Relapsing Polychondritis Foundation to Present Poster Highlighting Establishment of Penn RP Program at the EULAR 2021 Virtual Congress
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.
Relapsing Polychondritis Advocate Isabel Bautista Joins American College of Rheumatology Patient Perspectives Program Review Committee
Selected submissions are presented at the ACR annual meeting and published online and in Arthritis & Rheumatology, an official journal of the ACR.
Relapsing Polychondritis Patients and Advocates Emphasize the Benefits of Collaboration in Prestigious Patient Perspective Poster Program
This year’s American College of Rheumatology annual meeting featured five relapsing polychondritis (RP) patient poster submissions that were selected for presentation.
The RP Foundation Featured with Scuderia Corsa in the Ferrari Challenge at WeatherTech Raceway Laguna Seca
Ferrari Challenge drivers bring excitement and awareness to the track
KohR Motorsports, Kyle Marcelli and Nate Stacy Earn Breakthrough Win at Mid-Ohio While Jeff Westphal and Jon Morley Claim Double Podiums Including a TCR Win for Road Shagger Racing
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.
RP Advocate Spotlight: Michael Linn, Director / Vice Chair, Relapsing Polychondritis Foundation
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
RP Advocate Spotlight: David Bammert, Director / President, Relapsing Polychondritis Foundation
Do you have a friend or loved one suffering from RP? Dave Bammert, a Director and President of the Relapsing Polychondritis Foundation and Race for RP, knows firsthand what that is like.
RP Advocate Spotlight: Nancy Linn, Director / Chair, Relapsing Polychondritis Foundation
Race for RP’s founder, Nancy Linn, has been a catalyst of change in the community! She is a champion for facilitating research working to uncover the underlying cause and develop better treatments for RP.
RP Advocate Spotlight: Gonnie Imeson, Director / Chair, Canadian Society for Relapsing Polychondritis (CSRP)
The Canadian Society for Relapsing Polychondritis (CSRP) is an incredible partner in our mission to overcome RP.
Nancy Linn, Chair of the Relapsing Polychondritis Foundation and Founder of Race for RP, featured on WQBQ Triangle Spotlight
On 1 June 2020, Nancy Linn, Chair of the Relapsing Polychondritis Foundation and Founder of Race for RP, was featured on Triangle Spotlight on WQBQ. The program was originally broadcast on radio and available on WQBQ’s website. To watch the program, please see the video below:[vc_video link=”https://youtu.be/tL8ee35x0_Q”]Thank you Suzann Lynn, WQBQ and Triangle Media for […]
Relapsing Polychondritis Foundation Announces a Powerhouse Healthcare Coalition with the University of Pennsylvania and the National Institutes of Health (NIH) sponsored Vasculitis Clinical Research Consortium (VCRC)
The Relapsing Polychondritis (RP) Foundation has announced a generous gift to establish the Penn Relapsing Polychondritis Fund, which will support a unique partnership between the University of Pennsylvania RP Program and the National Institutes of Health (NIH) sponsored Vasculitis Clinical Research Consortium (VCRC).
RP Research Scientist Spotlight: Emily Rose, BS
Emily Rose is a medical student who is working tirelessly to research relapsing polychondritis (RP). Her work is helping to categorize RP in a more accurate way. This research draws information from all over the world and will provide the basis for clinical trials.