Well, since I last posted I spent a few days in the hospital. I went in to the Cystic Fibrosis clinic on Thursday and my lung function tests were lower, and I wasn't feeling too great...so they decided it's time for IVs. I was admitted and began to get to know our new hospital and the way they do things. It was good over all! The people were nice, and the nurses were alright, and my doctor is AMAZING! There are so many great CF doctors in this world, and I have had the blessing of working with a few of them, and now I'm working with another great doc!
The hospital itself is..well...it's old. So that comes with it's challenges. Like a bed that "creeks" when the respiratory therapists adjust it...etc
Yesterday I found myself laughing so hard! First, Peter saw a bug crawling in my bed (a silverfish bug)... so they gave me a whole new bed! wow! Then the nurse was making my bed and there was an adhessive heart monitor sticker fused to the blanket...o boy I laughed!
Peter and I had so much fun just being together on our mini "vacation" in the hospital!
The Lord has been our strength, and continues to be! To God be the glory great things He has done!