This website is dedicated to my nine-year-old cousin Shannon and the 2 million people worldwide who suffer from Neurofibromatosis.
Please take a moment to sign my Guest Book. Your thoughts and comments are appreciated.
Thank You!
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NF TEAM
Our NF Marathon Team
Who's missing from this picture?
You are!
Currently there is no cure or effective treatment for NF.
Our mission is to help change that but we need your help.
Are you ready to make a difference?
We need runners, walkers, and volunteers.
We'll be at the Walt Disney World Marathon on January 9th 2005.
This would be a great time to take that family vacation.
Come on out and cheer us on!
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