Dr. Rana Saha Reviews

A 7-year-old boy from an affluent family presented with recurrent febrile seizures; Dr. Saha identified an unusual electrolyte imbalance linked to his exclusive bottled water consumption, corrected it with dietary changes, and prevented further episodes without medication.

An impoverished 4-year-old girl with severe malnutrition and persistent cough was found to have multidrug-resistant tuberculosis; Dr. Saha coordinated with NGOs for free medication, provided nutritional guidance to her single mother, and achieved full recovery after 9 months of closely monitored treatment.

A 12-year-old aspiring athlete from a middle-class family developed unexplained fatigue; Dr. Saha diagnosed early-onset Addison's disease through meticulous hormone testing, initiated steroid replacement therapy, and gradually reintroduced athletic training under careful supervision.

A 3-day-old neonate from a remote village was rushed in with critical congenital heart disease; Dr. Saha arranged emergency transfer to a cardiac center, maintained communication with the anxious parents via daily updates, and the baby successfully underwent life-saving surgery.

A teenage girl from an educated family presented with psychosomatic abdominal pain; Dr. Saha discovered underlying school-related anxiety, involved both parents in counseling sessions, and implemented a holistic mind-body approach that resolved symptoms within weeks.

A 5-year-old boy with cerebral palsy from a low-income household developed severe contractures; Dr. Saha designed a home-based physiotherapy program using household items, trained his grandmother as primary caregiver, and significantly improved joint mobility over six months.

An 8-year-old adopted child with mysterious episodic rashes was diagnosed with rare mast cell activation syndrome; Dr. Saha created a personalized trigger-avoidance plan and emergency protocol, empowering the adoptive parents to manage flare-ups confidently.

A 10-year-old diabetic patient from a tech-savvy family was struggling with glucose control; Dr. Saha incorporated a continuous glucose monitor and smartphone app, involving the patient in his own data tracking, resulting in dramatically improved HbA1c levels.

A 2-year-old twins from a nuclear family presented with failure to thrive; Dr. Saha identified severe cow's milk protein allergy in both, switched them to specialized formula, and provided biweekly growth monitoring until they caught up to percentile curves.

A 15-year-old boy from a conservative family developed sudden neurological symptoms; Dr. Saha diagnosed autoimmune encephalitis, initiated immunosuppressive therapy against family initial reluctance, and achieved complete neurological recovery after three months.

A 6-month-old infant from a migrant worker family presented with developmental delays; Dr. Saha discovered congenital hypothyroidism missed in newborn screening, started immediate hormone replacement, and arranged community health worker follow-ups during family's seasonal migrations.

A 9-year-old girl with complex epilepsy from an upper-middle-class family was experiencing breakthrough seizures; Dr. Saha implemented ketogenic diet therapy with intensive dietary counseling, reducing seizure frequency by 80% without additional medications.

A 14-year-old with mysterious recurrent fevers was diagnosed with periodic fever syndrome; Dr. Saha prescribed targeted biologic therapy, coordinated with a rheumatologist, and helped the teenager resume normal school activities after years of disrupted education.