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Treatment Options

After an initial diagnosis of lupus, and depending on the length and severity of symptoms, your doctor may prescribe medication to help. But there are other ways you might control your symptoms.

Further Reading

Lupus Blog with Jeri Jewett-Tennant, MPH

New gene implicated in lupus

Friday September 5, 2008
A new gene variant linked to autoimmune response, known as TNFAIP3, is another link in the chain (literally) to stopping lupus. The variant was discovered by Patrick Gaffney, M.D., and Kathy Moser, Ph.D., of the Oklahoma Medical Research Foundation and has been shown to be one cause of preventing the immune system from turning itself off. In those without lupus, the gene produces a protein that lets the body know to shut down the immune response, but in those with lupus, it is thought that the gene either doesn't produce enough of the protein or produces an inferior protein. Of course, there are many genetic factors contributing to lupus, but it looks as we can count this as one more piece of the puzzle in finding a cure. For more about genes and lupus, visit the Lupus About site.

New information available for lupus clinical trials

Wednesday August 27, 2008
The Lupus Foundation of America is offering a new way for lupus sufferers to find and participate in clinical trials for their disease. The Center for Clinical Trials Education (CCTE) will feature a website and community education programs offered through the Foundation's chapter organizations. The CCTE website will even be able to link viewers with trials they feel may be right for them; a great service both for the clinical trial and potential participants. For more information about what clinical trials are and why it's vital to participate if you're able, click on the Lupus About site

Lupus Foundation of America Names New Chair

Friday August 22, 2008

The Lupus Foundation of America (LFA) has elected a new Chair of the Lupus Foundation of America, Inc. Board of Directors, Karen Evans of Baltimore, Md. She was elected during the LFA’s most recent annual meeting, held in San Antonio, Texas.

Evans has been a member of the LFA Board since 2003 and previously chaired the Board's Education Committee. In addition to her work with the LFA, Ms. Evans serves as Executive Director of the Will and Jada Smith Family Foundation. She previously was Executive Director of the Northwest Baltimore Corporation, and a founder and Chair of the Board of the Park Heights (Maryland) Community Health Association.

In her new role, she will lead the LFA Board's strategic initiatives to bring national attention and increased public and private resources to fight lupus.

Fluorescent Bulbs and Lupus

Thursday August 14, 2008

As you may know, in 2007 the Energy Independence and Security Act passed, part of which means lightbulbs as we know them (the incandescent kind) will be totally phased out of production by 2014. The alternative to these is compact fluorescent bulbs, which meet the new energy standards, but are fluorescent bulbs nonetheless, and can cause photosensitivity in those with lupus. And, so far, there has been no incandescent bulb replacement suggested.

The Lupus Foundation of America is currently developing public policy recommendations to send to Washington and says they will post these when complete, but in the meantime, what are your suggestions? We'll have an article soon on About Lupus and more information about how to make your voice heard on this issue.

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