This Is Your Brain on Mom, sibling co-hosts open up about the unexpected beginning of their mother’s dementia journey — a journey that didn’t start with obvious memory loss, but with a broken ankle. What followed were strange behaviors, unexplained shifts, and subtle cognitive changes that signaled something deeper was happening.
As a brother-and-sister caregiver team, we share the real-life dementia storyof how we first encountered our mom’s cognitive decline. From unusual reactions in the hospital to confusing days at home, we walk through the early signs of Alzheimer’s disease and how they can appear differently than you might expect. We also discuss the differences between dementia vs. Alzheimer’s and how confusing it is to understand the distinction.
This podcast highlights the emotional side of becoming sibling caregivers — the frustration, the gut instinct, and the bond that forms when adult children team up to care for a parent. We also share how we use humor as a survival tool, because sometimes the only way through the fear and confusion of the progression of Alzheimer’s disease is to laugh together.
By telling our caregiving story, we hope to normalize the chaos, confusion, and unexpected moments that caregivers face, and to create a space where others feel seen. We explain why we decided to start this podcast — to document the earliest moments of our journey and to give a voice to other sibling caregiversnavigating similar paths.
Whether you’re researching dementia vs. Alzheimer’s, searching for early signs of Alzheimer’s disease, curious about sibling caregivers, or looking for real-life dementia stories to relate to, this podcast offers a candid, relatable, and hopeful look at the very beginning of the caregiving journey.
All content for This is Your Brain on Mom is the property of Aflalo Communications Inc. and is served directly from their servers
with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
This Is Your Brain on Mom, sibling co-hosts open up about the unexpected beginning of their mother’s dementia journey — a journey that didn’t start with obvious memory loss, but with a broken ankle. What followed were strange behaviors, unexplained shifts, and subtle cognitive changes that signaled something deeper was happening.
As a brother-and-sister caregiver team, we share the real-life dementia storyof how we first encountered our mom’s cognitive decline. From unusual reactions in the hospital to confusing days at home, we walk through the early signs of Alzheimer’s disease and how they can appear differently than you might expect. We also discuss the differences between dementia vs. Alzheimer’s and how confusing it is to understand the distinction.
This podcast highlights the emotional side of becoming sibling caregivers — the frustration, the gut instinct, and the bond that forms when adult children team up to care for a parent. We also share how we use humor as a survival tool, because sometimes the only way through the fear and confusion of the progression of Alzheimer’s disease is to laugh together.
By telling our caregiving story, we hope to normalize the chaos, confusion, and unexpected moments that caregivers face, and to create a space where others feel seen. We explain why we decided to start this podcast — to document the earliest moments of our journey and to give a voice to other sibling caregiversnavigating similar paths.
Whether you’re researching dementia vs. Alzheimer’s, searching for early signs of Alzheimer’s disease, curious about sibling caregivers, or looking for real-life dementia stories to relate to, this podcast offers a candid, relatable, and hopeful look at the very beginning of the caregiving journey.
“You Should Visit More” and Other Things We Don’t Need to Hear
This is Your Brain on Mom
49 minutes
1 month ago
“You Should Visit More” and Other Things We Don’t Need to Hear
This week on This Is Your Brain On Mom, things take a hilarious turn — because apparently our mom has become… a joiner. Bingo champion. Artist. Bowling league member. Lead singer alongside a mysterious hallway guitarist. We don’t know who she is anymore — but honestly? We’re impressed.
In this episode, we catch up on mom’s surprisingly busy social life in memory care, upcoming travel plans, and Barry’s big family milestone. But beneath the laughter, we go somewhere real: the complicated emotional side of caregiving.
We talk about:
The isolation many caregivers feel
The frustration behind comments like “at least she still remembers you”
Unsolicited advice (especially from people who have never cared for someone living with dementia)
Toxic positivity, grief, resentment — and why humor sometimes saves us
The struggle with role reversal and language, including words like “diaper”
How routines shift when caregiving becomes part of everyday life
If you’re a caregiver for a parent with Alzheimer’s or dementia — or love someone who is — you’ll feel seen in this conversation. And you’ll probably laugh, because sometimes the only options are laughter… or chaos.
🎧 Listen now for honesty, humor, and the reminder that caregivers deserve compassion too.
Learn more about your ad choices. Visit megaphone.fm/adchoices
This is Your Brain on Mom
This Is Your Brain on Mom, sibling co-hosts open up about the unexpected beginning of their mother’s dementia journey — a journey that didn’t start with obvious memory loss, but with a broken ankle. What followed were strange behaviors, unexplained shifts, and subtle cognitive changes that signaled something deeper was happening.
As a brother-and-sister caregiver team, we share the real-life dementia storyof how we first encountered our mom’s cognitive decline. From unusual reactions in the hospital to confusing days at home, we walk through the early signs of Alzheimer’s disease and how they can appear differently than you might expect. We also discuss the differences between dementia vs. Alzheimer’s and how confusing it is to understand the distinction.
This podcast highlights the emotional side of becoming sibling caregivers — the frustration, the gut instinct, and the bond that forms when adult children team up to care for a parent. We also share how we use humor as a survival tool, because sometimes the only way through the fear and confusion of the progression of Alzheimer’s disease is to laugh together.
By telling our caregiving story, we hope to normalize the chaos, confusion, and unexpected moments that caregivers face, and to create a space where others feel seen. We explain why we decided to start this podcast — to document the earliest moments of our journey and to give a voice to other sibling caregiversnavigating similar paths.
Whether you’re researching dementia vs. Alzheimer’s, searching for early signs of Alzheimer’s disease, curious about sibling caregivers, or looking for real-life dementia stories to relate to, this podcast offers a candid, relatable, and hopeful look at the very beginning of the caregiving journey.
