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Post Traumatic Syringomyelia

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I found this site last nite and it is the best I have seen, I do not have Chiari

Malformation, but due have Syringomyelia.

Are my issues appropriate for this site? or is it just for CM, I would love to

be able to share my story and also seek help from others who suffer.

I am not very good with the computer and dont belong to any other groups, so

forgive my ignorance. If you havent heard it lately, thanks for your time, this

site seems like it would be a great benifit to those who need it.

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