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National Lupus Advocacy Summit

Learn. Connect. Advocate.

Join lupus warriors from all over the country for the largest lupus advocacy event of the year in Washington, DC! Summit attendees will learn from experts in the field about the latest in lupus research, connect with hundreds of their fellow lupus warriors and advocate for increased research funding, ensure access to care and advance policies to improve the lives of all people with lupus. Don’t miss your chance to turn Capitol Hill purple! The 2025 Summit will be held May 4-6. Stay tuned for registration early January 2025!

What you'll do at the National Lupus Advocacy Summit:

Each year, the National Lupus Advocacy Summit brings together the entire lupus community in pursuit of our shared goal: a world without lupus.

book
Learn.

Hear firsthand from the brightest minds researching and treating this disease and receive training on how to advocate for yourself and others with lupus throughout the entire year.

handshake
Connect.

There's no other event in the world that brings together as many people affected by lupus as the Summit. Be surrounded by those who understand your challenges and can help you manage them.

capitol
Advocate.

Meet with your members of Congress to tell your lupus story and urge them to join our fight against this terrible disease by supporting policies to improve the lives of all people affected by lupus.

The National Lupus Advocacy Summit is the keystone of our comprehensive advocacy program that has generated more than $768 million in federal funding for lupus research in the last five years.

Become an Advocate

Sign up to be an advocate and make your voice heard!

Thank you to our 2024 National Lupus Advocacy Summit Sponsors!


 

Capitol Sponsor

PhRMA

Summit Sponsors

Summit Sponsors 2024

Exhibit Sponsors 

Alexion
BIO
Cartesian Therapeutics
Dr. Reddy's Laboratories, Inc.
GSK
Lupus and Allied Diseases Association, Inc.
Mallinckrodt Pharmaceuticals
 

For questions about the National Lupus Advocacy Summit, please contact Sara Chang at chang@lupus.org.