$4.5 Million Appropriated to Continue Established MS Research Program

We are pleased to announce that $4.5 million has been appropriated within the FY 2010 Congressionally Directed Medical Research Programs (CDMRP) for multiple sclerosis research. This program is funded through the Defense Department at the direction of Congress and was signed today by the President. This latest appropriation is a continuation of the MS program that was founded in FY 2009.

“This continued opportunity is of great benefit to not only our nation’s 28,000 veterans living with MS, but to everyone and every family touched by the disease,” said Joyce Nelson, National MS Society’s President and CEO. “Emerging evidence has shown that combat veterans could be at an increased risk of developing MS. This important ongoing research being conducted under the CDMRP could help us move one step closer to better treatments and a better understanding of the disease.”

Congressman Russ Carnahan (MO-3) and Congressman Michael Burgess, M.D. (TX-26) have been strong advocates in this effort and have led a multi-Member letter of support for the appropriations request, garnering the signatures of more than 100 Members of Congress. “We owe it to the brave Gulf War veterans who have proudly served their nation to look into the causes of the higher rate of MS appearing in this population and to research possible cures,” said Congressman Russ Carnahan. “By shedding more light on the causes and treatments for MS those with combat service related MS as well as all others with the disease are given hope for a future cure.” Congressman Michael Burgess, M.D. continued, “Multiple sclerosis is a cruel disease, and one of the great unsolved mysteries of our day. As a medical doctor and a Member of Congress, I am proud to support work to research and help find cures and treatments for MS and other health care challenges that Americans, including our nation’s veterans, face.”

Beginning in 2006, MS activists went door to door and engaged online tools to collect more than 100,000 signatures supporting a research program for MS within the CDMRP. Building on this impetus, Society Chapters with their MS activists and our Federal Advocacy team in Washington, DC participated in hundreds of congressional meetings on the Hill and in home states. They took the case to the media, to town hall forums and testified before Congress. In addition, MS clinicians and people living with MS served on an Integration Panel, which helped to prioritize the MS research areas within the FY 2009 program. The first round of applications for 2010 that will be funded are expected to be announced this spring. “The tireless work of the thousands of MS activists who advocated across the country for these continued appropriations is a vivid example of the power that each of us have in working to create a world free of MS,” said David Chatel, National MS Society Executive Vice President, Advocacy.

Other allies who helped petition Congress for this new MS research funding included the American Academy of Neurology, the Paralyzed Veterans of America, United Spinal, AMVETS, the Vietnam Veterans of America, and the Disabled American Veterans.

Learn more about the National MS Society’s Government Affairs and Advocacy efforts.

Introducing Mark Scheerer, Programs Director

I am the Chapter Programs and Services Director; and have been with the chapter since 1993.  When I started with the chapter back in ’93 the first drug to actually treat MS had just been released and there was a lottery to determine who received the drug since there was a limited supply at that time.  That seems like a long time ago!  Over the years there have been so many changes in treating MS and it’s great to work for an organization that has helped spearhead many of the changes.

My experiences with the chapter have been both good as well as challenging.  I’ve been lucky to meet people who I consider my friends – both people with MS and also my co-workers.  Our staff is a dynamic one and I’m convinced one of the best in the country at working together to put an end to multiple sclerosis.  Challenges have come as I’ve seen some of my friends become increasingly affected by MS which makes me work even harder to contribute to the efforts of our chapter.  While I work directly with people living with MS, I also ride in our Bike MS: Tour to Tanglewood.  In this way I can share with other cyclists the ways their efforts are making a difference in the lives of over 2400 people living with MS in our chapter.

We are proud to announce that 107.5 WKZL and Rock 92 WKRR will be our new 2010 media sponsor for 25th Annual Bike MS: Tour to Tanglewood

November 12, (Triad, NC): The Central NC Chapter is proud to announce that 107.5 WKZL and Rock 92 WKRR will be our new 2010 media sponsor for 25^th Annual Bike MS: Tour to Tanglewood. Each station will have a team riding in the event and raising money. Mid-day DJ, Josie Paza, will be the team captain for 1075KZL and Ronie Alexander from the afternoon drive will be the team captain for Rock 92. Both stations will attend the Festival of Bikes kick off at the Festival of Lights at Tanglewood on January 5^th, training rides throughout the summer and ride in the event on September 25^th and 26^th. “We are so grateful and excited that 107.5 KZL and Rock 92 has joined us as our 2010 media sponsor”, says Stephanie Phipps, Marketing and PR Manager for the local chapter. “Together we can make a large impact in our community by raising awareness and valuable dollars towards creating a world free of MS.” The station’s sponsorship is valued at $51,650.

Bike MS is one of the Chapter’s two main charity events in addition to Walk MS. Raising over $1.12 million in 2008, this event is the Chapter’s largest fundraiser. 

Last year 1,700 cyclists participated in the event, both beginners and experienced riders.  The Chapter hopes to increase participation to 2,000 and donations this year to $1.2 million. 

All money raised during this event will be used by the Central North Carolina Chapter of the MS Society to help support families with MS and fund research to create a world free of MS.  For more information on the ride, call (336) 299-4136 or visit the website and register online at http://www.bikemsncc.org

About Multiple Sclerosis

Multiple sclerosis interrupts the flow of information from the brain to the body and stops people from moving. Every hour in the United States, someone is newly diagnosed with MS, an unpredictable, often disabling disease of the central nervous system. Symptoms range from numbness and tingling to blindness and paralysis. The progress, severity and specific symptoms of MS in any one person cannot yet be predicted, but advances in research and treatment are moving us closer to a world free of MS. Most people with MS are diagnosed between the ages of 20 and 50, with more than twice as many women as men being diagnosed with the disease. MS affects more than 400,000 people in the U.S., and 2.5 million worldwide.

About the Central NC Chapter
The Central North Carolina Chapter provides services and programs to nearly 2,400 people with MS and their families in fifteen North Carolina counties: Alamance, Alleghany, Ashe, Caswell, Davidson, Davie, Forsyth, Guilford, Randolph, Rockingham, Stokes, Surry, Watauga, Wilkes and Yadkin.

About the National Multiple Sclerosis Society

MS stops people from moving. The National MS Society exists to make sure it doesn’t. Our mission is to mobilize people and resources to drive research for a cure and to address the challenges of everyone affected by MS. We fund more MS research, provide more services to people with MS, offer more professional education and further more advocacy efforts than any other MS organization in the world. The Society is dedicated to achieving a world free of MS. We are people who want to do something about MS now. Join the movement at nationalmssociety.org.