Hi, where in the country are you? Maybe someone can direct you to a pediatric endo you can communicate with. When we brought my baby back to the hospital 2 weeks after she was born, they increased her meds in icu (hydrocortisone & florinef) until they felt comfortable lowering the dose that her body could stabilize on. In addition to this they I crushed up salt tablets and put them in her bottle and kept a diary of the times she would eat, the amount, and what she was eating. I’m glad they caught the CAH/saltwasting in time for your son. With boys it’s more difficult to see this condition right away and you are blessed that you didn’t lose him. With girls they see the ambiguous genitalia and immediately test for CAH. That’s why it’s so important for all states to mandate newborn testing for this medical condition. Talk to as many doctors as you can. Many prayers. God bless. Anne