“Relapsing polychondritis is a very hard disease to figure out and that’s where the Relapsing Polychondritis Foundation and the Race for RP really come in to play.”
RP is so rare that it’s easy to feel alone on your journey. But you’re not alone. Meet patients like you and the researchers working to find treatments.
We’re building a community of RP patients, families, doctors, and researchers. Do you have a story of hope you’d like to share with our RP community? If so, we’d love to hear it.