Episodes

Caregiving can feel like a private struggle, but the numbers and the lived reality say it’s a hidden crisis. We sit down with Diane, a nurse with 53 years of experience and the founder of CaregiverRelief.com, to talk about what dementia caregiving really does to families and why so many caregivers feel like they’re carrying the whole load alone. Diane traces her “why” back to her grandmother’s Alzheimer’s journey and the kind of moment every family hopes for: connection that still breaks throug...

Detroit is not playing around when it comes to dementia support, and we want you to see what we saw. We’re pulling back the curtain on our second Parenting Up tour stop in Detroit with Wayne State University and the team that helped make this three-part run happen. Along the way, we share the little moments that make tour life feel real plus the big moments that make you rethink what “living with dementia” can look like. The theme is simple and bold: Detroit cares about dementia. We talk about ...

A single ticket can feel like a confession when you’re a caregiver. I’m telling one of the most vulnerable stories I’ve shared yet: how I tried to take care of myself while parenting up and carrying the heavy reality of dementia caregiving after my father died. The only reason I’m responsible for my mama the way I am comes back to that loss, and the grief still shows up in unexpected places. When the New York Knicks finally made the NBA Finals and the schedule landed Game 4 on my dad’s birthday...

Alzheimer’s can make yesterday disappear, but it can also make love get very specific, very fast. I’m talking with Dan Phillips from the Georgia Chapter of the Alzheimer’s Association, and his story hits on every level: a grandmother diagnosed, a career pivot into advocacy, and then the brutal reality that multiple people he loves are living with the disease. We keep it real about what families actually face, including denial, confusion, and those moments when you realize you’re hearing heartbre...

If the words “dementia test” make you picture needles, scary machines, and a verdict you cannot take back, we get it. That fear keeps a lot of families stuck in delay, denial, and quiet panic. From Detroit’s Rosa Parks Geriatric Center at Wayne State University, we sit down with practitioners to make dementia screening feel simple, practical, and worth doing sooner than later. We walk through what a real memory screening looks like, including the Mini-Cog: three words, a clock drawing, and a qu...

Dementia doesn’t show up with a warning label, and it definitely doesn’t erase the person sitting right in front of you. We’re back in Detroit to hear directly from people living with dementia and the care partners walking beside them and the honesty is refreshing, specific, and sometimes even funny in the middle of the hard stuff. First, we talk with Dick and John (with Gerry bringing the real talk as a spouse and support system) about what made them finally say, “Something isn’t quite right.”...

If leaving the house feels like rolling the dice when dementia is in the picture, you are not alone and you are not overreacting. We record from Detroit during Brain Health Awareness Month with one big question on the table: where can people living with dementia go in public and truly be safe, welcomed, and understood? Not just at home, not just with a neighbor, but in everyday life like coffee shops, church, and movie theaters. We sit down with local leaders connected to the Alzheimer’s Associ...

Forget everything you think you know about “dementia daycare.” I went to Via Cognitive Health in Augusta, Georgia, and what I saw felt less like a holding space and more like a dignity-first cognitive health campus built for real life with dementia. Here, people aren’t called patients. They’re members. And that one word signals the bigger point: they belong, they’re respected, and the day is designed around what they can do right now, not what they’ve lost. We walk through programming that actu...

Caregiving can feel like you’re carrying a whole life on your back, then smiling through it so nobody worries. Today's episode highlights behind the scenes moments at our 2nd day at the 2026 Alter Dementia Summit--fast, powerful conversations that tell the truth about dementia caregiving and Alzheimer’s awareness, especially the parts families don’t always say out loud. We spoke down with Dr. Fayron Epps to talk about her book, From Faith To Action, and what it really takes to move from belief ...

Dementia doesn’t wait for the “right time,” and neither can we. I’m coming to you from Alter 2026, where Dr. Fayron Epps and her team turn a dementia summit into a real community experience: caregiving conversations, research access, faith-led support, and yes, enough joy to keep us standing when the topic gets heavy. We get into what makes Alter different, starting with the big idea of training the faith community to understand dementia and Alzheimer’s so they can take accurate information bac...

Season seven starts with the part of my story that still catches in my throat, even after 14 years: my dad died, and within months my mom began to fall apart in ways that grief alone couldn’t explain. People around her told me I was overreacting, that it was depression, that it was mourning. I had to trust what I knew about my mother, push for testing, and brace for the avalanche of becoming responsible for her care, her safety, and the life she used to run with ease. John from Georgia Focus as...

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Caregiving doesn’t just “get hard” over time. Sometimes it detonates your life overnight, and you’re left rebuilding your health, your career, and your family rules while dementia keeps moving the goalposts. That’s why this conversation with Jesse Jackson Jr. hits so deep. Jesse Jackson, Jr. had J Smiles as well as two other guests talk honestly about what it costs to care for a parent when the system quietly depends on your free labor, then acts surprised when families burn out. We get into th...

Forget the bubble-bath checklist. We dig into a practical, body-first approach to caregiver self-care that actually holds under pressure: better sleep, objective stress data, scaled movement, protected solitude, and preventive health that keeps you in the game. I share how a therapist’s tough wake-up call led me to a sleep study, what “daytime sleepiness” really means on the road, and how an oral appliance changed my oxygen, sleep quality, and mornings. We explore why you can feel exhausted afte...

In today's Season Finale, we recap our experience at Battle for the Brain 2026! We pulled up at the Coca-Cola Roxy for Battle for the Brain—Daughters Against Alzheimer's lip sync showdown, where corporate teams, cheerleaders, and neighbors channel pure joy into serious funding for Alzheimer’s research at Emory. We walk you through the night: teams that rehearse like Broadway hopefuls, a set list that jumps from the 50s to the 2000s, and a crowd that refuses to leave their seats. ...

In today's episode, you will hear all that went on for Alzheimer's Advocacy at the Georgia State Capital in Atlanta. We showed up with facts, handwritten notes, and a clear ask: allocate $2 million for caregiver support programs that keep families afloat and reduce avoidable health costs. That number might seem small until you compare it to what families already contribute—775 million hours of unpaid care in Georgia, valued at $13 billion. When you see that gap, the request becomes a re...

The honest part of caregiving isn’t just the long nights and endless appointments—it’s realizing you’ve become the project manager for a situation nobody trained you for. Family Caregivers take that and turn it into a plan, starting with the meds that don’t help or flat-out make things worse. In this episode, you’ll learn how to loop back to the exact prescriber with clear reports, and why your pharmacist may be your most valuable teammate for catching dangerous drug interactions. We also clear...

Caregiving comes with a stack of questions that rarely fit into neat answers—and that’s exactly where we go in this episode. We open up about the moments no one posts: the dark days, the quick resets that actually help, and the honest boundary decisions when history with a parent or partner is painful. If you’ve ever wondered how to stay steady, how to stop resenting the wrong things, or how anyone “does it all,” you’re in the right place. I share the mindset tools that keep me functional—grat...

What does perseverance look like when words are gone and the day goes sideways? We set out to honor a promise—no gray roots, ever—and walked straight into a masterclass on safety, dignity, and the tiny choices that keep identity alive. A new caregiver, a wardrobe wobble, and then the moment every caregiver dreads: knees buckling on a ramp and a slow fall to the ground. No injuries, just a spike of adrenaline and the question that lives in the gut—do we abort, or do we push through? I take you b...

What if the care system you need doesn’t exist yet? Chanda didn’t wait. In this episode, we speak with Chanda Hinton, founder of the Chanda Center for Health. After a childhood spinal cord injury and years of depending on medicines and medical care, Chanda found that daily movement, touch-based therapies, and a team that talks to each other worked to help her overcome challenges brought on by medicine. Then she pushed further—she helped pass a first-of-its-kind law in Colorado and built a disa...

A single shock can reorder a life. When my father passed suddenly and my mother’s Alzheimer’s deepened, I became the point person for everything. My pivot—raw, messy, and unplanned—sparked a mission: use comedy to have a positive outlet during those trying times. In this special mini episode, you'll hear me as I celebrate five years of our caregiver-centered podcast, ten years of stand-up, and my mom’s 77th lap around the sun, while pulling back the curtain on how humor, faith, and community tur...

Parenting Up Family! Tune in for a special episode during National Family Caregivers Month! We are usually bi-weekly, but thanks to the Alzheimer's Association of Georgia, we are releasing this bonus episode this month! In this episode, Actor Brandon Claybon joins us to unpack the shift that happens when family members forget your name and start losing their memory, with honesty and heart. He speaks with us about how Alzheimer’s touched both sides of his family, what he learned as a ten-year-ol...

What does it look like to choose love—and keep choosing it, day after day? We sit down with JET, a grandson who decided his grandmother with dementia wouldn’t go to a facility. He brought her into his home, rebuilt his life around her needs, and learned how dignity lives in small rituals: clean sheets, a sharp outfit, a slow stroll through every aisle at the market just to smell the spices. It’s funny, tender, and honest about what caretaking really takes. JET walks us through the first clues t...

The Promenade at Piedmont Park turned into a surge of color, courage, and hope at the Walk to End Alzheimer’s hosted by the Atlanta chapter of the Alzheimer's Association—and we brought our cameras and team to capture it all. From the first cheers to the last hug, we connected with caregivers, researchers, and supporters who refuse to let this disease define our futures. As a media sponsor, Parenting Up! dug into practical takeaways and lifted the voices that make this movement real. We spoke w...