Jim P
Well-known member
Hi Everyone,
I have now reached the 5-week point after AVR surgery (and 4 weeks since returning home from the hospital). Progress toward recovery has been remarkably good. I am feeling so much better than I did just 1-2 weeks ago. Even so, there are some days that are better and other days that are more discouraging. However, the trend is toward the better.
I discontinued the Percocet pain pills one week ago. I substituted Extra-Strength Tylenol for the Percocet and have only a little chest and back pain. More importantly, cutting out the Percocet finally relieved the (terrible) constipation problems I had before.
I am walking about 1½ - 2 miles per day (split between morning and afternoon), which is easy to do in the pleasant weather we have had recently in Florida.
I am still taking two meds prescribed by the cardiologist: Amiodarone (anti-arrhythmia), 200mg daily; and Lopressor (Beta-blocker), 25mg twice daily.
Concerns:
1. I have been steadily losing weight. So far, after 4 weeks, I have lost 20 pounds even though I am eating 3 square meals per day.
2. Big problems sleeping. Even though I am tired, I just cannot go to sleep at night, especially on my back. When I was taking the pain pills, I went immediately to sleep. Before surgery, I was one of those guys who fell asleep when my head hit the pillow and slept a full 8 hours. Now, I am averaging 3-4 hours sleep per night and no naps during the daytime. I find it most comfortable to sleep on my side on the living room sofa, with my back against the back of the sofa.
3. A high resting heart rate (about 90 - 100 bpm). Before surgery, I was never above a resting heart rate of 75 bpm.
4. Night sweats. I believe mine to be less than others on this site have described. However, it was never something I had a problem with before.
5. I have coughing attacks during or after every meal. I am still using my heart pillow, and it does not cause excess chest pain. I assume that my esophagus is not completely healed yet.
6. I have less energy than I would like and must pace myself daily to not over-exceed my current strength level.
I have thoroughly read most postings to the VR.com site for the past several months. It has given me strength and confidence to know that almost every OHS patient seems to have had similar concerns as I listed above during their recovery. Perhaps I just need to relax and let my body recover on its own.
However, I am most concerned that Amiodarone is a very strong medicine with some scary side effects, although I am taking a relatively low dosage. Many of my ?abnormalities? could be reactions to this medication. I already asked my cardiologist if I could stop taking it, and he wants me to continue for a few more weeks.
I wonder if any of you have stories to tell about Amiodarone, either positive or negative. If so, I would like to hear them, before I contact my cardiologist again.
I have set a goal of 3-4 months for when I should expect to feel close to ?normal? and 6 moths before becoming physically active again. I am trying to be patient, but I had hoped to feel a little better now than I do. My heart and chest feel good; it is just the other complications that are bothering me. Nonetheless, I am encouraged to be about halfway there (to the 3-month date).
Thank you again for the great encouragement and education you all provide to members of this site.
I have now reached the 5-week point after AVR surgery (and 4 weeks since returning home from the hospital). Progress toward recovery has been remarkably good. I am feeling so much better than I did just 1-2 weeks ago. Even so, there are some days that are better and other days that are more discouraging. However, the trend is toward the better.
I discontinued the Percocet pain pills one week ago. I substituted Extra-Strength Tylenol for the Percocet and have only a little chest and back pain. More importantly, cutting out the Percocet finally relieved the (terrible) constipation problems I had before.
I am walking about 1½ - 2 miles per day (split between morning and afternoon), which is easy to do in the pleasant weather we have had recently in Florida.
I am still taking two meds prescribed by the cardiologist: Amiodarone (anti-arrhythmia), 200mg daily; and Lopressor (Beta-blocker), 25mg twice daily.
Concerns:
1. I have been steadily losing weight. So far, after 4 weeks, I have lost 20 pounds even though I am eating 3 square meals per day.
2. Big problems sleeping. Even though I am tired, I just cannot go to sleep at night, especially on my back. When I was taking the pain pills, I went immediately to sleep. Before surgery, I was one of those guys who fell asleep when my head hit the pillow and slept a full 8 hours. Now, I am averaging 3-4 hours sleep per night and no naps during the daytime. I find it most comfortable to sleep on my side on the living room sofa, with my back against the back of the sofa.
3. A high resting heart rate (about 90 - 100 bpm). Before surgery, I was never above a resting heart rate of 75 bpm.
4. Night sweats. I believe mine to be less than others on this site have described. However, it was never something I had a problem with before.
5. I have coughing attacks during or after every meal. I am still using my heart pillow, and it does not cause excess chest pain. I assume that my esophagus is not completely healed yet.
6. I have less energy than I would like and must pace myself daily to not over-exceed my current strength level.
I have thoroughly read most postings to the VR.com site for the past several months. It has given me strength and confidence to know that almost every OHS patient seems to have had similar concerns as I listed above during their recovery. Perhaps I just need to relax and let my body recover on its own.
However, I am most concerned that Amiodarone is a very strong medicine with some scary side effects, although I am taking a relatively low dosage. Many of my ?abnormalities? could be reactions to this medication. I already asked my cardiologist if I could stop taking it, and he wants me to continue for a few more weeks.
I wonder if any of you have stories to tell about Amiodarone, either positive or negative. If so, I would like to hear them, before I contact my cardiologist again.
I have set a goal of 3-4 months for when I should expect to feel close to ?normal? and 6 moths before becoming physically active again. I am trying to be patient, but I had hoped to feel a little better now than I do. My heart and chest feel good; it is just the other complications that are bothering me. Nonetheless, I am encouraged to be about halfway there (to the 3-month date).
Thank you again for the great encouragement and education you all provide to members of this site.