We may be biased, but we believe our Indiana volunteers are the BEST. We truly couldn't be successful without YOU.
We must continue to make our voices heard and educate our elected officials about the impact of lupus on individuals and their families. The United States federal government continues to be one of the largest funders of lupus research in the world, so it is vital government officials hear from the lupus community throughout the year.Learn More
A place for you to read the stories of those who have lupus and who have been affected by lupus. We hope they bring you encouragement and hope. We hope they inspire you to share your own lupus journey.Read Stories
A registry is a place to store detailed information about individuals with a specific disease and their families. In this case, the Research.forME Lupus Registry is for individuals with a diagnosis of lupus. This registry will help researchers and people with lupus better understand the disease.Learn More
Every advance in the understanding of a disease such as lupus—its causes, its effects on the body, the development of new drugs and treatments—is based on research. By taking part in clinical trials, participants can play a more active role in their own health care. Most importantly, participating in clinical trials helps others by contributing to medical research.Learn More