The Lupus Foundation of America, Heartland Chapter envisions a world without lupus. We are part of a national force devoted to solving the cruel mystery of lupus while providing caring support to those who suffer from its brutal impact.
With the help of informed volunteers, lupus medical experts, and committed and caring supporters, we provide:
We answer questions about lupus, provide tools, resources, and referrals to doctors who treat lupus, and help guide individuals and families through the complexities of living with lupus and toward a better quality of life.
We conduct outreach efforts and share stories of those who suffer from lupus to increase awareness of lupus, bring greater attention to the disease and its devastating impact, and rally public support to join the fight to end lupus.
We advocate on behalf of all people with lupus, their families, and the health professionals who care for them. We educate government officials and industry leaders on the urgent need to expand public and private investment in lupus research, education programs, and support services.
We raise money to support research through the Lupus Foundation of America’s National Research program, Bringing Down the Barriers™, which aggressively pursues an agenda to find answers to the most difficult questions and advance the science and medicine of lupus.
If you join the fight, we will not have to concede victory to this terrible disease. With your support and involvement, we will be able to solve the cruel mystery of lupus in our lifetime and end its devastating impact on millions of lives.
LFA, Heartland Chapter
4640 Shenandoah Ave
Saint Louis, MO 63110
Below is an online copy of the 2012-13 Lupus Foundation of America, Heartland Chapter's Annual Report.
For a printed copy please contact us at 314-644-2222, 800-958-7876 or email us at email@example.com