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.

Wednesday, May 31, 2006

Matthew has been added to the portrait gallery of The Congenital Heart Information Network (TCHIN.org). Terri and I are members and donors to the non-profit organization and refer to their site quite often for information. Click Here to see photos and read Matthew's medical history.

1 comment:

Grandma Sue7:05 PM
Our little hero deserves to be in the portrait gallery so everyone can see his amazing story and how well he is doing. He is truly a miracle and we thank God for him every day.

He just gets cuter and cuter.

Love, Grandma Sue
ReplyDelete
Replies

Add comment

We never get tired of hearing how cute Matthew is. Go ahead :-)and tell us all about it!!

Let us know you came by.