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Researchers will meet to discuss comorbidities in MS
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February 2015
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Carlos, diagnosed in 2001

First Results Are Available from the MS Comorbidities Project

An international initiative identified the most prevalent disorders, autoimmune diseases, and cancers occurring alongside MS. Researchers will convene in the spring to determine next steps.
Live Webcast: Finding Answers for Progressive MS

Researchers to Share Insight Into Finding Answers for Progressive MS

Join us on March 4 for a live webcast featuring a panel of scientists and experts, who will discuss advancements and updates in Progressive MS research and treatment.

Register Today
Every Connection Counts During MS Awareness Week

Save the Date: MS Awareness Week is March 2 - 8

People everywhere are creating connections stronger than the ones MS destroys. During MS Awareness Week, take action to help others learn more about MS.

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Every Connection Counts

From fundraising events to influencing policy to giving financially, everyone can make a difference.
Joe, diagnosed in 2010
How to Balance Intimacy and Relationships

Find comfortable ways to talk about MS and tips for maintaining a healthy relationship.

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Brook, diagnosed in 2009
Change Lives All Year Long

Give monthly and make the biggest impact possible to help create a world free of MS.

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Kim, diagnosed in 1996
Connect to the Information You Need

Learn about managing MS and employment during this free phone program.

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This communication is partially sponsored through the generous support of Biogen Idec; Genzyme, a Sanofi company; Mylan Inc.; Novartis Pharmaceuticals Corporation; and
Teva Neuroscience, Inc.
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Novartis   Teva 

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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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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.

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