candid seal platinum 2024
penn youtube covers1

Stories of Hope

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.

dan smith 1


“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.”
“I want people to have hope. There is research going and things are going to be better for them. Thanks to the Relapsing Polychondritis Foundation and Race for RP, we’ve been able to make advances in diagnosing and helping people.”

Share Your Story of Hope

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.