Guest guest Posted July 6, 2009 Report Share Posted July 6, 2009 Thank you to all who replied to my earlier posting asking about how to test my 8 month old for " the gene " . One further question: has anyone had this test run via LabCorp? They are the only lab that my insurance will cover, so I wondered if they are viable? Or should I pay out of pocket for one of the places Pam listed? Thanks again! -laura Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 7, 2009 Report Share Posted July 7, 2009 My understanding is that there are multiple genes that play a part. I have some of them and my 4 year old has more of them than I do. The enterolab gene panel only requires a saliva swab (just like on CSI!), and not a blood test. You might find this helpful:https://www.enterolab.com/StaticPages/Frame_TestToOrder.htm#Genetic_testing-Luther On Tue, Jun 30, 2009 at 12:05 PM, lauracgadd <lauracgadd@...> wrote: Hi gang - I know this has been discussed on here over the years, but I'm not able to find the answer by searching the old postings. Can someone refresh my memory? Basically, I have Celiac Disease, and I have an 8.5 month old baby. I have been GF for 5 years, and have kept the baby GF thus far (my breastmilk is GF and making sure the commercial baby foods I feed her are GF). In a couple days, our pediatrician will do a blood test for iron and lead, and we have talked about her also requesting tests for CD. I know that the usual ELISA/IgG and IgA tests won't work since she's not being exposed to gluten, but I'm interested in seeing if she has " the gene " . Can someone please tell me exactly what test we're supposed to ask for (even a recommended lab??), and any other info about it? I read somewhere that 35% of the population may have the gene though it appears that 1 in 133 actually have CD...? Any other advice? Should I pay for it out of pocket so it won't be on her medical record in case it could ruin her insurability? Thanks! -laura Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 7, 2009 Report Share Posted July 7, 2009 I have heard of another test that was developed by the wife of the founder of Google. It is called 23andMe. The cost used to be over a thousand dollars, but now it is at $400.00. Time magazine did a piece on as one of the best inventions last year. They only need a saliva swab, mail it in and get the results. The website will have more info for you also. Eden > > > > > > > Hi gang - I know this has been discussed on here over the years, but I'm > > not able to find the answer by searching the old postings. Can someone > > refresh my memory? Basically, I have Celiac Disease, and I have an 8.5 month > > old baby. I have been GF for 5 years, and have kept the baby GF thus far (my > > breastmilk is GF and making sure the commercial baby foods I feed her are > > GF). In a couple days, our pediatrician will do a blood test for iron and > > lead, and we have talked about her also requesting tests for CD. I know that > > the usual ELISA/IgG and IgA tests won't work since she's not being exposed > > to gluten, but I'm interested in seeing if she has " the gene " . Can someone > > please tell me exactly what test we're supposed to ask for (even a > > recommended lab??), and any other info about it? I read somewhere that 35% > > of the population may have the gene though it appears that 1 in 133 actually > > have CD...? Any other advice? Should I pay for it out of pocket so it won't > > be on her medical record in case it could ruin her insurability? > > > > Thanks! > > -laura > > > > > > > Quote Link to comment Share on other sites More sharing options...
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