Nara Lokesh has stepped forward to support little Punarvika from Kurnool, who is battling a rare genetic disorder, Spinal Muscular Atrophy (SMA) Type-1. Sharing her story on social media, Lokesh appealed to the public to help raise the remaining funds needed for her life-saving treatment.
SMA Type-1 is a severe condition that weakens a child’s muscles over time. It gradually affects movement, breathing, and basic daily functions. Children diagnosed with this disorder require urgent and highly expensive medical intervention to survive.
₹16 Crore Injection Offers Hope
Punarvika’s treatment requires a one-time injection costing ₹16 crore. The amount is beyond the reach of most families. However, her story has moved thousands of people across Andhra Pradesh and beyond.
According to Lokesh, nearly ₹10 crore has already been raised through public contributions. He thanked every donor who stepped forward to support the child. He described Punarvika as a braveheart fighting an extraordinary battle at a very young age.
Appeal for Collective Support
Lokesh stated that it is now time to ensure the remaining ₹6 crore is arranged without delay. He urged authorities and supporters to coordinate efforts so the treatment can be administered at the earliest. He also appealed to citizens to continue contributing generously.
The call for help has gained traction on social media, where users are sharing the hashtag #GodBlessPunarvika to amplify the campaign. Many individuals have expressed solidarity with the family and pledged financial assistance.
A Race Against Time
Medical experts note that early treatment is critical in SMA Type-1 cases. Delays can significantly reduce the effectiveness of therapy. Therefore, supporters emphasise the need to mobilise resources quickly.
Punarvika’s fight has now become a collective mission for many compassionate citizens. With strong public backing and political support, hopes remain high that the required funds will soon be raised, giving the young child a renewed chance at life.
SMA Type-1 is a rare and devastating genetic condition that weakens a child’s muscles and slowly takes away the ability to move, breathe and live normally. Yet little Punarvika from Kurnool, AP, is a true braveheart – fighting this battle with extraordinary courage.
— Lokesh Nara (@naralokesh) February 25, 2026
