State of South Dakota
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EIGHTY-SIXTH SESSION LEGISLATIVE ASSEMBLY, 2011 |
922S0749 | HOUSE CONCURRENT RESOLUTION NO. 1005 |
Introduced by: Representative Rausch and Senators Rave and Peters
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A CONCURRENT RESOLUTION, Expressing support for raising public awareness of the
disease of lupus.
WHEREAS, Systemic Lupus Erythematosus, commonly known as lupus, is an acute,
chronic, complex, and often life-threatening autoimmune disease; and
WHEREAS, lupus can affect virtually every organ system in the body, including the skin,
lungs, heart, kidneys, and brain. The disease can cause seizures, strokes, heart attacks,
miscarriages, and organ failure; and
WHEREAS, the Lupus Foundation of America estimates that more than 1.5 million
Americans live with some form of lupus, including nearly four thousand people in South
Dakota; and
WHEREAS, while lupus strikes mostly women of childbearing age, no one is safe from the
disease. Women of color develop lupus at a rate of two to three times the rate of Caucasians -
a disparity that remains unexplained; and
WHEREAS, lupus can be particularly difficult to diagnose because its symptoms are similar
to those of many other illnesses and major gaps exist in understanding the causes and
consequences of lupus; and
WHEREAS, more than half of all people with lupus take four or more years and visit three
or more doctors before obtaining a correct diagnosis; and
WHEREAS, early diagnosis and proper treatments are critical to the improvement of the
quality of life and survival rate of those living with lupus; and
WHEREAS, lupus impacts more than just the life of the patient; it affects their family,
friends, coworkers, employers, and the community; and
WHEREAS, increased public awareness, education, and research are key to winning the
battle against lupus:
NOW, THEREFORE, BE IT RESOLVED, by the House of Representatives of the Eighty-sixth Legislature of the State of South Dakota, the Senate concurring therein, that the South
Dakota Legislature strongly urges all citizens of South Dakota to educate themselves on the
symptoms and impact of lupus and join with lupus advocacy groups such as the Lupus
Foundation of American in supporting programs of research, education, and community service.