We Are | Canada's Rare Voices | Rare Disease Day 2023 

Join patient advocate Meghan White and the rest of Canada's rare disease community as we raise our voices for Rare Disease Day 2023. Read our stories and educational Q&As at www.patientvoi....
Thank you to patient advocates from Stevens-Johnson Syndrome (SJS) Canada, Canadian XLH Network, Cure SMA Canada, The Sumaira Foundation, Thalassemia Foundation of Canada, Fighting Blindness Canada and CF Get Loud for participating in this awareness program.