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.

Tuesday, June 25, 2013

Neuro appointment!!

I had an excellent appointment today. My neurologist said I'm doing great. She said I'm progressing along wonderfully. She spent about 30 minutes with us talking, asking me questions, and observing. I talked to her the entire time and she noticed how much my speech has improved. She said that she would see us in December just to monitor my progress. I can't explain to you how much joy it brings to us to go to the neurologist and get nothing but good news. Not to mention we love our neurologist at Children's, she has gone above and beyond for us. After my appointment I got to go spend time with my cousins. My Aunt lives in the New Orleans area and she has a little boy and twin girls. I enjoyed getting to swim and play with them. We also stopped at Pizza Man in Covington on my way home. We love that place. If you've never been you should go. You can watch them cook the pizza through the window. I'm leaving you a few pictures of us today. As always, thank you so much for your prayers. Your prayers have helped my family greatly.

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