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Updated 23 Apr 2010 , 9:02pm
anyone here with or living with someone who has ACM and/or Syringomyelia?
well I am glad no one here suffers from it!! But we do need awareness. You can get info at World Arnold Chiari Malformation Association.Or watch House on May 3rd.Thank you.
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(if this is a private computer)
Yes please, register now!