I’m in SoCal (OC) so I’m not sure I’m going to be able to help with specifics on MDs. I will say, we interviewed 4 or 5 and had a lot of questions regarding how many procedures they’ve done, would it be them personally or a fellow, rates of recovery, nerve-sparing process, etc. I knew I didn’t want radiation therapy unless it absolutely looked necessary. From what I understand (by all means, do your research), RT is hard on you and mutates the tissue in the area such that if you do have to go in for a subsequent surgery, then there’s little chance of salvaging anything (particularly nerves) so “function” is highly unlikely and incontinence is highly likely. My thought was the chance for best outcome was surgery first and then RT if necessary.
If it can be a help to you or anyone else, I’m happy to share anything here about procedure itself, recovery, lingering effects (“function”, incontinence), things I didn’t expect, etc. So feel free to fire away as questions or concerns arise.