Guest guest Posted July 29, 2001 Report Share Posted July 29, 2001 <A HREF= " http://search.aol.com/redirect.adp?appname=QBP & query=%dc%9e%5d%53%71%7c%92\ %11%63%17%6d%1b%3e%d2%82%06%4c%f8%d3%ce%59%51%21%65%58%0d%63%83%36%97%53%41%5c%2\ 0%3d%f7%74%0b%57%fd%57%b8%ee%53%97%57%45%bb%e6%14%7e%57%d5%a1%97%ea%c1%1e%8f%b1%\ bc%15%69%16%48%6b%ff%25%89%8e%60%a8%51%60%38%60%28%62%d9%d1%2d%aa%81%16%9b%6a%db\ %c4%57%0e%ea%dd%44%b4%6c%a1%bb%4c%24%72%e2%7e%28%36%63%91%d5%69%45%e2%43%b7 " >Ame\ rican Syringomyelia Alliance Project</A> About 13 yrs ago a wonderful gal named Barbara White started a group of support, research and medical information for both Arnold-Chiari and Syringomyelia. Up until that time, there was virtually no information available ANYWHERE for either. Today, ASAP has over 4000 members, along with a team of neurosurgeon and other professionals on their board. Each year, ASAP sponsors a convention in which members and leading neurosurgeons all over the world, specializing in Arnold Chiari or Syringomyelia join together to share current information and strides made in the treatment of these conditions. This past week it was held in Los Angeles. Check out their website (there is also a mailing list for the group): Quote Link to comment Share on other sites More sharing options...
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