Hey everybody! We're at the hospital, Molly was admitted Tuesday. We have a loaner laptop from the hospital and for some crazy reason it won't allow me to sign into my blog so I can post. I can see my blog, and visit everyone else's though. So if anyone post comments I can read them.Steve is copying and pasteing this message for me. Molly's lung function was up a little when we came to clinic Tuesday but still not up where the docs would like her. You all know over the past few months we've been trying to fight things with oral antibiotics but with CF when it comes down to it you need those high powered iv antibiotics to get you really cleared out. So that's why we're here.She does seem much better already, and last night her o2 sats were at 99, yeaaaa! It was at 96 when we came in on Tuesday.For now the plan is for this to hopefully just be a 10 day stay, so we could get out of here July 3rd and be home for the 4th, we hope this really works out because spending the 4th in the hospital would be no fun. We're ready to get out of here and go swimming. We had planned on Molly getting a port put in this hospital stay but because it's summer and we love swimming we decided to wait until fall or winter time to send her to surgery for that, don't want anything to delay her from having fun once we get out of here. Steve had to leave us last night because he had to go back to work today after having 14 days off. We hated so bad he had to leave us and we miss him sooooooooooooo much already. You all just have no idea, he's just the best! Seriously he treats me and Molly like queens. We're soooooooooooooo lucky.3 nights down at the hospital and hopefully only 7 more to go..... sure hope they go fast. Tracy