RP Advocate Spotlight: Michael Linn, Director / Vice Chair, Relapsing Polychondritis Foundation

Do you want to share your gratitude for the amazing things people are doing to advance the cause of RP research? Likes, shares, and comments go a long way to help the RP community! Social media is an incredible way to spread awareness and information about RP.

Meet Mike Linn, the Vice Chair of the Relapsing Polychondritis Foundation. Mike says:

“We want to thank everybody who supports us – on and off the race tracks… It’s a broad community. It’s very inspiring…to have the alignment of interest to truly help the RP patients globally.”

We’ve come a long way, and there are so many people who make a difference. Thank you for your support!

One easy way to help RP patients is to increase awareness, whether through social media or by word of mouth. If you are able and willing to give a monetary donation, please donate by visiting

Michael Linn lends his insights in the “An Advocates’ View on Driving Relapsing Polychondritis Awareness and Accelerating Research” video, which is available below: