#ALS AWARENESS #LouGehrigsDisease #PARKINSONS
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#ALS AWARENESS #LouGehrigsDisease #PARKINSONS
Raising ALS | Lou Gehrigs Disease & Parkinsons Disease AWARENESS to the NEXT LEVEL!
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Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
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Call Congress Today! Ask Them To Vote YES for HR 6, the 21st Century Cures Act!

Call Congress Today! Ask Them To Vote YES for HR 6, the 21st Century Cures Act! | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it

HELP advance ALS research and  accelerate the advancement of new treatments.

CALL YOUR U.S. REPRESENTATIVE AND URGE HIM/HER TO VOTE YES TODAY!

 

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Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
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Congressional Legislation Will Fund ALS Research Through 2013 - The ALS Association

Congressional Legislation Will Fund ALS Research Through 2013 - The ALS Association | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
The ALS Association encourages scientific research to find a cure for ALS, heightens awareness of the nature of the disease, stimulates volunteerism and activism, and increases awareness of government leaders to encourage support of research and...
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Scooped by TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
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SENATE provides new incentives and opportunities to develop treatments for ALS.

SENATE provides new incentives and opportunities to develop treatments for ALS. | #ALS AWARENESS #LouGehrigsDisease #PARKINSONS | Scoop.it
Just before Congress adjourned for the year this week, Senators Michael Bennet (D-CO) and Orrin Hatch (R-UT) introduced the Senate version of the MODDERN Cures Act, legislation that would provide new incentives and opportunities to develop treatments for ALS.  Moreover, nearly 100 Representatives had cosponsored the House bill. These are significant milestones that not only indicate the legislation is gaining momentum, but also that Congress could take action on the bill early in 2015. 
    
Earlier this week, the President signed into law H.R. 83, the Consolidated and Further Continuing Appropriations Act, 2015, to fund the federal government through September 2015.  
 
As we reported in previous Advocacy Updates, the law provides $7,820,000 for the National ALS Registry in FY 2015, a more than 30% increase over last year! Additionally, the law includes $7,500,000 in continued funding for the ALS Research Program (ALSRP) at the Department of Defense.  The law provides $30 billion for the National Institutes of Health (NIH), $150 million more than last year, and specifically supports funding for ALS research.  Moreover, the law provides $1.6 billion for the National Institute of Neurological Disorders and Stroke (NINDS), which is $17 million more than last year. 
 
Thank you to everyone who reached out to Congress this year to make these and other successes possible!!!  

Happy Holidays!
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