7/9/14
Day 9 of recovery
Today has been a really hard & emotional day. We thought we were finally getting the pain
under control yesterday but we were wrong.
Alexa’s bowel movements have been really red for the past 3 days or so
& I have been really concerned about it.
They kept telling me it was just from some medicine they were giving her
that turns everything orange. They gave
her the last dose of that on Mon night or Tues morn & by tonight her bowels
were red as could be & I was positive that it was blood since about 4 days
ago they took a stool sample & said it came back positive for some
blood. I had her go in one of those hats
they use & when the aid came in to take the sample I asked her how long it
would take to get the results. She said
it depends on what they are testing for & when I told her blood she said, “It
shouldn’t take too long, it’s pretty obvious isn’t it?” We were also having probs with her g tube
again, it wasn’t draining properly & there was an excessive amount of
fluids coming out of that & her other tube on the other side of her
stomach. That little tube was having to
be emptied about 10 times today when the whole day yesterday it was only
emptied about 2 or 3 times. Ty & I
were just so worried about it. I went in
the bathroom & pretty much fell apart.
I knelt down & asked Heavenly Father to bless that something would
happen so that we could get her pain & nausea under control & we would
be able to figure out why all of this fluid was coming out so much. I asked for Dr. C to come. Dr. C told me at least 4 or 5 times before
surgery that if there was a prob with anything at all, even if it was just a
prob with the remote on the TV, to talk to him about it. He said there are so many doctors on the team
& there may be differing opinions but he is the boss & if there is a
prob we need to talk to him or it doesn’t exist. Within about ½ hr, in he walks!! As soon as he saw what was going on he told
us that she wasn’t absorbing her medicine & that it was passing right thru
her. He said sometimes this formula
causes diarrhea & that is the reason they haven’t been able to get her pain
under control. He ordered for her to be
changed back to IV pain meds & ordered her feeds to be reduced for the
night & had the nurse contact all of the other doctors & the dietician
& they are meeting here at 8:30 tomorrow morn to discuss what changes to
make. I was so relieved when the test
came back negative for blood but then it was pretty obvious that she hasn’t
been getting her pain meds hardly at all, they were just running right thru
her! Poor Alexa has been throwing up so
much today!!! It is so darn hard on us
to watch her go thru this!!! I have to
keep reminding myself about the blessings she has received. She has been blessed that she would return to
good health & have all of the strength & energy that she once
had!! When I start to panic, I repeat
that to myself & I also pull out my scriptures again! When Dr. C left the nurse said to me, “You
are so lucky he came this late in the afternoon, he doesn’t usually do that!” I said, “Well, I prayed him here!” She believed me & said, “That’s really
great! Really, he just doesn’t usually do this!” I am so grateful Heavenly Father once again
answered my prayer. Alexa is sleeping
peacefully now & is finally getting the pain meds that she needs. She is so exhausted from throwing up all
afternoon! She doesn’t just lie there in
pain, she gets so restless & has to stand up constantly & looks so
pitiful!!! Things are going to be ok
now. Ty & I were able to walk down
& get a bite to eat & reassure ourselves that we CAN get thru
this!! We are just completely amazed at
how quickly the days fly by. We were
sitting there about 7:00 tonight & Ty said, “Well, there’s another day gone
where I didn’t get anything done. I
checked my email for a bit & checked on payroll but that’s it.” I told him we are doing what we are supposed
to be doing right now, caring for our daughter.
I reminded him that he helped her go for a couple of walks, rubbed her
feet & held her hair back while she threw up. That’s really all we can do right now.
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