We are pleased to share that the RP Foundation is bringing RP and related autoimmune diseases to the forefront of ground-breaking scientific discoveries, thanks to the concerted efforts of the talented researchers that we’re investing in. Here’s an update from our partners on what they’ve been working on for the past 6 months.
The Ride of My Life documentary features Nancy Linn’s journey toward being diagnosed with Relapsing Polychondritis and her commitment to turn this potentially dire diagnosis into something positive by “living with purpose.”
The Relapsing Polychondritis (RP) Foundation is pleased to announce it will continue and expand its partnership with NYU Grossman School of Medicine to invest in and advance the next phase of collaborative VEXAS research.
We’re excited to share that we represented relapsing polychondritis at the NIH Rare Disease Day. The goal of this event is to raise rare disease awareness, spotlight those impacted by rare diseases, and NIH collaborations that advance research for new treatments.