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.

Sunday, August 15, 2010

Newspaper Article

Below is the article that will be in the newspaper. Just wanted to share with all of you.



Thank you to those who came out to support my cause last Saturday at Snow King, to those who donated to me personally, and to those who donated through my fund. Your generous donations will help in my journey to get well.I am very blessed to have so many people who love, care, and pray for me. I will travel to Boston Children's Hospital at the end of September. The out-pouring of donations will help me and my family with travel and medical expenses. My family and I could never thank you enough for all of your support. Thanks again for making my fundraiser a huge success!! Jadon Pailet
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