Years ago, a diagnosis of spinal muscular atrophy (SMA) meant uncertainty. Today, that story has changed. Individuals and families are finding new strength, research is advancing, and hope is real. Watch our 30-second teaser below to see the lives you have helped impact and the progress your generosity makes possible. The full video premieres later this week. Stay tuned 💜🧡 | Cure SMA

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Stem Cell Treatment for SMA - Spinal Muscular Atrophy

Meet Lyza. Lyza is 22 years old and has been on an approved treatment for spinal muscular atrophy (SMA) for over 7 years. While current treatments have helped her, she’s eager for more. “And there's so many things left to do. There is always room for more.” What would more mean to you? Visit Life Takes Muscle to explore what muscle strength means to people living with SMA: https://bit.ly/3P51CaB #SMAAwareness #CureSMA #SMAStrong | Life Takes Muscle

Spinal muscular atrophy (SMA) treatment has come a long way, from no options to three approved treatments and real hope. But access is still unequal across Canada. This SMA Awareness Month, we’re calling for fair treatment for every person with SMA. #SMAAwarenessMonth | Muscular Dystrophy Canada