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 | Firstpost

2.3M views · 10K reactions | Jaya Kishori Ji the spiritual speaker has joined the fight for baby kanav's life and requests you to come to his rescue. Jangra family is seeing their world slip away right in front of their eyes. Their baby’s SMA diagnosis has shattered thier heart. They need ₹17.50 crores to save their son’s life.Let’s save baby Kanav together from the deadly disease. Donate Now : https://bit.ly/3X2kj05 | Impact Guru | Facebook

💔 Save Baby Mahansh – 15 Months Old, Fighting a Rare Disease 🧬 This is not just another case. 👶 Mahansh, just 15 months old, has been diagnosed with Spinal Muscular Atrophy (SMA –) — a rare, genetic neuro-muscular disease that weakens muscles and can affect breathing, swallowing, and survival. 🩺 Dr. Neeraja shares Mahansh’s story to raise awareness and support. The treatment cost is in crores – and the family urgently needs help. 🤲 You can make a difference. 💳 Donate here: 🔗 https://www.i

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