“RP The Ride of My Life”

This powerful documentary about Nancy and her family’s journey through many years of struggling with painful and debilitating symptoms with an unknown cause, eventually being diagnosed with an extremely rare autoimmune disease, Relapsing Polychondritis (“RP”), and ultimately finding the strength and courage to persevere with a purpose to raise awareness about RP, help others in diagnosis and support, and advance research efforts about this and other autoimmune diseases in pursuit of treatments and cures.
NEWS
Thank you, WeatherTech Raceway Laguna Seca, Scuderia Corsa, Ferrari Challenge, and Ferrari North America for your excellent hospitality and the fantastic racing last weekend. We had a wonderful time and greatly appreciate your support for the Race for Relapsing Polychondritis (RP).
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.
Race for RP was represented by outstanding drivers and teams in the IMSA Michelin Pilot Challenge at Road America, driving awareness of relapsing polychondritis (RP).
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).
A live webinar on novelties about the diagnosis and therapeutic management of relapsing polychondritis in 2020 by Professor Laurent Arnaud, held on 23rd April 2020 for ERN ReCONNET.