Well, I am now almost 2 weeks post op. To tell you the truth I haven't felt at all like being around valvereplacement.com for the last week or so. I guess I just haven't really felt like sharing my experiences, but will do so now.
I met my surgeon (Indran Ramanathan) on the day before my operation, and my wife an I spent our 13th wedding anniversary discussing with him the options and waiting to get an urgent ct scan done to confirm if I needed the bentals proceedure as well as AVR. (Turns out that I didn't, although I didn't know that untill after the proceedure due to the late hour. Or maybe they told me, but have had to many drugs to remember)
We decided on the Medtronic Advantage valve, primarily because of the small size of my aortic root effectively ruling out my prefered On-X option. I was was worried about valve noise, and the surgeon felt that the Medtronic is quiter than the St Jude. I would have loved the luxury of meeting my surgeon weeks ahead of the operation, to come up with a list of questions, and go through everything in more detail, but I knew this man has a very high reputation (through someone I know on the cardiac care ward staff) and had confidence in him, even when he told me that due to complexity arrising from my previous AVR there was a chance (greater than 10%) that I wouldn't make it.
So that is why the initial operation took 8 hours.
In ICU I had excessive drainage from my chest drains, so they sent me back to theatre to open me up again and stop the bleeding.
Other than a brief period of atrial flutter about 4 days post op, recovery so far has been pretty smooth. Stangley I knew about the AF instantly and alerted the doctors, due to being able to hear the valve was no longer making it's regular tick, tick, tick. And then about 4 hours later, I knew exactly when it went back to normal, without having to look at the monitor screen. tick, tick, tick, tick.
About the ticking.......it was something I worried about pre-op (I am\was a light sleeper). And for the first week or so it kept me awake at night, but doesn't seem to any more. I can hear it clear as day, and not just in a quite room. I can't drown it out with my ipod, it's inside my head, always there. But I don't find it annoying, and I can't explain why (I really thought I would hate it! and I didn't think it would be this loud). At worst, it deminishes my enjoyment of music sometimes, but I think I can live with it.
I am progreesing well. Walking quite a lot. Sleeping OK. I do still stuggle with sleeping through the night, despite the best efforts of my doctor to drug me into a stupor (One of my friends has given me the nickname "the Pharmacist" and he is an anisthetics technician so is used to being around lots of drugs!) I still awaken at around 2am and can't get back to sleep. My body is just not used to sleeping all night on my back, and lying on my side or in other positions is not comfortable enough yet.
All in all I consider myself to be very lucky. I have survived, I am healing well, and I have the love and support of family and friends. My employer has also been extremely supportive, more than I would ever expect. So yes, I am lucky!