Chiari Malformation - Online Support Group
We are patients and survivors of Chiari (types I-IV), here for your support.
Northwest Regional Chapter - September 22, 2010 - Questions You Were Afraid to Ask About Chiari and Syringomyelia-Part II from csfinfo on Vimeo.
"Questions You Were Afraid to Ask About Chiari and Syringomyelia"
PART II
I really liked Dr. Richard Ellenbogen's presentation here!
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Comment by Debra Borrmann on March 1, 2011 at 2:09pm This community is part of the Ben's Friends network of patient communities. Learn more at bensfriends.org.
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