Bit of an update...
We have definitely found more of a routine with this. Emily has been very cooperative with the IV's, which helps, and was great for her dressing change.
The neverending vest nebs vest nebs vest nebs vest nebs has been incredibly wearing though~ it seems like she barely finishes one session and she's starting another. It's made a difference, though. She is coughing less and getting some energy back. They have us doing Pulmozyme twice a day (which she's never done before) alternating with the HTS twice a day, so it's all helping, despite the gruel of it.
I cannot wait for her followup on Tuesday. I hope they will tell us that it's enough, she can come off. I have no idea what to expect in that regard. Things are better but she's not close to her baseline and still having some chest tightness/pain (although she has some of that as her baseline too on occasion.) They will want her pft's back up to normal before letting her off, too, but I am not sure what they will consider her normal to be.