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My experience with encephalitis began in the summer of l960. I
was in the third grade in the Myrtle Beach, South Carolina area.
It was a hot summer and humid. We always had mosquitoes during
the warm months. A chicken appeared under our garage one-day.
The chicken would not move and appeared sick. I petted the chicken
and told my mother about it. Within a day or so, I began to
feel bad. We did not go to the doctor, except for vaccinations
once a year. I remember holding my head and yelling that the
pain was terrible, as I bent over a chair in the living room.
I remember to this day, it felt like someone had split my head
with an ax.
My mother got an appointment and we arrived at the office of
Dr. Smith, a wonderful child doctor and so caring toward me
on the exam table. He looked into my eyes, asked some questions
of me. In a few minutes, he had picked me up in his arms and
was carrying me down the street to the hospital. They explained
the spinal tap, and I remember two big men holding me gently
and telling me to lie still on the hospital table. I was put
into quarantine. One thing that I do laugh about was that I
was not an assertive child. I told them "no, I was not going
to be put in a crib", due to the shortage of hospital beds!
I remember hearing about icing me down in a tub. I was in the
hospital about eight days. The days were not very clear to me.
I returned home. They expected I would have to learn to walk
again, perhaps speech problems. I overheard these remarks. I
came home and was treated no differently by my parents. I returned
to fourth grade the next month.
After reading some of the other encephalitis stories, I saw
some similar problems that we have shared; I had problems understanding
math and algebra. I had to study two hours each afternoon on
my five book subjects. I would write on a pad, something I had
to learn over and over until I could retain it. I made good
grades, and it was a strict grading scale during the sixties.
I could not take college prep courses. I was not able to follow
as quickly as the other students that were in the advanced classes.
I took the general classes.
Bright lights always bothered me, noise startles me, I have
had depression, and a lot of insecurity and lack of self-confidence.
I since have been diagnosed with dystonia, it is in my maternal
side of the family, but the encephalitis may have triggered
it. I have chronic fatigue immune dysfunction and Fibromyalgia
now. I appear just like the picture of myself. I am in a lot
of pain, but I have a lot of determination.
I waited from eight years old until I was 46 years old to find
a survivor of encephalitis in which to share stories. I never could find
material on the illness until this won-derful site. I tried to contact Dr.
Smith this year. I never saw him again and never got to thank him as an
adult. I do care about all of you that went through this horrible illness.
Sheri Anderson Todd
Alabama, U.S.A.

Posted: July 2, 2000
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