A Cry for Hope: Baby Keerthana’s Fight Against a Rare Genetic Disorder

In the heart of Mysore, a young child named Baby Keerthana K, just 1 year and 11 months old, is facing a life-threatening battle with Spinal Muscular Atrophy (SMA) Type II—a rare and progressive neuromuscular disorder. Born on January 11, 2023, to parents Kirshore N and Nagashree H, Keerthana’s journey has taken a painful turn due to this debilitating disease that leads to gradual nerve degeneration in the spinal cord.

SMA Type II demands immediate and aggressive treatment, without which the condition can severely compromise her quality of life and survival. The prescribed drug, considered a life-saving therapy, is unfortunately not manufactured in India and comes at an astronomical cost of Rs. 16 crore (approximately 2.1 million USD).

The treatment, currently costing around Rs. 50 lakh per year, is only expected to rise as Keerthana grows. This immense financial burden is well beyond the means of her family.

But there is still hope.

We reach out to compassionate individuals, organizations, and well-wishers across the world to come forward and help mobilize funds. Your contribution, however big or small, can be a lifeline for Keerthana—offering her not just a chance to live, but to thrive.

By supporting her treatment, you aren’t just donating—you are becoming part of a life-saving mission. Let your kindness shine as a beacon of hope for this brave little girl and for many other families enduring similar struggles.

If you wish to contribute or learn more, please reach out to the family at:
📞 9901262206 / 9980690234

Together, let us give Keerthana a future full of dreams, smiles, and strength.