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Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

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Gordon
PostPosted: Fri Oct 01, 2010 1:30 pm 
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OMG

http://mssociety.ca/alberta/contact.htm
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TMrox
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PostPosted: Fri Oct 01, 2010 1:33 pm 
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finding a cure it seems...

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Diagnosed with Transverse Myelitis in December 2008. Inflammatory demyelination of the spinal cord (c3-c5). No MS, but still CCSVI.
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shye
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PostPosted: Fri Oct 01, 2010 4:35 pm 
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Location: NYC
at least getting a good salary, I'm sure...
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Shueywho
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PostPosted: Fri Oct 01, 2010 4:52 pm 
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Location: Brantford, Ontario
Bike tours?
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Merlyn
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PostPosted: Wed Oct 06, 2010 4:51 pm 
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From the New York Times readers comments: I believe this is the CEO of the US MS society, I have no idea what they are paying Canadian counterparts...

http://well.blogs.nytimes.com/2010/06/2 ... sclerosis/

It is public knowledge that Joyce Nelson makes just shy of half a million dollars a year as CEO. I think that is enough money to make sure she keeps in touch with the little people who have built the MS society into an organization that can afford to pay their CEO that kind of money.
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garyak
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PostPosted: Wed Oct 06, 2010 10:37 pm 
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Location: grande prairie , alberta,canada
There is only 24 listed , lol. In my town in Alberta every year for the ms walk they fly in 2 or 3 of the admin and put them up in hotels and meals so they can make an appearance. They basically hang out , take a few photos and don't even make a speach. I think that is a poor use of the money i raised. I will email Darrell Gregory and ask him what the annual payroll is and I will report back here.
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Gordon
PostPosted: Thu Oct 07, 2010 12:25 pm 
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http://www.thehistorychannel.co.uk/show ... about.html
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Gordon
 Post subject: Update required
PostPosted: Thu Oct 07, 2010 1:13 pm 
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ASK Gregory to provide a clear update what Metz and company are doing with the money they got from the BS society
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Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

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