My journey with Polycystic Kidney Disease began unexpectedly after the birth of my daughter. She arrived five weeks early via emergency C-section—a moment filled with urgency, fear, and overwhelming love. While she recovered beautifully, my body told a different story. Routine labs kept coming back abnormal, and what began as a few extra hospital days turned into months of scans, tests, and unanswered questions.

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After four months of CT scans, ultrasounds, and MRIs, I was officially diagnosed with Polycystic Kidney Disease and Chronic Kidney Disease. I was referred to a nephrologist in Beverly Hills who specializes in PKD, and treatment began immediately. Today, I manage my condition with Tolvaptan (Jynarque), blood pressure medication, and targeted supplements to support my body as much as possible as well as IV infusions for my lack of iron and anemic condition. As of 2025, my kidneys are nearly twice the normal size and functioning at approximately 25%.

I am currently classified as Stage 3B kidney failure and am navigating complications including anemia and elevated parathyroid levels. I share this not for sympathy, but for awareness—to shed light on the often invisible symptoms of PKD and to show what a “new normal” can truly look like..

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Instead of giving in to fear, I chose to take ownership of my health. . My hope is simple but powerful: to slow cyst growth, protect my remaining kidney function, and add meaningful years to my life with my family.

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This space exists to share resilience, education, and hope. I’m not giving up—and I want others facing PKD or CKD to know they don’t have to give up either. Even in the hardest moments, there is strength, choice, and light ahead.