I want to share with you some of the faces of heterotaxy and what this disease brings to different families. I am lucky that God has blessed my family and with a good prognosis. But, they are families out there who need your prayers too. They are happy and sad stories behind ever corner of the blog. No two children are the same and each child severity of illness is different from the next. Please take the time to read their blogs noted below.
http://noahsteven.blogspot.com/
http://sophiespleen.blogspot.com/search?updated-min=2007-01-01T00%3A00%3A00-06%3A00&updated-max=2008-01-01T00%3A00%3A00-06%3A00&max-results=25http://walkinglunaticfringe.blogspot.com/2008/02/i-heart-u.html
http://fourtran.com/2008/01/18/post-glenn-day-1/
http://morningramble.blogspot.com/2008/02/update-on-mei-ling.html
http://absolutegray.blogspot.com/2008/01/my-big-girl-turned-5-today.html
http://chicagobensons.blogspot.com/2008/01/we-have-diagnosis.html
No comments:
Post a Comment