Elcarim
Well-known member
Hi all. I've been reading through all my previous posts from the past 17 years that I have been a member here and decided that another post might be a good idea.
I am 46yo. I was born with a bicuspid aortic valve and had my first OHS in 2000 at 22yo. Five years later that tissue valve failed and I had a St Jude mechanical valve put in. I also ended up with heart block and a pacemaker. The PM lead has been interfering with my tricuspid valve ever since, causing severe regurgitation, which recently has led to the right side of my heart becoming enlarged. My cardiologist is referring me to a surgeon and expects them to make contact with me in the next few weeks. I'm guessing that surgery will be on the cards in the next few months.
I know that without surgery my heart will get worse and I'll get sicker until I die. I also know that tricuspid valve surgery is much riskier than aortic valve surgery, and 3rd OHS are riskier than first and second OHS.
I have a lot of memories from my previous surgeries, and as a result I am not only afraid that I won't survive another surgery, I'm afraid of going through the recovery again.
It took me a long time to get used to being on warfarin and having a pacemaker, but now all that is old hat. I self test and self dose my warfarin, which is going well, and I'm on pacemaker #3 with 9 years left on the battery. I dealt with bad anxiety for many years, but I have recently got that under some semblance of control.
I'm finding it hard to keep on keeping on knowing what is coming. I'm pretty well terrified. I'm trying to keep busy, but I get tired. This time of year, coming into winter, is always hard for me, but this year there is more to it. I feel like a deer in headlights a lot of the time. I find it hard to talk about it and don't want to have conversations with friends in case they bring it up.
I know time will bring it all to a head one way or another, but I am finding it incredibly hard to cope with at the moment.
I am 46yo. I was born with a bicuspid aortic valve and had my first OHS in 2000 at 22yo. Five years later that tissue valve failed and I had a St Jude mechanical valve put in. I also ended up with heart block and a pacemaker. The PM lead has been interfering with my tricuspid valve ever since, causing severe regurgitation, which recently has led to the right side of my heart becoming enlarged. My cardiologist is referring me to a surgeon and expects them to make contact with me in the next few weeks. I'm guessing that surgery will be on the cards in the next few months.
I know that without surgery my heart will get worse and I'll get sicker until I die. I also know that tricuspid valve surgery is much riskier than aortic valve surgery, and 3rd OHS are riskier than first and second OHS.
I have a lot of memories from my previous surgeries, and as a result I am not only afraid that I won't survive another surgery, I'm afraid of going through the recovery again.
It took me a long time to get used to being on warfarin and having a pacemaker, but now all that is old hat. I self test and self dose my warfarin, which is going well, and I'm on pacemaker #3 with 9 years left on the battery. I dealt with bad anxiety for many years, but I have recently got that under some semblance of control.
I'm finding it hard to keep on keeping on knowing what is coming. I'm pretty well terrified. I'm trying to keep busy, but I get tired. This time of year, coming into winter, is always hard for me, but this year there is more to it. I feel like a deer in headlights a lot of the time. I find it hard to talk about it and don't want to have conversations with friends in case they bring it up.
I know time will bring it all to a head one way or another, but I am finding it incredibly hard to cope with at the moment.