Sunday, July 02, 2006

In addition to showing off his burgeoning standing skills, Matthew has also begun grabbing everything that interests him...

1 comment:

Grandma Sue said...: You can tell by the look in his eyes that he's getting ready to get Terri's nose - and he did!

My gosh, what a difference a year makes. I remember our little flag waving hero from last year. Now he is almost standing up. God has been good to all of us.

I love you. Grandma Sue; 10:07 PM

Matthew's Blog

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.

To view more pictures of Matthew while at Stanford, you can expand the year of 2005 by first clicking on the arrow, then the month. He was at Stanford from July thru September of 2005. Matthew was transferred back to Sunrise hospital where he stayed until the end of October 2005.

His second open heart surgery at Stanford was March 16th of 2006.

We've been told he'll need a conduit change, on average, every three years. We are hoping technology will be on our side.

He's our amazing little soldier boy. Our miracle.

Sunday, July 02, 2006

1 comment:

Matthew's Blog

First picture

Day of birth ~ May 10th, 2005

Day of first surgery ~ July "05

After first surgery

Chest was just closed

BiPap mask

Getting ready for second surgery

After second surgery

Leaving Stanford after second surgery

Happy Days

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