About Us
After over 25 years of experience in the genetic and molecular diagnostics field and building strong networks with clinicians, national health ministry and its subsidiaries including district health authorities, NGOs, academics and companies, we feel a deep sense of responsibility to deliver to all the sections of the society. We realized that the most underserved and vulnerable populations, particularly those from economically weaker sections, are often the ones who need affordable diagnostic services the most. These communities, despite being the most in need, are frequently overlooked when it comes to vital healthcare.
Why Lightening Lives?
Welcome to Lightening Lives ! The company is built up around the principles of Golden circle that focusses on ‘Why’, ‘How’ and ‘What’ in that order to achieve a mission.
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WHY
We do what we believe in and we believe in challenging the status quo by thinking differently. The current burden of genetic disorders is huge and poses challenges such as accessibility, tailored testing, sample convenience, rapid reporting, infrastructure, and affordability.
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HOW
We intend to achieve our WHY by making genetic and molecular diagnostic and screening tests robust, simple, affordable, and user friendly with easy sampling and rapid reporting.
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WHAT
We believe these tests offer a compelling value proposition for healthcare stakeholders by streamlining the logistics of early diagnosis, particularly for newborn screening. This efficiency ensures the timely institution of appropriate treatment, directly enhancing patient outcomes. Additionally, early detection fosters a culture of genetic counseling, enabling the screening of at-risk populations. This comprehensive approach is essential for minimizing the burden of genetic disorders through effective carrier counseling and prenatal diagnosis.
Most organizations communicate from the outside in, starting with WHAT, then HOW, and rarely focusing on WHY. But at Lightening Lives, we follow WHY, HOW, and WHAT in that sequential order.
