Thursday, December 29, 2005

Matthew can almost sit up on his own.

1 comment:

Grandma Sue said...: What a big boy! He is growing up so fast.

I love you. Grandma Sue; 5:15 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.

Thursday, December 29, 2005

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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