We will be admitted to the paeds ward on February 25th, for some chest X-rays and other tests, and then her surgery will be some time on the 26th. After last time, nervous doesn't even begin to explain how I feel right now. I'm terrified that she will stop breathing again and they won't be quick enough. I feel like crying every time I think about it, so I don't know how I will be able to hand her over in two weeks time.
Ellie was born with a severe bilateral cleft lip and palate. This blog follows the ups and downs of her journey through the various stages of treatment, and offers some insight in to the life of a cleft-affected child. Being the parent of said child poses its own challenges, and updates are made when I can, not always as soon as something happens.
Saturday, 15 February 2014
16/02/14 - The date is set
While we were gallivanting around the Townsville country side on our well-earned family holiday, my phone rang. A new date had been set for Ellie's palate repair. There was a bit of confusion with the elective surgical nurse not actually believing me when I said she needed to be admitted the day before the operation, and trying to tell us we needed to come to Hobart a week before for pre-op, but of course when she checked with doctor Kimble and called me back the next day I was right.
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