Jadon's Infantile Spasms Story

I created this blog so that our friends and family will be able to follow Jadon as he fights to overcome Infantile Spasms. I also hope that if anyone else is going through this, they will find this site helpful. I have posted a video of what infantile spasms look like, as well as everything we are going through. I hope by posting this I am able to get help for other children who are having these spasms. The earlier this is diagnosed the better. Feel free to leave me comments. I love to hear from you. If you have any questions just email my mommy. She likes to help people in any way she can.

Monday, December 6, 2010

I'm updating from my phone so hopefully this works. I was admitted to
childrens hospital to start iv medicines to help lower my seizures. I
don't know how long we will be here. The neurologist said probably a
couple of days. I'll keep you updated. Please pray for me.
Sent from my iPhoner
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1 comment:

Unknown said...

Yes, Jadon. You are in my prayers. Catherine Esser

December 6, 2010 at 8:08 PM

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