As a father, there is nothing more devastating than watching your newborn fight for his life. My child is just 2 months old and has been diagnosed with Spinal Muscular Atrophy (SMA) Type 1 — one of the most severe and life-threatening genetic conditions a child can be born with. This disease rapidly destroys the nerve cells that control muscle movement, and without urgent intervention, the damage becomes irreversible within months.

The only treatment that can give my child a fighting chance is Zolgensma, a one-time gene therapy that must be administered as early as possible to prevent permanent muscle deterioration. The total estimated cost of this treatment is ₹17,00,00,000 — an amount that is completely beyond our reach as a family in Hyderabad, Telangana. We have exhausted every option available to us, and we are now turning to you with all the hope we have left. Medical reports confirming the diagnosis are attached to this campaign for full transparency.

Time is not on our side. Every day that passes without treatment increases the risk of irreversible harm to my baby boy. I am reaching out to every kind soul who can help — whether through a donation or simply by sharing this campaign. No contribution is too small. Please stand with our family in this impossible moment and help us give our child the chance to live, grow, and thrive. Your support can truly save a life.