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rare disease

Patient Access
Being Healthy Is a Privilege
Patient Access
Accelerating Canada's Rare Disease Drug Strategy, Post-Election
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Providing Critical Support and Research Funding for Alopecia Areata
Spinal Muscular Atrophy
How Rebecca Van Fraassen Battles SMA Every Day to Live Life to the Fullest
Spinal Muscular Atrophy
Research and Development Are Crucial to Discoveries in Rare Disease
Spinal Muscular Atrophy
New Treatments for SMA Provide Options for Patients
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