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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.
5 comments:
Yes, Matthew also loves to climb that white chair behind him and stand up!
Is that a little devilish look our sweet little angel? You bet it is. He's got us all buffaloed - or so he thinks. How did he get from crawling to those first steps to climbing over the rocker so fast?
I love humming along to Tumbling Tumbleweed while watching him ride his Zebra. I think I remember hearing that on the Roy Rogers show a few decades ago. Whatever he is doing is wonderful to see. He definitely brightens every day of my life - even if it is in pictures for now. I need to come see him soon.
I love you. Grandma Sue
Hi Kings...
He is so big and such a handsome little man, of course! Just wanted to say hello. Nothing new in California, except school and work. Send my love to your little man!
Love,
Christine
Matthew is just so cute! Everytime I click on your blog, there are new pics of his sweet face :)
Thanks so much for sharing the info about the VCUG. . . hopefully things will go smoothly on Thursday. They also put Bray-My on Spetra last week, which I thought was weird (an antibiotic??). I'm guessing that's pretty standard based on your comments, though.
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