Relapsing Polychondritis Foundation

Turning awareness into action.

The RP Foundation leads the effort to advance research, awareness and education for Relapsing Polychondritis.
Race for RP helps fuel that mission - one story, one partnership, one race at a time.

Thomas‘s mother, Jane Bowles, battled RP for eight years and believed deeply in better information and care for patients. In her honor, Thomas and seven friends created Prague for progress to support RP and autoimmune disease research.

Today, February 28, is Rare Disease Day. At the Relapsing Polychondritis Foundation, we stand with patients, caregivers, and researchers working toward better understanding, better care, and ultimately a cure. Rare may be the diagnosis, but no one should face it alone. Log onto polychondrtis.org to learn more or to donate.