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, March 25, 2013

Epilepsy Awareness!!

Epilepsy awareness day is tomorrow and I'm asking all my friends and family to wear purple to support epilepsy awareness. I'm so thankful that I no longer have epilepsy but as all of you know epilepsy has left its scar on me. I will never have 100% function of my right hand because I no longer have my motor cortex that controls movement on that side of my body. This is all side effects of my brain surgery that I had to have to save my life. We will never complain because we are truly grateful that I'm no longer having seizures daily. Oh and I can tell you that I give the best one handed hugs around :) I pray that one day there will be a cure for epilepsy so that none of my friends have to suffer another seizure. Until then I will do my best to tell my story and to spread epilepsy awareness. Thank you all so much for your support. I love you all!!! Jadon

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