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world’s largest MS conference

ECTRIMS 2011 Research results presented this week in Amsterdam
What’s new in the world-wide MS Research Revolution? Join About.com blogger Dr. Julie Stachowiak and producer / director Kate Milliken — both of whom live with MS — as they report live from ACTRIMS/ECTRIMS on cutting-edge MS research via the Society’s new blog. Tune in daily for a front-row seat to some of the most important and innovative research being reported.

Join Kate and Julie now  

 

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Earl Campbell

Football legend Earl Campbell and son Tyler
 
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Breanna Burkes

The Society’s 2012 Scholarship Program
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For a limited time only, your donation will be matched dollar for dollar. Your doubled gift will help us get that much closer to a world free of MS by funding research and supporting programs and services that touch the lives of people with MS and their families.

Donate Now

 

GeneticsStudy_teaser.jpgMS risk study seeks participants 

Harvard University researchers are recruiting 5,000 close relatives of people with MS for a study to determine risk factors that might make a person susceptible to developing MS. The study is being led by Dr. Philip De Jager, a Harry Weaver Neuroscience Scholar of the National MS Society.

Get the whole story

 

GetPlans_teaser.jpgGet Plans 

On October 20, Steve Nissen, MS, CRC, and Silvia Stazio, CFP, host Planning for Your Future: Careers and Finances, a Live Fully, Live Well webinar from the Society and Can Do MS for people living with MS and their support partners.

Register now

More MS News 

Oct 5: Results of successful phase III trial of oral teriflunomide for relapsing MS

Sep 21: Study comparing telephone-delivered self-management programs to improve MS symptoms launched

Read more about these and other recent reports

This communication is partially sponsored through the generous support of Biogen Idec;
EMD Serono and Pfizer, Inc; and Teva Neuroscience, Inc.
 

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MS stops people from moving. The National MS Society exists to make sure it doesn’t. We are a collective of passionate individuals, moving together to create a world free of MS.
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Please do not reply to this email as we are unable to quickly respond to messages sent to this address. To receive information about living with MS, Bike MS or Walk MS — or to contact National MS Society staff in your area — please
visit our Web site.

Early and ongoing treatment with an FDA-approved therapy can make a difference for people with multiple sclerosis. Learn about your options by talking to your health care professional and contacting the National MS Society at http://www.nationalmssociety.org/ or 1-800-344-4867.

National Multiple Sclerosis Society | 733 Third Avenue | New York, NY | 10017

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Early and ongoing treatment with an FDA-approved therapy can make a difference for people with multiple sclerosis. Learn about your options by talking to your health care professional and contacting the National MS Society at http://main.nationalmssociety.org/ or 1-800-FIGHT-MS (344-4867).

Our postal address is:
National Multiple Sclerosis Society
733 Third Avenue
New York, New York 10017

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