Little is known about Arnold Chiari Malformation and Syringomyelia, we would like to see this changed. Right now there is not much federal funding for Chiari and/or Syringomyelia. Thousands of people have chiari and many more are diagnosed each day. With more federal funding we could do more research, and possibly find a 100\% effective treatment. That would mean many people wouldn't have to live everyday full of pain and suffering. Please consider our request. Thank you very much.

For more information on Chiari and/or Syringomyelia please visit http://www.asap.org and http://www.wacma.com.