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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.
3 comments:
The look in Matthew's eyes clearly say, "bring it on, mom". Ha Ha
"I can take ya"! Let the games begin...... Ha Ha Love you my little "rocky". grandma w
There is definitely a challenge in his eyes.
Sometimes I wonder...
AM I EVER GOING TO GET THIS KID TO EAT?? I'm not having much luck..
I am able to get a bit in his mouth..
but most of it ends up all over his face, in his ears, nose... the highchair. He has quite the oral aversion.... who would ever think that a kid wouldn't want to eat or drink! I know a "heart" mom who said her boy didn't eat until he was about 3 years old.... he's 4 now and just had the G~tube removed. I'll just keep on plugging along... I'd like to quit those night feeds...
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