I'm a little biased, but I think he is perfect!!!
4/05/2009
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The mission of the Trisomy 18 Foundation is to improve the lives of families who receive a Trisomy 18 diagnosis for their child through national leadership in research, education and support, and advocacy. We have a vibrant online community of families supporting each other and a growing list of educational, research and legislative advocacy initiatives.
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- Just a nobody telling everybody about Somebody that can save anybody.
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4 comments:
To Michael Z's family! God bless you on the birth of your PERFECT little boy. We know that this is truly perfection. I can say this because I am the mommy to Annabel born and still living with Trisomy 18. I will be keeping up with your wonderful story and praying constantly for Michael and his strength. We found you on Zoe's blog.
He IS perfect and the most beautiful little face. Praying so hard for little Michael, that he proves to be a warrior and honor His God. I continue to pray for him and for all of you in this new journey. May God receive all the glory.
Love and Hugs, Laurie
He is beautiful. I will be keeping baby Michael Z. and your family in my thoughts and prayers.
He is BEAUTIFUL. I am a follower of the Bat Blog and have been following your story. Many prayers for Michael to prove the medical community wrong.
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