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rare disease

Patient Access

Being Healthy Is a Privilege

Patient Access

Accelerating Canada's Rare Disease Drug Strategy, Post-Election

Sponsored

Providing Critical Support and Research Funding for Alopecia Areata

Spinal Muscular Atrophy

Research and Development Are Crucial to Discoveries in Rare Disease

Spinal Muscular Atrophy

How Rebecca Van Fraassen Battles SMA Every Day to Live Life to the Fullest

Spinal Muscular Atrophy

New Treatments for SMA Provide Options for Patients

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