I had a patient in an ACLF today, and she told me she wanted to get better enough to go over to the memory care unit to work with them on dance exercises, I thought that was the coolest thing I have heard! having residents help with the memory unit.💓

Jeremy doesn’t just care for people—he creates pathways for care to flow where it’s needed most. As an activity specialist, caregiver advocate, Uber driver, storyteller, and community builder, Jeremy notices what others might miss: the quiet exhaustion in a caregiver’s voice, the loneliness behind a routine ride, the need for connection hiding inside ordinary moments. Instead of passing by, he pauses—and then he acts. Through projects like Caregivers in the Backseat, Mighty Caregivers, Beyond Bingo Support, Kindness in Action, podcasts, daily encouragements, and countless community initiatives, Jeremy helps caregivers feel seen, named, and valued. He reminds people they are more than their role—and that caregiving, in all its forms, is sacred work. Jeremy believes everyone is a Mighty Caregiver because everyone takes care of someone. His gift is helping people recognize that truth in themselves—and in each other. He doesn’t wear his cape loudly. He wears it consistently showing up, listening deeply, and building community where there once was isolation. Mighty Truth: Caregiving isn’t just something Jeremy does. It's the way he brings people together—and helps them remember who they are. Jeremy's superpower is connection—and it’s changing lives.

Your story is important. If you’d like to share it with other Mighty Caregivers, you can. And if writing feels hard, that's ok. just fill out a short questionnaire at the provided link—Jeremy will help shape your story using your words and experiences. Share Your Story | Edge UMC

Julie is the kind of caregiver who shows up with determination, purpose, and an unwavering sense of honor. Her caregiving journey is rooted deeply in service — both to her family and to those who have served our country. Julie cares for her father, who is living with dementia. In 2022, recognizing that he needed closer support, she made the life-changing decision to move him from California to Georgia so she could be actively involved in every aspect of his care. From medical needs to daily decisions, Julie stands firmly as her father’s advocate, ensuring he receives the dignity, attention, and compassion he deserves. Beyond caring for her father, Julie works for the Department of Veterans Affairs, serving veterans every day. In 2009, she left private practice with a clear calling — to give back to those who gave so much for our freedom. Her work at the VA allows her to walk alongside veterans and their families, especially those navigating the complexities of dementia care. Julie describes her caregiving style as determined. When obstacles appear, she doesn’t stop — she pushes forward. Navigating the VA system can be overwhelming, especially for families unfamiliar with it, and Julie has made it her mission to help other caregivers of veterans find the resources and support they need. She makes herself available, offering guidance, encouragement, and hard-won wisdom to those walking a similar road. To Julie, caregiving is more than responsibility — it is a privilege. Her message to other caregivers is powerful and heartfelt: “Don’t give up. Don’t get discouraged. You have been given the responsibility of being the advocate for your loved one. Look at it as a privilege to be there for them. What an honor to walk beside them in this journey.” A phrase that guides Julie’s heart was shared with her by someone who understood caregiving deeply: “You are walking him home.” Julie reflects on those words often — walking her father home. What an honor. What a blessing. What sacred work.

Judy’s caregiving journey began long before her mother was diagnosed with dementia. She grew up surrounded by a family that believed in showing up for one another—neighbors who checked in, church friends who listened deeply, and a grandmother who taught her that compassion is never wasted. These early caregivers shaped Judy’s heart, showing her what steady love looked like. When her mother’s memory began to fade, Judy stepped forward with the same quiet strength she had witnessed all her life. She didn’t hesitate. She simply said, “Mom cared for me. Now it’s my turn to care for her.” Judy cares for her mother at home—through the confusion, the repetition, the long nights, and the small victories. Her inspiration comes from a lifetime of watching others love generously. She often says, “I may not fix every moment, but I can make every moment feel safe.” To Judy, caregiving means being a steady place in someone else’s storm. It means patience when the story repeats for the fifth time that morning. It means gentleness when frustration rises. It means choosing connection—even when memory slips away. One of Judy’s greatest challenges is the emotional weight of watching her mother slowly change. There are days when the grief of “losing her a little at a time” feels overwhelming. But Judy finds strength in her routines, her faith, and the small sparks of recognition her mother still gives—a smile, a squeeze of her hand, or a soft “thank you” whispered at bedtime. The biggest joy Judy experiences is seeing moments of clarity when her mother’s true personality shines through. People often describe Judy as warm, patient, and deeply steady—a calming presence in a difficult season. She brightens her Mother’s Day with simple rituals: fresh flowers on the table, old gospel music playing during breakfast, and the soft comfort of reading beloved Bible verses aloud. Judy’s caregiving style is inspired by her grandmother, who believed that love is shown most powerfully in the everyday things—folding laundry, serving meals, sitting quietly beside someone who needs company.