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On Wednesday March 16th, he had his
previously scheduled 1-year check-up with his
regular pediatrician, Dr.
A. Gerald Reisman. When Dr. Reisman evaluated him,
he was concerned about the lump and said it was
getting no smaller and wanted them to have
additional blood work done, which was scheduled for
the following Friday.
After an all day visit to the lab on Friday, the
results of the blood work and ultrasound were
reported back to
Dr. Reisman with ‘concerned’ results. He then
scheduled them to report to the emergency room at
Scottish Rite hospital that night for
additional blood
work and a chest x-ray. The doctor also wanted a
cat scan immediately, but being that
Trenton was only a year old, he would need an
anesthesiologist and they were not there on Friday
nights. Therefore, the E.R. had the results of both
the additional blood work and chest x-ray results
immediately to Dr. Reisman and
Dr. Wasaluski
from the Pediatric Oncology Group, it was clear that
something was wrong.
So, in the cold confines of the emergency room
sometime around 11:30 p.m., the family was told the
news that no family ever wants to hear….your son has
CANCER. The initial diagnosis was Neuroblastoma.
Trenton was directly admitted into the 3rd
Floor Cancer floor to begin his full diagnosis.
A series of grueling tests were run and it was
determined that
Trenton had a solid mass tumor in his chest and
neck.
On March 21st he underwent surgery to
have a portion of the tumor under his arm
removed for a biopsy. Since that came back positive
for disease, they removed ¾ of the tumor under his
arm. At the same time
they took some bone marrow for testing and
Trenton had an External catheter
(also known as a VISCATH: BROVIAC®, HICKMAN®)
put in for the purpose of receiving medication and
blood and also for taking blood and bone marrow for
testing.
That afternoon his oncologist
Louis Rapkin, M.D. informed us that the frozen
section taken from the tumor (preliminary report)
and the rest of the tests confirmed that Trenton
indeed had Stage IV Neuroblastoma with High Risk. He
then scheduled to meet with the family on March 23rd
to lay out his plan for treatment.
Please see my “Treatment”
page for formal details of my planned treatment.
Not that I AM TOO HAPPY about all this, but I know
that Mommy and Daddy are making all the right
decisions for me to be CURED of this HUGE OWIE!!!
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