Lupus Foundation of America
Nonprofit organization / From Wikipedia, the free encyclopedia
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The Lupus Foundation of America (LFA), founded in 1977, is a national voluntary health organization based in Washington, D.C., with a network of chapters, offices and support groups located in communities throughout the United States. The Foundation is devoted to solving the mystery of lupus. Its mission is to improve the quality of life for all people affected by lupus through programs of research, education, support and advocacy.
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Founded | 1977; 47 years ago (1977) |
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Focus | "Improve the quality of life for all people affected by lupus through programs of research, education, support and advocacy." |
Location | |
Area served | United States |
Key people | Dr. Susan Manzi (Board Chair) |
Website | www |
The Lupus Foundation of America is a charitable organization with tax-exempt status granted under Section 501(c)(3) of the Internal Revenue Code. The foundation is a BBB Accredited Charity[1] and highly rated by Charity Navigator.[2]