we've just been texting to each other
she texted me at 4am telling me her red sox won
well, i know that, i did'nt have to be waked-up to know that
-but it's so great getting ANY communication from her
so this morning we've been texting back and forth
she's just laying in bed watching tv and she sez
she's got her mask on
i think that means no breathing machine
just an oxygen mask ...so she's breathing on her own again
she sounds happy and refuses to root for the steelers
she's a strong young lady and she's always looking forward
she's been through so much but she's always ready to do it
and then move on
i believe she knows who's at the controls of her life
and is willing to take what comes because
she's always looking forward to a brighter tomorrow
Sunday, October 28, 2007
Saturday, October 27, 2007
lots going on
this nurse this morning was a wealth of information
she said they're getting ready to take another(longer)walk
and that she's off the vent tube again today
and that her kidneys are starting to work again
(little by little)
and that they are gonna start feeding her differently
because she seems to be able to handle it
she said they're working her hard
because they want to get her out of CTICU and get her upstairs
'upstairs?'
that's were the rehabilition really gets going
she told me so many things that will start to happen there
way too much to handle
this is a long long process
and everything is being done for acacia's best results
the nurses and doctors at this place are truly incredible
i wish you'd include them in your prayers
Friday, October 26, 2007
she's trying
the 'trials' continued today
because she's stable and things look good
-that's where they take her off the breathing machine
and let her and her new lungs breath by themselves
i know that this is not easy for her
it takes a lot out of her, almost like learning to breath
she did it today for over six hours
good girl
the nurse said they've given her a lil' something
to help her sleep tonight (no game, travel day)
so she should be raring to go tomorrow
because she's stable and things look good
-that's where they take her off the breathing machine
and let her and her new lungs breath by themselves
i know that this is not easy for her
it takes a lot out of her, almost like learning to breath
she did it today for over six hours
good girl
the nurse said they've given her a lil' something
to help her sleep tonight (no game, travel day)
so she should be raring to go tomorrow
more heavy breathing
this morning the nurse said she's doing good
no fever, up in her chair
watching a movie with her mom
they have her on yet another 'trial'
-having her breathe on her own
this is rough on her, they make her do all the work
no machine assisting her breathing
so she has to do the huffing and puffing herself
she'll stay off the machine for as long as she can
little by little
day by day
Thursday, October 25, 2007
one step at a time
this morning she took a little walk!
really
step by step
the nurses thought that she could do it
so when they got her up to move her to her chair
-they took her for a little walk
'round her room and to the door
a little peek outside then back
she did really well they said
and now that everybody has seen her do that
they've all been in to see her and talk to her
she said 'can i get some sleep now?'
i guess so, being up all night texting her dad
little baby steps...
changes in her feed tube
changes in her oxygen levels and the amount of pressure
changes in her dialysis (she's on again today)
they are all very happy how she's doing
her strength, fortitude, patience and steadfastness
are all a miracle and proves the power of your prayers
thank you
really
step by step
the nurses thought that she could do it
so when they got her up to move her to her chair
-they took her for a little walk
'round her room and to the door
a little peek outside then back
she did really well they said
and now that everybody has seen her do that
they've all been in to see her and talk to her
she said 'can i get some sleep now?'
i guess so, being up all night texting her dad
little baby steps...
changes in her feed tube
changes in her oxygen levels and the amount of pressure
changes in her dialysis (she's on again today)
they are all very happy how she's doing
her strength, fortitude, patience and steadfastness
are all a miracle and proves the power of your prayers
thank you
Wednesday, October 24, 2007
past your bedtime
so here we are
texting back and forth and back and forth
and it' 2 in the morning back there in pittsburgh
as you know...
you can't sleep in the hospital, only when they knock you out
so we're texting about how good she's doing
and the red sox clubbering the rockies
and how happy she is about getting off her 'flolan' pump
ya know, she's been hooked up to a pump
day and night for the last 5 years
and this medicine was doing lots more than keeping her alive
it had lots of side effects that weren't good
all gone
and she's thrilled
she's so sweet
laying in bed, 2am, texting her dad
i couldn't be more blessed
but, i can't wait to see what The Almighty will do NEXT
another day
kim, her nurse said:
she's (still) responding well to the rejection treatments
they gave her 'a gram' of steriods yesterday and again today
she said her spirits are good
sitting up in a chair and listening to her iPod
this is great!
she's been talking to her nurse about tonight's big game
GAME 1
well, that's great, let's hope that these treatments work
i'll post again when there's a change
(or if her red sox win)
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