PFFD Type 1b |
Nash is doing great with his shoe! He's walking along the funiture already so we're very happy he's getting used to it. I'll try to get some video of it and post it...its super cute :)
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!!
PFFD Type 1b |
Thank you for the update!! We love and are thinking of you all! xoxo
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