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

Skyhook Interactive
January 12, 2017

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.

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[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]

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Relapsing Polychondritis Foundation
6137 Crawfordsville Road
Suite F #232
Speedway, Indiana 46224

Federal Tax ID 46-2458916

admin@polychondritis.org

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All content of this web site, such as text, graphics, images, or any other material contained in this website are for informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. We do not recommend the self-management of health problems. We cannot and do not give you medical advice. If you think you may have a medical emergency, call your doctor or 911 immediately. The Relapsing Polychondritis Foundation, Inc. is a nonprofit 501(c)3 corporation. Donations are tax deductible as allowed by law.