<<Disclaimer: Verify this information before applying it to your situation.>> Summary regarding MyCeliacID saliva test: Thank you ALL for the great feedback. I received many responses and the majority seems to indicate that the saliva test is probably worth exploring further. I got several responses comparing it to the Enterolabs stool test and the antibody test from Canada. From what I understand the Enterolabs version tests for gluten sensitivity and the one in Canada tests for antibodies and the MyCeliacID one tests for the Celiac gene itself. I guess my takeaway from it all is this: 1. It would be nice to do the test at home and find out a bit more before our insurance company knows her status. 2. It would be nice to feel reasonably comfortable ruling it out if it came back negative or being more aggressive about treatment if not. Some examples of responses include: I haven't tried it, but I trust the company, Prometheus, who is marketing it. They have been experts in the field of celiac disease for many many years so I would trust them. I don't know anything about the test, but thought I'd let you know in case you aren't aware that UCSD has a Celiac Disease Center and a new pediatric specialist. They might be a good resource for you - http://celiaccenter.ucsd.edu/ <http://celiaccenter.ucsd.edu/> I did the saliva test for myself and found it to be a good experience -- company sent everything I needed, no dr's orders needed, no blood draw, the results were clear and easy to understand. This test cost you $369, I suggest you click on the FAQ tab and it answers all your questions and its painless. My understanding is that if your daughter does not have the genes you can almost certainly rule out celiac and move on to other things. If she does test positive for the genes, then further exploration is merited – and she still might not have celiac -- even with the genes. I am very interested in this – however, I am trying to find out how this one compare to the original in Canada and why that one cost $50 and I believe this one cost over $300. The test would show if she carries the gene. If she does, it means that at sometime in her life, she COULD develop celiac. It does not mean that she already has celiac. If she does not carry the gene the odds are almost impossible that she would ever develop celiac. The home test from Prometheus is only a genetic test that screens for DQ2 and DQ8. Although DQ8 and DQ2 are associated with 95-98% of those with CD, there is a small chance one could have CD without those genes. I highly recommend the genetic testing through Kimball labs and U of Chicago Celiac center http://www.celiacdisease.net/testing <http://www.celiacdisease.net/testing> I don't know anything about the test, but thought I'd let you know in case you aren't aware that UCSD has a Celiac Disease Center and a new pediatric specialist. They might be a good resource for you - http://celiaccenter.ucsd.edu/ <http://celiaccenter.ucsd.edu/> ….suggest that you contact Dr. Kimberly Newton, pediatric/gastroenterologist at Rady Children’s Hospital, San Diego 858 966-4003. Dr. Newton sees children under the age of 18 and she is associated with the Wm. K. Warren Medical Research Center for Celiac Disease at UCSD 858 822-1022. Visit the Celiac Web Page at Http://www.enabling.org/ia/celiac/index.html Archives are at: Http://Listserv.icors.org/SCRIPTS/WA-ICORS.EXE?LIST=CELIAC