Relapsing Polychondritis Awareness and Support Foundation Releases “RP The Ride of My Life”

The Relapsing Polychondritis Awareness and Support Foundation is proud to release its first documentary, “RP The Ride of My Life,” chronicling one woman’s journey to live life with purpose while suffering from Relapsing Polychondritis (RP), a rare autoimmune disease. [imic_button colour=”btn-default” type=”enabled” link=”https://globalgenes.org/raredaily/relapsing-polychondritis-awareness-and-support-foundation-releases-rp-the-ride-of-my-life/” target=”_blank” extraclass=”” size=”btn-lg”]Learn More[/imic_button] [imic_button colour=”btn-default” type=”enabled” link=”https://rpf-new-staging.skybox2.com/the-ride-of-my-life/” target=”_blank” extraclass=”” size=”btn-lg”]Watch Video[/imic_button]