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SCCWS

Well-known member
Joined
Jun 26, 2012
Messages
51
Location
Rhode Island
I had AVR replacement surgery the beginning of last September. I bumped into a good friend I had not seen for a few months last week and he asked how I was doing. At first I wasn't sure what he meant but then realized he was asking about my recovery. Funny, but unless someone brings it up, I don't even think about it.
I started seeing a cardiologist 5 years ago after my MD decided the results of my annual echo had reached the point where I needed a specialist. When I went to the Cardio 5 years ago, he looked at the echo and said I would probably need surgery in 3-5 years. When I went last June-2012 for the results of my echo, he said I would most likely need the surgery this spring or summer ( Year 5). Luckily I felt great and was speed walking 30 minutes a day. I also had a first grandchild who was turning 1 last August. So I decided I did not want to wait another 9-12 months but rather go in September 2012 and get it over with. I thought since I felt great it made more sense to go in then since I assumed it would help recovery. Also, as I saw my grandaughter growing quickly, I wanted to get it over with and enjoy her more. In hindsight it was a great decision. I posted numerous posts on this site last year. but it hit me last week that next month will be a year. I can do anything I want and I hardly even think about the surgery. The only inconvenience I have is a daily water pill which my Cardio said he likes to continue for one year after surgery or till he sees the first echo which is scheduled next month. Just a few things I posted last year that hopefully will help:

1. I was 63 going in and had never spent one night in a hospital.
2 I put numerous warnings on this site that a key thing is to warn your significant other that their first glimse ( 2 hours or so post) of you after surgery is not pretty. It really upset my wife even though I had warned her based on tips from this site. I guess all the tubes still connected does not help the look. Having said that, my wife was stunned how good I looked at noon the day after. I was sittting up in a chair by 10:00am that morning and stayed up till dinner time.
3. The 2nd day after surgery I was released to the step down unit and released on the 5th day after..... Surgery Wednesday afternoon and released Monday morning.
4.I chose the bovine valve despite being 63. I was convinced that the next time the procedure will be less invasive. After having the surgery, I felt it was not a major problem anyway. I am no hero, but I did not need any painkillers after the first dose I was given in recovery. The nurse kept asking but I said wait until I feel pain. I never did.
5. Worse part of the whole procedure was the cough which started a few days after I got home. It was awful for a week. In fact, my MD told me to start taking the painkillers for the cough that I didn't need for the pain.
6. I had a bout with A-Fib which was aggravating. I was on Cumidin from mid Oct-mid Dec. It was frustrating like the cough problem but I got through it.

I am so happy I went early. Looking back it was not a major inconvenience. I am retired ( which probably helped not worrying about work) but am very active. The purpose of this long rant is to once again provide some tips and hopefully provide some encouragement. If a valve is in your future, I think it is very important to stay in the best shape you can before going in. Finally my first visit to a hospital was wonderful. The procedure was less than I envisioned, the recovery had some bumps but was not too bad. I sent a letter to the Hospital afterwards complementing 4 different nurses who treated me like I was a family member. I did not have one nurse who I found any fault with. Maybe I just got lucky.
 
From a fellow cow-valver, it's great to hear that you are doing well. Keep enjoying that grand-daughter. Your post will sure help all those in the waiting room to know that this procedure is a do-able situation. Best Wishes on your first valversary and wishing you many many more.
 
Another cow valver here happy to hear how well you are doing........

I also am so fortunate that I've done extremely well despite the replacement having been my second OHS.

Keep up the good work.
 
Your note could not have been better timed for me! I am literally in the waiting room, undergoing my pre-op tests and waiting to speak with the cardiac anesthesiologist. I was checking this site for the list of things to ask during the pre-surgical consult, and saw your post. You made my day, and I congratulate you on your successful surgery and thank you for your thoughtfulness in stopping by!
 
Your note could not have been better timed for me! I am literally in the waiting room, undergoing my pre-op tests and waiting to speak with the cardiac anesthesiologist. I was checking this site for the list of things to ask during the pre-surgical consult, and saw your post. You made my day, and I congratulate you on your successful surgery and thank you for your thoughtfulness in stopping by!

I will keep you in my thoughts and prayers and will check back to see your post-op posting.
 
MOO! Another cow valver checking in. I, too, was 63 at time of implant. I'm hoping that the newest generation of bovine valves will attain their "planned" life span - that period being longer than the last generation. That's all we can ask. I'll take my chances on re-op when the time comes.

Glad you're here and enjoying life after valve surgery. Your post sure helps the folks in The Waiting Room to realize that life can be great after surgery.
 
Skeptic, if you don't mind me asking, how long has your valve been 1.1cm? Did your docs give you any idea when they think you'll need surgery? I can't even get a consistent estimate from mine. I know it's all guess work and everyone's different.
 
Agian -- I think it's all very individual. As one example, mine was 1.1 cm for over 10 years. Then it dipped to .9, where it hung out for three more years. This past year it went rather abruptly to .69, and I'm having surgery next week. So long plateaus are possible in the progression of this condition. Just keep living your life and getting it checked once a year (or twice, if your doctor recommends it), is my advice!!!
 
Heather: Make sure you write into Post-Op about how your surgery goes once you have recovered. I am sure you can provide some valuable tips to others who are waiting.
 
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