Three weeks post op and feeling great!

Valve Replacement Forums

Help Support Valve Replacement Forums:

This site may earn a commission from merchant affiliate links, including eBay, Amazon, and others.
R

RickKiem

I thought I would let everyone know that I am doing fine. I listened to everyone's advice and everyone was right, time is all it takes. I feel so much better than I did a week ago that I just can't believe it. All my follow up Doctors visits have gone well. Cardiac rehab is great. I feel like I can push myself a little harder than I do at home due to being monitored. The staff there is so caring and it is comforting that several of the people who are there are people who helped me while I was in the hospital.

I must admit that my hospital stay was very difficult. Day after my first surgery they had to go back in because of some fluid pooling around my heart. This was the only time that I was really frightened. I was still on the resperator but I could not breath. There were so many people by my bed that I knew something was wrong but I could not figure out what. The last thing I remember is one of my surgical team standing over me and telling me that everything was all right but that they need to take back to surgery. I wanted to tell him fine just knock me out now! when I woke up I was back in my room and my wife was there and other that still being on the respirator I felt fine. They finally removed the breathing tube the next morning. I remember dreaming about drinking an ice cold Sprite that last night that I was on it.

I was in CCU for seven days and I am not sure if I ever slept for more than 30 minutes at a time from day 3 thru 7. The pain medication had me seeing things(scary things) whenever I would close my eyes. Things like demons sitting in the chairs next to my bed and all kinds of other wierd stuff. Did anyone else have this happen to them? I finally slept through the night on my eighth day. When I woke up I was so excited.

My wife is easing back into her job and so I am alone for the first time since surgery. Not really a problem except that I am getting a touch of cabin fever. My pain has almost completely gone away except for when I cough. You know, I hear how much sneezing hurts but I have not sneezed once since my surgery. Three weeks no sneezing? (knocking on wood) Kind of strange...I must be living right. I received a carbomedics mechanical valve and they repaired my anuerysm with a graft. That valve is LOUD. My wife can hear it clicking when I lay next to her in bed. How long does it take to get used to that clicking? Well I have rambled on enough. Thanks once again for all the great advice, support, and in some cases just listening. This is a great forum and wish that anyone who has to go through with this find it before hand as it really does help.

Rick
 
Sounds great Rick. Don't get too far ahead of yourself though. You can still backslide. Your not that far out of the gate yet. Keep progressing slowly and easily and don't push too much. Just little bits at a time will get you there.

Keep up the good work. ;)

I think we should start a thread on our "Visions" but alot of people don't like to talk about what they saw or felt. I know my first round is still locked in my mind and I really don't want to let it out. Second time around was a little better but not much.
 
Hey Rick,
Glad to hear how well you are doing. Like Ross said, you still need to take it easy and slow. After 7 months out I still find myself overdoing it at times, like the other day I decided to run the snowblower, can't be that bad because I have been pushing the lawn mower. Well I found out I should of listened to Gina. I had to show my wife how to use it if the boys are working.
As far as getting use to your clicking sound, I think it all depends on how a person deals with it. I still hear mine but I have come to the conclusion that if it is clicking I am alive.
Again Rick, I am glad you are doing so good!
Take Care

Dave
___________________________
Surgery: 4/21/03
Aortic Aneurysm Repair
AVR, with a St. Jude Mechanical
 
Hi!

Sounds like you are coming along just fine. Don't try to over do it. Breathe, walk, nap!

I am 6 months post op and I still hear mine most of the time. I think the only time I don't is when I am at work since it is always noisy there.

Take care,
 
Hi Rick-

Congratulations on feeling so well. Things do fall into place a little at a time.

You aren't the only one who has had halucinations with pain medications. I think there are quite a few who have mentioned them. Joe has had them too. They do use some strong stuff..

It's nice to hear good news.
 
Hi Rick,

Glad to hear things are going so well. I think you will be able to feel improvement each week, but if you overdo you may pay with a few days progress. Just enjoy life and progress as you feel able. No one wants to sit at home recuperating forever. Just take the time you need!!!! Pain meds don't give me wierd dreams, just make me sick!!! I didn't take them after 2 days....
Best wishes and get lots of rest...you still need it!

Heather
 
Hi Rick , Glad your home and well, take it easy your body needs time to heal.hfk
 
You just don't know how lucky you are not to have experienced the great sneeze...I think I blew mine the third day! Ouch!

Keep on healing as dandily as you are. You may have some zinger pains when your nerves start healing, but the big stuff will be fading in the past.

Good luck.
 
Rick:

Where in TX are you? Trees in photo look like those around San Antonio or the Hill Country.

My sister, niece, nephew and husband have heard my Timex ticking away. I called St. Jude to comment about the noise and was told that some people complain they never hear their mech. valve. I was told chest cavity physiology can affect sound transmission.
The valve isn't as noisy as it was immediately post-op. I hear it when the surroundings are very very quiet.
 
Rick

Rick

Glad to hear that you are doing fine. I am two weeks post op and I had to laugh when you asked how long it takes to get used to the clicking sound.

I had my mechanical valve for 21 years. Two weeks ago they replaced it with a tissue valve. I am lost without the clicking! I can't tell one arrhythmia from another without the clicking tone. My doctor yesterday asked me if I had experienced any Wincheback (arrhythmia) and I told him I couldn't tell! I would always be able to tell if I was having a PVC, or PAC, or Winchebach, but I can't tell anymore. When I went into A-fib in the hospital I knew I felt some weirdness in my chest but I didn't have a clue that what it was. Now I have to learn all over how interpret what I am feeling. Don't worry, you'll get used to the clicking. :D :D
 

Latest posts

Back
Top