Guest guest Posted October 25, 2006 Report Share Posted October 25, 2006 The simplest thing might be to just go gluten-free for a trial. My daughter also had high IgG to gliadin, as well as gluten, wheat and relatives of wheat, and dairy products were totally off the charts. She is not currently GFCF, but it was only after implementing the diet that she was able to potty train. Kerri > > Hi all > > I have been so busy lately (vacation, IEP, therapies) that I have not > been able to keep up with messages. > I do have some lab results back and I could use some help > interpreting. Of course nothing is obviously wrong (that would be to > easy) and my pediatrician isn't looking beyond the basics. > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All other - > gliadin IGA, reticulin IGA and endomysial IGA are in the normal range. > > What does the elevated gliadin IGG mean? From my google search it can > be a false positive for celiac. Should we see another dr? Who? an > allergist/immunologist or a gstroenterologist? > > Thanks for the input!! > > Martha > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2006 Report Share Posted October 25, 2006 In the past a positive IgG with negative TTG and other celiac markers was considered a " false positive'. But WAY TOO MANY of our kids with apraxia have a positive anti gliadin IgG. Since this antibody can cross react to cells of the brain as if it were gluten it is very suspect that all these kids have positive gliadin antibodies. I'm wondering if this is part of the apraxia picture for many kids???? Did you have other fat soluble vitamins checked? I would suggest you trial a gluten/dairy free diet for a month or 2 and keep a diary of any changes you see. Some changes that seem subtle initially are obviously changes down the road. If nothing happens after this time, return to your previous diet. Does your child have any gastrointestinal symptoms? Like diarrhea, constipation, reflux, abd pain...food allergies, asthma etc? Just wondering. Some people would recommend a biopsy of the gut to rule out celiac disease, but I suspect it would be negative...unless there are other risk factors for celiac disease...like symptoms, failure to thrive or family history. - > Hi all > > I have been so busy lately (vacation, IEP, therapies) that I have not > been able to keep up with messages. > I do have some lab results back and I could use some help > interpreting. Of course nothing is obviously wrong (that would be to > easy) and my pediatrician isn't looking beyond the basics. > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All other - > gliadin IGA, reticulin IGA and endomysial IGA are in the normal range. > > What does the elevated gliadin IGG mean? From my google search it can > be a false positive for celiac. Should we see another dr? Who? an > allergist/immunologist or a gstroenterologist? > > Thanks for the input!! > > Martha > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2006 Report Share Posted October 26, 2006 The simplest thing might be to just go gluten-free for a trial. My daughter also had high IgG to gliadin, as well as gluten, wheat and relatives of wheat, and dairy products were totally off the charts. She is not currently GFCF, but it was only after implementing the diet that she was able to potty train. Kerri > > Hi all > > I have been so busy lately (vacation, IEP, therapies) that I have not > been able to keep up with messages. > I do have some lab results back and I could use some help > interpreting. Of course nothing is obviously wrong (that would be to > easy) and my pediatrician isn't looking beyond the basics. > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All other - > gliadin IGA, reticulin IGA and endomysial IGA are in the normal range. > > What does the elevated gliadin IGG mean? From my google search it can > be a false positive for celiac. Should we see another dr? Who? an > allergist/immunologist or a gstroenterologist? > > Thanks for the input!! > > Martha > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2006 Report Share Posted October 26, 2006 In the past a positive IgG with negative TTG and other celiac markers was considered a " false positive'. But WAY TOO MANY of our kids with apraxia have a positive anti gliadin IgG. Since this antibody can cross react to cells of the brain as if it were gluten it is very suspect that all these kids have positive gliadin antibodies. I'm wondering if this is part of the apraxia picture for many kids???? Did you have other fat soluble vitamins checked? I would suggest you trial a gluten/dairy free diet for a month or 2 and keep a diary of any changes you see. Some changes that seem subtle initially are obviously changes down the road. If nothing happens after this time, return to your previous diet. Does your child have any gastrointestinal symptoms? Like diarrhea, constipation, reflux, abd pain...food allergies, asthma etc? Just wondering. Some people would recommend a biopsy of the gut to rule out celiac disease, but I suspect it would be negative...unless there are other risk factors for celiac disease...like symptoms, failure to thrive or family history. - > Hi all > > I have been so busy lately (vacation, IEP, therapies) that I have not > been able to keep up with messages. > I do have some lab results back and I could use some help > interpreting. Of course nothing is obviously wrong (that would be to > easy) and my pediatrician isn't looking beyond the basics. > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All other - > gliadin IGA, reticulin IGA and endomysial IGA are in the normal range. > > What does the elevated gliadin IGG mean? From my google search it can > be a false positive for celiac. Should we see another dr? Who? an > allergist/immunologist or a gstroenterologist? > > Thanks for the input!! > > Martha > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2006 Report Share Posted October 26, 2006 Clauia - Is reflux very prevalent among people with celiac disease? I've seen it listed as a possible sign but no more than that. My son has had reflux his whole life and has been taking Zantac to control it since he was 3 months old (he's 3 years, 4 months now). He also has a peanut allergy. When I was nursing it seemed that everything I ate hurt his tummy but it seemed to correspond more to acidic (e.g.orange juice) and spicy (e.g.spaghetti), so I lived on turkey sandwiches for a year. I never cut out gluten - never even gave it a thought. I picked up Drs. orders today to have blood work done for " everything " (I requested a list of tests that you had posted earlier - thank you! The ped didn't question me on bit on any of them. It includes a celiac panel. My son and I both went gluten free 1.5 weeks ago but I've reintroduced a some back into his diet so we can get more reliable results. We've kept the dairy in. BTW - I feel GREAT on a gluten-free diet! I'm sure I'll need to post our results and ask your advice as our ped has already told me he expects to get a low yield of info from it but supports it so that " I'll know " and won't have to keep wondering. I'm really hoping to prove him wrong. > In the past a positive IgG with negative TTG and other celiac > markers was considered a " false positive'. But WAY TOO MANY of our > kids with apraxia have a positive anti gliadin IgG. Since this > antibody can cross react to cells of the brain as if it were gluten > it is very suspect that all these kids have positive gliadin > antibodies. I'm wondering if this is part of the apraxia picture for > many kids???? Did you have other fat soluble vitamins checked? > > I would suggest you trial a gluten/dairy free diet for a month or 2 > and keep a diary of any changes you see. Some changes that seem > subtle initially are obviously changes down the road. If nothing > happens after this time, return to your previous diet. > > Does your child have any gastrointestinal symptoms? Like diarrhea, > constipation, reflux, abd pain...food allergies, asthma etc? Just > wondering. Some people would recommend a biopsy of the gut to rule > out celiac disease, but I suspect it would be negative...unless > there are other risk factors for celiac disease...like symptoms, > failure to thrive or family history. - > > > > Hi all > > > > I have been so busy lately (vacation, IEP, therapies) that I have > not > > been able to keep up with messages. > > I do have some lab results back and I could use some help > > interpreting. Of course nothing is obviously wrong (that would be > to > > easy) and my pediatrician isn't looking beyond the basics. > > > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All other - > > > gliadin IGA, reticulin IGA and endomysial IGA are in the normal > range. > > > > What does the elevated gliadin IGG mean? From my google search it > can > > be a false positive for celiac. Should we see another dr? Who? an > > allergist/immunologist or a gstroenterologist? > > > > Thanks for the input!! > > > > Martha > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2006 Report Share Posted October 26, 2006 I did get other tests - carnitine (free, total & esthers), Vits D, K, A & E were all normal. Howver E & K could be considered low side of normal. Lead was negative for a recent exposure (but haven't done hair yet). I did read on celiac.com that something like 20% of people with a positive gliadin Igg antibodies have some other intestinal disorder. hmmmmmm I have been reading " Children with Starving Brains " and this makes me wonder about overall intestinal health. I just don't know where to go with the info. My pediatrician is just not on board with all of this and there are no DAN doctors in the area - and if we have to travel I want to be sure it is necessary and worthwhile. I am willing to try GF but does it have to be GF/CF? Oh man that will be tough. I can hit the healthfood store to get alternative products but my son literally only eats gluten!!! He actually likes raw instant oatmeal!!!! I had beeen hoping the test would shed some light without putting our household through that level of stress. Martha In , " claudia.morris " <claudia.morris@...> wrote: > > > In the past a positive IgG with negative TTG and other celiac > markers was considered a " false positive'. But WAY TOO MANY of our > kids with apraxia have a positive anti gliadin IgG. Since this > antibody can cross react to cells of the brain as if it were gluten > it is very suspect that all these kids have positive gliadin > antibodies. I'm wondering if this is part of the apraxia picture for > many kids???? Did you have other fat soluble vitamins checked? > > I would suggest you trial a gluten/dairy free diet for a month or 2 > and keep a diary of any changes you see. Some changes that seem > subtle initially are obviously changes down the road. If nothing > happens after this time, return to your previous diet. > > Does your child have any gastrointestinal symptoms? Like diarrhea, > constipation, reflux, abd pain...food allergies, asthma etc? Just > wondering. Some people would recommend a biopsy of the gut to rule > out celiac disease, but I suspect it would be negative...unless > there are other risk factors for celiac disease...like symptoms, > failure to thrive or family history. - > > > > Hi all > > > > I have been so busy lately (vacation, IEP, therapies) that I have > not > > been able to keep up with messages. > > I do have some lab results back and I could use some help > > interpreting. Of course nothing is obviously wrong (that would be > to > > easy) and my pediatrician isn't looking beyond the basics. > > > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All other - > > > gliadin IGA, reticulin IGA and endomysial IGA are in the normal > range. > > > > What does the elevated gliadin IGG mean? From my google search it > can > > be a false positive for celiac. Should we see another dr? Who? an > > allergist/immunologist or a gstroenterologist? > > > > Thanks for the input!! > > > > Martha > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2006 Report Share Posted October 26, 2006 I'll be honest and say that I have not read the entire chain of posts here, but I can comment on the gfcf and reflux. My son joey now 3 1/2 is on a gfcf diet and it virtually eliminated all reflux and constipation within a few weeks of starting the diet. He was tested at just under 2 1/2 for food sensitives via blood and also for the possiblity of celiac disease. His blood tests showed a sensitivity to all gluten containing grains, eggs, milk, corn, rice, most nuts, etc. He also was said to have mild to moderate gluten sensitivity but not necessarily Celiac if that makes sense. Just to let you know that has never taken any reflux meds and this diet did the trick - it was absolutely amazing. Katrina and > > In the past a positive IgG with negative TTG and other celiac > > markers was considered a " false positive'. But WAY TOO MANY of our > > kids with apraxia have a positive anti gliadin IgG. Since this > > antibody can cross react to cells of the brain as if it were gluten > > it is very suspect that all these kids have positive gliadin > > antibodies. I'm wondering if this is part of the apraxia picture > for > > many kids???? Did you have other fat soluble vitamins checked? > > > > I would suggest you trial a gluten/dairy free diet for a month or 2 > > and keep a diary of any changes you see. Some changes that seem > > subtle initially are obviously changes down the road. If nothing > > happens after this time, return to your previous diet. > > > > Does your child have any gastrointestinal symptoms? Like diarrhea, > > constipation, reflux, abd pain...food allergies, asthma etc? Just > > wondering. Some people would recommend a biopsy of the gut to rule > > out celiac disease, but I suspect it would be negative...unless > > there are other risk factors for celiac disease...like symptoms, > > failure to thrive or family history. - > > > > > > > Hi all > > > > > > I have been so busy lately (vacation, IEP, therapies) that I have > > not > > > been able to keep up with messages. > > > I do have some lab results back and I could use some help > > > interpreting. Of course nothing is obviously wrong (that would be > > to > > > easy) and my pediatrician isn't looking beyond the basics. > > > > > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All > other - > > > > > gliadin IGA, reticulin IGA and endomysial IGA are in the normal > > range. > > > > > > What does the elevated gliadin IGG mean? From my google search it > > can > > > be a false positive for celiac. Should we see another dr? Who? an > > > allergist/immunologist or a gstroenterologist? > > > > > > Thanks for the input!! > > > > > > Martha > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2006 Report Share Posted October 26, 2006 Clauia - Is reflux very prevalent among people with celiac disease? I've seen it listed as a possible sign but no more than that. My son has had reflux his whole life and has been taking Zantac to control it since he was 3 months old (he's 3 years, 4 months now). He also has a peanut allergy. When I was nursing it seemed that everything I ate hurt his tummy but it seemed to correspond more to acidic (e.g.orange juice) and spicy (e.g.spaghetti), so I lived on turkey sandwiches for a year. I never cut out gluten - never even gave it a thought. I picked up Drs. orders today to have blood work done for " everything " (I requested a list of tests that you had posted earlier - thank you! The ped didn't question me on bit on any of them. It includes a celiac panel. My son and I both went gluten free 1.5 weeks ago but I've reintroduced a some back into his diet so we can get more reliable results. We've kept the dairy in. BTW - I feel GREAT on a gluten-free diet! I'm sure I'll need to post our results and ask your advice as our ped has already told me he expects to get a low yield of info from it but supports it so that " I'll know " and won't have to keep wondering. I'm really hoping to prove him wrong. > In the past a positive IgG with negative TTG and other celiac > markers was considered a " false positive'. But WAY TOO MANY of our > kids with apraxia have a positive anti gliadin IgG. Since this > antibody can cross react to cells of the brain as if it were gluten > it is very suspect that all these kids have positive gliadin > antibodies. I'm wondering if this is part of the apraxia picture for > many kids???? Did you have other fat soluble vitamins checked? > > I would suggest you trial a gluten/dairy free diet for a month or 2 > and keep a diary of any changes you see. Some changes that seem > subtle initially are obviously changes down the road. If nothing > happens after this time, return to your previous diet. > > Does your child have any gastrointestinal symptoms? Like diarrhea, > constipation, reflux, abd pain...food allergies, asthma etc? Just > wondering. Some people would recommend a biopsy of the gut to rule > out celiac disease, but I suspect it would be negative...unless > there are other risk factors for celiac disease...like symptoms, > failure to thrive or family history. - > > > > Hi all > > > > I have been so busy lately (vacation, IEP, therapies) that I have > not > > been able to keep up with messages. > > I do have some lab results back and I could use some help > > interpreting. Of course nothing is obviously wrong (that would be > to > > easy) and my pediatrician isn't looking beyond the basics. > > > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All other - > > > gliadin IGA, reticulin IGA and endomysial IGA are in the normal > range. > > > > What does the elevated gliadin IGG mean? From my google search it > can > > be a false positive for celiac. Should we see another dr? Who? an > > allergist/immunologist or a gstroenterologist? > > > > Thanks for the input!! > > > > Martha > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2006 Report Share Posted October 26, 2006 I did get other tests - carnitine (free, total & esthers), Vits D, K, A & E were all normal. Howver E & K could be considered low side of normal. Lead was negative for a recent exposure (but haven't done hair yet). I did read on celiac.com that something like 20% of people with a positive gliadin Igg antibodies have some other intestinal disorder. hmmmmmm I have been reading " Children with Starving Brains " and this makes me wonder about overall intestinal health. I just don't know where to go with the info. My pediatrician is just not on board with all of this and there are no DAN doctors in the area - and if we have to travel I want to be sure it is necessary and worthwhile. I am willing to try GF but does it have to be GF/CF? Oh man that will be tough. I can hit the healthfood store to get alternative products but my son literally only eats gluten!!! He actually likes raw instant oatmeal!!!! I had beeen hoping the test would shed some light without putting our household through that level of stress. Martha In , " claudia.morris " <claudia.morris@...> wrote: > > > In the past a positive IgG with negative TTG and other celiac > markers was considered a " false positive'. But WAY TOO MANY of our > kids with apraxia have a positive anti gliadin IgG. Since this > antibody can cross react to cells of the brain as if it were gluten > it is very suspect that all these kids have positive gliadin > antibodies. I'm wondering if this is part of the apraxia picture for > many kids???? Did you have other fat soluble vitamins checked? > > I would suggest you trial a gluten/dairy free diet for a month or 2 > and keep a diary of any changes you see. Some changes that seem > subtle initially are obviously changes down the road. If nothing > happens after this time, return to your previous diet. > > Does your child have any gastrointestinal symptoms? Like diarrhea, > constipation, reflux, abd pain...food allergies, asthma etc? Just > wondering. Some people would recommend a biopsy of the gut to rule > out celiac disease, but I suspect it would be negative...unless > there are other risk factors for celiac disease...like symptoms, > failure to thrive or family history. - > > > > Hi all > > > > I have been so busy lately (vacation, IEP, therapies) that I have > not > > been able to keep up with messages. > > I do have some lab results back and I could use some help > > interpreting. Of course nothing is obviously wrong (that would be > to > > easy) and my pediatrician isn't looking beyond the basics. > > > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All other - > > > gliadin IGA, reticulin IGA and endomysial IGA are in the normal > range. > > > > What does the elevated gliadin IGG mean? From my google search it > can > > be a false positive for celiac. Should we see another dr? Who? an > > allergist/immunologist or a gstroenterologist? > > > > Thanks for the input!! > > > > Martha > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 27, 2006 Report Share Posted October 27, 2006 I'll be honest and say that I have not read the entire chain of posts here, but I can comment on the gfcf and reflux. My son joey now 3 1/2 is on a gfcf diet and it virtually eliminated all reflux and constipation within a few weeks of starting the diet. He was tested at just under 2 1/2 for food sensitives via blood and also for the possiblity of celiac disease. His blood tests showed a sensitivity to all gluten containing grains, eggs, milk, corn, rice, most nuts, etc. He also was said to have mild to moderate gluten sensitivity but not necessarily Celiac if that makes sense. Just to let you know that has never taken any reflux meds and this diet did the trick - it was absolutely amazing. Katrina and > > In the past a positive IgG with negative TTG and other celiac > > markers was considered a " false positive'. But WAY TOO MANY of our > > kids with apraxia have a positive anti gliadin IgG. Since this > > antibody can cross react to cells of the brain as if it were gluten > > it is very suspect that all these kids have positive gliadin > > antibodies. I'm wondering if this is part of the apraxia picture > for > > many kids???? Did you have other fat soluble vitamins checked? > > > > I would suggest you trial a gluten/dairy free diet for a month or 2 > > and keep a diary of any changes you see. Some changes that seem > > subtle initially are obviously changes down the road. If nothing > > happens after this time, return to your previous diet. > > > > Does your child have any gastrointestinal symptoms? Like diarrhea, > > constipation, reflux, abd pain...food allergies, asthma etc? Just > > wondering. Some people would recommend a biopsy of the gut to rule > > out celiac disease, but I suspect it would be negative...unless > > there are other risk factors for celiac disease...like symptoms, > > failure to thrive or family history. - > > > > > > > Hi all > > > > > > I have been so busy lately (vacation, IEP, therapies) that I have > > not > > > been able to keep up with messages. > > > I do have some lab results back and I could use some help > > > interpreting. Of course nothing is obviously wrong (that would be > > to > > > easy) and my pediatrician isn't looking beyond the basics. > > > > > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All > other - > > > > > gliadin IGA, reticulin IGA and endomysial IGA are in the normal > > range. > > > > > > What does the elevated gliadin IGG mean? From my google search it > > can > > > be a false positive for celiac. Should we see another dr? Who? an > > > allergist/immunologist or a gstroenterologist? > > > > > > Thanks for the input!! > > > > > > Martha > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 27, 2006 Report Share Posted October 27, 2006 > > In the past a positive IgG with negative TTG and other celiac > > markers was considered a " false positive'. But WAY TOO MANY of our > > kids with apraxia have a positive anti gliadin IgG. Since this > > antibody can cross react to cells of the brain as if it were gluten > > it is very suspect that all these kids have positive gliadin > > antibodies. I'm wondering if this is part of the apraxia picture > for > > many kids???? Did you have other fat soluble vitamins checked? > > > > I would suggest you trial a gluten/dairy free diet for a month or 2 > > and keep a diary of any changes you see. Some changes that seem > > subtle initially are obviously changes down the road. If nothing > > happens after this time, return to your previous diet. > > > > Does your child have any gastrointestinal symptoms? Like diarrhea, > > constipation, reflux, abd pain...food allergies, asthma etc? Just > > wondering. Some people would recommend a biopsy of the gut to rule > > out celiac disease, but I suspect it would be negative...unless > > there are other risk factors for celiac disease...like symptoms, > > failure to thrive or family history. - > > > > > > > Hi all > > > > > > I have been so busy lately (vacation, IEP, therapies) that I have > > not > > > been able to keep up with messages. > > > I do have some lab results back and I could use some help > > > interpreting. Of course nothing is obviously wrong (that would be > > to > > > easy) and my pediatrician isn't looking beyond the basics. > > > > > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All > other - > > > > > gliadin IGA, reticulin IGA and endomysial IGA are in the normal > > range. > > > > > > What does the elevated gliadin IGG mean? From my google search it > > can > > > be a false positive for celiac. Should we see another dr? Who? an > > > allergist/immunologist or a gstroenterologist? > > > > > > Thanks for the input!! > > > > > > Martha > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 27, 2006 Report Share Posted October 27, 2006 > > In the past a positive IgG with negative TTG and other celiac > > markers was considered a " false positive'. But WAY TOO MANY of our > > kids with apraxia have a positive anti gliadin IgG. Since this > > antibody can cross react to cells of the brain as if it were gluten > > it is very suspect that all these kids have positive gliadin > > antibodies. I'm wondering if this is part of the apraxia picture > for > > many kids???? Did you have other fat soluble vitamins checked? > > > > I would suggest you trial a gluten/dairy free diet for a month or 2 > > and keep a diary of any changes you see. Some changes that seem > > subtle initially are obviously changes down the road. If nothing > > happens after this time, return to your previous diet. > > > > Does your child have any gastrointestinal symptoms? Like diarrhea, > > constipation, reflux, abd pain...food allergies, asthma etc? Just > > wondering. Some people would recommend a biopsy of the gut to rule > > out celiac disease, but I suspect it would be negative...unless > > there are other risk factors for celiac disease...like symptoms, > > failure to thrive or family history. - > > > > > > > Hi all > > > > > > I have been so busy lately (vacation, IEP, therapies) that I have > > not > > > been able to keep up with messages. > > > I do have some lab results back and I could use some help > > > interpreting. Of course nothing is obviously wrong (that would be > > to > > > easy) and my pediatrician isn't looking beyond the basics. > > > > > > Will's gliadin IGG is 14.1 (the lab has <10 as normal). All > other - > > > > > gliadin IGA, reticulin IGA and endomysial IGA are in the normal > > range. > > > > > > What does the elevated gliadin IGG mean? From my google search it > > can > > > be a false positive for celiac. Should we see another dr? Who? an > > > allergist/immunologist or a gstroenterologist? > > > > > > Thanks for the input!! > > > > > > Martha > > > > > > Quote Link to comment Share on other sites More sharing options...
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