Eve,
Thanks for clearing it up the "who's" who for me.
And thank you for bringing Denise's story over to TIMS for all of us to read and follow. I think it's good to read about everyone's journey through the liberation procedure. This is how we all learn. Some of these stories are almost too good to be true and some are sad when no improvements are marked right away.
And all the personal experiences after the procedure, the good, the exhilarating, the scary, and yes, even the bad are of great importance to all of us. It will help us when our time comes to remember what we've read is "normal" after the procedure and what is not. And which symptoms are, head straight back to the hospital type of symptoms, and which are telling us to slow down and rest
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There have been quit a few MS'ers going abroad for procedures, so these post-procedure posts are probably helpful to them as well. Even some done here in the US are done far from a person's home and can make you feel all alone and without support after you return home.
I know personally, just having MS is, in a lot of ways, a very confusing and scary disease. Often we're confronted with a new medication that we are given and have to work our personal way through it's side effects and decide whats normal and whats not.
When I started shooting Avonex into my body, I got the shakes so bad. They were similar to when I came out of anesthesia from an operation. But Biogen did have a telephone number you called that had support folks on the other end, who walked me through.
With CCSVI, we don't have a telephone number, but we do have other MS'ers here at TIMS as our support group. And thanks to Dr. Sclafani, we even have some medical presence. All of this helps so very much.
Lora