Solutions We Provide
Genetic & Molecular Testing
Affordable screening panels for carriers, patients, newborns, and communities.
Preventive & Community Health
Awareness camps and counseling to prevent genetic disorders.
Research & Development
Developing rapid and robust kits for genetic disorders/NCDs and access to Biobank research data.
Training & Capacity Building
Workshops and skill-building for labs and healthcare professionals.
Partnerships & Consultancy
Collaborations and expert guidance for hospitals, NGOs, and public health programs.
About Us
Why LLP exists?
Welcome to Lightening Lives ! The company is built up around the principles of Golden circle that focusses on ‘Why’, ‘What’ and ‘How’ in that order to achieve a mission.
- WHAT: Every company or individual knows what they do, whether it's a product, service, or job role. This is easy to identify.
- HOW: Some people or organizations understand how they do what they do—this could be a unique process or selling point, but it's not as obvious as WHAT.
- WHY: Few can clearly explain why they do what they do. The WHY isn't about making money—it's about the purpose, cause, or belief driving their actions. WHY is the core motivation.
Most organizations communicate from the outside in, starting with WHAT, then HOW, and rarely focusing on WHY. But at Lightening Lives we follow Why, What and How in the sequential order. Here is our Why, What and How
Impact Stories From Lightening Lives
Each story reminds us why we began—every child’s smile, every family’s relief, and every life changed fills us with gratitude. At Lightening Lives, we are humbled to serve humanity by bringing hope where it’s needed the most through science and innovation.
In a small tribal village of Madhya Pradesh, a 3-year-old boy was showing signs of muscle weakness. His family had no access to specialized hospitals and assumed it was just a nutritional issue. Through an NGO, they came across Lightening Lives’s affordable molecular test, and he was quickly diagnosed with Duchenne Muscular Dystrophy (DMD). Timely diagnosis allowed the family to start supportive therapy early, join patient support groups, and prevent years of uncertainty. For the first time, they felt empowered with knowledge, not fear.
A tribal couple from Chhattisgarh lost their first child to Spinal Muscular Atrophy (SMA) without ever knowing the cause. When they approached us through a government screening platform, during their second pregnancy, we carried out carrier testing. Results showed both parents carried the SMA mutation. With genetic counseling and early testing, they made an informed decision that prevented the recurrence of this devastating disease. Today, they have a healthy child, and the couple often says—“We didn’t just save a child, we saved our family’s future.”
In a tribal hamlet of Odisha, a young couple came to us after noticing similar breathing difficulties, muscle weakness, severe anaemia and prolonged repeated infections in two children in their extended family. Our robust molecular testing revealed both were carriers of Sickle Cell Anaemia (SCA). With this knowledge, they were able to avoid passing the condition on to their children. This simple, quick test broke a generational cycle of suffering that the community thought was “fate.” For the first time, science brought hope.
A tribal mother in Jharkhand brought her 6-year-old daughter to a local health camp where we were conducting awareness and testing. The girl was diagnosed with DMD at an early stage. The mother also underwent carrier testing and was found positive. With this crucial knowledge, the family received counseling and could make informed choices for future pregnancies. They told us, “We never knew such testing existed for people like us. You have given us knowledge that will save our next child.”
Products
CSIR-SCAN
SickThal/
DualHemoDetect
AccelHemo/
HemoSwift
OmniAllInOneLyo
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Affordable & Innovative Diagnostic Solutions for All
Cutting-edge Genetic Tests
From carrier screening to newborn testing, we provide accurate, rapid, and low-cost molecular diagnostics tailored to community needs.
Innovative Diagnostic Kits
Our CSIR-SCAN, SickThal, and HemoSwift kits ensure faster, more reliable results—empowering labs, hospitals, and communities with accessible solutions.
Why Choose Us
Why We Started Lightening Lives
After over 25 years of experience in the diagnostics field and building strong networks with clinicians, national health ministers, NGOs, academics, and companies, we felt a deep responsibility to give back 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.
Our Mission
We partner with clinicians, NGOs, and health ministries to expand newborn screening and genetic counseling. Our one-drop blood test delivers fast, painless, and accurate results within a day—bringing early diagnosis to underserved communities.
What We Do
We provide affordable and reliable tests for hemoglobinopathies and musculopathies, ensuring underprivileged communities get access to early detection and timely care for better health and quality of life.
