This blog is a creation of the Heartland Chapter of the Lupus Foundation of America (LFA) . As many of you already know the LFA was found in 1974 here in St. Louis and has grown to a national foundation serving the needs of Lupus. We are part of the nation’s leading non-profit voluntary health organization dedicated to improving the diagnosis and treatment of lupus, supporting individuals and families affected by the disease, increasing awareness of lupus among health professionals and the public, and finding the cure.

It is our desire to spread awareness of Lupus and disseminate factual information that can help those with this disease cope better. However, we want to do more and share our personal stories and those of others to help share our collective experiences. As such, we will be inviting guest writers from time to time and highly encourage you to share your stories with us and comment as often as you like. If you would like us to tell your story please write us at info@lfaheartland.org.


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