Senate Appropriations Committee approves a draft of the fiscal year (FY) 2014 Labor-Health and Human Services-Education appropriations bill.
Lupus Advocates Paint Capitol Hill Purple
March 04, 2011
Lupus Foundation of America Holds Thirteenth Annual Advocacy Day
(Washington, DC) Members of Congress received more than 2500 emails, messages, and stories from lupus advocates across the country during the Lupus Foundation of America’s Thirteenth Annual Advocacy Day held February 28-March 1, 2011. More than 200 individuals met in person with their Congressional Representatives and staff on Capitol Hill, and countless others called, wrote letters, or helped spread the word online through Facebook and Twitter, to raise awareness about the need for increased federal funding for lupus research, education, and awareness programs.
During the first day of the action-packed program, Lupus Advocacy Day attendees were armed with information on how to educate their elected officials about lupus, and why federal support is critical to the biomedical research effort on lupus and improving the quality of life of those living with the disease. In these challenging economic times, it is more important than ever that lupus advocates continue to bring to the forefront the needs of the 1.5 million Americans living with lupus and their family members. On the second day, lupus advocates put their purple on and united on Capitol Hill to meet with their Members of Congress.
Lupus advocates also honored Senator Claire McCaskill (D-MO) and Representative Bill Young (R-FL-10) with the prestigious Distinguished Leadership Award. Senator McCaskill was honored for her friendship with the Lupus Foundation of America and her dedicated work to health care reform. Representative Young was honored for his dedication to biomedical research.
It’s not too late to take action. Spread the word among friends and family. To send an email to your Members of Congress, visit www.capwiz.com/lfa.
About the LFA
The Lupus Foundation of America is the foremost national nonprofit organization dedicated to finding the causes of and cure for lupus, and providing support, services, and hope to all people affected by lupus. The LFA and its national network of chapters, support groups, and local representatives conduct programs of research, education, and advocacy.
Lupus is an unpredictable and potentially fatal autoimmune disease in which the immune system is out of balance, causing inflammation and tissue damage to any organ system in the body. The health effects of lupus include heart attacks, strokes, seizures, and organ failure. An estimated 1.5 million Americans and at least five million people worldwide have a form of lupus. For more information, visit www.lupus.org.
A new medical education curriculum to help medical professionals make early diagnosis of lupus has been unveiled by representatives of The Lupus Initiative in Washington, DC.