I joined KTG because I strongly believe in the power of the community to raise awareness and support for rare diseases. My journey with KTG began after witnessing the impact of Retinoblastoma in my own community in a small village in India, which opened my eyes to the need for education, advocacy, and accessible resources in our region. I have seen firsthand how lack of awareness can affect patients and their loved ones. Through KTG, I hope to contribute by spreading knowledge towards preventable causes of child mortality, supporting affected families, and helping build a stronger network of understanding in my part of the world.
Outside of KTG, I come from a family that values education, empathy, and resilience. I have pursued my medical school & pediatric training in India, which has helped me develop skills in child advocacy, having trained in high pressure, resource-limited settings, which I am profoundly proud of. Outside of medicine, I enjoy content writing about policies, communities and patient care. I am committed to using my experiences, both personal and professional, to make a meaningful impact and to continue learning from the incredible community that KTG has built.
