Hello, Thank you for this message board. I am a little unusual, I guess. At 43 years old, I was diagnosed with true CAH. Apparently, I had just been misdiagnosed. So I don't know whether I fit into the "late onset" aspect, but I need this board, if I may. I am now 52 years old. At 43, all my problems had been gynecological in nature, however, I had always been infertile. I had all the symptoms as a child, but it was just missed. I had two surgeries on my vagina as an adult and surgery on polycystic ovaries. Meanwhile, frankly, my clitoris was enlarging and finally my gynecologist wanted me to see an endocrinologist. I have now seen 3 who all confirm the CAH from birth. I had a cortrosyn stimulation test which confirmed the diagnosis. I first took Decadron and later was switched to Prednisone as it was easier to fine tune the dosage. I now take 5 mg. daily. I had numerous changes to my body and mind and became fertile at 43 years of age. We adopted a child as my uterus and ovaries were too small. Years of being told I had an ovarian problem only to change and have it become CAH threw me. I have suffered emotionally over this with depression and anxiety. I have many medical problems. Is there anyone out there who has gone so late in life to suddenly receiving this diagnosis. I seem to be an oddity which does not help me. What is now being done for infants and children is wonderful. I would like to hear from anyone. Thank you.