i'll have to check tomorrow when i'm at my daughter's house.i know jess is an "extreme" salt-waster and i guess that may be why his endo keeps him on the sodium in addition to his florinef in the am and his hydrocordisol in the am and in the pm. his next blood work=up is the first week in feb (he is checked every 4 months) so i'll be anxious to see if his levels are stable and his meds are continued as they have been for some time. he seems to be doing fine, but what is "fine" for children with cah. i often wonder if they ever feel "great" or if they have felt the way they do all their lives and know no other feeling. i just hope his endo is on target with his meds, etc. i know the dr. is good and dr. maria new sees jess annually so i pray with his local dr. and dr. new overseeing his progress he is truly doing well. he is 6 1/2 is right on target for his bone age, is very intellegent, and a typical active 1st grader. he is very slim, but that may be genetic as i understand his father was a tall slim child growing up. we had never heard of cah before jess' birth and still don't know everything there is to know, but we're learning and are always open to comments and suggestions from other parents. happy holidays to you and your family