JM Punarvika Shri
8 months old · Kurnool, AP
JM Suresh Kumar
Father & Campaigner
📸 Punarvika's Journey
🏥 Medical Diagnosis
Source: Rainbow Children's Hospital, MedGenome Labs & Malaysia Health Association
📋 Medical Certificates
💔 A Father's Plea
When Punarvika was just 5 months old, we noticed something was wrong. She was losing weight, struggling to breathe, and her tiny stomach was growing bigger. The doctors diagnosed SMA Type 1 - Spinal Muscular Atrophy.
SMA is a rare genetic disorder that slowly takes away a child's ability to eat, breathe, and move freely. Since June 2025, Punarvika has been fighting this battle. She cannot move her legs, has no neck control, and needs constant care.
Gene Therapy: Zolgensma
FDA-approved treatment that can CURE SMA
(approx ₹1.05 Crore for the drug alone)
We cannot manage the extremely high cost of this treatment alone. Our daughter needs your help to have a normal life.
"Punarvika Shri is currently undergoing ongoing treatment with regular physiotherapy and medication (Risdiplam). Her recovery requires continuous care and supervision. Your continued prayers and generous support mean so much."
— JM Suresh Kumar
💬 Donor Comments
God bless you Punarvika....
Done from my side. God bless her!
✓ Promise of Authenticity
All medical certificates from Rainbow Hospital, MedGenome Labs, and Malaysia Health Association are verified.
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