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.
Sunday, January 8, 2012
Big decisions tomorrow.
Not much time but I have a prayer request. Tomorrow is the day that we will be given the surgery options. Please pray for the doctors as they meet in the morning. They will discuss my case at 10:30. 9:30 our time. We will not know anything until around 1:30,12:30 your time. Please pray that they can get all of these seizures without having to take out my motor cortex. Thanks for praying. I believe we are all fixing to witness a miracle. Just so you know. I had a great day today. I even smiled and laughed for my daddy. I'll update you tomorrow when we know the plan. Love ya, Jadon