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Lokesh Commits to Raise ₹6 Crore for SMA Treatment

Lokesh Pledges ₹6 Crore to Save Kurnool Girl Battling Rare SMA, Donors Rally Nationwide

Vijayawada: IT and education Minister Nara Lokesh on Tuesday pledged to mobilise `6 crore required for the life-saving treatment of Punarvika, a young girl from Kurnool diagnosed with Spinal Muscular Atrophy (SMA) Type-1, a rare and severe genetic disorder.

The announcement followed an appeal made by Punarvika’s parents on social media, seeking help for their daughter’s treatment, which requires an injection costing Rs 16 crore. They stated that public contributions had already helped them raise nearly ₹10 crore.
Responding to the appeal, Lokesh said SMA Type-1 is a debilitating condition that gradually weakens muscles and affects vital functions. He said it was now his responsibility to help raise the remaining ₹6 crore and directed his office to immediately coordinate efforts for the fundraising.
The minister also acknowledged the support extended by donors across the country and praised their generosity in coming forward to support the child.
The announcement drew widespread appreciation, with actor Manchu Manoj and others taking to social media to commend the minister’s swift response and to further amplify the campaign.


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