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, January 2, 2012
Tomorrow is the day
We are leaving for Detroit tomorrow. I can't believe it is already here. I really don't have much to say because this is starting to feel like a dream. Anyway we are having a prayer send off tomorrow at 2:00 in the parking lot at house on the rock. We would love to see you there. I'm very excited that the community can all come together as one and pray for me. It's awesome and I can't wait to see everyone before I leave. Well I'll update you once we get to Detroit. Right now I'm going to snuggle with my mom in the rocking chair while she holds me just a little tighter tonight. Thanks all of you for your prayers. I can't believe how many people are praying for me and how many people truly love me. Love you all!!! Jadon
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1 comment:
I can't be there for the send off, but KNOW that I am there in spirit. I L O V E you guys and pray that this surgery will be a huge success for Jadon and your entire family.
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