Last Friday (May 14) I was admitted to the hospital. I thought my cardiologist would think it was something significant, but that I would be out on pills for a while to relax the breathing. It astounded all of us just how drastically my aortic valve stenosis (thickening) went from mild to very severe (3 years for me, often 20-30 gradual years for everyone else.
Saturday night mom and dad flew up from Homer and picked up Quin. They then all drove in my car to Seward to pick up stuff for her and then they drove on to Homer. They have all been having a good time--she is still there & mom send me pictures every other day of what they have been doing.
After they left (last Saturday) around noon they took me for an angiogram to see if my heart was strong enough.
Technique
Access to the valve was gained through the right femoral artery, to look at the left side of the heart and the arterial system as well as pushed into the lungs. Using a system of guide wires and catheters (pushed up through that artery all the way though the cambers of the heart, a type of contrast agent (which shows up by absorbing the x-rays), is added to the blood to make it visible on the x-ray images. ~adapted for wikipedia
They found that everything looked good--strong heart muscles, clean veins & arteries. My aortic root above the valve was found to be enlarged (at least doubled in size) and they thought they might have to repair or replace that part as well.
Sunday I just had some x-rays and blood work done. The surgeon cam in several time to talk with me and show me the different types of valves. Because of my young age, we opted for the mechanical vale. It is wrapped w/carbon filament and is the most long lasting.
It has taken me 25 minutes just two write all of this so far--I am not on my own computer & am on pain killers.Monday Phil showed up at 6:30 a.m. They took me at about 7:30 a.m. I remember entering the room and some gentle preparation--nothing more.
I woke up in the ICU. I had a breathing tube down my throat which was very uncomfortable and meant I couldn't talk. Phil was right there, looking down at me, squeezing my hand and being very reassuring,
I am finding it increasingly hard to type, so I will expand on this tomorrow. Just quickly, I was in the ICU 2 days, then the normal care unit for 4 days and was discharged yesterday. I am in lot of pain, as they cut though your sternum & it take a long time to fix that. Thank goodness for pain killers. I was discharged late afternoon Sunday. We are staying t the Hickel House (click on the link to see) until at least Tuesday to follow up with the surgeon. It is nice here. Finally today, after a week, I can take a shower and have no needles in me.
I am very grateful for the hospital staff, for my parents and to Phil who has been a friend and a help to his "patient".
I now have a big, new, red scar 9 inches down my chest and some smaller scars below from the drainage tubes and from where they pulled out the pacer wires (for a temporary external pacemaker). I gained about 18 pounds from surgery from all the fluids pumped in, so I am on medicine to get me to pee a lot to reduce the water swelling,
The wedding is still planned for July 9 in Homer.