I have a repair Tetralogy of Fallot (February, 1970) and porcine pulmonary valve replacement (May, 2005).
I started C25K first week of August and doing okay (getting ready for Wk5 Day1 tonight). I would be interested in hearing experiences from any other ACHD individuals working through this program. I currently experience about 12% leakage in my pulmonary valve -- I wish I had a way of recognizing what impact that really has on my stamina, O2 supply to my muscles, etc.
Things I am learning:
I run REALLY slowly combined 16min mile run/walk in week 4
Mentally (even at 46 years old) I struggle with resisting the urge to stop when I begin to get winded (my childhood programmed me to do this)
Shin splints suck
I find myself wondering if my body is even capable of running for 30 minutes non-stop
Now that I am hitting week 5 (after 6 1/2 weeks), I laugh at myself for fearing the runs back in weeks 2 and 3 - although at the time they were hard
Figuring out the proper pace to allow timed finishes is hard
My goal is to run a 5k without having to walk any of it. I would REALLY like to not be the last in my age group, but am really only racing against one person that I will tie (me).
Although my cardiologist did not specifically prescribe this program, it seems perfect for what I need to do. I am loving the runs!
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