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

RP Advocate Spotlight: David Bammert, Director / President, Relapsing Polychondritis Foundation

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

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)

The Canadian Society for Relapsing Polychondritis (CSRP) is an incredible partner in our mission to overcome RP.