Wednesday, May 19, 2010
Thursday, May 13, 2010
Monday, May 10, 2010
Monday, May 3, 2010
15 month stats
Height: 31.5"
Weight: 24 lbs 4 oz.
(Photo credit: Thanks to Mike O'Donnell, who managed to snap amazing pics of not one, but five (5!) kiddos on the move)
Sunday, April 25, 2010
Julia!
Our new niece, Julia Alexandra Bright arrived on March 28th, 2010.
Congratulations to Becky and Steven!
Congratulations to Becky and Steven!
Wednesday, April 14, 2010
Friday, April 9, 2010
Thursday, April 8, 2010
Feet First
Jay taught Owen to climb off the couch feet first,
but he seems to use the technique indiscriminately
(The first 15 seconds are where the action is...the rest is a bit boring).
Wednesday, April 7, 2010
Monday, March 22, 2010
Playground
We hit the playground on a beautiful day in March.
Owen discovered that he can do laps on the slide all by himself
(click here for the video).
Click the image for additional photos.
Tuesday, March 9, 2010
Monday, March 8, 2010
Monday, February 22, 2010
Race Day
Thanks to everybody who donated, I was able to raise over $1400!
Owen came out for the big day
Owen came out for the big day
With Laura (aka speedy gonzalez)...who suggested the race in the first place,
swore up and down that she didn't train enough,
and then beat me...by 13 minutes!
Tuesday, February 16, 2010
Winter 2010
Click image for additional photos
This album is updated all the time so be sure to check back for more pictures!
Wednesday, February 10, 2010
Tuesday, February 9, 2010
Laughing
Owen thought it was hilarious when I smacked my head on one of his toys.
So I spent the next 10 minutes smacking my head just to get the laughs, but it was worth it.
Monday, February 8, 2010
Sunday, February 7, 2010
Friday, January 22, 2010
Tuesday, January 12, 2010
I need your support!
On February 21st, 2010 I will be running a 10 mile race in Prospect Park to raise money for my cousin and his family. My cousin, Michael, was diagnosed with ALS, also known as Lou Gehrig's disease. ALS in a degenerative and progressive neurological disease and there is no known cure. Motor cells in the spinal cord and brain degenerate, leading to muscle weakness and loss of mobility, speech, swallowing, and respiratory function. Michael is now in a wheelchair and uses a speech assistive device to communicate. Please support me in helping Mike, his wife, Chris, and their three children, Sarah, Alex, and Lizzy, cope with this disease. Medical care, home care, assistive technologies and equipment are just a few of the mounting expenses that Mike and Chris have. Any amount is truly appreciated.
Click this button to make your donation today!
Also, click here for the ALS Association Greater Philadelphia Chapter, Mike and Chris' local ALS foundation, for additional information on how you can help families that are coping with ALS.
Click this button to make your donation today!
Also, click here for the ALS Association Greater Philadelphia Chapter, Mike and Chris' local ALS foundation, for additional information on how you can help families that are coping with ALS.
Monday, December 28, 2009
Wednesday, December 16, 2009
Tuesday, December 15, 2009
Monday, December 14, 2009
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