The art of caring well…

Where connection grows deep, and support feels like home.

Our Mission

The Remember Me Foundation supports families navigating neurodegenerative disease by offering emotional care, practical resources, and space for restoration. We honor both caregivers and the ones they love, fostering a community rooted in lived experience, human connection and understanding, and the art of caring well—for you and for them.

How we started

The Remember Me story began the way so many caregiver stories do—quietly, unexpectedly, and out of need. In 2020, two daughters caring for parents with FTD found each other through a simple Instagram exchange. Living on opposite coasts, they were navigating the same unfamiliar terrain: grief layered with responsibility, love mixed with loss, and the constant question of how to keep going.

What began as a simple conversation quickly became a lifeline. In sharing their experiences, they found understanding, relief, and a sense of recognition that felt rare and deeply needed. Out of that connection, The Remember Me Podcast was born—a space for honest conversations, shared experiences, and the kind of understanding that can only come from living it.

As more caregivers found their way to the podcast, the community grew organically. Stories were shared. Voices were amplified. And again and again, caregivers were reminded they weren’t alone—that their experiences mattered, and that there was a way to approach this work with tenderness, intention, and the art of caring well.

Where we’re heading

As the Remember Me community grew, one truth became impossible to ignore: you cannot truly care for someone else without also caring for yourself. Caregiving is demanding, tender, and relentless—and those who show up for others deserve support, space, and restoration in equal measure.

The Remember Me Foundation exists to honor that balance. We hold both the caregiver and the person being cared for at the center, recognizing that real care flows in both directions. Emotional support, practical resources, and financial relief are all offered not as luxuries, but as necessities—for caregivers to breathe, feel held, and show up fully, and for the people they love.

This is a community rooted in lived experience, in the quiet strength of showing up, and in the belief that human connection sustains and transforms. Here, caring well is a practice, not a burden—a dance of tending to yourself and the one you love simultaneously.

Looking forward, our mission is simple: to expand this care, deepen this connection, and create spaces where caregivers can be steadied, restored, and seen—because caring is not just something we do—it’s something we learn, we practice, and we honor as the art of caring well.

Our plans for supporting you

  • Support circles, respite care, writing prompts, grief support for during and after — are just a few of the things you can expect as we build out our resources for you - the caregiver.

  • Meaningful, curated compassionate resources — so you don’t spend hours googling. Information on

  • Through all of the resources we provide — there will be community woven throughout — support curated by people who have been there — advice from former caregivers. This is a place for our community to thrive.