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My name is Van Brown, I'm 44 years old and from Alabama.
I contracted Guillian Barre' Syndrome in September 2000 (one
week before my 42nd Birthday).
My story begins in the gym on a Friday afternoon. I walked
3 miles at lunch and returned to the gym after work for my
afternoon gym time. At 41, I was healthier than I'd been in
years. I cared for elderly family members for years and following
my Grandmother's passing, and a bout with a ruptured disk,
swore it was my time and I'd make the most of it. I looked
and felt better about myself than I had ever felt.
The night before my onset I was very restless and couldn't
sleep, come to think of this the entire week before the onset,
my sleeplessness became more and more. I'd traveled Labor
Day weekend, and like my companions, gotten a sinus infection.
My ENT prescribed antibiotics and a steroid the previous Monday
and of course, the seasonal allergy shot.
While lifting weights I became very fatigued and headed home
early, as I really felt some oncoming weakness. The trip home
was very strange and my driving skills became increasingly
poor. As the evening progressed, my hands become numb and
I had a rough time in the shower raising them above my chest.
I'm not much of a drinker and always had numbness after a
glass of wine, so, at first, I laughed it off. My housemate
returned home at 10:30pm and I told him something strange
was happening to me. Throughout the night my trips to the
bathroom became abnormally frequent and my inability to walk
increased.
The following day, I seemed to be a little better and thought
this weakness just a reaction to medications. At the advice
of some physician buddies, I stopped taking any medications.
Walking became more difficult and eating/holding a cup became
almost impossible. The following morning I could no longer
bathe myself or walk without help. I panicked as I knew the
medications should be weakening after 10 hours. I was admitted
to a local emergency room and within an hour, informed I had
the beginning symptoms of Guillian Barre'.
The emergency room physician listened and questioned me on
every statement. He didn't have much bedside manners and without
much concern informed me what he thought I had and what I
should expect to happen. I wouldn't trade him for the friendliest
doc in town today. A neurologist was called in and before
a definite diagnosis could be made using the spinal tap, she
started the treatments of plasma drips which would last for
5 days.
The longest 6 days of my life were spent in that Critical
Care unit. I saw first hand the helplessness my family must
have experienced during their illnesses and my only comfort
was that they never feared that they would be taken care of.
Thanks to some very quick thinking doctors for starting treatment
so quickly and a healthy body, I was only paralyzed for 5
days.
The 3 months of outpatient therapy that followed are somewhat
of a blur. I was transported to a rehab hospital a week later
and spent a while there. I learned to walk with a walker,
dress and feed myself, and the hardest thing of all, look
in a mirror to view what had been a healthy 41 year old who
became a very old 42 overnight.
I returned to work one week before Christmas. I made it for
the planned trip to Ft Lauderdale for New Year but as a different
person.
I've left a lot of baggage behind now and I live for today
and not tomorrow. As of June, my doc says I've made a complete
recovery, well physically anyway. Recovery has been ongoing
for the last 3 years. I'm 95% well today.
I've never been a very competitive person. I attribute my
nearly complete recovery to my physical condition at the time
of the onset and to a quick thinking emergency room doctor
who had a very good prognosis within the first hour in the
hospital emergency room. As fate would have it, he contacted
a Neurologist who was also quick thinking, she began the treatments
even before complete testing was done as I entered the hospital
on Sunday and most tests couldn't be run until the following
day. She was also 9 months pregnant. I remember praying the
baby wouldn't come before she got me through my week in intensive
care!
I do realize just how very fortunate I've been as I read
testimonials from others recovering from GBS. My illness can't
compare in length to many of you, but the trauma has been
just as great. I remember so clearly struggling with using
my fingers, awakening of my toes, the Frankenstien walk,and
the terrible depression which outlasted the physical aspect
of the illness.
I've learned how quickly your health can be taken from you.
Physical healing can be seen by the eyes but emotional healing
is long felt by the heart. My life has been forever changed.
I still catch myself watching my feet move in amazement or
practice my finger exercises I learned as a little boy and
relearned as an adult to help in coordination. I know there's
always the possibility of return and each day that goes by,
I wake up and say a little prayer when my feet touch the floor.
To each of you who are healing, have healed, or trying to
resolve the emotional issues that come with this illness,
my prayers are with you. There is healing in time.
Looking back, I never realized just how sick I was. Sometimes
I think the brain allows us to filter emotions and helps us
not deal with issues in order to act as a buffer. As a caretaker
for 3 elderly relatives during my younger years, my most dreaded
fear was such an ordeal as being paralyzed. Those same fears
allowed me to take comfort and learn to let go of control.
I would be most grateful if relaying my experiences with someone
would assist in their recovery.
If I could share one thing which attributed to my success
in recovery, it would be that I was told early in my recovery
stage that I should actively work hard in rehabilitation as
I would make the most significant recovery within the first
3 months. The physician in charge of rehab felt that after
that time recovery would be more difficult, and that very
likely after 3 months I'd probably have to live with weaknesses.
I'm not sure if that is truly the case as I've been recovering
for 3 years, but I do know it provided me with much determination.
I'm currently working out 6 days a week, and you'd never know
I had such an unusual disheartening illness.
Thanks for the opportunity to tell my story, Sharon.
Van Brown, GBS 09/00
06.2003
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