ILoVeNY25
Well-known member
Hello Everyone,
Hope this post finds everyone healthy and happy. I'm sorry I haven't posted in a while. Life has been very hectic. I've had a few ER visits with SOB, dizziness, and blurred vision. I went on a holter monitor and I am having difficulties with some arrhythmias. I will be going to two cardiologists on July 7th and 8th. But my main concern is that my PCP ran some tests and says my red blood cell count is very low and he believes they are being destroyed by the mechanical valves. Has anyone else had experience with this or anyone have any good websites or articles on this? I haven't been able to find much info. The doctors have also put me on 50mg of Lopressor 2x a day which seems to be putting me in the dumps. I'm exhausted all the time and have had to ask my boss to cut back my hours. I'm very frustrated with all this and it's sad to say I feel worse now, 14 months after my surgery than when I was in Class IV CHF. I find it very ironic that the surgery I had to feel better is actually making me worse. Any insight would be greatly appreciated. Again I'm sorry for being a stranger and hope all is well. Talk to you all soon. Take Care!
Hope this post finds everyone healthy and happy. I'm sorry I haven't posted in a while. Life has been very hectic. I've had a few ER visits with SOB, dizziness, and blurred vision. I went on a holter monitor and I am having difficulties with some arrhythmias. I will be going to two cardiologists on July 7th and 8th. But my main concern is that my PCP ran some tests and says my red blood cell count is very low and he believes they are being destroyed by the mechanical valves. Has anyone else had experience with this or anyone have any good websites or articles on this? I haven't been able to find much info. The doctors have also put me on 50mg of Lopressor 2x a day which seems to be putting me in the dumps. I'm exhausted all the time and have had to ask my boss to cut back my hours. I'm very frustrated with all this and it's sad to say I feel worse now, 14 months after my surgery than when I was in Class IV CHF. I find it very ironic that the surgery I had to feel better is actually making me worse. Any insight would be greatly appreciated. Again I'm sorry for being a stranger and hope all is well. Talk to you all soon. Take Care!