Hi All, I am in the very early stages of trying to have CAH added to the new born testing in Missouri. I have received some information from Cathy at MAGIC. But I have yet to find the right people at the state level to see if this has been attempted before, is it in the works, etc. At the next ped endo appointment I am hoping to have the chance to talk with the doctor and to the endocrine nurse to see if they know anything and will help (I am assuming they will!) I know I will need help from other Missourians! The larger the group trying to get this done, the better. But also, this might not be a problem, but depending on the officials we need to work with it might. I don't have a compelling birth story -- Olivia was adopted at the age of 7 months. And from what I have been able to get from other places, the new born screening test would not have helped to diagnose Olivia -- the screen is for 21-hydroxylase deficiency and she has 11-beta-hydroxylase deficiency. So, if you are from Missouri and would like to help, please let me know. Also, if anyone else has information that they used in working with their state I would be interested in it. Thanks!