The Relapsing Polychondritis Awareness and Support Foundation (RPASF) is pleased to present a story of the challenges, disappointments, hopes and dreams of living a life with purpose while suffering from the rare disease, relapsing polychondritis, which is commonly known as “RP.”
Please View:
“RP The Ride of My Life”
A documentary about Relapsing Polychondritis, a rare autoimmune disease.
Click here to watch the entire video
Click here to watch the trailer
Visit The Foundation At: polychondritis.org
For more information contact: rideofmylife@polychondritis.org
Won’t you please help us achieve our purpose by making a donation now?
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A 501(c)(3) Organization