I met Evan at Cali Kari's house right after his diagnosis and he was so damn cute. In learning his story and how even small things can help (not just Evan but all kids who are ill), I realized that hair was "something that I can do" with little effort from me. It's a gimmie, no excuse not to do it.
I've joked with Kari about waiting for the call from the bone marrow registry, logically knowing that it will probably never come, but sometimes I can't get over thinking that it can truly come at any moment. It's really an awesome thought knowing you're in the pool to be the one to save someone. You are my motivation and so is your son.
Your friend who's praying and pulling for your family,
Jill
P.S. Thanks for the tip on John Russo Dexter, I have an appointment to donate blood for him on for Feb 18th.
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