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WELCOME to Stu's Views & MS News. A product of MS Views and News, a Not-for-Profit [501c3] organization. Founded in 2008, we provide educational Multiple Sclerosis information via live seminars and via the internet.

Key-Notes: Our live seminars average approx 60 people per educational program. Our blog is visited over 2900 times per week and our website is visited by thousands each month.

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Disclaimer: "Stu's Views & MS News" / 'MS Views and News' does not endorse any products or services found on this blog. It is up to you to seek advice from your healthcare provider. The intent of this blog is to provide information on various medical conditions, medications, treatments, and procedures for your personal knowledge and to keep you informed of current health-related issues. It is not intended to be complete or exhaustive, nor is it a substitute for the advice of your physician. Should you or your family members have any specific medical problem, seek medical care promptly

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Tuesday, May 10, 2011

Help Urgently Needed to Maintain MS Research Funding Take Action!





Because of the hard work of MS activists across the country,  approximately $17 million has been allocated to MS research under the Congressionally Directed Medical Research Programs (CDMRP) over the past four years.  The CDMRP is a Department of Defense (DoD) program that is funded annually via the Defense Appropriations Act. It is important that you act now to ensure this funding stream for MS research is maintained!

We need your help to secure funding for MS research under the CDMRP. Ask your Representative to support a $15 million appropriation under the CDMRP that will help scientists to better understand the causes of MS and help find a cure. The large number of grant proposals submitted each year to the DoD for MS projects indicate that there is a clear need for more funding for MS research.

Because the timeline for requests has been condensed this year, Members of the House must submit their requests for Department of Defense appropriations by this Friday. Click here to contact your Representative today and ask them to show their support for people living with MS by signing onto a bipartisan Dear Colleague letter circulated by Representatives Burgess (TX-26) and Carnahan (MO-3), in addition to including the MS program in the CDMRP in their DoD appropriations request. 

A similar letter will be circulated shortly in the Senate, so watch out for another legislative alert and opportunity to take action and support MS research!
To keep future MS activism messages out of your junk folder, add the following address to your contacts or safe sender list: MSActionNetwork@nmss.org
    Take Action!    




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Disclaimer:  'MS Views and News' (MSVN), does not endorse any products or services found on this blog. It is up to you to seek advice from your healthcare provider. The intent of this blog is to provide information on various medical conditions, medications, treatments, and procedures for your personal knowledge and to keep you informed of current health-related issues. It is not intended to be complete or exhaustive, nor is it a substitute for the advice of your physician. Should you or your family members have any specific medical problem, seek medical care promptly.

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