My name is Muthukrishnan, and I am raising urgent funds for my beloved son  (1 year 10 months), who has been diagnosed with Spinal Muscular Atrophy (SMA Type 2) — a rare, life-threatening genetic disorder that weakens his muscles and affects essential functions like breathing and swallowing. SMA progressively worsens without treatment, and while physiotherapy helps manage symptoms, it cannot stop the disease. 

After thorough medical evaluation, doctors have advised a life-saving gene therapy — Zolgensma, a one-time treatment that delivers a functional copy of the defective SMN gene and can halt the progression of SMA and give him a chance at a healthy, independent life. However, the cost of this treatment is approximately USD 2.1 million (about ₹16–18 crore) — far beyond our family’s financial capacity.
He is currently under care at Bangalore Baptist Hospital, Bengaluru, Karnataka, and every prayer and contribution strengthens our hope. Your support — whether through donation, sharing our campaign, or spreading awareness — is more than financial help; it is a gift of time, strength, and a future for our little boy who deserves a chance to live and thrive. With hope in our hearts and faith in humanity, we humbly ask for your support. 🙏