We are new to the internet. We were happy to find a site for people with CAH. Our son was born with salt-wasting CAH. He is now 3 years old. His last blood work found that his renin was undetectable. He has been taken off his Florinef for a trial of three weeks. We are waiting to hear back from his doctor to see if he is no longer salt-wasting. Has anyone heard of a child that has stopped salt-wasting? We have never had a problem with his blood pressure and his height seems to be right on. Anyway, we are glad to see so much information being passed back and forth. We live in a small community where CAH is not common, i.e., the emergency physician nor the family doctor had never seen it, so as much information as we get is a help.