Agenda Post navigationPreviousPrevious post:‘This disease will slowly rob me of everything’: Why are Canadians living with rare diseases waiting for treatment?NextNext post:Activist Sammy Cavallaro awarded Quebec National Assembly Medal of HonourRelated PostsSPACESAugust 15, 2022August is Spinal Muscular Atrophy (SMA) Awareness month!August 15, 2022Activist Sammy Cavallaro awarded Quebec National Assembly Medal of HonourJuly 18, 2022‘This disease will slowly rob me of everything’: Why are Canadians living with rare diseases waiting for treatment?March 1, 2022Health Canada approves Risdiplam!April 16, 2021Interim access to Zolgensma for Alberta childrenJanuary 28, 2021
‘This disease will slowly rob me of everything’: Why are Canadians living with rare diseases waiting for treatment?March 1, 2022
