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PostPosted: Sun Feb 07, 2010 10:29 am 
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Hello all,
I'm a semi-retired husband with SPMS. I was Dx'ed in '01 after a looong and tiring battle. I have all the usual symptoms, fatigue, spasticity, bladder, etc. I am putting a lot of faith in this newer CCVSI, am I being too optimistic?

ToddH :D


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PostPosted: Sun Feb 07, 2010 11:31 am 
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Welcome ToddH!!! You have come to the right place for support and a if neccesary a place to vent! Welcome.


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PostPosted: Tue Feb 09, 2010 5:55 am 
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Welcome toddh , I too am a bluenoser you have come to a great place there is alot of information and support here :)


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PostPosted: Tue Feb 09, 2010 6:07 am 
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Hi Todd, welcome to TIMS. As far as CCSVI goes, I would say be cautiously optimistic. From the sounds of the Buffalo testing, I think we can say at this stage you likely would find some evidence of CCSVI on testing. I don't imagine we can say whether your particular scenario will be easily treated. If you have not already done so, you can read about the experiences of other SPMS-ers post surgery, on the CCSVI tracking project 'sticky'. http://www.thisisms.com/ftopic-8346-0-d ... -spms.html
HTH!

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my approach: no meds so far - just balanced whole foods (partial 'paleo', much less outright elimination), science, supplements, & bloodwork
my regimen - www.thisisms.com/ftopict-2489.html
www.whfoods.com, www.nutritiondata.com


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 Post subject: Thanks
PostPosted: Tue Feb 09, 2010 1:34 pm 
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jimmylegs, I checked out that link and read some great news! I know it is different for everyone, but I think this may be worth checking into deeper.

lubylu, do you still live in NS? I am in Truro.

scorpion, I promise not to be too vocal in my rants. hehe

thanks all :D


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PostPosted: Tue Feb 09, 2010 3:59 pm 
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No i now live in alberta but lived in dartmouth area until 2006. Really miss the maritimes. :(


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 Post subject: From Nova Scotia
PostPosted: Mon Mar 01, 2010 3:44 pm 
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Hi Toddh, I saw your posting and wanted to let you know that I am also from Nova Scotia, Cape Breton actually. Have had MS for 14 years, just joined today and looking for information on CCSVI.

Liz


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PostPosted: Wed Mar 03, 2010 8:14 am 
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HI Todd....
another bluenoser here.... live in Yar. CO........
diagnosed since 05......
i visit the halifax clinic as you do to i am sure....
i am hopeful for this new finding as well.....
i am one of 4 in my family with MS.....


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PostPosted: Fri Mar 12, 2010 4:47 am 
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Hi globab, yes my hfx visits to my neuro Dr. Bahn I hate so much. It reminds me of how sick I am.

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"I am aware that I am less than some people prefer me to be, but most people are unaware that I am so much more than what they see." - douglas pagels


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PostPosted: Fri Mar 12, 2010 7:49 am 
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Location: Ireland
Hi All,
Excuse my ignorance - what is a blue noser??


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PostPosted: Fri Mar 12, 2010 3:39 pm 
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A person from Nova Scotia, we had a sailboat named the Bluenose. It was fast in it day. :)

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"I am aware that I am less than some people prefer me to be, but most people are unaware that I am so much more than what they see." - douglas pagels


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