About

In 2019, I lost both of my parents within one month - a heartbreaking season that revealed how deeply caregiving can drain you physically, emotionally, mentally, and financially when you’re carrying it largely on your own. My father had been my mother’s caregiver for many years, and when he passed away first, everything shifted overnight. Suddenly, I found myself in the deep end of eldercare planning - navigating hospitals, healthcare systems, paperwork, and decisions I didn’t feel prepared to make.

The impact of those years didn’t fade when caregiving ended. My own health was affected, and it reshaped how I understand wellness, support, and the urgent need for clear, accessible information. While sharing my story on a podcast, I realized something meaningful: this was more than a personal experience - it was a calling to help others navigate their own caregiving journeys.

As a caregiver navigator, I bring the fragmented aging-care world into one coordinated conversation.

My Story

The Vision

We envision a world where family caregivers are not invisible, unsupported, or forced to navigate crisis alone.

In this world, caregivers are recognized early, guided clearly, and supported consistently - not only in moments of emergency, but throughout the full arc of their journey. They have access to understandable information, compassionate systems, and communities that acknowledge both the responsibility they carry and the emotional cost of carrying it. Caregiving is no longer isolating or reactive, but sustainable, respected, and grounded in dignity.