Greg
Tomalesky
Hi Everyone:
My name is Greg
Tomalesky. I am 50 years old
(soon to be 51). I work as a
software engineer for an
industrial process control
company in Maryland. I
currently reside in
Pennsylvania with my wife and
son.
I "discovered" my
condition in July of 2001
during a routine physical. I
say "discovered" because that
is when the symptoms(shortness
of breath, etc...) began to
assert themselves. Up until
that time, I was aware only
that I had a heart murmur. It
was only after my cath &
subsequent MRI that I learned
that my aorta was constricted
just beyond the carotid artery
and slightly enlarged
immediately after the valve.
The aortic valve was still
tricuspid but with moderate to
severe stenosis. Between July
of 2001 and April of 2002, I
dug up as much information as
I could on the Internet. My
cardiologist said that I
shouldn't but I felt the need
to be as informed as possible.
I still believe that gathering
all the information that I did
helped in may ways. The
biggest help was in preparing
my mind for surgery. I knew
that the surgeons would take
care of my body so it was up
to me to prepare my mind. By
the time my surgery date
arrived, I was ready to go.
My surgeon (Dr.
John V. Conte @ JHU in
Maryland) was (is) a very nice
person. He displayed an
amount of confidence in his
work that put both me and my
wife at ease. He was quick to
suggest a mechanical valve
because of my age. After all
my research I was in complete
agreement.
I did not really
have much in the way of
medication prior to surgery.
This may have been due in part
to the fact that I had no
other illness of condition
other that needing a valve. On
the morning of my surgery I
scrubbed my self in the shower
and waited for the nurses to
arrive to transport me to the
OR. Today's anesthetics are
truly amazing. As far as I was
concerned, no time passed from
the time I was brought into
the OR until I was waking up
in the CICU. I don't even
remember the time spent in the
CICU. So my first recollection
of my surroundings and family
was in the step-down room the
next day. My wife said that
when she and my son arrived
after surgery, that I looked
as though I had been hit by a
bus! It was really scary for
them both.
Allow me to take
this opportunity to heap some
praise on the staff at Johns
Hopkins Hospital. There was
never a time in my entire stay
there (6
days) when I wasn't made to
feel as though I was the only
one they needed to care for.
They were always helpful and
answered all my questions.
They were also very helpful
and understanding to my wife
and son during the times they
were visiting me.
I am into my third
week after surgery. My biggest
problem is convincing myself
that the pains in my chest are
the result of the surgery and
NOT the result of any further
heart problems. I have been
dutifully monitoring my AM &
PM temperature as well as any
weight gain and BP. Everything
seems to be in order. When I
was first in the recovery
room, I was receiving oxygen
but that was soon removed
because I was breathing well
enough on my own. I am taking
Toprol XL to regulate my heart
beat and keep my BP down. My
cardiologist said that this
will become unnecessary after
2 weeks or so. Of course I am
taking Coumadin and having
blood test almost daily to
establish the dosage. I am
going for a baseline
echocardiogram next
week(6-May-2002).
One final note: I
cannot stress the importance
of a loving and caring wife.
She stoically put up with my
increasingly grouchy behavior
in the months prior to my
surgery and has been by my
side during my recovery. She
even learned how to mow the
lawn on our 2 1/2 acre "estate"(ha
ha). I can truthfully say that
recovery would be next to
impossible without her.
Here are some
pictures of me in the hospital
and at home.

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