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My name is Sheri and my son Dylan got encephalitis at the age of 15 months of age. It happened Sept. 15,2001. He had showed
no signs of being sick before hand. He was visiting some grandparents and was put down for a nap. When I got there I had decided to go and wake him up because he had been sleeping for a long time and when I did he was lethargic. He wouldn't wake up. After trying for a while we decided to take him to the ER. He was running a fever and had vomited.
They ran a lot of tests then transferred him to another hospital.
It took several cat scans and MRI's and spinal taps and nothing
would show up. After five weeks in ICU a MRI showed that he
did in fact have encephalitis. He was not responsive at all.
He was on a breathing machine, feeding tube and would only stare
to one side. We were all so scared and didn't know if he was
going to make it. He kept having seizers.
It all happened so fast he didn't show any signs before this,
he was walking and played like any other day. They ran several
tests to find out how he contracted it but everything came back
negative. We still do not know only that a virus caused it.
It was very frustrating. After two months of being in the hospital,
they were transferring him to a rehabilitation center in Orange
County. He stayed in rehab for about six weeks and still was
not making very much progress. He could not sit up, barely rolled
over, and was still not really responsive. We later found out
that the latest MRI showed that his brain had shrunk and that
he had lost some brain cells but they didn't know which ones.
We were discharged on Nov.27th, 2001 to bring him home. There
was nothing else they could do for him. It was like a just wait
and time will tell how far he is going to come back.
Since we have been home it has been amazing. Dylan is the strongest
person that I know. At first he was progressing slowly. Rolling
over was his mode of transportation. He sees physical therapy;
occupational therapy and we take him to a special therapy called
feldenkrais, which I would recommend to anyone, I give Elinor
most of the credit for his progress.
It is now May 2002, and he recently started army crawling, sitting
up and is attempting to pull himself up onto things. I have
such tremendous hope that he is going to be just like he was
but if not I am just happy to have him with me. He is a blessing
and I will take him anyway I get him. There is so much that
I left out but I tried to just sum it up as short as I can.
I just want to tell anyone out there who is going through this
to never give up hope and to give as much love as possible to
your child. If anyone wants to contact me, my e-mail address
is below.
Thank you,
Sheri
Huntington Beach, California, U.S.A.

Posted: May 1, 2002
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