RP Advocate Spotlight: Michael Linn, Director / Vice Chair, Relapsing Polychondritis Foundation
![M Linn 3x2 1](https://polychondritis.org/wp-content/uploads/2022/06/M-Linn-3x2-1-1024x683.jpg)
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
RP Advocate Spotlight: David Bammert, Director / President, Relapsing Polychondritis Foundation
![bammert](https://polychondritis.org/wp-content/uploads/2022/06/bammert-web-3x2-1-1024x683.jpg)
Do you have a friend or loved one suffering from RP? Dave Bammert, a Director and President of the Relapsing Polychondritis Foundation and Race for RP, knows firsthand what that is like.
RP Advocate Spotlight: Nancy Linn, Director / Chair, Relapsing Polychondritis Foundation
![nancy web](https://polychondritis.org/wp-content/uploads/2022/06/nancy-web-1024x683.jpg)
Race for RP’s founder, Nancy Linn, has been a catalyst of change in the community! She is a champion for facilitating research working to uncover the underlying cause and develop better treatments for RP.
RP Advocate Spotlight: Gonnie Imeson, Director / Chair, Canadian Society for Relapsing Polychondritis (CSRP)
![gonnie 3x2 web scaled 1](https://polychondritis.org/wp-content/uploads/2022/06/gonnie-3x2-web-scaled-1-1024x683.jpg)
The Canadian Society for Relapsing Polychondritis (CSRP) is an incredible partner in our mission to overcome RP.