Riley's Diagnosis

Riley James Faiai is my 2 year old son who was born with Craniosynostosis and probable Pfeiffer syndrome. When he was 5 months old, Riley had surgery to reconstruct his skull. This blog is the journal, story, and timeline that has helped me put Riley's Journey into words. Browse around the archives and feel free to contact me for more info or support! -Lauren (lfaiai@gmail.com)

Saturday, January 20, 2007

1/20/07

No words needed for this update!




5 comments:

TK said...

Oh my gosh sooooo cute!! I just want to kiss him.

Glad you had some time today to hang out with two of your boys.

Anonymous said...

he looks more and more good looking just like his uncle.

your lucky he has a little bit of my blook in him.

-Landon

Lindsay Jo said...

I wonder what landon's "blook" is. ... no idea.
All I gotta say is that he definatly got his good looks from his aunt.

Becky said...

With your camera phone? Amazing and totally adorable.

Loretta said...

Lauren and Steve,

You are totally blessed with your two little boys! Looks like Riley is recovering nicely!

Isn't it amazing how resilient babies are? We think of them as these helpless little creatures. Yet, they continue to amaze us, with their ability to thrive, in spite of their circumstances!

It is obvious, Lauren and Steve, that Riley will have a speedy recovery. Just look at him! He is amazing!

God bless Cameron for being such a loving big brother during this entire process!

Our lives will never be the same again! This journey has completely transformed lives! It has taught us about love, about faith, about community, about ourselves, our inner struggles, about acceptance, and about rejoicing.

Lauren, Steve, Cameron and Riley, you are such an example to others! You exude life and all that we have to be thankful for!