We have created this blog to help keep all of our family and friends updated on Pearson's progress as he begins to take his first baby steps in life. As most of you know, Pearson has a birth defect known as CDH and will have to overcome many challenges over the next several months. We thank you for visiting our blog and encourage you to leave comments as often as you would like. We look forward to hearing from you!
Thursday, March 31, 2011
CDH Awareness Day!
Today is CDH Awareness Day!!! I would love for you all to say a special prayer today for all the families who are fighting or have fought this terrible illness! These kids are very special!!!
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So typical of you and Matt... to think of everyone else fighting a CDH battle on this very Special Day of recognition. The selflessness of the two of you just never ends. As you watch your very own Child fight for his Life on this Day... you are still thinking of others!!! However I know we are one of the few fortunate to have a Dr as SPECIAL as Dr Kays who has a sixth sense when it comes to these Babies. Not only do we Praise our God for the many Blessing but we need to lift up our Dr Kays who has undoubtedly been given a Gift from God to give these Children a chance at Life! So to reiterate the CDH Awareness Day on this March 31,2011... I would ask that everyone would take a moment to lift up their Dr's, Nurses and everyone involved who make it possible for those of us to have each day with our most Precious Gift of Life... These Children!
ReplyDeleteLove, MaGa (Grandmother to Pearson)