So this is what filled our
Monday morning.
We woke up super early and
were one of the first cases of the day.
5:45 we entered the
hospital. We got checked in and waited for our beeper to buzz.
They took me back to prep
me. Urine samples, blood samples, weight check and verify medical
history.
I had a wonderful nurse
and a great technician to draw my blood. I met my Nurse Anesthetist
and then the Anesthesiologist. I met my Surgical Nurse. They
finally they let Andrew come sit. I had to repeat to everyone why I
was there and after the 4th or 5th times I kind
of teared up explaining it. My Neurosurgeon finally came did his 30
second bit and said, 'See you in there.'
The Nurse Anesthetist
slipped me an sedative and I said, “Goodbye” to Andrew.
They wheeled me to the OR
and I mentioned how crazy cold it was in there. They asked me to
move to the OR table then told me to move my arms to the side while
they put this big pink boards on the side of the table and then I was
in recovery.
I was watched closely by a
very nice man. He kept asking me my name, where was I, what
procedure I had done and what day it was. He would often get on the
phone that was attached to the column next to him. Then repeat his
questions. He asked me if I was a runner of any sorts since my heart
rate was maintaining in the 50's. I told him, “I used to be. I
don't run like I used to, but I want to again.”
The CT was open so it was
my turn to go. That was a quick scan and I told them, “That was
way better than the MRI.” (time wise) The took me back to PACU and
after a nurse calling around looking for my bed and fussing people
out. They wheeled in my bed, moved me to it and took me to my room
on the Neuroscience floor.
I was greeted by Andrew,
Mom, Dad and Mr. R. The nurse (who was looking for my bed) and the
man ( I assume a nurse) who stayed by my side instructed them all to
leave the room while they got me in and set up.
They decided I no longer
needed to keep the nasal cannula. They reported my stats to the
medical staff on the floor then finally let everyone in.
I was tired. They all
stared and we had awkward conversation.
I finally asked, “Do I
have a headband on?
They all laughed and said,
“No.”
I said,”It feels like I
am wearing one.”
With a sterotactic biopsy.
They attach a frame/cage to my scalp in various places and use that
plus the brain lab series (3D image of my brain) to guide the needle
most accurately into the tumor. The “pins” for the frame are
quite sharp and left three open sores on my head. They also numb
your entire scalp in preparation of the cage.
That is what I was
feeling..or not feeling..it was a numb head.
Odd.
I had to have a
“clear/liquid” lunch. GROSS! I am not a jello fan. I don't
want a cup of broth. Oh yes and they cut my “chewing” muscle so
it hurts to open my mouth and chew.
I slept on and off all
afternoon, they monitored my stats and gave me pain meds.
Andrew got the nurse when
I got nauseous and lost feeling in my head/face. Neurologically
everything was fine she said when the nerves regenerate, some people
feel numb, tingling, sharp pains or nothing at all. I was getting
the numb/tingly all over my face..it creeped me out especially when
the right side of my face got numb too.
The nausea eventually
passed. They said I could go home but needed some antibiotics before
I go. Well, that took FOREVER...one to get the antibiotics then for
them to go through my IV. Finally well after 7p I was able to be
discharged if I wanted. Andrew and I talked and we thought we
would try it.
She walked us through our
discharge instructions. One thing she mentioned that I had already
noticed was not laying flat and not holding my head up. The amount
of pressure that would come was terrible. My head felt as heavy as a
bowling ball too.
I got dressed and Andrew
then went to get the van.
Enter nausea bout number
2. The Nurse Mario went to get me a wheelchair. I began to feel
horrible and went into the bathroom. I couldn't get any closer to
being sick. After a few gags I stopped and felt a little better. I
went to find Mario and sit in my chair.
Too bad the nausea lasted
the entire time in the van. We stopped by the pharmacy to fill my
prescriptions, one was for nausea. I requested Andrew park across 4
spots as to not turn the van. They did not take long to fill but it
sucked for me. I eventually got a bag to hold onto in the event I
got sick. Well maybe 2 miles from our house it took me over. Andrew
was great. We got home and I headed straight to our room and rinsed
out my mouth.
I slept on and off all
night constantly changing positions due to a pretty sore head.
Medical wise I handled it
great. It could take anywhere from 1-2 weeks to hear the results.
They said they would call me when they got them. I get my stitch out
Wednesday and have a follow up on February 19th. I should
find out before the 19th. ( I sure hope so.)
Again, I pray that they
are able to get a diagnosis from the biopsy and we can move on from
there. I want to get this done and over with. I know it's not that
simple but if it needs to be removed I want to go ahead and get that
done with.
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| Here is what it looked like right after surgery. Since I couldn't feel my head and I definitely couldn't see it..I asked Andrew to take a photo for me.. |


1 comment:
Thanks for sharing Carrie. I continue to pray that this all turns out the best it can.
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