The following excerpt is taken from Chapter
6 of Childhood Leukemia: A Guide for Families, Friends, and Caregivers, 2nd
Edition by Nancy Keene, copyright 1999 by O'Reilly & Associates, Inc.
For book orders/information, call (800) 998-9938. Permission is granted to print
and distribute this excerpt for noncommercial use as long as the above source is
included. The information in this article is meant to educate and should not be
used as an alternative for professional medical care.
There are primarily
three types of relationships that develop between physicians and parents:
After we left Children's and
returned home for outpatient treatment, the local pediatrician's nurse called
and said, "Doctor wanted me to tell you that the blood results were
normal." I thought that unlikely since she was on high-dose chemotherapy,
so I politely asked for the actual numbers for my records. She read them off and
my daughter's ANC (absolute neutrophil count) had dropped far below 500. I said,
"Would you tell the doctor that her counts have dropped dramatically from
last week?" She said in a frosty voice, "Doctor said they were
fine." So I called Children's, and they told me to keep her at home, take
her off all medications for a week, and then have her blood retested. I was glad
that I paid attention to the counts.
A surprising number of parents are
intimidated by doctors and express the fear that if they question the doctors
their child will suffer. This type of behavior robs the child of an adult
advocate who speaks up when something seems wrong.
I knew one family who just hated
the Children's Hospital. They called it the "House of Horrors" or the
"torture chamber" in front of their children. Small wonder that their
children were terrified.
We had a wonderful relationship
with the oncologist assigned to us. He blended perfectly the science and the art
of medicine. His manner with our daughter was warm, he was extremely well
qualified professionally, and he was very easy to talk to. I could bring in
articles to discuss with him, and he welcomed the discussion. Although he was
busy, he never rushed us. I laughed when I saw that he had written in the chart,
"Mother asks innumerable appropriate questions."
• • •
• •
Justin's oncologist had remarkable
interpersonal skills. At our first meeting he said, "Justin has leukemia.
There are two kinds of leukemia, and both of them are treatable." So right
away he emphasized the positive. He then wrote on his notepad what all of
Justin's blood counts were, he told us what normal counts were and explained
clearly what we said that it was safe and he would allow his own daughter to
have one. He was very reassuring. It has been years since that day, and he has
always been very caring. He still frequently calls us on the phone.
Another mother relates a different
experience:
We tried very hard to form a
partnership with the medical team but failed. The staff seemed very guarded and
distant, almost wary of a parent wanting to participate in the decisions made
for the child. I learned to use the medical library and took research reports in
to them to get some help for side effects and get some drug dosages reduced.
Things improved, but I was never considered a partner in the healthcare team; I
was viewed as a problem.