Yes....but it’s a little complicated because of my severe hypertension that is and has been fairly unresponsive to many anti-hypertensive treatment regimens. I am told that I am at a much higher risk of stroke during the surgery. And,  it’s hard to deceipher whether the tumor is actually secreting ACTH on its own, or if the tumor is there as a result of chronic hyperstimulation of the pituitary from lack of treatment of CAH for 25 years. Also,  since CAH affects the results of certain tests used to confirm ACTH secreting tumors, such as  the dexamethasone-CRH stimulation test and Petro sinus sampling with CRH stimulation, a clear diagnosis of the tumor’s nature is difficult. From what I’m being told from docs at NYU Hopsital, Yale University Hospital and the Mayo Clinic....the comibination of CAH with Pituitary ACTH secreting tumor (aka Cushing’s Disease) is extremely rare. However, CAH is known to cause pit abnormality and even small tumors when underdiagnosed. So, if the CAH caused the pit tumor, and I no longer can be successfully treated with more than adequate doses of dexamethsone (1-1.5mg dex a day), they’re thinking that by removing my adrenals, my CAH and possible Cushing’s disease would be resolved. Thanks for your response Laura and if anyone else has further feedback, I would really appreciate it.