The Lupus Alliance of America is a group of agencies that have come together for the express purpose of providing needed services to those affected by lupus within their local communities. Our mission is “To ensure the delivery of services to those affected by lupus through affiliate members and other agencies and to fund research efforts.”

Amanda Greene enjoys connecting and sharing her passions with others. She is a advocate for Lupus, an autoimmune disease which afflicts more than 1.5 million people in the United States. As “LA Lupus Lady”, she raises awareness and support for Lupus and the Lupus community...

We are a new organised campaign aiming high to raise awareness of the disease Lupus. To find out more about us why not take a look!

Purple Rose is committed to spreading awareness about the disease and providing support to those who have it. There are currently approximately 1.5 million Americans Nation wide affected by Lupus. The foundation is currently active, motivated, and focused on fundraising efforts; thus providing academic scholarships to students with lupus as well as dependants of those fighting the disease.

"On June 17, of 2009, I had my first of many ER Visits to the hospital. Eight months later on February 12, 2010 I was diagnosed with Polymyositis, and on August 25, 2010 I was diagnosed with Lupus. Because of my illness I was forced to quit my job. I am now legally disabled. I now spend my time as a self employed Author and Artist. I also spend my time helping to spread the awareness of Auto Immune Diseases."

The Lupus Magazine is 100% voluntarily, ad-free and independent for those with lupus, by those with lupus. Dirty Dog Media + Publishing proudly provides this informative website free of charge for the global lupus community.  To acknowledge our publisher, simply visit their website...