The plan was for Steven and me to take off since I haven't slept since Thursday night. However, we waited around until she was settled in, had at least one more breathing treatment, and were confident that Mark was sufficiently up to speed.
She is scheduled to have treatments every three hours (so she should have just had one), and they started her on steroids. When I checked in with Mark, she was playing but starting to slow down, which was good since she only slept until 1:30 or so last night and then took a 1 1/2 hour nap in the ER before they transferred her to her room.
The current plan is for Steven and me to catch up on some sleep and then head back to the hospital. Either Mark will return home with Steven or he'll go to a friend's house. We're just waiting to see how things go.
I was told this morning that Michelle would be there overnight. We're praying that she isn't there longer. At this point, they don't know what is causing the breathing problems. They have ruled out pneumonia through chest x-rays (so fun to do at 2:30 in the morning!). We really believe that it's asthma, but the doctors are hesitant on that right now. From what I understand, they don't like to diagnose it before the age of 3. However, with her medical history, it makes sense. Her allergist all but said that she'd develop asthma and that it was just a question of when, not if. At this point, there is no indication that this is an allergic reaction.
Thank you for praying for Michelle, for us, for the medical staff, for Steven, and for our families. My dad has been sending out updates through Facebook and Twitter, and I'll do my best to update when I can. However, I'm hoping to be asleep for quite a few hours :)
1 comment:
So sorry to hear that Michelle is in the hospital! We went through this very same thing with Owen, twice. The doctors were also hesitant to diagnose asthma so they called it "pre-asthmatic." Praying she gets well and is able to go home soon!
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