Relapsing Polychondritis Foundation Announces Appointment of Frances Sweeney to Board of Directors
The Relapsing Polychondritis Foundation (RP Foundation) is pleased to announce the appointment of Frances “Fran” Sweeney to its Board of Directors effective December 11, 2022.
Thank You for an Exceptional 2022
In these final weeks of 2022, as you connect with family and friends to celebrate the holiday seasons, the RP Foundation and Race for RP extend our heartfelt thanks for the partnership and support you generously share with us.
2022: Celebrating A Year Filled with Progress and Discoveries!
In 2022, the Relapsing Polychondritis Foundation, Race for RP, and our incredible partners helped drive RP and related autoimmune diseases to the forefront of ground-breaking scientific discoveries. We also improved patient access to specialized, multi-disciplinary teams of clinicians and fostered a greater understanding of RP among clinicians, scientists, and the broader community.
Race for RP Partners with Podium eSports and Monday Night Racing for Special eRacing Charity Event
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.