Lupus community members Brianna Fitzpatrick, Shanelle Gabriel, and Gayle Taliaferro share their individual perspectives about what having lupus is like for each of them, and how being part of the lupus community and working with the LRA empowers them to be the best versions of themselves.
LRA President and CEO Albert T. Roy speaks about our funded research that is leading to real results for people living with lupus.
Learn more about lupus and the LRA: lupusresearch.org
Lupus affects millions worldwide, and there is no cure. Please help the Lupus Research Alliance to raise awareness and funds for lupus research.
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