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Karen Lynn Vidra, The Texas Tornado

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     Young Lucas, who has fibrodysplasia, and his family cope with his condition as best as he can, given the circumstances.

Image (C) 2009, Karla Dorman.

Lucas Drake Ibbotson is my name.  I live in Carlsbad, New Mexico, with my family.  I am eight years old.  I have two sisters, who are older.  Their names are Larkspur and Kiera, and they are ten and thirteen.  I'm eight, as I just said.

I am not like most kids.  I have a disease that is causing me to turn into stone.  I fell off a slide when I was three years old, and for some weird reason, my body went nuts.  You know how your body heals after you break a bone?  Well, that's how it is with me:  my body keeps "making" new bone, and for some reason, it can't stop.  For this reason, I have a lot of trouble walking or moving around, and I'm often in a lot of pain.  It's no fun having this disease; it's really a pain!

The disease I have is called fibrodysplasia ossificans progressiva, but that is way too hard for me to say (or spell), so I just call it FOP for short.  It's a lot easier that way.  Anyway, most people have never heard of it, and most kids don't understand why I hurt all the time or have trouble getting around.  Eventually, I might need a wheelchair, but for now I can walk.  I just wish I could run around like my friends; I hate not being able to play baseball or football with them!

While my friends are running around outside, I'm usually doing something like reading a book, playing on my laptop computer, or writing stories or poems.  I'm a very good writer.  I'm also a very good speller.  My mom and dad tell me I'm very smart.  I had to become smart, so I could learn all about this disease that I have, this FOP.

My disease will eventually kill me, as more bone grows and develops.  Every month, I have to see my special doctor, to see how I'm doing, to see if any more bone is growing inside me.  Sometimes there is, but often times, there's not.  When there's new bone, I get worried because if I get too much, it could crowd my heart or lungs, and it would kill me.  I'm only eight years old; I don't want to think about dying at such a young age!  I'm only a little boy!  I should be thinking about what I want to do in life, not thinking about my funeral or how I am going to die!!

The reason I can't do a lot of running around is because I could fall, and that could make the bone in my body grow faster.  So I have to be very careful and watch what I do.

I stay still so I don't fall and die sooner than I'm going to!  If I fell, that would be bad.  That would be very bad!!

Larkspur and Kiera are very patient with me, but they sometimes say I drive them crazy.  Well, what about them?  Sometimes they pick on me or call me names like "Squirt" or "Maggothead", which I don't like!  When they do this, I smack them one or tell them to leave me alone, but most of the time, we get along good.

Well, we gotta eat and get ready for church, so I will go for now.  I will write in here again; if not, my mom or dad will.  Until then, this is your friend, Lucas Ibbotson, saying so long!  God bless!

~Lucas Drake Ibbotson.  :)

*to be continued.* 

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Reviewed by Karla Dorman, The StormSpinner 2/8/2010
Sadness, yet courage, in these lines, Karen, well done.

(((HUGS))) and love, karla.
Reviewed by Michelle Kidwell Power In The Pen 2/8/2010
Its hard for a child to deal with the fact that knowing they have a condition that will evnetually kill them but the Lord is able
In Christs Love
Michelle~
Reviewed by Margaret Mullings 2/7/2010
Karen this is a very heartfelt moving story of hope
because God is able, and prayer changes things. Thank
you so much for sharing..written with excellence!



Much Love,
Margaret
Reviewed by Rose Rideout 2/7/2010
Poor little guy don't really have too much too look forward to other then work on staying alive, very, very sad indeed Karen.

Newfie Hugs are on the way, Rose
Reviewed by Mark Lichterman 2/7/2010
What a story for such an unknown, deadly disease. This boy, this Lucas sounds like one hell of a good kid and I can only hope for the best that his life can offer.
Your friend in Southern California, Mark
Reviewed by Emile Tubiana 2/7/2010
Dear Karen Lynn, This is a sad story. I hope that none of your kids have this disease. I pray for all the kids who have such a disease that the cure will be found soon. Love Emile
Reviewed by Paul Berube 2/7/2010
Quite the informative update, Karen. Very sad too. God bless.
Reviewed by Georg Mateos 2/7/2010
After the economic debacle, one would have thought that the people holding the strings of the purse will think other thoughts, the ones that not go all off to save banks and arm dealers, but go to the rescue of researchers looking for a cure. Then again, doctors and hospitals wouldn't want it to happen, do they?

Georg

Reviewed by Cindy Tuttle 2/7/2010
I hope some day they find a cure for this. I can't imagine what that would be like for a child and their family.As always you imform us in a very creative way about challenges people have. Thank you Karen.
With Love,
Cindy

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