Hello, my daughter Alexandra was born July 6, 2000, soon after I was told she had CAH. These last few weeks have been hell. Dealing with a newborn is hard enough. They were taking her blood almost everyday, now its down to three times a week. They said she has the salt-wasting form, and to give her 1/4 tsp three times a day plus the other meds. Has any other mothers experienced giving table salt to their newborn and if so, is there an easier way? I guess my question is..... Does it get better/easier??? I am also wondering about the surgery part. Will my daughter live a normal life?