P
plexxer
Hello all, my name is Joel, I am 35 years old and I am having surgery on the 26th of October.
I started reading this site when I was first diagnosed with Aortic Stenosis in late spring of 2003. I sprained my ankle and went to my PCP when he off-handedly asked me if anyone ever told me I had a heart murmur. A echocardiogram and cardiac catheterization over that summer indicated my condition, an until-then undiagnosed bicuspid valve, but that it wasn't bad enough to warrant immediate surgery. I had the bi-yearly cardiologist visits along with annual echos and stress tests and, until this fall, everything seemed to be okay.
Now, after an echo indicating severe regurgitation and significant narrowing, a stress test that did not fit the profile of a person my age and a confirmation through a second cardiac catheterization procedure, my cardiologist suggested surgery, and I agreed. Unfortunately, it meant withdrawing from college for the semester (I am a non-traditional student seeking my degree in Scientific Computing from the Univ. of Pittsburgh), and as things seem to be ramping up, I am both confident and scared witless.
I must admit, I haven't been reading this site much over the past couple years I was in the diagnosed-but-not-severe holding pattern that many in my condition live with, but I have been checking it regularly within the past few weeks. The stories have been very encouraging. If anything, while I have a wonderful support system through my family, it has helped me feel not as "alone" knowing how many more there are out there living wonderful lives in the same boat as me.
As for the details of the surgery, I have decided to have my surgery out of the hospital that my cardiologist works out of. It isn't the biggest hospitial in the area, and they have only started doing OH procedures for about 5 years, but it is near to my family, which was a big factor in my decision. I decided on a surgeon who also works out of the hospital, but who is also a chief surgeon for the cardiac hospital in the UPMC group. He has over 30 years of experience and even received a glowing review from Catheran at MCRI when I spoke with her.
After doing a lot of research, I decided upon the On-X valve, most notably because of its ability of reducing clot formation and the good datas relating to pannus formation. The choice of going with a mechanical valve was the result of the good information I read on this site regarding coumadin.
So, that's it. A little over a week to go. Most of the unanswered questions I have revolve life immediately after surgery. I am married, and my wife is the primary bread winner in the family currently (highschool librarian) and we have a 16 month-old son (http://www.flickr.com/photos/parkersparents). How much will I be able to help around the house when I get back? Is there a lot of appointments afterwards?
Thanks for reading,
Joel
I started reading this site when I was first diagnosed with Aortic Stenosis in late spring of 2003. I sprained my ankle and went to my PCP when he off-handedly asked me if anyone ever told me I had a heart murmur. A echocardiogram and cardiac catheterization over that summer indicated my condition, an until-then undiagnosed bicuspid valve, but that it wasn't bad enough to warrant immediate surgery. I had the bi-yearly cardiologist visits along with annual echos and stress tests and, until this fall, everything seemed to be okay.
Now, after an echo indicating severe regurgitation and significant narrowing, a stress test that did not fit the profile of a person my age and a confirmation through a second cardiac catheterization procedure, my cardiologist suggested surgery, and I agreed. Unfortunately, it meant withdrawing from college for the semester (I am a non-traditional student seeking my degree in Scientific Computing from the Univ. of Pittsburgh), and as things seem to be ramping up, I am both confident and scared witless.
I must admit, I haven't been reading this site much over the past couple years I was in the diagnosed-but-not-severe holding pattern that many in my condition live with, but I have been checking it regularly within the past few weeks. The stories have been very encouraging. If anything, while I have a wonderful support system through my family, it has helped me feel not as "alone" knowing how many more there are out there living wonderful lives in the same boat as me.
As for the details of the surgery, I have decided to have my surgery out of the hospital that my cardiologist works out of. It isn't the biggest hospitial in the area, and they have only started doing OH procedures for about 5 years, but it is near to my family, which was a big factor in my decision. I decided on a surgeon who also works out of the hospital, but who is also a chief surgeon for the cardiac hospital in the UPMC group. He has over 30 years of experience and even received a glowing review from Catheran at MCRI when I spoke with her.
After doing a lot of research, I decided upon the On-X valve, most notably because of its ability of reducing clot formation and the good datas relating to pannus formation. The choice of going with a mechanical valve was the result of the good information I read on this site regarding coumadin.
So, that's it. A little over a week to go. Most of the unanswered questions I have revolve life immediately after surgery. I am married, and my wife is the primary bread winner in the family currently (highschool librarian) and we have a 16 month-old son (http://www.flickr.com/photos/parkersparents). How much will I be able to help around the house when I get back? Is there a lot of appointments afterwards?
Thanks for reading,
Joel