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....
We’re pleased that a poster abstract about the founding and launch of the Penn RP Program (Philadelphia, PA) has been accepted for presentation by the European Alliance of Associations for Rheumatology (EULAR) 2021 Virtual Congress....
This year’s American College of Rheumatology annual meeting featured five relapsing polychondritis (RP) patient poster submissions that were selected for presentation....
Thanks to its excellent drivers and teams, Race for RP had an exhilarating weekend in Rounds 6 and 7 of the IMSA Michelin Pilot Challenge at Mid-Ohio Sports Car Course....
Do you want to share your gratitude for the amazing things people are doing to advance the cause of RP research? Likes, shares, and comments go a long way to help the RP community...
