...Meets girl? (Played by the beautiful Ali Hazelwood)
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2 weeks before he was born ~ we did not know of his defect until he was 4 days old
4lbs 1oz ~ born at 32 weeks
"Unifocalization" ~ 9 hours by Dr. Frank Hanley
Chest was open for 4 days ~ hence the gauze on top
Still on a ventilator (remained on vent for another few weeks)
Mask would assist him to breathe in and out
Waiting for the surgery team to take him off
And still he smiles...
Happy day ~ Look no oxygen!
So much to be thankful for!
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.
First picture
2 weeks before he was born ~ we did not know of his defect until he was 4 days old
Day of birth ~ May 10th, 2005
4lbs 1oz ~ born at 32 weeks
Day of first surgery ~ July "05
"Unifocalization" ~ 9 hours by Dr. Frank Hanley
After first surgery
Chest was open for 4 days ~ hence the gauze on top
Chest was just closed
Still on a ventilator (remained on vent for another few weeks)
BiPap mask
Mask would assist him to breathe in and out
Getting ready for second surgery
Waiting for the surgery team to take him off
After second surgery
And still he smiles...
Leaving Stanford after second surgery
Happy day ~ Look no oxygen!
Happy Days
So much to be thankful for!
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.
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.
Blog Archive
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2006
(680)
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August
(30)
- We've recently had several requests to link Matthe...
- After his bath, Matthew and I enjoyed some cuddle ...
- When Matthew is in such a good mood it is hard to ...
- Last weekend we traveled to California for Grandma...
- ...Meets girl? (Played by the beautiful Ali Hazelw...
- It makes for great pictures. But, would there be m...
- Here Ali looks as if she wants to massage Matthew'...
- ...Turned into a full on hair-pull. Ali grabbed an...
- When all the adults ran over to intervene on Matth...
- Summer, the Hazelwood's loyal companion, came over...
- Matthew was enamored with all of Ali's toys. There...
- "What? You want me to share? With a girl?"
- Matthew was recently featured on professor Elizabe...
- A friend from Stanford posted this on her carepage...
- This morning Matthew took the time to "stretch out...
- Matthew is very close to being able to pull himsel...
- After all that hard work, Matthew needed a little ...
- Once recharged, Matthew was ready for some push-ups.
- When bedtime came, Matthew was still ready to play...
- "Peek-A-Boo"
- "I see you."
- Matthew was reaching for the camera as if to say, ...
- When Terri makes a "roar" sound, Matthew belts out...
- Today, our "Man about Town" attended Luke Daynes' ...
- While steadying themselves at the coffee table, Ma...
- Luke couldn't wait to show Matthew the features on...
- Luke was also born with a heart defect. We met the...
- While Matthew still doesn't crawl or walk, he has ...
- Hey little Mister, the song says, "With a knick-kn...
- In the end Matthew picked the newest and most inte...
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August
(30)
3 comments:
There she is, Miss Hazelwood. We all said what a darling little girl she is, but Daddy Johnny wants us to refer to her as a baby for just a little while longer. She is growing up too fast for him. Johnny & Cheryl have a beautiful little princess and they are great with her.
By the way, Happy Anniversary to Johnny & Cheryl - August 24th, right?
Love, Susan (Grandma Sue)
Ali is a beautiful "little Princess". You are right to enjoy your baby as long as you can. They grown up so fast, too fast. How will Johnny ever be able to say "NO" to those big blue eyes? Probably as "easy" as Michael will be able to say "NO" to Matthew's big blue eyes... Ha Ha. Love you little Princess, Ali. grandma w
We love having Mikey, Terri, and Matthew over to vist. It's amazing to see just how quickly Matthew is recovering. The setbacks in development he's had due to the surgerys are being very quickly overcome and he's near ready to be walking around (which is yet another exciting adventure). You will always have a bedroom with your name on it, and we encourage you to visit as often as you can. We are looking forward to having many a family vacation with you all (Disneyland anyone?? :)
Thanks for the anniversary wish, can't believe it's been 9 years. I have a feeling that between Matthew and Ali's growth we will wonder where time has gone so quickly.
Love you guys!
John, Cheryl, and Princess Ali
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