In loving memory of a 5 year old diva with Spinal Muscular Atrophy Type 1 who changed our lives forever
Tuesday, January 13, 2009
At the Hospital, DAY 6
Not much to add... Deedee still fighting the bugs, and we officially got the notice that they may try extubing by the weekend (which is good, early extubation with so much secretions had me nervous). If everything keeps going well, maybe it's a matter of just one more week... We are preparing our minds for 2 nevertheless. Better safe than sorry.
Deedee was cranky today, watched Aladin and after reading about shapes she fall asleep for a long while. She's getting her respiratory treatment every 4 hours (two days in a row, I'm amazed! Seems that Daddy's talk with the doctor worked well). Yeah, last night I was feeling useless, they actually did everything... LOL
Bach and Lou passed by today, a quick in and out. Oxygen is at 21%, and everything else seems stable, so there were no further comments. No more surprises for the day, which is good. We don't want more surprises.
Daddy stayed the night today. Gotta go rest. Thanks for all good vibes and prayers, as all work its wonders. We strongly believe so.
10-4
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1 comment:
Thinking of you guys! You are doing great! Keep it up and know we are thinking of you all! If you ever need anything, we are here for ya!
Sarah and Stella www.caringbridge.org/visit/stellaturnbullturnbull
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