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National Multiple Sclerosis Society
National Multiple Sclerosis Society:

MS stops people from moving. The National MS Society exists to make sure it doesn’t. Most people with MS are diagnosed between the ages of 20 and 50, with at least two to three times more women than men being diagnosed with the disease. MS affects more than 400,000 people in the U.S., and 2.1 million worldwide.

We help each person address the challenges of living with MS. Through our national office and 50-state network of chapters, the Society funds more MS research, provides more services to people with MS, offers more professional education and furthers more advocacy efforts than any other MS organization in the world.

In 2011 alone, the Society devoted $164 million to programs and services that assisted more than a million people. To move us closer to a world free of MS, the Society also invested $40 million to support more than 325 research projects around the world.

Current Campaigns:
Whatever It Takes
Whatever It Takes
Past Campaigns:
Surfer/Dancer Together We Are Stronger
Surfer/Dancer Together We Are Stronger
2012 Connect PSA Campaign
2012 Connect PSA Campaign
PSA Digital » National Multiple Sclerosis Society Campaigns » 2012 Connect PSA Campaign
2012 Connect PSA Campaign 2012 Connect PSA Campaign

The National Multiple Sclerosis Society has launched a multi-media PSA campaign which reflects the stark reality of what MS does, but more importantly, how the challenges of MS can be overcome by strengthening and growing our connections.

With these PSAs, the Society seeks to encourage people to connect to end MS by visiting a special website that has been created for the campaign at www.msconnection.org. The Society believes that by combining effort, knowledge and hope, the connections we make can become more powerful than the connections MS destroys.

The campaign features people living with MS as well as those whose lives have been affected by the disease. Each person in the campaign reflects the human spirit of the many authentic stories and experiences across the movement, and how connections help individuals address the impact of the disease and move their lives, and others, forward.

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