Patient Experience
A 63-year-old retired schoolteacher with multiple comorbidities including diabetes and hypertension developed Fournier's gangrene. Dr. Manikandan led an emergency multidisciplinary team for aggressive debridement and reconstruction. After three months of wound care and multiple procedures, the patient made a remarkable recovery with minimal functional impairment.
A 34-year-old ******* woman undergoing gender affirmation therapy developed urethral complications. Dr. Manikandan collaborated with plastic surgeons to perform complex urethral reconstruction using buccal mucosa graft. The innovative approach resulted in successful voiding function after four months of staged procedures.
A 51-year-old corporate executive presented with renal calculi but was found to have an incidental small renal mass. Dr. Manikandan performed partial nephrectomy using ice-slush renal cooling technique, preserving 90% of renal function. The executive returned to international business travel within a month.
A 19-year-old college athlete from a middle-class family developed testicular torsion during cricket practice. Dr. Manikandan performed emergency detorsion and bilateral orchidopexy within the critical window, saving testicular function. The patient returned to competitive sports after three months with no limitations.
An 81-year-old grandmother with dementia and recurrent UTIs was brought by her grandchildren. Dr. Manikandan implemented a comprehensive management plan including behavioral modifications, timed voiding, and low-dose prophylaxis. Family education resulted in 90% reduction in infections over six months.
A 42-year-old rickshaw driver presented with chronic pelvic pain syndrome. Instead of immediate intervention, Dr. Manikandan prescribed a multimodal approach including physical therapy, dietary changes, and stress management. Significant improvement was noted within eight weeks without surgical intervention.
A 7-year-old boy from a tribal community with posterior urethral valves was airlifted to MIOT. Dr. Manikandan performed endoscopic valve ablation and managed subsequent renal impairment with careful monitoring. The child's renal function stabilized over two years with ongoing follow-up.
A 58-year-old woman with neurogenic bladder from spinal cord injury developed autonomic dysreflexia during urodynamics. Dr. Manikandan's team managed the emergency seamlessly and subsequently implanted a sacral neuromodulator, dramatically improving her quality of life with reduced catheter dependence.
A 31-year-old research scholar from Germany, visiting Chennai, developed emphysematous pyelonephritis. Dr. Manikandan performed emergency percutaneous drainage followed by staged nephrectomy, coordinating care between local and international medical teams for seamless continuation of treatment back home.
Dr. riya achamma daniel provided exceptional care for my dental surgery condition. The treatment was personalized and effective.
As a 72-year-old retired botanist with unexplained neurological decline, I was misdiagnosed for years until Dr. Grace Swarna Priya identified my rare ATXN2 gene mutation. Her personalized management plan at MIOT Hospital has slowed my progression remarkably, I can now enjoy gardening again with adapted tools.
Our 6-month-old daughter stopped meeting developmental milestones, and multiple doctors were baffled. Dr. Priya's whole-exome sequencing revealed a novel GRIN1 variant. Her compassionate guidance through experimental treatment access gave our family hope where there was none.
A construction worker at 38, I suddenly developed unusual cardiac symptoms. Dr. Priya diagnosed familial amyloidosis through genetic testing and coordinated a liver transplant before irreversible damage. Her emergency intervention saved my life and three relatives who were subsequently diagnosed.
After losing three pregnancies, we found Dr. Priya who discovered a balanced translocation through advanced karyotyping. Her preimplantation genetic diagnosis guidance resulted in our healthy twins, she didn't just treat a condition but built our family.
As a 19-year-old college athlete, my sudden vision changes were diagnosed as Leber's hereditary optic neuropathy by Dr. Priya. Her gene therapy trial enrollment preserved vision in my other eye, I'm now studying genetic counseling inspired by her work.
Our 8-year-old son's mysterious seizures were solved by Dr. Priya's identification of a SCN1A mutation. Her tailored ketogenic diet and medication protocol reduced episodes by 90%. She even educated his school teachers about his condition.
A 55-year-old with family history of early cancers, Dr. Priya found my Lynch syndrome mutation and implemented surveillance that caught colon cancer at stage 1. Her preventive approach literally saved me from chemotherapy.
When my 13-year-old developed sudden psychiatric symptoms, Dr. Priya diagnosed Wilson's disease through genetic testing, a complete paradigm shift from initial psychiatric diagnoses. Chelation therapy reversed symptoms completely within months.
As identical twins at 65, we both developed different cancers. Dr. Priya's investigation revealed we were actually chimeric twins with different genetic profiles, revolutionizing our treatment plans at MIOT Hospital.
I was impressed by the professional approach at Miot Hospital Chennai. Dr. karthik sudhan mathivanan explained everything clearly and made me feel comfortable.