At the end of a VERY busy day with docs/specialists, more x-rays and blood tests, I was finally moved to the "CF Floor". This floor is a MUCH quieter floor with lots of nurses and respiratory therapists that are comfortable and knowledgeable about Cystic Fibrosis. I've heard great things about this floor, so I am glad to be here and even more glad that I'm at the end of the hall with no noise outside my door... :)
I'm also starting to feel better, for the first time i'm taking deeper breaths and getting more oxygen- so we'll see if this helps me get home soon! I'll keep my blog updated.
Here's to some good sleep tonight!
~Em
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