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It was May 2, 1988. Life was a bed of roses for me. I was a successful sportswriter-
columnist, I had just bought my first home and I was only 28-years-old.
I was the only bilingual sportswriter at the city's main news-paper in New
Orleans, La. and that gave me a tremend-ous advantage in the department.
I was ready to take on the world. Unfortunately, fate dealt me a hand that
I didn't expect.
The day I was moving into my "new" home, I fell ill. While I was moving the furniture
into the house with a friend, I began to feel the chills, headaches, aching
in my bones and since we were close to a hospital, my friend suggested that
we go there to see what they thought. Initially, they gave me a quick routine
exam and de-termined that I was coming down with the flu. They gave me two
flu antibiotics and I was promptly released.
That night, I slept in my new home for the first and only time. The following day, I was awakened by the sound of my doorbell. I got up from my bed to answer the door and when I opened it, I collapsed. I had experienced the first of what would become hundreds of seizures up until this very day. The person who rang the doorbell called an ambulance and I was taken to a nearby hospital, where I was kept under observation for six weeks.
Anyone familiar with this illness knows the routine: MRI's, EEG's etc. At the
beginning, the neurologists weren't sure if I had meningitis but finally
I was diag-nosed with viral encephalitis. I had violent grand mal seizures
during that first six-week period and it got so bad that I had to be restrained
in a strait jacket. Finally, after a month and a half, I was released.
But I walked out a different man into a different world being viewed as a different person, whether your friends want to admit it or not. I bear no grudges because it's difficult being with someone not knowing when or if they will have a violent spell in public. Perhaps that's why only about two of the many friends I had prior to my virus are still in contact with me today. It's as if you've returned into the infancy stage. The first five to six years are the most emotionally trying, more so for my family than for myself.
My employers gave me every opportunity to return to work after about three months. But that experiment lasted for only three months. But I continually made errors in my stories and repeatedly had seizures in the office. I was an award-winning columnist prior to my illness. Finally, I was called over by the sports editor: "Mario, we need to talk". I responded by saying that there was no need for that conversation; that I was surprised the paper had kept me on for as long as they did. "We've always liked you and we were all hoping you'd improve...now, we just don't know how long this is going to go on." I said that there was nothing left for him to say, and that I understood completely.
Well, it's been more than 21 years now and I've been living with my wonderful mother since my illness began. The first 14 years, my mom was fortunate enough to still have my father to help her with the enormous burden of my seizures. Since my dad died in 2002, my darling mother - who's almost 77 now - has been carrying the crux of my problem although my sister has been a tremendous help despite having a family of her own to raise.
My situation has improved somewhat these last few years although I continue to
have the spells, can't drive and well, have been stripped of everything
that con-stitutes a person's independence. I've been a virtual prisoner
in my own body although I realize I have soooo much to be grateful for.
I still have a virtual pharmacy that I take twice daily for my seizures.
I don't have them as often or as intensely as I did those first five to
seven years. If you see me on the street and talk to me, you'd never guess
I have a disability.
My speech isn't as slurred as it was during those early years but my memory continues to be a big problem (the medication I imagine). But after reading many of the stories on this web site, I simply thank God that I'm alive and that I have a wonderful family to support me. Thank you so much for the opportunity for allowing me to share my story with you.
Mario
Louisiana, U.S.A.

Posted: April 16, 2009
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