Saturday, February 25, 2012
Peaceful Day
Today Kristina has been resting peacefully. We tried to wake her, she has her days and night confused. She sleeps much during the day and awake at night. Which is not good. We usually leave the hospital around 9pm at night, after visiting hours. Sometimes Kristina is up when we leave and becomes sad and cries. It'll be best if she slept when we aren't here and awake during the day so we could keep her company. Kristina's respiration and vital signs are all good.
Thanks again for all of your calls, texts, emails, and prayers.
Our family appreciates all of the love and support.
A Letter for Kristina
Dear Christian friends,
I am a doctoral
candidate at Emory University, and am writing to you to introduce you
to my wife's niece, Kristina Jones, 27yrs, who is being currently
treated in Atlanta, Georgia, for a brain stem tumor, a Glioma.
Kristina was diagnosed in 2010, and underwent radiation therapy
treatment in Savannah. The tumor responded to said treatment,
and shrank. About a year later, in September 2011, incredibly, the
tumor was back. Kristina’s Savannah and Atlanta doctors have
advised her family that surgery is not an option, and they are
disinclined to do any more radiation, since she was given the maximum
dosage allowable, last year. At Emory University hospital, Atlanta,
in January 2012, Kristina was able to see one of the top
neurosurgeons in the world, and a top-notch oncologist, who suggested
chemotherapy. She was administered her first dose of chemotherapy on
Friday, January 20th
and seemed to do well. Unfortunately, she was rushed to a hospital
the next evening, with breathing problems—which she had experienced
before—possibly due to complications from the tumor, and, or the
chemotherapy.
Currently,
Kristina is in a Critical Care Unit near Atlanta, fully
conscious, mentally, but being
assisted by a breathing machine/life support system. The tumor,
located at the junction of Kristina’s spinal column and the base of
her brain, is adversely affecting the nerves that control Kristina’s
breathing, among other things. She has near-paralysis on her entire
left side and her right side is weak. She can responds “yes”
or “no” to questions by shaking her head and blinking her
eyelids. While the doctors and nurses at all the hospitals so far
have been very helpful and supportive, it has become apparent that
their general disposition is that the family might do well to
consider removing Kristina from the life support system, provide her
with “comfort measures,” and let her pass on. This is, of course,
a very difficult situation for her family to consider—Kristina is
young, and
a mother,
herself, of two young boys, aged nine and six, who need her alive!
She also has sisters and a brother, aunts, uncles, grandparents,
nephews, nieces, and a mother and father, all who love her! Given the
fact that Kristina’s mind is still as aware of her surroundings as
you are, reading this letter, it seems unconscionably cruel to have
to consider “letting her go,”
as the doctors and nurses euphemistically advise us!
It has become
apparent that IF
Kristina had been covered by regular medical insurance (she has
Medicaid/Medicare), she could have access to, perhaps, an indefinite
time on the life support system, at a long-term care facility like
Kindred Hospital, also in Atlanta, while her family tries promising,
new, emerging treatments, and, or Kristina receives a miracle. Her
brother recently found out about a treatment called oncolytic,
for just her type of tumor—something the family would like to try.
We need to “buy time” for Kristina, and to be able also to buy
the medication. There is also a doctor that we would like Kristina to
see in Texas, Dr. Burzynski at the Burzynski Clinic. The family has
been told, in many ways, that her time at the hospital where she is
now is just about over, they having done all that they can, and they
have encouraged us to seek care at a long-term care facility. We have
been advised that IF she is admissible at the long-term care
facility, she has only twenty days
there—that Medicaid/Medicare
will ONLY
pay for twenty days of her care on a respirator/life-support system!
Hence our letter
to you—we would like you
to consider helping the family in any way that you can, to facilitate
getting the time and medication for Kristina. You might be able to
help financially, or you might have access and connections to medical
personnel, facilities and equipment; or you might be able to spread
word about Kristina’s situation through your church, organizations,
families and friends, or social networks. Above all, we ask that you
keep Kristina and her sons, especially, in your thoughts and prayers.
As a family, we look forward to hearing from you at your earliest
opportunity, and thank you in advance for your kind consideration.
Below are appended additional “letters” from other members of the
family, including Kristina’s siblings, parents, aunts and uncles,
and other family members and friends. Again, thank you, and may God
bless you and yours.
Sincerely,
Kwesi J.
DeGraft-Hanson
Thursday, February 23, 2012
Peaceful day
Today has been a very relaxing day for Kristina. She's still on the vent, some days they attempt to ween her off the vent. The longest she has been off the vent has been 9 hours, praying tomorrow would be longer. Yesterday we massaged her legs and arms and painted her toenail bright orange. I think she enjoyed that. Please continue to pray for Kristina, prayer changes things.
Psalms 91
~We read Psalms 91 to Kristina everyday.
Psalms 91
~We read Psalms 91 to Kristina everyday.
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