Hi friends. I have a question. I don’t think I asked it here and I won’t see the Dr. for another month so here goes. In January I received a PCD. About 3 weeks ago I began a cardiac-rehab program. Two things stand out BIG TIME!
The first thing I notice is that I do not experience the chest pain I have had for the last 12 years. I have exercised more in these last three weeks than I have in 12 years and I don’t hurt! Admittedly this is inside and away from the elements, but the reduction is pain is about 97% compared to before. Secondly, my SOB symptoms are greatly reduced (I’d say about 75%). I find I can talk better now while exercising than I could in the mid-eighties before I even knew I had HCM.
They tell me I am pacing almost full time when I exercise and they expect that is due to the beta-blockers I’m on. The device recognizes that my heart needs to pick up some speed and evidently does it for me. Would this make the difference?
Has anyone else experienced a relief from symptoms after getting a pacer? I am quite pleased with this unexpected quality of life increase!
Peace,
Leon
The first thing I notice is that I do not experience the chest pain I have had for the last 12 years. I have exercised more in these last three weeks than I have in 12 years and I don’t hurt! Admittedly this is inside and away from the elements, but the reduction is pain is about 97% compared to before. Secondly, my SOB symptoms are greatly reduced (I’d say about 75%). I find I can talk better now while exercising than I could in the mid-eighties before I even knew I had HCM.
They tell me I am pacing almost full time when I exercise and they expect that is due to the beta-blockers I’m on. The device recognizes that my heart needs to pick up some speed and evidently does it for me. Would this make the difference?
Has anyone else experienced a relief from symptoms after getting a pacer? I am quite pleased with this unexpected quality of life increase!

Peace,
Leon
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