Courage doesn't always roar. Sometimes courage is the little voice at the end of the day that says I'll try again tomorrow. - Mary Anne Rademacher

Wednesday, December 15, 2010

Dr. Bill Code, Canadian doctor and MS medical expert, treated for CCSVI


by CCSVI at UBC MS Clinic - Information and Support on Tuesday, November 30, 2010 at 10:13pm



Dr. Bill Code is treated for CCSVI!

We now have a Canadian specialist physician ~ one who has studied circulation and the brain and written numerous books on multiple sclerosis and brain recovery ~ to fight for our cause from a very personal perspective.

On November 29, 2010, Dr. Bill Code was treated for CCSVI in California. Dr. Bill had received his diagnosis of CCSVI when he went to Dr. Zivadinov's facilities in Buffalo over the summer. With that information, he carefully planned his next step to get the problems fixed through angioplasty.

We were honoured to have Dr. Bill as our medical expert at our August 9, 2010 Victoria CCSVI Information Session and our recent November 16, 2010 Vancouver CCSVI Information Session. Just last Friday, Dr. Bill served as a medical expert again at our November 26 Vancouver CCSVI Roundtable with Kirsty Duncan, MP. And now...Dr. Bill has been treated for his CCSVI!

In his own words sent via iPhone after treatment last night:

"Hi, All 3 veins treated today with much improved flow. No stents required. I firmly believe this is the place to go.

They [Pacific Interventionalists] follow the Kuwait concept that it is primarily a valve  problem. I agree. Also, that CCSVI should be treated as a vascular issue in it's own right rather than a treatment for MS. I agree.

My head feels less pressured already. Cheers, Bill"

Please join me by sending Dr. Bill your messages of hope and congratulations below. I will pass your messages onto Bill when he returns from California. We now have a renewed, re-energized, and committed CCSVI friend and ally ~ who is also an insider to our medical system ~ who now knows what it feels like to have blood flowing freely. Not only is this a terrific personal victory for Dr. Bill in his battle against symptoms he thought were MS, this is a victory for all of us.

~Sandra


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