I've been surmising my reply to an email I rec'd. regarding my latest liberation treatment. My answer prompted her to say" I guess that's why Canada has stringent tests". Question was " how did it go in California?"

Why I went to Cal. It was my 2nd procedure. My 1st was in Costa Rica.

Question should have been " Why did u get the "Lib.... Procedure?"

My right leg had been a problem since 2004. dx 2008 PPMS, ...Spring 2010,Right hand starts to noticeably get dysfunctional late in day. My pal Al and I had been researching and following the problem of CCSVI since 2009. He knows my Friend Jenny died at age 50 same disease. I will be 49 this fall.

So would u try being a Pioneer instead of dying at age 50?

U Betcha.

The 1st procedure (there was nothing in the states at that time) in Costa Rica (Nov 21/10 ) I had to stay an extra nite because the balloon caused my vein to tear. Still the eventual  result  was very true to the name (Liberation) Balance (I got to dance! with my pal Al)., walking, Ticklish, brighter, warmer. etc. 

So, I felt immediate results, the tops was NO PAIN.

But 3months later  MRV test that I had, showed my right jugular was 100% occluded and my left was 99% occluded.

How muAnd Dr. Hewett from Synergy Health Concepts, who had a consultation with while he was in Vancouver, said he thought he could help.

Costa Mesa is alot closer to home (Vancouver Canada). FYI, Google Synergy, or Renaissance Surgiclal @Newport Harbour.

So 2nd procedure. Here's the outcome -

1.Talking with Dr. Harris post op, he told me they did finally have success with left but not even finding the right jugular.

Anyways, long story short, my hands still work, 1 bum leg, and I am really healthy except for my MS and a missing right internal jugular.

Would I have waited to lose my hands while Canada's Neuro's make up their minds about bloodflow swamps at the base of my brain?

No.

Could my right jugular been saved if I had proper follow up in Canada?

We won't know.

My friend asked me a question 2 yrs ago. Would I research and be willing to try something? anything to add some years to my life?

I told him yes, I would try. Hell, they's ain't no pills for me doctor. and I don't want to be a corpse with bad blood flow to be studied.

Pioneers go where people in comfort Zones don't. They have no choice.

So, I know liberation thru venoplasty worked for me.

I am convinced that better blood flow alieviates my MS symptoms.

I've got PPMS. Other than Diet, I have no other options.

Tired of words.