Matt had a busy morning! No wonder Noel had trouble updating the Blog. His "fluid output" rate is very high because they're giving him a lot of fluids due to the chemo drugs. Because of this, they have decided to put in a Foley catheter. This will stop him from being wet all of the time. They told me that some of the chemo drugs come out in the urine and that is bad for his skin.
We had a bang-up physical therapy session. He didn't want to do anything at first but then got into it and took about 4 steps (with help). He also sat up on the edge of the bed for a while and sat in the wheelchair.
Still waiting on doctors to make rounds. Will post more later.
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