Donors have the power to get MS research underway

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.
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PointsNorth
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Donors have the power to get MS research underway

Post by PointsNorth »

Excellent article.

Source: Charity Intelligence Canada (10/03/10)

http://www.msrc.co.uk/index.cfm?fuseact ... ageid=2954
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fiddler
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Better Link

Post by fiddler »

Hi PN,

It is a great article and a great endorsement. However, here is a better link to the full article: http://charityintelligence.ca/pdfs/Ci_C ... aimer.pdf..

Also, there is a good justification of their stance from the managing director of Ci in another thread and on my blog: http://my-darn-ms.blogspot.com/2010/03/ ... nt-of.html.

And, finally, there is an explanation of what Ci is all about from a Ci volunteer in the "making charitable donations" sticky: http://www.thisisms.com/ftopict-9768.html

I know that there are similar "charity vetting" organizations in the US and elsewhere - perhaps others who know similar organizations in their countries should try to get them to look at this, as well.

...Ted
Dx SPMS in 2004.  Liberated 29/04/2010.
My blog: www.my-darn-ms.blogspot.com
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