Two months
ago my wife was diagnosed with breast cancer.
She is a private person so I will not post her personal experience; but
I feel I might cover the procedure, giving a non-medical account for anyone
about to go through, or with a friend or love one about to experience this
traumatic disease.
The cancer
was found by comparing routine mammograms; this is why women should conform to
a yearly breast exam schedule. Within a
week my wife had returned for a second exam, an ultrasound and a needle biopsy. The biopsy result was an invasive lobular
cancer, but it had been caught at a very early stage and was quite small.
We met with
the surgeon and he explained the procedure for removal of the cancer. The hospital assigned my wife a great support
person that has been actively with us throughout this whole time.
We scheduled
the surgery and all went well. An area
about the size of an egg was removed from my wife’s breast along with four
lymph nodes under the arm – this is done to see if the cancer is traveling
beyond the breast. The removed tissue
and lymph nodes were sent to the lab for diagnosis and came back with the best
possible outcome… the cancer had not spread to the lymph nodes.
After the
surgery we met with our oncologist – a doctor that specializes in the treatment
of cancer. She will be the doctor that
coordinates treatment and monitors my wife into the future.
A sample of
tissue was sent off to California for an oncotype
dx test to determine the potential for re-occurrence, and whether the
patient would be best treated with radiation therapy or chemotherapy.
You are
given the choice of mastectomy- complete or partial; chemotherapy; radiation or
no treatment. Viewing the results of the
oncotype dx test we decided that
radiation therapy would be appropriate – and our oncologist agreed.
Next we met
with the radiation oncologist who performs radiation therapy. He reviewed our records and our oncologist
recommendations and agrees with our preference of treatment.
This past
Thursday we were called back in for the preliminary procedure prior to the
actual radiation treatments.
The nearest
cancer center in 35 miles away. We
arrived before noon and again met with the radiation oncologist and he
explained the procedure along with percentages of all the scary possible side
effects.
Next we met
with two nurses that escorted us to a treatment room with modified cat scan
equipment. The nurses were very
supportive, they explained the procedure about to take place, reviewed the process
and answered our questions. This is not
the radiation treatment, but the process necessary to program the machine.
I was shooed
out of the room, my wife put on a hospital robe. She was placed on a table with her arms
raised where she would pass through a doughnut shaped x-ray. She said the only thing bothering about the
procedure was her arms were placed in restrains to prevent her from
moving. It only took a few minutes for
the doctor to get the information he needed.
The purpose
of the procedure is to predetermine the exact focus of the machine that will
administer the radiation. The focused
is critical so the cancer area and not the heart or lungs receive the radiation
dosage. When the exact location was
determined a small dot was tattooed on the right and left side and middle of my
wife’s chest. This will be used for
focusing the radiation machine. This
whole process took about twenty minutes, but my wife said it felt much
longer.
When the
procedure was over and my wife was dressed the nurses led us to the room where
she will be actually receiving the radiation treatments. The machine and procedure was explained and
all our questions were answered.
I can’t
emphasize how supportive, caring and professional the nurses and staff
were. They made this scary pre-radiation
therapy appointment seem very personal and doable.
My wife will
not start the actual treatment for another week as the radiation oncologist
will be on vacation this week and we do not want to be passed to a stand-in
doctor for the first week of treatment.
The
radiation treatment will be five days a week for three weeks and then we will
meet back with our primary oncologist and she will direct the rest of the
treatment and observation over the next five years.
I will
continue to relate our experience for the edification of others that may be
facing this scary disease.
We are very
fortunate to be living in this era. Twenty
years ago the treatment and outcome would have been indeterminable – now cancer
is considered a curable condition if detected early enough.
I love my
wife above my own life. I am much older
then she and I have always expected that at some time I would face a terminal
condition – but not her. This has
scared the hell out of me.
the Ol’Buzzard
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