Since Terri's not feeling well today and we're all STARVING for more of the little guy... I thought I'd post a couple of pics.
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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.
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January
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- Isn't this soo cute... Spookie hung out w/ Matthew...
- This was in 1965, Terri was 5 years old. The pict...
- Look at this smug mug
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- THIS JUST IN... Matthew has discovered his mouth.
- This is from earlier today. Magoo's daddy let him...
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- Since Terri's not feeling well today and we're all...
- A couple pics to hold you over until I can get the...
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January
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4 comments:
such a cute pic..
I just made Mike run to Longs and get me some DayQuil and Nyquil ..
my head is going to explode...
Yes.. I have what Matthew had...
now I see why he was so darn grumpy.
Magoo is beginning to look such the little man!! Thanks for taking the reins and posting, Kim! You two are a beautiful auntie and nephew!!
Auntie Kim to the rescue!!!!!
Thanks Kim for posting the new pictures of Matthew. I believe these were from our Thanksgiving family get together at your home. It was a fun time for all with, as always, too much to eat. hee hee
The pictures are all great and all of you just get better looking every day. Both houses look wonderful. Matthew just gets bigger and bigger and cuter and cuter.
Sorry to hear that Terri hasn't been feeling well. It's tough not feeling well when you have a busy little boy to entertain.
Love to all of you and Happy New Year (a little late).
Grandma Sue
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