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.

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.

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.

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. ❤️