If I can do one thing, it is tell you that CCSVI has worked miracles for me.
This is not a dream I ever had, since I only learned about CCSVI last Aug or Sept. I forget. But then I was screened and treated Oct. 20, 2009 so that was fast, but my heart told me GO.
I hate to hear about everyone having to wait so long but I do believe that the MD who does the screening needs to be one of the best, lest the screenings/findings become inaccurate and the treatments inaccurate.
Does that make sense?
I think the slowing of MSers being screened and treated is a discouraging feeling right now. I know I am discouraged that not everyone is lined up for screening at a minimum. But I have faith that it will pick up again. I mean we are not going away, right?? MS being what it is, so unpredictable and difficult to diagnose, makes it a quagmire, for sure.
But we will prevail. I do believe this. and I hope we ALL do.