Relapsing Polychondritis Foundation

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The RP Foundation’s purpose is to facilitate awareness, education, and research to improve the quality of life for patients with relapsing polychondritis (RP). We are raising awareness of relapsing polychondritis (RP) and fueling autoimmune disease research. The purpose of the Relapsing Polychondritis Foundation is to facilitate awareness, education, and research to improve the quality of life for patients with relapsing polychondritis (RP) and advance a cure for this disease. RP is a debilitating and sometimes fatal systemic inflammatory disease that is characterized by recurrent inflammation of cartilage and other tissues throughout the body. This disease affects multiple organs, particularly cartilaginous structures such as the ears, nose, airways and joints as well as eyes, skin, heart valves and brain. The cause of RP is unknown and there currently is no cure for the disease.

Founded

2014

Facebook

4000

X (Twitter)

1343

Address

Speedway

Address: 6137 Crawfordsville Road Suite F #232, SpeedwayWeb: Sign in to see organisation websiteFacebook: RelapsingPolychondritisX (Twitter): RP_OrganizationEmployees: 1Revenue: 641371ICO: 462458916

A Source of Hope | Relapsing Polychondritis (RP) Foundation Matching Your Courage with Hope The Relapsing Polychondritis RP Foundation is a champion for patients a source of support for family members and a driving force for research and awareness focusing on this debilitating autoimmune disease. We discover sources of hope to match your courage. What is Relapsing Polychondritis RP. Relapsing Polychondritis RP is a severe chronic autoimmune disease in which cartilage throughout the body becomes inflamed and breaks down over time.

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Victoria

1. What innovative strategies can NGOs employ to effectively raise awareness about less-known autoimmune diseases like Relapsing Polychondritis and engage a wider audience in the conversation?

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Helen

❤️ Thank you for shining a light on relapsing polychondritis! Awareness is the first step towards finding support and solutions for those affected. Let's keep pushing for research and hope!

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Kate

2. How can the Relapsing Polychondritis Foundation collaborate with research institutions to accelerate the development of targeted treatments for patients suffering from this disease?

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Lucille

👏 Grateful for the RP Foundation's tireless efforts to help patients and their families! Together, we can raise awareness and fuel the search for effective treatments. Every bit counts!

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