Facts Cola on Instagram: "Please DO NOT SKIP this video. This is not a request for money, but a desperate plea for a single SHARE that could save an 8-month-old baby girl's life. 🙏😭 #reels # Trending Meet Baby Punarvika, who is battling a deadly and rare genetic disorder called Spinal Muscular Atrophy (SMA Type 1). This terrifying disease silently destroys a baby's nervous system, leaving them unable to swallow milk, cry, or even breathe properly. The parents are watching their little angel fade away in front of their eyes, completely helpless. The Cure Exists, But It Costs ₹16 Crores! There is a life-saving medicine called the 'Zolgensma' injection, but it costs a staggering 16 Crore Rupees. Even if the parents sell everything they own, they cannot afford this massive amount. How YOU Can Save Her Without Giving a Single Rupee: We are not asking for your money. We have not attached any account numbers or QR codes. All we ask from you with folded hands is to SHARE this video. Share it on your WhatsApp Status. Share it in your family and friends groups. Tag government officials, NGOs, and philanthropists in the comments. Your one share could act as a messenger of God. If this video reaches the Government, the Chief Minister, or kind-hearted leaders like Sonu Sood, Baby Punarvika can get the medical help she urgently needs. Please take 10 seconds of your time. Let us use the power of social media for humanity. Let's unite to give this baby a chance to live! 🥺🙏 Please tag @SonuSood, @PMOIndia, and local government officials in the comments! #SavePunarvika #SMAType1 #Zolgensma #FactsCola HumanityFirst SaveALife RareDisease MedicalEmergency CrowdfundingIndia SonuSood HelpPunarvika SocialMediaForGood ViralForACause Disclaimer: This video is created solely for public awareness to support 8-month-old Baby Punarvika, who is diagnosed with Spinal Muscular Atrophy (SMA Type 1). This channel is not directly collecting any funds, running a financial campaign, or managing donations. Our only goal is to amplify the family's plea so it reaches government authorities, NGOs, and philanthropists for urgent medical intervention."
107K likes, 3,012 comments - facts_cola on February 24, 2026: "Please DO NOT SKIP this video. This is not a request for money, but a desperate plea for a single SHARE that could save an 8-month-old baby girl's life. 🙏😭
#reels # Trending
Meet Baby Punarvika, who is battling a deadly and rare genetic disorder called Spinal Muscular Atrophy (SMA Type 1). This terrifying disease silently destroys a baby's nervous system, leaving them unable to swallow milk, cry, or even breathe properly. The parents are watching their little angel fade away in front of their eyes, completely helpless.
The Cure Exists, But It Costs ₹16 Crores!
There is a life-saving medicine called the 'Zolgensma' injection, but it costs a staggering 16 Crore Rupees. Even
