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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. 

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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