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, September 6, 2010
I will never understand.
I will never understand why children have to get sick. I will never understand why a seizure medicine can have the opposite effect. I will never never understand why so many children have to suffer from sickness. I will definitely never understand why God needs a child in heaven more than a mother needs her child. Yesterday our Amite family lost a beautiful, brave, and loving little girl. She was one of the bravest people I know. I am asking that you please pray for this family. I can't imagine the heartache they are going through. They need strength right now. Also pray for this little girls friends. Friends shouldn't have to lose friends at such a young age. Though I will never understand these things I know God has a reason for them. I also know that God received a beautiful angel yesterday. She is now pain free. So today I'm leaving you a picture of this beautiful little girl and her family. Please pray for them. Caroline you will never be forgotten. You touched many lives while you were here. Rest in peace beautiful girl.