal nausea and diarrhea) she only had a low level stomach ache and just didn't feel so good. I think she was getting a more constant low level exposure where she wouldn't get all of her normal symptoms, but just felt mildly icky. Some other possibilities to check into at school are: How often is her desk cleaned? While your child might not be playing with playdough or cookies, the other kids are and they often go around putting their hands on ALL of the desks. Ask to let her/him be allowed to wash off their desk daily. Let the teacher know this could be an issue and ask when would be a good time for them to clean the desk. I have sent in baby wipes (the ones with just a bit of soap on them) for this purpose instead of just the antibacterial ones. Does your child's class use hand sanitizer before going to lunch, or do they actually wash their hands? Many classes use the hand sanitizer because it is quicker than getting 20+ kids to wash their hands. While Purell itself has been found to be GF, it's mode of action is to kill bacteria, not deactivate proteins such as gluten. I suspect there may still be some gluten on their little hands that they can react to. I have brought this to our child's teacher and now our daughter is sent to the sink instead of the hand sanitizer bottle. The lunch table. Again, a prime place for little glutened hands to be touching everywhere. Also usually subject to sanitizer, NOT soap and water. We have had our little one get in the habit of spreading a napkin out over her place or to wash it off for herself. I send the little wet nap wipes with their lunches. Make sure your little one learns that what brand name something is DOES make a difference. My daughter made that mistake at first. She knew we had little fruit snacks at hime and so she took some from a friend at school. Wrong brand of course and she paid for it with 3 weeks of diarrhea. She has been learning to read labels for herself and we work a lot of what gluten might be called. I actually work on it at the grocery store with them. Our 9 yr old has gotten pretty good at it, though once in a while, he misses something. These were some possible sources that we didn't think of at first, but I think they did contribute to her sore tummy. We worked at correcting these and her tummy aches improved. Also, I have had to remind both my children and the teachers after longer breaks like winter, easter and spring vacations. Things have a tendancy to get a bit too lax after such periods. Hope this helps. Cheryl in Tampa > > Hello! My 6 yr. old has had celiac diagnosed for 3 months. Our whole > house is gf and we are very careful!!! Her first level at diagnosis > was 22. Now, her level is 17. The doctor didn't seem too concerned and > said that she was " moving in the right direction " . He said that 6 > months from now, he wants her to be under 12. 17 did not seem like it > had come down too much. Is that the norm? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 7, 2006 Report Share Posted May 7, 2006 Thanks for your help. I am a neurotic RN and mom who has deal with diabetes and health issues with my daughter since age 2. Her teacher fully understands. We have her wash her hands with soap and water before snacks and lunch; we cleaned out all of the playdough and replaced with GF dough; I also cleaned the entire room play areas, games, toys, etc. that may have come into contact with playdough ever; before her snacks, the table is cleaned with clorox wipes (as well as after neighbors eat their snacks to remove their gluten); I replaced EVERYONE in her room's art supplies with GF varieties (because they often share them); we stay away from stickers and lotions of any kind; at lunch the tables are cleaned down before she eats, she has a disposable place mat to eat on and even sits on a covered stool (because the kids all twist and touch the stools); I call every new product to inquire (even if the label seems GF); I read every label every time; we use GF hair products, lipglosses, tooth paste, kiddie makeup, etc.; we do not eat out much at all because of my neurotic fear!!!; I am her room mom, Daisy leader, Sunday school teacher, at every party, etc. (because I've had to be with her diabetes); we have no gluten in our house; she's not allowed to eat at other's houses; I mean, my husband calls me the gluten police!!!! Therefore, I can not imagine that there is anything possibly else that I can do or change that would help. Can anyone else think of anything else I'm forgetting? Thank you all for your help. It's great to know that there are others like you all to rely on!!! > > > > Hello! My 6 yr. old has had celiac diagnosed for 3 months. Our whole > > house is gf and we are very careful!!! Her first level at diagnosis > > was 22. Now, her level is 17. The doctor didn't seem too concerned and > > said that she was " moving in the right direction " . He said that 6 > > months from now, he wants her to be under 12. 17 did not seem like it > > had come down too much. Is that the norm? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2006 Report Share Posted May 8, 2006 While I don't have answers, I am facing a similar dilemma. My son was diagnosed with celiac around Thanskgiving with a level of 100. While I cannot claim to have been as attentive as you have been, we have vastly changed his diet and behavior (altering all food and cleaning products, meeting with school teachers and supplying substitutes for everything, etc). He is now essentially asymptomatic, his vitamin absorption levels are all normal and his coloring has visibly improved, yet his 3-month labs were still 100---NO CHANGE! We have further tightened our regimes and are staying tuned for the next blood test; having spoken with others about this, one other person's daughter took a long time to react to the diet as well. Carla Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2006 Report Share Posted May 8, 2006 One solution for having young celiacs eat over at friends' houses (which might not be an issue now but might become increasingly important to her as she gets older) is to have her bring her own food. Of course you may want to talk to her friend's parents before any kind of extended visit, especially any visit involving food. This is what I do sometimes, just bring an amy's microwavable meal, if there is going to be a meal that I'm not sure I can eat, even as an adult. Of course it will become easier as she gets older and able to protect herself from the " gluten goblins " we have no gluten in our house; she's not allowed to eat at other's houses; Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2006 Report Share Posted May 8, 2006 One solution for having young celiacs eat over at friends' houses (which might not be an issue now but might become increasingly important to her as she gets older) is to have her bring her own food. Of course you may want to talk to her friend's parents before any kind of extended visit, especially any visit involving food. This is what I do sometimes, just bring an amy's microwavable meal, if there is going to be a meal that I'm not sure I can eat, even as an adult. Of course it will become easier as she gets older and able to protect herself from the " gluten goblins " we have no gluten in our house; she's not allowed to eat at other's houses; Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2006 Report Share Posted May 8, 2006 One solution for having young celiacs eat over at friends' houses (which might not be an issue now but might become increasingly important to her as she gets older) is to have her bring her own food. Of course you may want to talk to her friend's parents before any kind of extended visit, especially any visit involving food. This is what I do sometimes, just bring an amy's microwavable meal, if there is going to be a meal that I'm not sure I can eat, even as an adult. Of course it will become easier as she gets older and able to protect herself from the " gluten goblins " we have no gluten in our house; she's not allowed to eat at other's houses; Quote Link to comment Share on other sites More sharing options...
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