CCSVI in MS Testimonial – Tracy Cooke

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I was diagnosed in 2003 and have Secondary Progressive MS.  I decided to have venoplasty treatment for CCSVI in Melbourne in 2012.  My jugular veins were blocked on both sides but the right was worse (almost completely blocked!).
Before venoplasty I had a pain in the back of my left leg, upper left arm and a cold right foot.  These symptoms went almost immediately and have never returned.
I had other very good changes with my legs and I could move them well.  This unfortunately only lasted a week.
I felt that my veins had restenosed so I decided to start on the antibiotic protocol for Chlamydophila pneumoniae (CPn).  I am going back to be re-scanned and have venoplasty treatment again.
The more research I do the more convinced I am that this can be a great help to me.

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