<<Disclaimer: Verify this information before applying it to your situation.>> To the list. So many people sent similar stories of how the medical profession was unable to meet the needs of CD patients. For so many of you who asked me to share the findings, here's some really good references. Michael Jones sent me this list of very important and interesting files. I did not know that these files were available or what they pertained to in the list. I am going to list them for those who did not know they were available. I have transferred them to my Word for Windows file, pressed reformat, and printed them out and copied them. There is about 38 pages of information, much info would be important to a doctor. I am bringing them to my doctors and sending one to our local paper that has a doctor that does a column on medical conditions, as well as sending them to my adult children for them to give to their doctors and their children's doctors. I believe that all of us should have a copy on hand when we switch doctors or need medical treatment. Thank Michael Jones! Send an e-mail to: [log in to unmask] Send these lines in the e-mail: GET CELIAC DIAG-TST GET CELIAC SUMMARY GET CELIAC INCIDENC GET CELIAC MEDCARE GET CELIAC SPECTRUM Other helpful sites that I have never seen are www.celiac.com http://www.panix.com/~donwiss/ CSA was listed as a source also. This address was given for information from Ireland. The Coeliac Society of Ireland Carmichael House 4 North Brunswick Street Dublin 7 Tel. 01-8721471 (10am-1pm Mon-Fri) Fax. 01-8735737 (Carmichael House) plus international prefixes Thanks so much for the valuable information from everyone Carol in NJ