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18 August 2010

Life is a Gift

This post is for everyone...but especially for my Congenital Myasthenic Syndrome friends (via blogs) Kyla and Luke.  (Hey guys!)

Anyway...seriously, like I said.  This is for EVERYONE.  I ran into this video on Facebook this morning.



I don't even know what to say.  There are so many things to say but I think I will say them later.  First I just want anyone who just watched the video above to let Nick's words resonate within you.

Love and peace to everyone.

Lauren

1 comment:

  1. Thank you Lauren! How inspirational and life changing! Such a good reminder to shoot for the stars!

    Sabrina Carter
    Kyla's mom

    ReplyDelete