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Mar 9th - Feb 8th, 2008 |
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Rabekah's condition has not changed. We tried
backing off the vent and she is unable to
control her breathing at this time. The plan is
to try again tomorrow after introducing a
different medication, and weening her off the
meds that are keeping her in a sedative state.
We are asking that wherever you are tonight at
10:00 pm, please pray for Rabekah, pray for
guidance, healing and direction. We thank you
all for your love and support during this
continued fight. Much love - The Hicks Family
Rabekah is resting in the hospital and is very
restless. She has perked up over the last 5
hours. I think it is the most excitement we have
seen out of her in weeks. Even being on sedation
she is breathing over the vent and is wanting
the tube out. The Doctors will not pull the tube
here, they want to get her to Maine before doing
so. Glenn, Bekah, Daniella and I have a 10 am
Medical flight tomorrow morning that will
transport us back to our Hospital in Maine. We
will consult with her Doctors there and decide
what is best for Bekah and where to go from
there. Lots of battles were fought today within
our family, Emotional and spiritual. We spent
the day preparing for the worst but tonight (as
usual ) Bekah told us a different story. She
certainly has a strong will and is not cowering
to this fight. Even at the most painful moments
she still finds a way to make us smile.
Especially today since she managed to tell off
anyone who walked in the room. She wasn't able
to make the words but you knew she meant
business. That's our Bekah!! We are asking for
prayers of guidance and direction and for her
complete healing. We will update once again when
we are settled in Bangor.
Much Love,
Team Hicks
Rabekah was admitted at Arnold Palmer Women's
and Children's Hospital this evening. She did
not have a very good day and was really having a
hard time breathing. A CT Scan was done and
there have been no changes since last Friday but
after speaking with our Neurosurgeon in Maine by
phone everyone agrees this is progression of the
Tumor. She is able to breath in oxygen the
problem is she cannot blow it out. Her CO2 level
was 100, the normal is 40. She is very sick.
Glenn and I have decided to intubate and give
her a high dose of steroids as well as fluids
and some time for her body to rest. It is our
hope that this will be effective and she will
perk up long enough to get her back to Maine.
Thinking on the positive side,,, this very thing
has happened twice before and we hope this turns
into another viral infection that she just needs
to overcome. We made it to Florida but not to
Disney, guess she wants to wait a bit longer to
tackle the parks! A Princess has to be able to
Dance at her Castle right? We just have so much
hope and so little strength. My oldest daughter
Kaylee is so sad and scared that she might loose
her best friend. She told me she had a dream
that Bekah came to her School and she was
walking again. She also put her arm around me
tonight and rubbed my shoulder and said, it's
okay Mommy, Bekah will be alright. Such honest
trust. Our hearts are breaking, it's hard to
imagine that God would allow one of his own to
bare this kind of pain. We pray for wisdom,
guidance and understanding of the path he has
chosen for our family. We know Rabekah has
painted our life with so many Beautiful colors
and she has reached out and painted every one of
yours as well. Say a prayer for her tonight, but
not just any prayer. Let her colors fill the
words you use and let her fight become your
surrender to God. Much Love,
The Hicks Family
Hi Everyone, Rabekah is doing better today.
Praise the Lord. We believe He is answering all
of our prayers. We certainly feel the strength
and energy that is being sent out to her and
hope that within her precious little body, a
miracle is unfolding. We are still planning on
heading to Florida, as long as her health
continues to get better. She said three times
this morning, I want to go to Disney!!! So
here we go. We are so looking forward to this
trip as a family. We hope and pray all goes well
and Bekah's energy holds strong. We look forward
to these next two weeks to give us memories we
will cherish forever. There is a song that we
would like to share with all of you. Martina
McBride - Anyway. This song shines hope on the
face of our daughter and gives us the strength
and courage we need to keep our heads up and
believe that God's plan is worth waiting for.
Just seeing the passion Rabekah has when she
tries to sing this song among the few favorites
of hers is what keeps us going. It is our hope
that someday, she will sing for all of you! We
leave for Florida Tuesday afternoon and will be
updating and hopefully posting some pictures of
the first day at Disney. We love you all and
Thank you for sharing your prayers with our
family.
Much Love, Glenn, Shannon, Kaylee, Bekah, Abby &
Dani
Rabekah has been having some trouble the last
few days. Yesterday before we left for NY we
took her to have a CT Scan done just to make
sure the shunt was still working. Everything
looked good. The Neurosurgeon said it looked
like the cyst was causing the problems. We upped
her dose of Steroid to 1 mg and today she has
been having some difficulty breathing. She is
still breathing okay and is getting enough
oxygen but she cannot really talk and she said
it's hard for her to swallow. She is in good
spirits and will have nothing to do with going
to the Hospital. We feel it is extremely
important to keep her resting, quiet and happy.
When she gets worked up she doesn't do well. We
spoke again with the Doctor this morning and she
said it does sound like the Tumor is the cause.
We have upped her Steroid again to 3 mg a day.
Right now all of our plans are on hold until we
feel she is doing better. We may be at the point
where we need prayer for direction in decision
making. Quality of like is most important for
her. Our plead to God of all things is that his
hand be tipped to fill our daughter with good
health, restore the peace within our home and
make her the example for all to see, that we all
carry within ourselves the ability to change
things with positive, continual prayer and
thinking. This truly is a test for us all. Times
when we know God is close he still feels too far
away. We pray for direction, wisdom and
understanding and hold her outstretched before
God begging for his Mercy. We will update again
tomorrow.
Much Love,
Glenn, Shannon and The Girls
Well, Rabekah is home now and doing much better.
She had a few very challenging days but made it
through. We just need to be extremely careful
with the whole germ thing. A small cold for her
ends up in a Hospital stay. We hope and pray she
gets over this cold quickly and is able to
travel. The Disney trip is coming up so we all
need to be healthy. She is looking forward to
this trip as well as the rest of us. We all need
a break and are looking forward to spending some
FUN TIME together. Thank you all so very much
for continuing to pray for Rabekah's complete
healing. We have faith and trust in the Lords
hands and know that better days are still ahead.
We will update you from Disney and hopefully add
a picture or two.
Much Love,
The Hicks Family
Rabekah was admitted to the PICU at EMMC early
Monday morning and was intabaited due to poor
Respiratory Response. She was tested for RSV,
Influenza and just about anything else you can
think of. All came back negative except for the
Sputum (mucos) grew out a bug, and basically she
does have an infection in her lung. She has been
on Antibiotic for over 24 hrs now and has been
on lots of pain and sedation meds to keep her
calm and resting while the Breathing Tube is in.
They are all set to pull the tube and see how
she does but,,,, Rabekah has decided she wants
to make them wait and is still sleeping. If you
know Bekah, she likes to do things on her
terms!!!! That is a great sign. This does not
seem to be an effect of the Tumor, just a really
yucky cold. Because her Respiratory System is
sensative and she is immune-compromised she just
can't handle the extra secretions that the body
makes when it is sick. We ask that you cotinue
to keep her in prayer and we will update again
to let you all know how things are going.
Rabekah had her Shunt Revision this morning. She
had a rough go in the beginning with the
anesthesiologist trying to access the port. He
was unsuccessful after 3 tries and lots of
aggravation and discomfort they ended up doing a
regular IV in the arm. The procedure went well,
no complications!! Praise the Lord. The Dr found
that the valve in her head was completely
blocked and there was alot of pressure. The Dr
did give us a little good news, most patients
are completely shunt dependant which means if
there is blockage they would generally get very
sick within a day and possibly go into a coma
and die, where in Bekah's case she is only
partially dependant meaning that she is able to
pass and absorb some of that fluid on her own.
This is a good thing!!! She was supposed to stay
in the Hospital for 24 hrs but wanted to come
home right after she came to so,,,, they did a
CT Scan and everything looked good, no bleeding
and shunt is in good position so they let her
come home. She is very happy, resting and was
excited to see her sisters and Bella. She looks
really good, her eyes look straighter and less
bloodshot. She is drinking and eating as normal
and hasn't complained of any aches or pains at
all. God certainly has his hand upon her. Thank
you all for the prayers and wishes of good luck.
We have been trying to put pictures on the
website but have been having trouble. Hopefully
they will post soon. We will keep you updated on
how she does the next few days.
Much love,
The Hicks Family
Hi all,
I know you all are wondering why I haven't
updated yet. I have it just takes at least 12
hrs for the update to post. Bekah was very brave
and did great during her CT Scan, only a two
minute scan but to a child,,,, it's forever. We
then went to meet with her Neurosurgeon to
discuss the scan. She did find that the shunt is
not working well. There is blockage and a very
large amount of fluid in her ventricles which is
why we have been noticing some minor setbacks in
her lately. She is scheduled for surgery at 8:15
Monday morning to have a Shunt Revision.
Basically the same operation she had when the
shunt was placed only this time they think the
blockage of the valve is located in the head
some if that is the case they will only need to
make the one incision there. If they find
blockage elsewhere they will then go in at the
two other locations, another on her head and on
her stomach. Hopefully that won't be the case.
This was in a way comforting for us to hear, the
fact that this is a fairly easy fix and not
Tumor Activity is such a blessing. She will only
need to stay in the Hospital over night and if
all is well the next morning she will be able to
come home. Doing this procedure will help Bekah
to feel better and hopefully give her more
strength and energy once again. She remains
strong willed and cannot wait for her Disney
Trip. She has been asking everyday, how many
more days till we go Mommy? Ariel has called her
from the Castle 3 times and she is so excited to
meet her!!! Keep her close in your prayers and
ask that God's hand be used for wisdom Monday
morning and that he fill her with the renewal
breath of strength and complete healing. We know
in our hearts that Gods lessons are great and
now we look forward to a Beautiful New Year of
his Miracles. Much love from our family to you
and thank you all for believing in Gods unseen
Miracle, for it is then that the miracle is seen.
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