I had CCSVI done about a year and a had ago in California. It improved my quality of life very positively.My MS went back a good ten years in symptom relief. Have had a few new symptoms, since the procedure. But I am no way near the amount of disability I presented with before CCSVI.

Had significant stenosis of left femoral, left kidney, right int. jugular and azygous veins. 100% occlusion of left into. jugular. Was part of research protocol that terminated study early due to lack of evidence that procedure is effective.

I was very excited about it at the time, especially because of all the you tube videos. i keep looking for new research on cures. My first cousin who is in a wheelchair also had CCSVI and she felt nothing.

Had it twice with no discernable results...

I did notice my headaches stopped and the coldness in my left foot stopped.No way to tell if this will continue.The reason for 3xs I had a stent put in my L Jugular and there was failure Now on Plavix to keep blood thin through stent.