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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:
Matthew will never be able to get away with any kind of mischief with "those" facial expressions of his. He loves to play with his buddy Quixa who is so unsuspecting of any mischief in the planning. LOL love you sweet baby
He is so darn cute and such a big boy. I got the surprise of my life on Saturday when my sister had a 65th birthday party for me and the "guest of honor" was Matthew Michael King. He brought along his Mom and Dad also. They were out of site in the back yard and I walked out there I couldn't believe my eyes. It was the best birthday present I could have asked for.
Leo took some pictures and hopefully Michael will be able to put some on the blog. They are just kind of a roaming view of the whole family, instead of some posed family shots.
Then we went to breakfast on Sunday with Johnny, Cheryl and Aly and I got to hold Matthew the whole time. It wasn't hard to choose between a waffle or our little hero. Who needs food when you are being entertained by such a little doll.
He showed off big time. I'm sure Grandma Wright can attest to that. I'm thinking maybe she taught him some of the cute things he does.
Love, Grandma Sue
Hi, my name is Julia and I found your blog through Wisdom Heart's blog. Our son was born with TGA and corrected at 2 weeks of age. I enjoy meeting new heart families and reading about the amazing courage of these kids. Your son looks amazing! :) You are welcome to stop by my blog if you like (just fun stuff with some update on my son, and other), his story is on my side bar. I would love to link to your blog in my heart kids link section if that would be okay.
What an amazing story you have shared here of your son! My name is Sarah and I found your blog link on Miles Suggs blog. My son was born with Tetralogy of Fallot and is now 2 1/2 years old. These heart kids are so amazing! I also keep a blog and would love to link yours to mine, if that is okay let me know. evanbraveheart.blogspot.com
Thanks,
Sarah - Mommy to Evan
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