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How Rebecca Van Fraassen Battles SMA Every Day to Live Life to the Fullest
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Accessibility
Asthma, Allergies & Better Breathing
Blood Health
Brain Health
Cancer Care
Careers in Health Care
Empowering Aging Canadians
Exploring Your Gut & Microbiome
Future of Health Care
Future of Pharmacy
Heart Health
Immune Health & Wellness
Managing MS
Men's Cancers
Men's Health Care
Mental Health
Pathways to Parenthood
Patient Access & Health Equity
Rare Disease
Sexual & Reproductive Health
Stress Management
Supporting Canadian Caregivers
The Skin We're In
Understanding Neurological Conditions
Women's Health Care
ISSUE: Spinal Muscular Atrophy (2021)
Spinal Muscular Atrophy
How Rebecca Van Fraassen Battles SMA Every Day to Live Life to the Fullest
When Rebecca Van Fraassen was two years old she was diagnosed with spinal muscular atrophy (SMA), a rare genetic disorder.
Spinal Muscular Atrophy
Research and Development Are Crucial to Discoveries in Rare Disease
Spinal Muscular Atrophy
New Treatments for SMA Provide Options for Patients
Campaigns
Living with Spinal Muscular Atrophy
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