Advocacy: Forging Critical Public-Private Partnership
Thanks to the relentless and coordinated outreach to members of Congress by advocates from the Lupus Research Alliance community...

April 3, 2020
The Lupus Research Alliance (LRA) hosted a live webcast April 2, 2020 on COVID-19 for people with lupus that you won’t want to miss – so click here to view the full video recording.
The webast addressed the most frequently asked questions doctors are hearing from people with lupus, put the hydroxychloroquine shortage into perspective, and highlighted LRA actions on behalf of the community.
Hundreds of people, including many healthcare professionals, attended, and the response was overwhelmingly positive.
Moderated by Brenda Blackmon, former news anchor and LRA board member, the expert panel included: