I knew nothing about MS, until I got it. Little of the general public knows about MS and fewer know about the CCSVI situations we are dealing with. We would have more voices on our side, if they knew.

And, they could see how, and who, are resisting, misleading, and denying, a safer and much less costly treatment option for MS. And, how all MS drug options, have little benefit and real dangers for many PwMS, which primarily are kept as uncommon knowledge. Let's let more public know of our MS mess!