<div>Our baby boy, Moksha, is just 4 months old — a tiny soul who should only know love, laughter, and lullabies right now. But life had other plans. He’s been diagnosed with Spinal Muscular Atrophy (SMA), a rare genetic disease that weakens muscles and can even take away the ability to move or breathe.
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<div>There is hope — a one-time gene therapy can save his life. But this treatment costs several crores in India (around  $1.8M in USD) and must be given urgently. Every single day matters.
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<div>As parents, it’s heartbreaking to know that our baby’s chance at life depends on how quickly we can raise the funds. We’re doing everything we can, but we can’t do it alone.
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<div>Please help us give Moksha the chance to live, smile, and grow up like every child deserves — by donating or sharing his story. Your support means the world to us and could truly save his life. ❤️
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Anonymous

Anand Chiluka

Shaswati Mukherjee

Ravindra Penugonda

Supriya Gowda

Bhanu Prasad

Gerald Carvalho

Yuvaan Gowda

RAMESH R KETHIREDDI

Naveen Kumar Balaneni

Nagendar Thallam

Satwik Mancholla

Ashley Bose

Saranya Mandava

Ankith Mandugula

Gene Therapy for Moksha's SMA Battle

Gene Therapy for Moksha's SMA Battle

Still $1,748,070 to go. Help us build momentum.