Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero!!
Monday, June 27, 2011
Trying this walking thing...
We've been practicing walking a lot lately and he's getting really good at it. He even let go a couple times today and was standing alone!! He seems to like the shoe lift better, and walks around more, when I don't put his left shoe on so whatever works!?! He's doing great!!! He even put a few dance moves in there for ya! :)
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Thanks for the update! I've been thinking about you guys a lot lately and it's so nice to be able to catch up on your blog! I love how happy Nash is in every pic - he's so handsome!!! Mss you!
ReplyDeletethis just made my day. i am so in love with that little man. he melts my heart.
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