American Syringomyelia and Chiari Alliance Project Fundraiser

by Cindy Crysler Two years ago my youngest daughter was diagnosed w/Chiari I Malformation.  Around the same time, my friend’s daughter was diagnosed w/the same thing.  That’s 2 little girls w/this same rare brain disorder in our little town of just over 1,100 people.  I can’t change that, but I am doing what I can …