• Home
  • Information
    • What is RP?
    • About the CSRP
  • Travel Bursary
  • Support the CSRP
    • Mabels Labels
    • #CANforRP Events
    • Rare Disease Day 2021
  • Videos
  • Articles and Publications
  • Links
    • Race for RP
    • RPASF
  • More
    • Home
    • Information
      • What is RP?
      • About the CSRP
    • Travel Bursary
    • Support the CSRP
      • Mabels Labels
      • #CANforRP Events
      • Rare Disease Day 2021
    • Videos
    • Articles and Publications
    • Links
      • Race for RP
      • RPASF
  • Home
  • Information
    • What is RP?
    • About the CSRP
  • Travel Bursary
  • Support the CSRP
    • Mabels Labels
    • #CANforRP Events
    • Rare Disease Day 2021
  • Videos
  • Articles and Publications
  • Links
    • Race for RP
    • RPASF

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




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