Stillgoing
New member
Thanks to all of you for such great ideas.
I will definitely bring her enzymes with me. I hadn't thought of that. I figured they would be ready for us since they had 24 hours notice of our arrival. That probably isn't how it works, is it?
I didn't think of bringing wipes either. What a great idea! She doesn't need to pick up a new bug a the hospital.
They will be starting a PICC line tomorrow. The good thing for her is that they will insert the PICC line while she is out for the bronch. (I act like I know what I am talking about here. I am really just echoing what the doctor said.) She will get stuck twice - once today to start the IVs and then again tomorrow - but she will only be awake for one of them.
Gina mentioned doing PT once a day - I never even thought of that. I had been racking my brain trying to think of ways to keep her physically active. I never thought of it being included as part of the program. I will be sure to ask about that.
The doctor talked about doing four treatments a day. I am hoping they will be during normal waking hours. I don't want them to wake her up in the middle of the night for a treatment. Is that unreasonable?
Thanks for all your great ideas!!
Kathleen
Mom to Lauren 7 w/CF and JJ 9 no CF
I will definitely bring her enzymes with me. I hadn't thought of that. I figured they would be ready for us since they had 24 hours notice of our arrival. That probably isn't how it works, is it?
I didn't think of bringing wipes either. What a great idea! She doesn't need to pick up a new bug a the hospital.
They will be starting a PICC line tomorrow. The good thing for her is that they will insert the PICC line while she is out for the bronch. (I act like I know what I am talking about here. I am really just echoing what the doctor said.) She will get stuck twice - once today to start the IVs and then again tomorrow - but she will only be awake for one of them.
Gina mentioned doing PT once a day - I never even thought of that. I had been racking my brain trying to think of ways to keep her physically active. I never thought of it being included as part of the program. I will be sure to ask about that.
The doctor talked about doing four treatments a day. I am hoping they will be during normal waking hours. I don't want them to wake her up in the middle of the night for a treatment. Is that unreasonable?
Thanks for all your great ideas!!
Kathleen
Mom to Lauren 7 w/CF and JJ 9 no CF