Dr. Namita Jaggi Reviews

A 72-year-old retired schoolteacher from rural Haryana, with no prior medical history, presented with unexplained weight loss and fatigue. Dr. Jaggi's team detected abnormal protein levels in serum electrophoresis, leading to a multiple myeloma diagnosis. She coordinated with oncology for timely treatment, and the patient achieved remission after six months of therapy, now enjoying gardening with her grandchildren.

An 18-year-old college athlete from an affluent Delhi family collapsed during a marathon. Dr. Jaggi's laboratory identified rhabdomyolysis through elevated creatine kinase and myoglobin levels. Her rapid diagnosis enabled immediate fluid resuscitation and renal protection, resulting in full recovery within two weeks and the patient returning to competitive sports with modified training.

A 45-year-old street vendor with limited financial resources was found to have persistent eosinophilia during a routine camp screening. Dr. Jaggi personally supervised specialized stool tests that revealed strongyloides stercoralis infection. She arranged for donated medication, and after three weeks of treatment, his eosinophil count normalized, significantly improving his quality of life.

A 33-year-old pregnant woman from a middle-class background showed abnormal liver enzymes in prenatal testing. Dr. Jaggi's team diagnosed intrahepatic cholestasis of pregnancy through bile acid testing. Close monitoring allowed for scheduled early delivery at 37 weeks, preventing fetal complications, with both mother and baby thriving postpartum.

A 60-year-old businessman with extensive travel history presented with recurrent fevers. Dr. Jaggi implemented advanced molecular testing that identified babesiosis, rarely seen in urban India. Her diagnosis led to targeted antimicrobial therapy, with complete symptom resolution in three weeks, enabling his return to international work.

A 28-year-old software engineer with family history of thyroid disorders had confusing thyroid function tests. Dr. Jaggi identified heterophile antibody interference and validated results with alternative platforms. This prevented unnecessary medication, and the patient was discharged with reassurance and annual monitoring recommendations.

A 9-year-old girl from an underserved community presented with developmental delay and seizures. Dr. Jaggi's metabolic workup revealed phenylketonuria through plasma amino acid chromatography. She connected the family with nutritional support programs, and with dietary modification, the child showed improved cognitive function within months.

A 52-year-old heart transplant recipient on immunosuppressants developed mysterious neurological symptoms. Dr. Jaggi's cerebrospinal fluid analysis detected JC virus, indicating PML. Though the prognosis was guarded, her early diagnosis allowed for modified immunosuppression, stabilizing the condition and extending meaningful life.

A 41-year-old homemaker with rheumatoid arthritis had abnormal kidney function during routine monitoring. Dr. Jaggi identified amyloidosis through abdominal fat pad biopsy analysis. This changed her disease management strategy significantly, with palliative care improving her comfort despite the progressive nature of her condition.

A 67-year-old retired army officer with diabetes presented with non-healing foot ulcers. Dr. Jaggi's microbiology team cultured burkholderia cepacia, requiring specific antibiotics. Her targeted approach led to ulcer healing in eight weeks, preventing amputation and preserving mobility.

A 25-year-old medical student suspected self-administration of insulin despite normal glucose levels. Dr. Jaggi confirmed factitious disorder through C-peptide and insulin antibody testing. She facilitated psychiatric referral, and with therapy, the patient returned to studies after three months of treatment.

A newborn from a high-risk pregnancy showed feeding difficulties and hypotonia. Dr. Jaggi's urgent genetic testing revealed Prader-Willi syndrome. Early diagnosis enabled immediate intervention and family counseling, helping parents adapt to their child's special needs from infancy.

A 58-year-old factory worker with occupational chemical exposure developed pancytopenia. Dr. Jaggi's bone marrow analysis confirmed aplastic anemia. She coordinated with hematology for immunosuppressive therapy, resulting in partial recovery after six months, allowing limited return to work with protective measures.

A 31-year-old immigrant construction worker from Bangladesh presented with chronic cough. Dr. Jaggi's TB PCR testing detected multidrug-resistant tuberculosis when conventional methods failed. Her rapid diagnosis initiated appropriate second-line therapy, with culture conversion achieved in two months.

A 47-year-old woman with family history of cancer had rising tumor markers during surveillance. Dr. Jaggi's circulating tumor DNA analysis detected recurrence before imaging showed changes. This ultra-early detection allowed for prompt intervention, potentially extending survival significantly.