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.

lines
Avery
“RP foundation is making everything more accessible; through information, through other people’s stories, and through what they are trying to do in bringing awareness. It allows patients and others to recognize and take a step back and say, I might have that.”
Holli
“Relapsing polychondritis is a rare disease that can affect even the simplest moments of everyday life—especially during severe flare-ups.”
dan smith 1

Dan

“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.”

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.