I am curious to get information from anyone who has had experience with Prednisone.  My 10 yr. old daughter with SWCAH has had an extremely easy time so far living with CAH.  She has been on Cortef and Florinef for 10yrs with hardly an abnormal lab.  At her last endo visit, her 17OHP came back at 2500.  They sent me a prescription in the mail for Prednisone 2.5mg twice a day.  We have been on this for one week and will go back in 5 more weeks for another blood draw to see if the Prednisone is bringing her levels back down. 

Does anyone have any information or experience to share about this medication?  I'm probably just obsessing but it's so hard to change something that's worked for so long....

Thank you,

Monica