Below is the update that my Mom wrote for KC's caringbridge page.
We are gearing up to walk through the fire yet again with Mr. KC :(
He has been having some troubles for the last month or so and they continue to get worse in spite of Mommy's best efforts to slay the dragon that keeps bothering her boy.
Among the current issues are sleeplessness, extreme mood swings, biting, hitting and scratching himself and Mommy, stuttering, talking gibberish and then getting agitated that Mommy doesn't understand, lots of ear flapping and hitting himself in the head, irrational periods lasting from 5 to 30 minutes during which he needs to be restrained to keep him from hurting himself or the closest person to him, rigidness that is getting more consistent even to include a requirement that we enter in the same door we exited. Oh, and some seizing too! The list goes on but these are currently the major issues.
Poor KC and POOR Mommy! The fear surrounding what could be wrong this time and what uncovering what the problem is will entail, is overwhelming to us all. Frustration abounds, tears are flowing, and worrying is constant.
Please pray that the wonderful doctors at the U of C will swiftly find out what the problem is and how to best solve it so our little boy can enjoy his life more consistently again.

All truth goes through three stages. First it is ridiculed. Then it is violently opposed. Finally, it is accepted as self-evident . Facts are stubborn, and refusal to accept them does not avoid their inexorable effects-the tragic consequences are now upon us - Hellen Keller. The time has come for everyone to step up and be an advocate for our children. It is no longer enough to simply ask questions. We need to demand answers.
Showing posts with label Sensory Processing Disorder. Show all posts
Showing posts with label Sensory Processing Disorder. Show all posts
Sunday, November 8, 2009
The Caringbridge Update...
What is this post about?
Autism,
Infantile Spasms,
Sensory Processing Disorder
Tuesday, August 18, 2009
Is there blood on your hands?
Sorry I haven't posted in a while.
I don't know why....
No energy for the fight maybe? That's a cop-out and I know it, but it is what it is. I lost it somewhere between therapy sessions, and follow up EEG's, and trips to Detroit, and meetings with specialists.
I'm struggling to get it back...because I need it.
I have six months worth of excitement, progress, fear and heartache inside, all bottled up. So I'm workin on it. I updated some things, such as my profile. It's a start anyway.
In the mean time, check out this post from a fellow blogger...
either copy and paste below OR just click on my title "Is there blood on your hands?"
http://crystaldavidsonengler.blogspot.com/2009/08/1-in-100-when-will-you-listen.html
Love the message...and the graphics!
For now...
Karen
What is this post about?
Autism,
Sensory Processing Disorder,
Vaccines
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