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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.

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naomi
“The research that we’re doing is helping us learn more about this disease (RP) and then develop effective therapies.”
miriam
“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.”
patty
“When I went to the NIH and I saw the things that they have the ability to do, the research that they’re doing now – that wasn’t there 10 years ago.”

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.