Well, we are undersurpressed, and discouraged. Her OHP levels came back at a number of 6760. A little high wouldn't ya say? I know I shouldn't be discouraged because I did expect some change. After all we did go from giving my daughter almost 13 mgs. a day to 5mg a day. I have an appointment with her endocrologist next Thursday. I will have a LONG list of questions for him. We have upped her to 7.5 mgs a day now. We are back to the three times a day dosing much to my dismay. Dosing her twice a day took away the mid-day reminder that she had this crummy disease/disorder. Yet on the other end, I feel a little better to have the meds in her all day. I never did find my answer to why it was ok to give the pill form only twice a day. Another question to be answered next week. Although, she did just fine physically and mentally with the twice a day dosage. Argh. (bang, bang, bang) (sound of my head banging against desk) Thank God literally, for EMULA cream. I have a feeling we are going to be taking stock in that stuff. I will update all of you with the answers to my list of questions I plan to ask her endo next Thurs. Then I will update you on the next blood draw (in 30 days) I am sorry for sounding discouraged. It rips me after finally getting perfect OHP levels from last endo visit to getting these high levels today. I am sure I would be taking this much better if I did not have so many outside worries dragging on me. Chin up. Onward and upward to the next blood draw. Anyone else with results yet?