Скачать или смотреть SAVE PUNARVIKA | WHY GOVERNMENT NOT RESPONDING? 😭

This video is not for entertainment… this is a public awareness request 🙏.
Baby Punarvika from Andhra Pradesh is fighting a rare and life-threatening disease called Spinal Muscular Atrophy (SMA Type-1). This condition slowly weakens muscles and breathing. Doctors advised a special gene therapy injection, but the cost is around ₹16 crore, which her family cannot afford.

Many students, youth, and common people are coming forward to help. But this issue should not be limited to one child only. There are many children in India suffering from rare diseases. This video is created to raise awareness and request government authorities, celebrities, and responsible people to take action and support such children.

Even if you cannot donate, your one share can reach thousands and help save a life. Please watch, share, and spread this message so that it reaches CM and Deputy CM and creates a permanent solution for rare disease treatment in India.

Let us show that humanity is still alive ❤️.
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⚠️ Disclaimer

This video is made only for awareness and educational purposes.
The information shared is collected from public and social media sources. The intention of this video is not to criticize, defame, or hurt any individual, government, organization, or celebrity. It is purely to spread awareness and request support for rare disease patients.


📌 Copyright

This content is created under fair use for awareness, education, and public interest.
All images, clips, and references used belong to their respective owners. If any owner has concerns, please contact us for credit or removal.

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