Guest guest Posted October 11, 2010 Report Share Posted October 11, 2010 Hi Alan You should get onto Facebook or do some research on the net about it. As I'm an Aussie living in the UK, I've concentrated on the happenings here in England lately. You could go to: http://csvi-ms.net/en/content/who-is-who http://www.ccsvifoundation.org/index.php http://www.multiplesclerosissurgery.com/where-tested-ccsvi.html These may give you further information too, but I think it best to look into the places available through Facebook - each different area of the US has a CCSVI group or can tell you where to get it done. 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 11, 2010 Report Share Posted October 11, 2010 Hi Alan You should get onto Facebook or do some research on the net about it. As I'm an Aussie living in the UK, I've concentrated on the happenings here in England lately. You could go to: http://csvi-ms.net/en/content/who-is-who http://www.ccsvifoundation.org/index.php http://www.multiplesclerosissurgery.com/where-tested-ccsvi.html These may give you further information too, but I think it best to look into the places available through Facebook - each different area of the US has a CCSVI group or can tell you where to get it done. 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 12, 2010 Report Share Posted October 12, 2010 i had my treatment in august at the arizona heart institute by dr. dietrich. hi nurse is teresa capriotti. since he is the founder of the hospital he is able to do what he finds reasonable without fearing he may be shut down. the entire staff is wonderful and they are genuinely concerned with helping everyone with ms. the wait time is short compared with other places. give them a call and ask for teresa. you won't be sorry. Re: Re: CCSVI & MS: FIbrin, Sleep apnea, systemic proteolytic enzymes, venous stenosis I am a bit confused. I had read on this site a while aback that CCSVI treatment was only available in the U.S. in two places: one place in CA and one place in NY, but then both of those closed down. and that it was not available in the U.S. at all .... But now people have been writing that they are getting the treatment (not just the testing) in various places in the U.S. such as NY, Phoenix, and several other places in the U.S. So is this treatment available in the U.S. now, and how does one who lives in the U.S. go about finding the closest center to get not just the testing but also the treatment? Thanks. Quote Link to comment Share on other sites More sharing options...
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