RP Foundation
Non-Profit & Charitable Organizations · Indiana, United States · 1-10 Employees
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Overview
Headquarters
6137 Crawfordsville Rd Ste F 232, Speedw...Website
www.polychondritis.orgRevenue
<$5 MillionIndustry
ZI Rank: 1
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ZI Rank
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About RP Foundation
The Relapsing Polychondritis (RP) Foundation is dedicated to supporting patients and families affected by the chronic autoimmune disease, Relapsing Polychondritis. It serves as a catalyst for research and awareness, funding numerous projects aimed at improving treatment options and quality of life for those impacted by RP. The foundation collaborates with various partners to drive innovative research and patient care initiatives. Through events like Race for RP, it seeks to raise awareness and foster community engagement around this rare condition.Explore more
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RP Foundation is experiencing very low activity levels compared to other companies in the Organizations sector.
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RP Foundation News & Media
Relapsing Polychondritis Foundation Renews Partnership with NYU Grossman School of Medicine to Invest in Next Phase of VEXAS Research
This information is from the Relapsing Polychondritis Foundation Inc. (RP Foundation) with Race for RP. (PRWeb March 28, 2023) Read the full story at https://www.prweb.com/releases/relapsing_polychondritis_foundation_renews_partnership_with_nyu_grossman_school_of_medicine_to_invest_in_next_phase_of_vexas_research/prweb19249809.htmRelapsing Polychondritis Foundation Announces Appointment of Frances Sweeney to Board of Directors
This information is from the Relapsing Polychondritis Foundation Inc. with Race for RP. (PRWeb January 09, 2023) Read the full story at https://www.prweb.com/releases/relapsing_polychondritis_foundation_announces_appointment_of_frances_sweeney_to_board_of_directors/prweb19103070.htmThe Relapsing Polychondritis Foundation Invests in the Next Phase of VEXAS Research
The Relapsing Polychondritis Foundation is partnering with the researchers at NYU Langone Health and the NIH who, in 2020, discovered a new autoimmune disease named VEXAS Syndrome, to build upon this exciting and potentially ground-breaking work. (PRWeb March 31, 2022) Read the full story at https://www.prweb.com/releases/the_relapsing_polychondritis_foundation_invests_in_the_next_phase_of_vexas_research/prweb18589849.htmRelapsing Polychondritis Advocate Isabel Bautista Joins American College of Rheumatology Patient Perspectives Program Review Committee
This information is from the Relapsing Polychondritis Foundation Inc. with Race for RP and is not sponsored by, nor a part of, the American College of Rheumatology. (PRWeb May 11, 2021) Read the full story at https://www.prweb.com/releases/relapsing_polychondritis_advocate_isabel_bautista_joins_american_college_of_rheumatology_patient_perspectives_program_review_committee/prweb17926940.htm
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The Relapsing Polychondritis (RP) Foundation is dedicated to supporting patients and families affected by the chronic autoimmune disease, Relapsing Polychondritis. It serves as a catalyst for research and awareness, funding numerous projects aimed at improving treatment options and quality of life for those impacted by RP. The foundation collaborat... Read More
