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Foundation News​

We’re busy creating research partnerships and advancing awareness for RP. Here’s a look at what we’ve been up to.
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Thank you to everyone who attended this one-of-a-kind event that rasied over $26,000 for RP and related autoimmune research.
New York – January 25, 2023 – This information is from the Relapsing Polychondritis Foundation Inc. (RP Foundation) with Race for RP. A new study by investigators from the National Institutes of Health (NIH) and New York University Grossman School of Medicine (NYU Grossman), published online in the Journal of the American Medical Association (JAMA) on January 24, found that the recently discovered inflammatory disease VEXAS syndrome is more common than previously understood.