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hopeforcj.blogspot.com

Christopher's New Journey

This is a blog about Christopher's new diagnosis. We want to update our family, friends and other families we have connected with that have injured children or a child with a rare disease. I am hoping this blog will help all understand what it is like to be blessed with such a child.

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Christopher's New Journey | hopeforcj.blogspot.com Reviews
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This is a blog about Christopher&#39;s new diagnosis. We want to update our family, friends and other families we have connected with that have injured children or a child with a rare disease. I am hoping this blog will help all understand what it is like to be blessed with such a child.
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Christopher's New Journey | hopeforcj.blogspot.com Reviews

https://hopeforcj.blogspot.com

This is a blog about Christopher&#39;s new diagnosis. We want to update our family, friends and other families we have connected with that have injured children or a child with a rare disease. I am hoping this blog will help all understand what it is like to be blessed with such a child.

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hopeforcj.blogspot.com hopeforcj.blogspot.com
1

Christopher's New Journey: July 2010

http://hopeforcj.blogspot.com/2010_07_01_archive.html

This is a blog about Christopher's new diagnosis. We want to update our family, friends and other families we have connected with that have injured children or a child with a rare disease. I am hoping this blog will help all understand what it is like to be blessed with such a child. Monday, July 5, 2010. Hope Everyone Had a Happy 4th of July! We had a great day! Then I had family over for a BBQ. Nana babysat and my husband and I went fishing! He bought some bait and it was a total surprise! Http:/ www&#...

2

Christopher's New Journey: Cj's 8 years old!

http://hopeforcj.blogspot.com/2011/06/cjs-is-8.html

This is a blog about Christopher's new diagnosis. We want to update our family, friends and other families we have connected with that have injured children or a child with a rare disease. I am hoping this blog will help all understand what it is like to be blessed with such a child. Friday, June 3, 2011. Cj's 8 years old! I can not believe Cj. Is eight years old and Ryan is six. He had the best time at his Birthday party, the best party yet! As you can see, Ryan now insist. It's a dream, but you can dre...

3

Christopher's New Journey: August 2010

http://hopeforcj.blogspot.com/2010_08_01_archive.html

This is a blog about Christopher's new diagnosis. We want to update our family, friends and other families we have connected with that have injured children or a child with a rare disease. I am hoping this blog will help all understand what it is like to be blessed with such a child. Thursday, August 26, 2010. HERE WE GO AGAIN :(. I am so worried about him! Last Wednesday I noticed he was really working his mouth with his tongue and his loose top tooth! Labels: HERE WE GO AGAIN :(. Monday, August 16, 2010.

4

Christopher's New Journey: A DREAM COME TRUE!

http://hopeforcj.blogspot.com/2011/11/dream-come-true.html

This is a blog about Christopher's new diagnosis. We want to update our family, friends and other families we have connected with that have injured children or a child with a rare disease. I am hoping this blog will help all understand what it is like to be blessed with such a child. Friday, November 4, 2011. A DREAM COME TRUE! He always giggles and beams when I say "Who knows, maybe you will be the president of the USA someday.". So watch out world! November 5, 2011 at 8:33 AM. So very happy that you ha...

5

Christopher's New Journey: April 2011

http://hopeforcj.blogspot.com/2011_04_01_archive.html

This is a blog about Christopher's new diagnosis. We want to update our family, friends and other families we have connected with that have injured children or a child with a rare disease. I am hoping this blog will help all understand what it is like to be blessed with such a child. Wednesday, April 27, 2011. I must tell you, I am still overwhelmed with happiness about Cj's IEP meeting! I wish my husband was there. Chris was at work, as I usually do all the talking! Past IEP's were not that bad, I've be...

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Our ABR Journey | Kellys Corner

https://pittsburghkellys.wordpress.com/2011/01/06/our-abr-journey

The comings and goings of the Kellys along with our ABR Journey With Ryan. Laquo; The Whole Testa Gang! January 6, 2011 by pittsburghkellys. On March 14, 2011 at 1:34 pm. Hi Sue, I remember you from Canada. Ryan was walking so well in the video clip a few years back! Wow, I bet he is doing much better now. I am also happy he is doing so well on the Dynavox! Funny about the girl, watch out! I can’t wait for Cj to start using the Dynavox! I would love to see Ryan walking now! You should post a new video!

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