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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....

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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...

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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....

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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...

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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....

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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....

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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....

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Nancy Linn, Chair of the Relapsing Polychondritis Foundation and Founder of Race for RP, featured on WQBQ Triangle Spotlight

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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)....

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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....

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All content of this web site, such as text, graphics, images, or any other material contained in this website are for informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. We do not recommend the self-management of health problems. We cannot and do not give you medical advice.If you think you may have a medical emergency, call your doctor or 911 immediately. The Relapsing Polychondritis Foundation, Inc is a nonprofit 501(c)3 corporation. Donations are tax deductible as allowed by law.

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