Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile
Relapsing Polychondritis Foundation

@rp_organization

The RP Foundation’s purpose is to facilitate awareness, education, and research to improve the quality of life for patients with relapsing polychondritis (RP).

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linkhttp://give.polychondritis.org calendar_today21-07-2018 15:19:32

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Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

There's just 3 days left to participate in this year's RP Warrior Walk! Have you signed up yet? It's not too late to get involved. Check out our page to sign up or make your donation now. Click here to get started: give.polychondritis.org/event/2024-rp-…

There's just 3 days left to participate in this year's RP Warrior Walk! Have you signed up yet?

It's not too late to get involved. Check out our page to sign up or make your donation now.

Click here to get started:  give.polychondritis.org/event/2024-rp-…
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

Thanks to a generous, anonymous donor, donations made to the RP Warrior Walk between now and Sunday, November 3 will be doubled up to a total of $25,000! Will you help us reach our goal of raising $50,000? Give Now: give.polychondritis.org/event/2024-rp-…

Thanks to a generous, anonymous donor, donations made to the RP Warrior Walk between now and Sunday, November 3 will be doubled up to a total of $25,000! 

Will you help us reach our goal of raising $50,000?

Give Now:  give.polychondritis.org/event/2024-rp-…
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

This year's RP Warrior 5K Walk was a huge success because of YOU! Thank you to everyone who walked and gave to this year's event. Together, we raised $38,658 to benefit disease awareness and research! Learn more: polychondritis.org/2024/11/relaps…

This year's RP Warrior 5K Walk was a huge success because of YOU!

Thank you to everyone who walked and gave to this year's event.

Together, we raised $38,658 to benefit disease awareness and research!

Learn more:  polychondritis.org/2024/11/relaps…
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

Dec. 3 is #GivingTuesday and The RP Foundation invites you to plan your gift now! Much research is needed to understand better how to diagnose, treat, and cure patients. Where there's research, there's hope. give.polychondritis.org/GivingTuesday2…

Dec. 3 is #GivingTuesday and The RP Foundation invites you to plan your gift now! Much research is needed to understand better how to diagnose, treat, and cure patients. Where there's research, there's hope. give.polychondritis.org/GivingTuesday2…
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

Tomorrow is #GivingTuesday. Don’t forget to plan your impact today and give tomorrow. Your gift has the power to advance relapsing polychondritis and related autoimmune disease research, and improve the lives of patients battling RP. give.polychondritis.org/GivingTuesday2…

Tomorrow is #GivingTuesday. Don’t forget to plan your impact today and give tomorrow. Your gift has the power to advance relapsing polychondritis and related autoimmune disease research, and improve the lives of patients battling RP. give.polychondritis.org/GivingTuesday2…
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

Today is #GivingTuesday. Will you help change a community for the better?  Your gift will fuel relapsing polychondritis and autoimmune-related research to improve the lives of patients. Please consider making your tax-deductible donation now. give.polychondritis.org/GivingTuesday2…

Today is #GivingTuesday. Will you help change a community for the better?  Your gift will fuel relapsing polychondritis and autoimmune-related research to improve the lives of patients. Please consider making your tax-deductible donation now. give.polychondritis.org/GivingTuesday2…
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

As 2024 draws to a close, we'd like to take a moment to extend our most heartfelt thank you for your interest and investment in our organizations. We look forward to building a brighter, healthier future for patients suffering from RP and related autoimmune diseases in 2025.

As 2024 draws to a close, we'd like to take a moment to extend our most heartfelt thank you for your interest and investment in our organizations. We look forward to building a brighter, healthier future for patients suffering from RP and related autoimmune diseases in 2025.
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

Wishing everyone a safe and Happy New Year! Thanks to your continued support, we’ve made great strides in raising awareness and advancing research into RP and other related autoimmune diseases. Check out our progress in our 2024 End-of-Year Message! polychondritis.org/2024/12/2024-e…

Wishing everyone a safe and Happy New Year! Thanks to your continued support, we’ve made great strides in raising awareness and advancing research into RP and other related autoimmune diseases. Check out our progress in our 2024 End-of-Year Message! polychondritis.org/2024/12/2024-e…
Race for RP (@raceforrp) 's Twitter Profile Photo

After an incredible run in the Ferrari Challenge series that generated great awareness for the RP Foundation, “Neilio” Langberg is racing toward a new adventure. Will we see him back on track soon? Exciting news is coming! #RPFoundation #RelapsingPolychondritis

Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

As a founding stakeholder in the Penn Medicine RP Program, the RP Foundation continues to invest in the Penn RP Center. Recently, the center hosted a series of meetings to provide the RP patient community updates from experts in the field. Learn more: med.upenn.edu/pennvasculitis…

As a founding stakeholder in the Penn Medicine RP Program, the RP Foundation continues to invest in the Penn RP Center.  Recently, the center hosted a series of meetings to provide the RP patient community updates from experts in the field. Learn more: med.upenn.edu/pennvasculitis…
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

We are thrilled to congratulate Dr. Merkel on his appointment to lead the Colton Center for Autoimmunity at Penn! As a proud founding partner of the Penn RP Center & long-time collaborator in Dr. Merkel’s groundbreaking research, we're excited to be part of this inspired project.

We are thrilled to congratulate Dr. Merkel on his appointment to lead the Colton Center for Autoimmunity at Penn! As a proud founding partner of the Penn RP Center & long-time collaborator in Dr. Merkel’s groundbreaking research, we're excited to be part of this inspired project.
Race for RP (@raceforrp) 's Twitter Profile Photo

Announcing the new Director's Cut of "The Race Of Our Lives" - now available on RaceforRP.org or at youtu.be/Y0tZYRazk8U #autoimmuneawareness #relapsingpolychondritis #Documentary #directorscut

Race for RP (@raceforrp) 's Twitter Profile Photo

Race for RP partners with McLaren Trophy America as official charity partner! Let’s go!! Read more here: polychondritis.org/2025/03/race-f… #raceforrp #relapsingpolychondritis #autoimmuneawareness

Race for RP partners with McLaren Trophy America as official charity partner! Let’s go!! Read more here: polychondritis.org/2025/03/race-f…
#raceforrp #relapsingpolychondritis #autoimmuneawareness
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

We're proud to support the PURPOSE Biobank & Data Repository. The PURPOSE Biobank is a direct-to-patient initiative to collect blood specimens and medical info from patients with RP and related autoimmune diseases to accelerate discovery &therapies, & ultimately find a cure.

We're proud to support the PURPOSE Biobank & Data Repository. The PURPOSE Biobank is a direct-to-patient initiative to collect blood specimens and medical info from patients with RP and related autoimmune diseases to accelerate discovery &therapies, & ultimately find a cure.
Relapsing Polychondritis Foundation (@rp_organization) 's Twitter Profile Photo

Over 50M Americans live with an autoimmune disease & there are over 100 different types, including Relapsing Polychondritis (RP). We are committed to raising awareness, advancing research & advocating for those impacted. Where there’s research, there’s hope.

Over 50M Americans live with an autoimmune disease & there are over 100 different types, including Relapsing Polychondritis (RP). We are committed to raising awareness, advancing research & advocating for those impacted. Where there’s research, there’s hope.