Take it to the Hill and Advocate for Lupus Research 2022

If you have registered to participate in LRA's "Advocate for Lupus Research 2022", please login using the email you registered with to access all the resources you need to meet with members of Congress and their staff virtually.

About LRA

The Lupus Research Alliance is the largest non-governmental, non-profit funder of lupus research worldwide. The organization aims to transform treatment while advancing toward a cure by funding the most innovative lupus research, fostering diverse scientific talent, stimulating collaborations, and driving discovery toward better diagnostics, improved treatments and ultimately a cure for lupus. Because the Lupus Research Alliance’s Board of Directors fund all administrative and fundraising costs, 100% of all donations goes to support lupus research programs.

Sponsors

Thank you to Aurinia Pharmaceuticals and the PA Fund for Patient Advocacy at the LRA for helping make possible this 2022 program. We are especially grateful to the PA Fund for Patient Advocacy for their support over the past seven years in helping the LRA to bring the voices of people with lupus to Capitol Hill.

This site provides resources for advocates who signed up in advance to meet with their members of Congress and their staff virtually. For those who did not register by the Feb. 22 deadline, you can still make a difference and have your voice heard in Congress. Visit our Legislative Action Center starting on March 28 and use the tools provided to reach your legislators to increase lupus awareness and the need for increased research funding.