ABOUT this BLOG and How to use it

WELCOME to Stu's Views & MS News. A product of MS Views and News, a Not-for-Profit [501c3] organization. Founded in 2008, we provide educational Multiple Sclerosis information via live seminars and via the internet.

Key-Notes: Our live seminars average approx 60 people per educational program. Our blog is visited over 2900 times per week and our website is visited by thousands each month.

Register at our website to receive our globally transmitted Multiple Sclerosis e-newsletter, currently being received in (90) Countries.

On this blog see our Directory, Archives, recent Blog Posts & so much more. Use the Blog Search box (enter a keyword). See our Facebook information AND Links to other MS Organizations & bloggers. Scroll through entire page, to find information that could EMPOWER You. At the Bottom of this page, see informational videos and some for fun.

Disclaimer: "Stu's Views & MS News" / 'MS Views and News' does not endorse any products or services found on this blog. It is up to you to seek advice from your healthcare provider. The intent of this blog is to provide information on various medical conditions, medications, treatments, and procedures for your personal knowledge and to keep you informed of current health-related issues. It is not intended to be complete or exhaustive, nor is it a substitute for the advice of your physician. Should you or your family members have any specific medical problem, seek medical care promptly

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Like this blog? - CLICK "LIKE"

Monday, November 23, 2009

Breaking News: MS Society of Canada announces request for research operating grants related to CCSVI and MS

I just received the following message from the MS Society Canada

The message found below, was sent to their own staff

Dear staff:

As many of you know, we have received tremendous interest and excitement about the chronic cerebrospinal venous insufficiency (CCSVI) and MS story that appeared on CTV’s W5 this weekend. While Dr. Zamboni is the first to comment that these early results require additional study, it will please you to know that the MS Society of Canada has just confirmed that it will launch a competition to fund operating grants related to CCSVI and MS. To read about this announcement please link here.


In the meantime we recommend that you learn more about CCSVI and MS.


Thanks to your dedication, we will continue to play a leading role in ending MS.

Stewart


The Stewart found above, is not the Stuart, who posts these messages. This is a new topic for me too, and I am trying as fast as my brain allows, to catch up on this new information.



============================================