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One boy's long road to recovery. Matthew was born two months premature with a rare fourfold heart defect known as Tetralogy of Fallot with Pulmonary Atresia and MAPCA's, and Ventricular Septal Defect. He's had two open heart surgeries and will need additional heart surgeries in the future. To appreciate the absolute miracle of this "3 plus million dollar boy", you'd need to look into the "Archives" beginning after his first 9 hr open heart surgery at Stanford, August 2005.
2 comments:
Oh, how cute is that! What a smile he has for his new friend.
I love you Matthew.
Grandma Sue
Terri, Mike and MATTHEW "the KING ANGEL", Kim & Janet:
Just wanted you all to know what a fantastic and thorough job you and
Kim and your Mom are doing on the Blog and the Nannigrams!
YOU WILL RECEIVE YOUR REQUESTED MIRACLES! BELIEVE! Too many people PRAYING and GIVING THANKS TO GOD FOR ALL MATTHEW HAS ECEIVED AND WILL GET IN THE FUTURE!
He and all of you are always KEPT IN PRAYERS! GIVE GOD THANKS
FOR WHAT HE WILL GRANT UNTO YOU - ALL MATTHEW NEEDS!
Our Grandson MARK is 16 yrs. old now after his "hard start" and is Our Blessing!
Prayers & Love, Sandy Parker
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