I’m raising urgent funds for my beloved son, Sammya, who has been diagnosed with a rare and life-threatening genetic disorder called Spinal Muscular Atrophy Type 1 (SMA Type 1).
Sammya is just 8 months old and is already fighting a battle no child should ever face. SMA Type 1 affects his muscles, making it difficult for him to move, eat, or even breathe properly. Without immediate treatment, his condition will continue to worsen.
The only hope for Sammya is gene therapy, which costs over ₹16 crore. This is far beyond what we can afford on our own. That’s why we are reaching out to you—with all our hope and heart.