“The only thing worse than being
blind is having sight but no vision." Helen Keller
These words mean so much to me today
and after reading this perhaps you will know why. My name is Kimberly and I have Congenital
Glaucoma and Rieger’s Anomaly (scarred cornea tissue). I was
thought to be completely blind at birth. However my Mother noticed my
responses to different color and light. Our family made our way to Kansas
City's Mercy Children's Hospital and so my journey began.
My first surgery was at six months
old to relocate my pupil in my good eye and by the age of three i had several
eye surgeries. It was discovered i had very little sight in my right but the
left eye had promise. My parents totted me to the hospital nearly every thirty
days for a checkup. In 1979 little was known about what causes my type of
Glaucoma and educated doctors were few and far between.
Fast forward 34 years, I'm now
37 years old, live is SW Florida and this past year has been one of the most
difficult years of my life. I've had three major eye surgeries in the
past two years and have become what is considered legally blind in my good
eye.
In my lifetime
i have had over 20 major eye operations, faced many obstacles one encounters with
having a disability and trudged through life like everyone else. In the past
year I've given up driving due to my vision loss. I've learned a few
things along the way and that is to ask for help, to educate myself and to be
my own advocate. My perception is to keep an open mind, to be willing to
learn and to be honest with myself and others about my experience. I've
decided that i will not let my disabilities define my existence (I also
have hearing impairment). Instead I prefer to be positive, to be
accepting of life and its opportunities. I prefer to find solutions instead of
dwelling on the problems. It isn’t always easy and how I handle things is
always the best way to go about things.
I’ve learned that reaching out to those who are similar to me. It is a wonderful feeling to know I'm not
alone with this disability and others have much to share with me. So when a friend suggested that i share my story
on a blog, I thought it was a marvelous idea.
But I have a tendency to jump into things without thinking it
through. So I thought about it for some
time and asked the advice of those closest to me and I sat still and prayed
about it. Today I decided to start my blog Vision not Sight. My hope and my vision is to share my
experience, strength and hope about being a person with visual disability.
I plan to share the information I’ve obtained along my journey and to offer the
world an insight into what it’s like to be me. If this blog helps but
just one person with a disability that it will have served its purpose.
I’ll close with another quote that
has come to be close to my heart……..
“The real problem of blindness is not the loss of eyesight. The real problem is the misunderstanding and lack of information that exist. If a blind person has proper training and opportunity, blindness can be reduced to a physical nuisance.”
National Federation of the Blind
You are an inspiration to me, Kimberly. Thank you for sharing. Keep on posting. If I ever can help you with a ride an ear to hear you share live, please don't hesitate to call.
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