What is the Canadian Society for Relapsing Polychondritis (CSRP)?
We are a non-profit organization that focuses on education, awareness, and support for RP patients, their families, and the medical community.
Meet Your Board
From left to right;
Denise Lau (BC) Director/Co-Chair
Grace Alarcon-Isla (AB) Mother of RP Patient - Director/Treasurer
Gonnie Imeson (AB) RP Patient - Director/Chair
Tamara Tejada (AB) Director/Secretary