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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 little girl with multiple disabilities brings joy to her family.

 

Our oldest child, Teagan Ravelle, is six, and the light of our lives.  We can't imagine our world without her; she means that much to us.

Teagan was born with multiple disabilities.  She is unable to see, walk, or even talk; yet she expresses herself very well, much to the amazement of other people whenever they come into contact with her.  She is definitely one of a kind.

Teagan was born with cerebral palsy that's affected all four of her limbs.  She is unable to sit up without help, and she is nonverbal, blind, and almost totally deaf.  She sits in a wheelchair when up; when down for the night she lies in her hospital bed, where she plays until she goes to sleep.

Teagan loves to do many things:  listen to music (she can hear via powerful hearing aids), listen to the sounds around her, be held in people's arms or laps, be read to, tickled, taken places.  Wherever there's people, this is when her happy, bubbly personality is most evident.

There are days where she gets grumpy; fortunately, those are few and far between.  She mainly laughs or sings in her special, silent way; for her a great big "Ahhhh!" is sufficient enough.

Sometimes our daughter gets sick (due to her inability to chew or swallow); she often ends up in the hospital with pneumonia or any other respiratory type illness.  It is always a scary time whnever this happens because we are so scared she's going to die (she's come close to dying several times, but thankfully she came back; she's still with us by the grace of God!).

She is unable to eat:  for this reason, she's fed by way of a special tube that's been placed into her stomach; we pour her nutrition suppliments (or her medications) down this tube; the stuff then goes directly to her stomach, where it's supposed to go.  We do this every four hours, day and night, without fail; this is how we keep her hydrated, fed, medicated.

We have to do this or she will die. 

Life with a child like Teagan isn't easy, but we've managed this far for six years; what's to say we won't have many more happy years together?? Only God knows the answer to that one; as long as we have her in our lives, we intend on enjoying Teagan as an integral part of our lives!

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Reviewed by Bonnie May 10/2/2008
The saying "God never gives us more than we can handle"...but sometimes I do question, how one person or one family should have so much. Sorry, this is tough. Love, Bonnie
Reviewed by Mr. Ed 10/2/2008
Your heartfelt story reminded me of young Cole who also has cerebral palsy and is helped by his faithful dog.
Reviewed by Rose Rideout 10/2/2008
Thank you again Karen for keeping us informed with the lives that others have to endure.

Newfie Hugs are on the way, Rose
Reviewed by Georg Mateos 10/2/2008
Giving up is the weakeness of the strong, never giving up is the strength of the weaks ones.

Georg
Reviewed by Michelle Kidwell Power In The Pen 10/1/2008
Teagan sounds like a very special little girl, thank you for sharing, and may the Lord bless you in your writings
In Christs Love
Michelle~
Reviewed by Mary Coe 10/1/2008
You write such interesting stories. keep up the good work.
Reviewed by Micki Peluso 10/1/2008
Dear Karen,
How I admire you for having the love and patience to raise a special child like your wonderful daughter. It takes a particular person to do this 24-7 and I can only surmise that your strength comes from God. Bless you and your sweet daughter--know you both will be in my prayers. My daughter-in-law to be has cerebral palsey but is functional and forces herself to walk by twisting her hips--she refuses to end up in a wheel chair. I am proud of her for her bravery as she just graduated college. I pray for a miracle for her and I will ask the same for Teagan.

Love, Micki Peluso
Reviewed by Sandie May Joyce 10/1/2008
I'm so glad that Teagan's parents are there for her. Wonderful write, Karen!!!

Sandie Angel :o)
Reviewed by 000 000 10/1/2008
We do not know what we have..until it is gone.There will be strength as this family struggles.
Reviewed by Carole Mathys 10/1/2008
A powerful and heartfelt write, Karen...
peace and love, Carole~
Reviewed by Felix Perry 10/1/2008
I tip my hat to the courage and fortitude, not to mention the love, that these parents have for their children.

Fee
Reviewed by Karla Dorman, The StormSpinner 10/1/2008
Teagan's family is a whole lot stronger than I could ever be ... I couldn't do it. Powerfully penned, Karen. Well done.

(((HUGS))) and love, Karla.

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