ALL of my MDs tell me CCSVI is in no way the cause of MS sx, but then I see so many videos of folks who almost jump off the recovery room stretcher to sprint to the parking lot. I want to see more videos of them 3 months out and 6 months out and 12 months out. I have seen several that have had it done 2 or 3 times and keep having to have those veins reopened. Its so scary! I want so badly for this to be a real answer, but I too am chicken and want better answers. I want to see more research being done, and not just searching thru youtube videos to find info.

MS has been a big money maker and there is no profit in a cure, but I simply cant imagine that if a cure existed that they would hide it. That the humanitarian side of those folks in R&D wouldnt win out and find a way to get that study published.

I hate this stupid disease.