lilmanmaxsjourney blogspot.com

Little Man Maxs Amazing Journey

My son Max has been diagnosed with Bilateral Persistent Fetal Vasculature. He is visually impaired. I was inspired to start this after reading a blog by a woman named Jessica with a 3 year old son named Thomas with the same condition. After reading their story and gaining so much hope and relief from it I wanted to do the same for someone else and hope this blog about my sweet Max provides that for someone.

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Little Man Maxs Amazing Journey

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My son Max has been diagnosed with Bilateral Persistent Fetal Vasculature. He is visually impaired. I was inspired to start this after reading a blog by a woman named Jessica with a 3 year old son named Thomas with the same condition. After reading their story and gaining so much hope and relief from it I wanted to do the same for someone else and hope this blog about my sweet Max provides that for someone.

CONTENT

This web page lilmanmaxsjourney.blogspot.com states the following, "My son Max has been diagnosed with Bilateral Persistent Fetal Vasculature." We saw that the webpage said " I was inspired to start this after reading a blog by a woman named Jessica with a 3 year old son named Thomas with the same condition." It also said " After reading their story and gaining so much hope and relief from it I wanted to do the same for someone else and hope this blog about my sweet Max provides that for someone. Sunday, February 12, 2012."

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