Dr. Nakamura prescribed this vibrating chest vest for little Magoo to help loosen up the junk in his lungs. Here he is sporting the latest fashion in pulmonary wellness while receiving his breathing treatment.
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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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2009
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May
(26)
- Almost finished w/ the steroids. THANK GOD.
- A couple pics from the past couple days
- Just got home from hospital ... all hooked up to o...
- Not a good night last night for Matt and Mike
- Here it is... the shot we all dread in the hospita...
- Face of an Angel, Heart of a Soldier
- More strolls around the halls
- I just love this!
- The Elephant Mask
- Even the lion needed a breathing treatment today
- Matthew is very proactive in his care
- Reading Time
- Matthew finally gets out for a walk in the halls
- Mommy's sick too!!
- Sunday Update
- Just got home from hospital. Mike just got off wo...
- Couple of smiles today :)
- Dr. Seuss helps too!
- Vibrating Chest Vest
- Matthew Update
- Gwenna is an angel
- Charlotte's Web video has captured his attention a...
- Finally... a very short nap.
- This is how the poor little guy has looked for a c...
- Picture taken within the last hour. They've start...
- Matthew is in hospital
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May
(26)
6 comments:
Matthew LOVES chest compressions...so I bet he's really loving the vibrating vest...
he is funny... He loves getting his little "puffer" treatments too...
LOL
Well Terri was doing a great job on the chest compressions at home, but this is really something. He is so good about having his treatments and hopefully he will be home soon.
Love, Grandma Sue
He actually hates this vest. It's a lot more vibration than we thought it would be. It fills up with air and has little baffels in it that really move. The entire bed vibrates.
He probably would laugh if he wasn't so sick. He stays right there in bed and doesn't even try to get out of bed. A sure sign of not feeling good.
This is more than vibrating... LOL...
it's like a bucking bronco vest...
bounces him all over the bed...
Rather cool blog you've got here. Thanks for it. I like such topics and anything that is connected to this matter. I would like to read a bit more on that blog soon.
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