Скачать или смотреть Support for SMA Patient | The Real Cost Behind Life-Saving Medicine 💊 | Dr. Neeraja Appeals

A heartfelt appeal from Dr. Neeraja, Consultant Neurologist.

🧬 Spinal Muscular Atrophy (SMA) is a rare and life-threatening genetic condition — and for some families, hope comes with an unimaginable price tag.

Today, we revisit the story of Baby Mahansh (15 months), diagnosed with SMA Type 1 — a condition that needs urgent treatment. The life-saving drug costs high. And that’s not just for the medicine —
🔸 Research & development
🔸 Licensing
🔸 Manufacturing rare-dose medications
🔸 Cold-chain transport
🔸 Expert administration
All these contribute to the cost. This isn’t a scam — this is how rare disease medicine actually works.

🎯 We are not asking for sympathy.
We are requesting a small act of solidarity. Even a small amount can create a ripple.

#drneeraja #neurologistguntur #neurocareindia #doctorexplains #neurologyexplained #healtheducationindia #brainhealthindia #parkinsonsawareness

🔗 Donate Now:
👉 https://www.impactguru.com/fundraiser...

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🧠 As a neurologist, I’ve seen pain I couldn’t cure — but I’ve also seen miracles happen through people like you.

🙏 Please watch, share, and support.
Let’s stand together — not just for Mahansh, but for every rare-disease warrior.