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, May 31, 2011
Getting admitted in the morning.
I'm getting admitted in the morning to Children's Hospital in New Orleans. They are going to do the 5 day steroid treatment. My seizures started increasing Sunday and they haven't slowed down. My neurologist wants to go ahead and try the steroid treatment. Please pray for me. We would love for this to stop these seizures. We know God has a plan and we are just trusting him right now. I will keep everyone posted while I'm in the hospital. Thanks for praying. If you can say a prayer around 8:30 in the morning. That's what time we have to be there. I'm leaving you a picture of me sleeping with my big brother. I'm sure going to miss him this week. Talk to ya soon. Love you all, Jadon