RP Research Scientist Spotlight: Emily Rose, BS

Skyhook Interactive
May 24, 2020

[vc_single_image image=”2745″ img_size=”large” alignment=”center”]The Relapsing Polychondritis Foundation actively pursues effective treatments for relapsing polychondritis. Fortunately, there are amazing researchers all over the world who are using their expertise to help patients with RP.

We are pleased to recognize Emily Rose, a medical student, who works with skill and enthusiasm on RP research. Emily played a key role at the RP Investigators Meeting in Atlanta on 9 November 2019.

We are grateful for Emily’s contributions to date and are highly confident she will have an excellent career helping patients worldwide.

Please join us in salute of Emily and all others who support the RP community by sharing this post (and others) on social media.Emily Rose and other experts generously share their insights in “The Need for New Treatments for Relapsing Polychondritis and the Next Steps” video below:[vc_video link=”https://youtu.be/XW11uARMX2Y”]

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Relapsing Polychondritis Foundation
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All content of this web site, such as text, graphics, images, or any other material contained in this website are for informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. We do not recommend the self-management of health problems. We cannot and do not give you medical advice. If you think you may have a medical emergency, call your doctor or 911 immediately. The Relapsing Polychondritis Foundation, Inc. is a nonprofit 501(c)3 corporation. Donations are tax deductible as allowed by law.