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Karen Lynn Vidra, The Texas Tornado

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Karen Lynn Vidra, The Texas Tornado, click here to update your pages on AuthorsDen.




     A young preteen copes with living with epilepsy. His mother tells his story.

My son, Jeremy Micah, looks like any other thirteen-and-a-half year-old:  tall, thin, almost to the point of being too skinny (due to his height), long, dark-brown hair that falls into his eyes, and rather gregarious in nature at times.  One minute he can be very sweet and loving; the next, he tests your patience with his attitude.

He loves to do many things:  read, draw, create games on his computer, skateboard, swim, and hang out with his friends; however, one thing sets him apart from most kids his age, in particular, his friends:  he has epilepsy.

He has had epilepsy since he was two years old, after he fell off a kiddie slide and landed on his head.  He was briefly knocked out and didn't appear to be too terribly injured (much to our relief), but shortly after the incident, he'd fall down without warning and start shaking all over.  It was terrifying to see.  We immediately rushed him to the ER after the first episode; we went back there several more times, to see if there was anything anyone could do to help him.

After extensive testing was performed, doctors informed us that Jeremy had epilepsy.  The news stunned us because up to that point, he had been exceedingly healthy, unlike his younger brother, Colby Shane, who was always going to the Emergency Room for one thing or another. 

We could picture a boy shaking uncontrollably in a seizure or a boy who wouldn't be able to get a job because nobody would hire him once he became an adult:  he'd live out the rest of his days at home as a recluse, friendless, alone, depressed.  It was awful!

Yet the doctors gave us hope:  they said that there were medications on the market that could control the seizures, or if not, at least, keep them to a minimum.  He could work once the medications took effect and once the side effects could be curtailed.  He could have a very happy, normal life and live it out as any other child.

It's been 11 years since that fateful diagnosis, and while he has experienced some seizure-related episodes in the past that required a trip in an ambulance to the hospital, he has otherwise done whatever he wanted (excepting for contact sports, of course, as any blow to the head could make his epilepsy worse).

Nothing has really stopped Jeremy Micah.

We have tried to treat him like a normal child all these years.  It's worked wonders (for the most part, excepting for when he springs one of his attitudes).  We don't let him get away with anything just because he has a condition that could seriously curtail his life if we let it. 

Now if we could only do the same with Colby Shane, his younger brother, who, at the age of nine, is a walking accident-waiting-to-happen ...  

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Reviewed by Patrick Granfors 1/8/2010
Thank goodness for the medications! Patrick
Reviewed by Carole Mathys 1/8/2010
Thank you for writing with a sensitive pen about a loving family with a couple of health issues, but what family doesn't have some type of problems...well done, Karen
peace, Carole~
Reviewed by Georg Mateos 1/8/2010
I have read so much about stem-cells applied directly to the brain for Epilepsy, Parkinson and other ailments with fantastic results that I can't understand why the condemnation about researching and using it!

Georg

Reviewed by Mary Coe 1/8/2010
Well done!
Reviewed by Cindy Tuttle 1/7/2010
They seem like wonderful parents. Another story helping us realize the struggles familes have when they have a child with a disabilty.Thank you Karen.
With Love,
Cindy
Reviewed by Michelle Kidwell Power In The Pen 1/7/2010
This is an excellent write, thank you for sharing, I truly enjoyed reading this story
In Christs Love
Michelle~
Reviewed by Karla Dorman, The StormSpinner 1/7/2010
A sensitive, beautiful write of a boy living with a disability instead of being lived by it. Well done, Karen!

(((HUGS))) and love, Karla.
Reviewed by Paul Berube 1/7/2010
Having had suffered from Epilepsy myself for over 13 years, I can appreciate this story, Karen. More people need to be aware of this little spoken of, treatable, and even curable disease. Mine was cured through radical brain surgery is January of 2001.

Well done, my friend and may God bless.

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