Patient Experience
A 67-year-old street vendor with no fixed address was brought in with severe anemia. The laboratory identified a rare hemoglobin variant through capillary electrophoresis that explained lifelong mild symptoms that suddenly worsened. Simple nutritional intervention and regular monitoring at a nearby clinic produced dramatic improvement within weeks.
A 19-year-old college athlete collapsed during training with rhabdomyolysis. Dr. Shankaranarayana's team used rapid mitochondrial enzyme testing to diagnose an inherited metabolic disorder, allowing tailored rehabilitation that enabled return to modified athletic activity within four months with extensive family support system.
A 52-year-old homemaker from a traditional joint family presented with recurrent infections. Advanced flow cytometry revealed a previously undiagnosed primary immunodeficiency. Subcutaneous immunoglobulin therapy initiated by Dr. Shankaranarayana's recommendations transformed her quality of life over eight months, with daughters learning administration techniques.
A 34-year-old migrant worker from Northeast India had persistent fever unresponsive to standard treatments. The laboratory cultured a rare antibiotic-resistant bacterium using specialized media, guiding targeted therapy that resolved the infection when broad-spectrum antibiotics had failed for weeks.
A 61-year-old retired banker with complex polypharmacy developed unexplained liver dysfunction. Dr. Shankaranarayana's team used mass spectrometry to identify a dangerous drug interaction missed by electronic systems, leading to medication reconciliation and complete liver recovery within three weeks without family involvement.
A 5-year-old adopted child from conflict zone presented with developmental delays. Chromosomal microarray analysis revealed a novel microdeletion syndrome, providing answers to years of diagnostic uncertainty and enabling targeted early intervention therapies with dramatic developmental progress over six months.
A 39-year-old vegan nutritionist developed severe neurological symptoms. The laboratory's sophisticated B12 deficiency testing revealed a genetic absorption disorder, requiring monthly injections that produced remarkable symptom reversal within two months, challenging the patient's professional beliefs about nutrition.
A 71-year-old farmer with chronic kidney disease showed paradoxical lab results. Dr. Shankaranarayana personally investigated and discovered laboratory interference from agricultural chemical exposure, developing a new testing protocol that accurately monitored his condition while addressing environmental health concerns.
A 23-year-old medical student self-referred with concerns about hereditary cancer risk. Advanced genetic panel testing coordinated by Dr. Shankaranarayana revealed a low-penetrance variant, providing reassurance and personalized screening recommendations that allowed continuation of medical studies without anxiety.
Our newborn daughter was diagnosed with congenital diaphragmatic hernia and required immediate surgery. Dr. Koushik Herle performed the delicate procedure with such precision and care. His calm demeanor reassured us during the most terrifying hours of our lives. Today, our baby is thriving and hitting all her milestones, thanks to his expertise.
As parents of a 12-year-old with severe pectus excavatum, we consulted multiple surgeons before meeting Dr. Herle. His innovative minimally invasive approach and detailed explanation won our confidence. The surgery was a success, and our son's confidence has soared along with his improved breathing capacity.
Our 3-year-old accidentally swallowed a button battery - every parent's nightmare. Dr. Herle's team at Manipal Hospital acted swiftly, performing an emergency endoscopy to remove it. His quick thinking prevented serious tissue damage, and he personally called us twice daily during recovery to check on our child.
When our teenage daughter needed surgery for ovarian torsion, we were hesitant about a pediatric surgeon. Dr. Herle's expertise in adolescent gynecological surgery and his respectful approach made all the difference. He preserved her fertility and helped her recover with minimal scarring.
Our 7-year-old with Hirschsprung's disease had failed previous surgeries elsewhere. Dr. Herle revised the procedure with remarkable skill, using advanced laparoscopic techniques. For the first time, our child is experiencing normal bowel function and quality of life.
During a routine checkup, Dr. Herle detected an undiagnosed heart murmur in our 5-year-old that turned out to be a congenital defect requiring immediate attention. His thorough examination and referral to the right cardiac specialist saved our child from potential complications.
Our infant son was born with an abdominal wall defect that required complex reconstruction. Dr. Herle's surgical artistry is evident in how beautifully the incision has healed. His follow-up care has been exceptional, always available for our concerns no matter how small.
When our 15-year-old needed emergency appendectomy during exam season, Dr. Herle coordinated with the hospital to create a quiet recovery environment where she could study. His understanding of adolescent needs went beyond medical care to holistic patient support.
Our 8-year-old with chronic constipation had been through multiple treatments without success. Dr. Herle diagnosed an underlying anatomical issue and performed a corrective surgery that transformed our child's life. His patience in explaining the condition to our child was remarkable.
After a terrible accident, our 6-year-old needed complex hand reconstruction. Dr. Herle's microsurgical skills restored function and sensation perfectly. His compassionate approach to our frightened child made the hospital experience much less traumatic.
Our premature twins both required hernia repairs. Dr. Herle scheduled their surgeries strategically and managed their care with incredible attention to detail. His experience with multiple birth complications was evident throughout their treatment.