Foundation News

Race for RP Partners with Podium eSports and Monday Night Racing for Special eRacing Charity Event

The eRace for RP will be held on the iRacing platform on Wednesday, September 14th, 2022 at 7:30pm ET. Funds raised through the event will be used to invest in ground-breaking autoimmune disease research.

FULL THROTTLE, Powered by Race for RP, Premieres Hosted by Greg Creamer Covering IMSA and Other Motorsports Alongside Segments Featuring the Relapsing Polychondritis Foundation and Race for RP

The Relapsing Polychondritis Foundation is supporting a study to advance autoimmune disease research and bring science closer to the discovery of a biomarker for RP.

The Relapsing Polychondritis Foundation Invests in Potentially Groundbreaking Collaborative Research

The Relapsing Polychondritis Foundation is supporting a study to advance autoimmune disease research and bring science closer to the discovery of a biomarker for RP.

The Relapsing Polychondritis Foundation Invests in the Next Phase of VEXAS Research

The Relapsing Polychondritis Foundation is partnering with the researchers at NYU Langone Health and the NIH who, in 2020, discovered a new autoimmune disease named VEXAS Syndrome, to build upon this exciting and potentially ground-breaking work.

Relapsing Polychondritis Patients, Advocates, and Researchers Emphasize Awareness, Partnership, and Collaboration with Exhibits on Rare Disease Day 2022 at the National Institutes of Health

This year’s Rare Disease Day exhibits supported by the Relapsing Polychondritis Foundation included presentations by patients, advocates, and researchers.

Relapsing Polychondritis Foundation: Year in Review

Fueled by bold thinking, purposeful action, and inspiration, 2021 was a transformational year for patients with Relapsing Polychondritis (RP), the RP Foundation, and Race for RP.