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Karnataka hemophilia society

Dr. Suresh Hanagavadi, was born into a family where health challenges were prevalent, and he faced the harsh realities of Hemophilia early on. His journey took a pivotal turn when his maternal uncle, also afflicted with Hemophilia, died due to a life-threatening bleed without timely medical intervention. This traumatic experience ignited a passion in Dr. Suresh to pursue a career in medicine, driven by a desire to ensure that no one else would have to face such a tragedy.

    Navigating his own condition, he not only focused on his education but also became acutely aware of the systemic gaps in healthcare for patients with bleeding disorders. In 1989, he founded the Karnataka Hemophilia Society (KHS) to provide support, education, and treatment options for individuals with Hemophilia. His advocacy work has been instrumental in securing government support for the procurement of expensive treatments, making Karnataka a model for Hemophilia care across India.

    Through the years, Dr. Suresh has remained a compassionate leader, providing free consultations and services to patients while also engaging in extensive research and awareness campaigns. His personal journey is a testament to his commitment to transforming the landscape of Hemophilia care, inspired by the memory of his uncle and fueled by his own experiences.

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