Unfurling the hidden truths about the rare disease, Spinal muscular atrophy (SMA). Tune in on Saturday at 4.30 PM. #CelebrateLife #RocheCares #SMAWarriors #CareForRare #SMAAwareness | News18
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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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Spinal muscular Atrophy (SMA) is a group of genetic diseases that cause muscle weakness and wasting (atrophy) due to the loss of specialized nerve cells called motor neurons. These motor neurons, located in the spinal cord and brainstem, are crucial for controlling voluntary muscle movements like walking, breathing, and swallowing. SMA is primarily caused by mutations in the SMN1 gene, which lead to a deficiency in the SMN protein, essential for motor neuron survival and function. Key aspects of
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