Hello all. I'm brand knew to the group. The warm welcome I've recieved has
been just wonderful! I've been living with CES for three years next month.
Although I'd heard my doctor say the phrase "Cauda Equina Syndrome", I had no
clue it was a condition (much less MY condition) until very recently. I posted
pretty much my whole story on my personal web page a few months ago and would
love for anyone who's interested to take a look at it. The URL is:
Again, thank you for making me feel so welcome.