Tuesday, July 26, 2016

Christmas In July : Fight MS with information and your donation

As you can guess I get a lot of newsletters about things I care about. One of those is MS. I have met people and am related to people whom have MS.
Please consider donating today.

National MS Society eNews
July 2016
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More MS NewsJoin the CommunityFind an EventAdvocate for ChangeIn Your Area
Dave, diagnosed in 1974

Gut Bacteria Linked to MS Inflammation

Harvard researchers found significant differences between the gut bacteria of people with MS and without MS — and between treated and untreated MS — adding to growing evidence of the possible influence of gut bacteria on immune activity.
Get the Details
William, diagnosed in 2002

Speak for Yourself

25-50% of people with MS report speech or voice changes during their disease, and 30-60% experience cognitive changes that impede communication.
Learn More
Doctor writing a prescription

FDA Approves Zinbryta™ for Relapsing MS

The latest immune-modulating therapy approved by the FDA for people with relapsing forms of MS, Zinbryta™ is a concentrated form of daclizumab taken every four weeks.
Read More

Every Connection Counts

From fundraising events to influencing policy to giving financially, everyone can make a difference.
Michelle, diagnosed in 2001
Workout Your Worries
Be our guest on August 9 to learn more about easing the symptoms of depression and anxiety with movement.
Register Now
Hand holding labeled test tubes
Breakthroughs Start with You
The Society is the catalyst for all major advancements in MS research. Until July 29, 100% of your gift goes to research.
Help Today
Jennifer, diagnosed in 2000
Dealing with Spasticity
Join the discussion — how do you manage these involuntary muscle spasms and the stiffness, tightness and/or pain they cause?
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This communication is partially sponsored through the generous support of Biogen; Mylan Inc.; Novartis Pharmaceuticals Corporation; Sanofi Genzyme;  and Teva Neuroscience.
BiogenMylan Seeing is BelievingNovartis Sanofi Genzyme
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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