Sorry I haven't been writing, there just hasn't been much to write about.
I keep getting good reports from the transplant doctors. I have now started going to clinic only once a week, compared to two weeks ago when I was going twice a week. I also started taking Pulmonary Function Tests every time I go to clinic now and the doctor said they look great.
I have continued to have physical therapy, and I am improving every time I go (which is every time I go to clinic). Last week I took the stairs from the third floor to the eighth floor, back down to the third floor, and then up to the fourth floor and back down to the third; this was all after walking 1.5 miles in about 30 minutes. My physical therapist said I was walking 3 miles an hour. Hopefully I continue to improve so I can run the Cystic Fibrosis walk at the end of April in San Dimas.
This is my family at the walk last year. (I couldn't go because I was in the hospital).
Bree-meister, that is all fantastic! Always praying for you. Much love to you and your family.
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