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Finally, a doctor listened to me!

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I don't know if anyone else has had a problem with a rapid heart rate during and after chemo and radiation. but this has been an ongoing problem for me. I have been mentioning it to my oncologist for the last few months and he just keeps saying "it will get better". My resting heart rate has been 100-115 and when I walk (slowly), it goes up to 120-150 and I also get short of breath. They did an ECG a while back and it showed a normal ryhthm and tachycardia. I went to see my reg doc last week because I wanted her input on this. She followed me around with a pulse oxy meter and my O2 dropped the higher my heart rate got. Within a couple of minutes or less, my heart rate was over 150 and the O2 was in the low 80's. She wanted me to see a pulmonologist and possibly start on O2. I told her I wanted to think about it and see what my oncologist thought. I emailed his nurse coodinator with the info about the heart rate and O2 level....Lo, and behold, I got a response immediately. He wants me to see the pulmonologist that works with LC patients tomorrow. I guess sometimes you have to advocate for yourself a bit harder in order to get attention. I think it will get better too, but it is preventing me from regaining strength and if there is anything I can do in the short time to facilitate that. I will do it. I didn't have this problem before the LC and I have not had surgery....inoperable Stage 3a with a para aortic lymph node involved.

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Surgery Lopressor

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This sounds very similar to some problems my husband has been having since chemo and radiation. We've just been discussing whether he should try to get to the bottom of this thing. I would be very interested in hearing how things go and whether you're able to get an answer and a good solution.

bev

I'll certainly let you know how things go. Tomorrow they scheduled me for a chest xray, a visit with the LC pulmonologist and my oncologist. I was already scheduled for my first followup with the radiation oncologist. I am going to have to go alone since my husband can't get off with this short notice. I think they missed the part that I get out of breath if I walk very far at all! I'll be from one building to another.

I had experienced a resting pulse of 100-120 right after my surgery. It persisted on and off for a year. My pulmonologist put me on Lopressor and it has made such a difference. They rold me that my heart has shifted since the surgery on RLL. Anyone else had this problem. I am sure that they will be able to give you a beta blocker to decrease your heart rate and make you feel comfortable. Good luck and God Bless...Dianne

My mom had the same problem she also was put on Lopressor and it helped her tremendously

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