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Part of a projected 2016 investment of $54 million to support more than 380 new and ongoing studies around the world.
National MS Society eNews
April 2016
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Rebecca, diagnosed in 2013

Stop. Restore. End.

The MS Society has invested more than $25 million into 60 new research projects and clinical training awards. Projects include online treatment for MS-related depression; evaluating whether low vitamin D in early life increases the risk of developing MS; myelin repair; understanding MS progression; and more.
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Lisa, diagnosed in 2005

Coping with dual diagnoses

Are you blaming MS for new or worsening symptoms? It could be something else.

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Dan, diagnosed in 2009


Be inspired, discover how others overcome challenges, and share your solutions that defy MS. Like Dan, who found a way to keep “getting the hook in the water.”

Discover Solutions

Every Connection Counts

From fundraising events to influencing policy to giving financially, everyone can make a difference.
Mike, diagnosed in 1983
Stress management and relaxation

Join a free telelearning on how to reduce and more effectively manage stress on May 10.

Register Now
Angela, diagnosed in 2007
Walk to create a world
free of MS

Team up with friends, loved ones and co-workers and become a powerful force.

Sign Up
Michelle, diagnosed in 2001

Join the discussion — how do you cope with the invisible symptoms of MS?

Connect Here
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This communication is partially sponsored through the generous support of Biogen; Sanofi Genzyme; Mylan Inc.; Novartis Pharmaceuticals Corporation; Teva Neuroscience.
Biogen  Sanofi Genzyme Mylan Seeing is Believing Novartis

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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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