Hey, Ward
Hey, Ward
Not sure if I can help much with the A-FIB, but I'll tell you about a couple of emergency post-op experiences I had and hopefully this will make ya feel a bit better.
I am 16 months post-op just as of yesterday. I had both Mitral and Aortic valves replaced at the same time with St. Jude's titaniums. (My story is on the VR.com site).
Last summer I was experiencing weird sensations on the left side of my chest that felt like a "lady-wrestler-with-huge-finger-nails" was grabbing me there! This is exactly what I told the emergency room docs, and I saw them TWO TIMES! These pains would come and go intermittently and sometimes not happen for days or weeks. I believe they happened like 3 or 4 months post-op and again about 8 or 9 months. Weird, huh?
Both visits to emergency turned out to be non-threatening and I'd feel very bad having spent valuable time (both times were a 3 hour visit!) of emergency personnel. Although they'd run a battery of tests (heck of a way to get an unscheduled Protime test!) they'd send me home with the conclusion that my problem was "nerve endings."
It's been awhile since I've experienced anything close to these pains, so I "believe" it is over. Man, you're only 3 weeks post-op! Hang in there! It will take time. I was told in re-hab to expect at least 6 months for a "full" recovery. Surgeons and doctors aren't going to give you too much information unless you have specific questions that they have to answer. It just takes time! Perhaps some of your a-fibs are due to impatience and anxiety?
If I had to do it over again (oh sure, I'd love to!), I'd set some solid goals and stick to them. I wasted stupid time after surgery and really regret it!
#1 GOAL: get through re-hab then IMMEDIATELY join a health club and continue the re-hab routines and add to them as you progress. (I'm walking about 2 to 3 miles a day now and it feels pretty good). GOAL 2: your lifestyle HAS changed and you have to submit to it. Seminars and cardiac informational meetings have helped me a lot. Go to as many of these meetings as you can. GOAL #3: Concentrate on your DIET. See a dietician. Learn about food and vitamins and herbal supplements. If you're on Coumadin you have to watch what you eat anyway so you might as well change it now for the better! One of the VR.COM members says his A-FIB's are virtually history due to Magnesium. Sorry I can't think at this time who that is, but I'll re-direct you to his string another time. I found a wonderful physical therapist in Libertyville (after re-hab) and her treatments were very helpful. GOAL 4: keep Coumadin therapy under control. My anxiety over the routine blood draw was terrible. I went numb one time when I was poked by a part-time intern. I thought I was going to have a heart attack right there in the lab! While I still don't like it, I tolerate it! My thoughts and test anxiety is focussed now on the "positive" aspect of getting off of work a few hours early at least once a month to go for my PT!
Ward, I hope this is helping? I believe you are on the right track by at least talking about your situation. This website is a great tool with people of all walks, some with more details than others, nevertheless, all of us are here today because of valve replacement.
I live just over the Wisconsin border in Vernon Hills, IL. Please feel free to e-mail or call.
Take care and please keep in touch.
Perry Anderson
847-377-0825-direct line at work (I work in Waukegan)
[email protected]