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