Wednesday, December 13, 2006
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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, he will love these pictures when he gets bigger. Well, I love every picture and getting to see every thing he does every day. I guess I could say it's the next best thing to being there, but I'm hoping it won't be too long before I can come see him very often.
I love you Matthew. Grandma Sue
Now this is a typical look that Matthew is famous for. That lower lip of his juts forward when he is up to something... perhaps splashing the camera??? Ha Ha You hardly even notice his Mickey Button. It is just a part of Matthew. I still wish my kids had one. Giving Matthew his meds is wonderful. I use to wear half of my kids vitamins.
You would never know to look at this "hunk" there was ever a thing wrong with his precious heart. Stay tuned for the results of all the tests he went through this past week. Please pray to God that he won't be needing a third heart surgery any time soon.
I am happy to see others starting to add comments to Matthew's blog. He loves to hear from his "Prayer Warriors". hint, hint.
Love my sweet baby, grandma w
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