Carol Hanson
Hi. My name is Carol Hanson. I'm 47 years old and until June
of this year I worked at the local newspaper where I wrote the
people news and obituaries. I'm married and have two sons, 20
and 18.
I first found out about my heart condition in 1988 when my
heart skipped beats during minor surgery. I had not experienced
any previous symptoms. I was sent to a cardiologist who
discovered that I had mitral valve regurgitation and
cardiomyopathy. I took no medications and my condition was
monitored by an echocardiogram every year. Because of changes in
my work I missed going to the cardiologist for four years, but
this past year I began to experience shortness of breath and
fatigue, but decided that was due to the fact that I smoked and
my job was very stressful. I experienced an anxiety attack at
work one day in May and went to see my primary care physician
who suggested that I have a complete physical. It was during
this time that I confessed to my doctor that I had not seen the
cardiologist for four years. He set up an appointment with me
for the following week.
That weekend I experienced pain in my chest and went to the
emergency room. The doctor who took care of me the next day told
me that I had had an esophageal spasm (I suffer from GERD) and
sent me home. I saw my cardiologist and had an echo two days
later. On Friday of that week the cardio called me and said that
I needed to have open heart surgery and that his office would
set up an appointment for me with a surgeon. He said that my
mitral valve was in bad shape and stressed that the surgery
needed to be performed within a year. The echo showed my
ejection fraction to be 20%. The appointment with the surgeon
was set for July 20.
After a TEE and heart cath, surgery was scheduled for July 25
at Sacred Heart Medical Center in Spokane, Washington. My
surgeon, Dr. Timothy Icenogle, and I decided that if a valve
replacement was necessary that I would receive the St. Jude
Mechanical, but surgery was cancelled because my white count was
20,000, not optimal for heart surgery. After examination by an
infectious disease specialist found nothing amiss surgery was
scheduled for that Friday. On Thursday night, while talking with
my surgeon, I experienced a pain in my head. A CT Scan showed
that I had a sinus infection and surgery was rescheduled for
August 19. Meanwhile my primary care doc and cardio decided that
I needed to see an ear, nose and throat doc for the sinus
infection. He cancelled the surgery. During this time my blood
was drawn every week for the WBC but never got below 13,000.
Finally one day my white count was a normal 9.6 and surgery was
scheduled for September 26. We checked into the hospital the day
before where a blood sample was taken and it was found that my
white count had again soared to 19,000. I called my surgeon's
office and told his assistant about this new development. The
surgeon was in Florida so they left a message with his answering
service to call me that night when he was due back.
Unfortunately, the service got the message wrong and told him
that my white count was 9.6.
The next morning we arrived at the hospital and told them
about the white count, but they prepped me and waited for Dr.
Icenogle to decide what to do. So there I was in pre-op with
five doctors standing around me discussing what to do with
me.... send me home or keep me in the hospital as my cardio
suggested. He won.
Dr. Icenogle told me that people who have white counts that
high usually have either leukemia, a tumor somewhere or they
were dead. A battery of tests could not determine the cause of
the high white count, so after a week in the hospital surgery
was finally performed October 3. Surgery went well (he was able
to repair my mitral valve using an annulplasty ring) until they
removed me from the bypass and I started hemorrhaging and
required four units of blood. I also required a lot of
anesthesia and as a result didn't wake up until the following
afternoon. A few days after the surgery I experienced trouble
breathing until it was discovered that I was allergic to drugs
used during respiratory therapy. I went home seven days after my
surgery. I never really experienced any pain from my incision
but have had trouble with fluid retention. I returned to the
hospital for three days with fluid on my heart and two weeks
later I was admitted with fluid on my lung, which required a
four-day stay.
I wish that this was the end of the story, but during my last
visit to my cardiologist he told me that my heart is now
"Global" his term for the fact that there is no part
of my heart unaffected by heart disease. I will now probably
require a heart transplant.
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