Drug researcher disputes rare disease medication pricing. Post navigationPreviousPrevious post:HOW MUCH LONGER WILL SMA PATIENTS HAVE TO WAIT TO GET THE APPROVED TREATMENT?NextNext post:Cure SMA Canada has been working feverishly in our fight for broad access to treatment. Related PostsGovernment of Canada improves access to affordable and effective drugs for rare diseasesMarch 27, 2023SPACESAugust 15, 2022August is Spinal Muscular Atrophy (SMA) Awareness month!August 15, 2022Activist Sammy Cavallaro awarded Quebec National Assembly Medal of HonourJuly 18, 2022Cure SMA Canada Conference August 10-14th in Hope, BC.July 6, 2022‘This disease will slowly rob me of everything’: Why are Canadians living with rare diseases waiting for treatment?March 1, 2022
Government of Canada improves access to affordable and effective drugs for rare diseasesMarch 27, 2023
‘This disease will slowly rob me of everything’: Why are Canadians living with rare diseases waiting for treatment?March 1, 2022
