Charlotte went for her post-surgery exercise stress test yesterday. If you recall, she had a baseline test in January. For the details of the visit itself, check out that blog post–I was pretty specific about the machines, the hook-ups, etc. and how it all worked.
In January she was only able to move (a slow, steep walk into a steeper run) for about 7 minutes. She had to stop because she began to have pain in her chest, or in her heart as she put it. Her lung capacity was 71%, lower than the average 80% for kids her age.
Yesterday she continued on to 10 minutes. She only stopped because the tube she had to breathe into was terribly uncomfortable–she was drooling around it, but her mouth was dry–and the knee she skinned on a carpet was really bugging her.
Unlike the test in January, the cardiologist in the room did not give us the full detail of lung function, etc. He just said that everything looked good and that he wasn’t worried about anything. We’ll expect a more full report from Dr. Young when she has a chance to read the EKG and other data.
We weren’t terribly surprised by what we did hear, though we loved hearing it. Charlotte is training for the Girls on the Run 5K which she and I will run on November 21. She regularly is asked to run for as long as she can in gym and usually gets to at least 12 minutes. She tells me that is longer than some of her other classmates.
She was thrilled to go to school for a half day on her half birthday! I was thrilled that all is as it should be: Her heart surgery in February is a memory, the scar is fading to white (finally), and our daughter is again thriving and keeping up with her friends. A good day.