Newsletter June 2008

Personal Stories

Every voice matters.
Every story counts.

Hundreds of real stories from people living with MS, their families and friends.

share your story

MS Fact

Every hour in the United States, another person is diagnosed with MS.

more facts

In the News

New Study Suggests Immune Genes Help Determine Sites of MS Damage and Symptoms

more news

Miles Walked

Due to a technical error, you may have mistakenly received a Spokes Report e-newsletter during the last week of May. We apologize for this inconvenience.


Research News

Research Photo

$24 Million in New Research Projects
More than $24 million in new funding has recently been dedicated to MS research and treatment projects. This is just half of what the National MS Society hopes to invest this year. Read more about the latest in MS research >>

Getting Results

Advocacy

MS Activists Go to Washington
In early May, thousands of MS activists visited and contacted their legislators in Washington about the need to increase federal investment in MS research. Read more about our success >>

Moving Forward

Knowledge is Power

How Knowledge Is Power Helps Stephanie Stay in Control of her MS
Knowledge Is Power program is a free, at-home educational series for people newly diagnosed with MS and their families. When Stephanie first learned she had MS, she thought her life was over. Learn how this program convinced her otherwise >>

Get Involved

Sharon Dodge

Sharon,
Diagnosed in 1996

Give Today and Your Gift will be Doubled
Join Sharon Dodge in making twice the impact for people living with MS. For a limited time, your gift will make double the difference!

Give Now

Bike MS
Walk MS
Society Store

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.
JOIN THE MOVEMENT

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 www.nationalMSsociety.org or 1-800-344-4867.

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