scotttnz
Well-known member
Hi, I'm Scott, and I'm new around here,so thought I'd introduce myself.
I live in Auckland, New Zealand. City of Sails, and vacated home of the Americas Cup. (And if they ever get out of court we might have a shot at getting it back!)
Anyway, I was born with a dodgy aortic valve, which was mildly restrictive when I was growing up. When I was 17 I had an aortic homograft done which was great, and terrible at the same time. It all went pretty well, but sure was traumatic at the time. Since then I have led a pretty normal life, and have been lucky that the homograft has lasted for over 19 years.
About 4 months ago I started developing shortness of breath and tireness etc, and after visits to the doctor, cardioligist, ultrasound, and angiogram learned last week that my valve is now severly constricted. So I'm now on the waiting list for a new valve. (I don't know about the rest of the world, but here no insurance company will cover someone born with a dodgy valve for anything to do with the heart, so I'm stuck with the public health system.)
My cardiologist does not expect me to be waiting long, 3 months at the most.
So, I've been lurking around learning what I can about valve selection etc, but I guess I need to wait untill I see my cardiologist again to find out what options are open to me in the New Zealand public health system. I'm leaning towards a mechanical valve, but don't know yet what types are available to me.
This site is great as it will help me know the right questions to ask!
I live in Auckland, New Zealand. City of Sails, and vacated home of the Americas Cup. (And if they ever get out of court we might have a shot at getting it back!)
Anyway, I was born with a dodgy aortic valve, which was mildly restrictive when I was growing up. When I was 17 I had an aortic homograft done which was great, and terrible at the same time. It all went pretty well, but sure was traumatic at the time. Since then I have led a pretty normal life, and have been lucky that the homograft has lasted for over 19 years.
About 4 months ago I started developing shortness of breath and tireness etc, and after visits to the doctor, cardioligist, ultrasound, and angiogram learned last week that my valve is now severly constricted. So I'm now on the waiting list for a new valve. (I don't know about the rest of the world, but here no insurance company will cover someone born with a dodgy valve for anything to do with the heart, so I'm stuck with the public health system.)
My cardiologist does not expect me to be waiting long, 3 months at the most.
So, I've been lurking around learning what I can about valve selection etc, but I guess I need to wait untill I see my cardiologist again to find out what options are open to me in the New Zealand public health system. I'm leaning towards a mechanical valve, but don't know yet what types are available to me.
This site is great as it will help me know the right questions to ask!