Dementia Caregiver’s Corner

Episode Title: Mild Cognitive Impairment vs Dementia: What’s the Difference? Sharon Lukert’s Story of Hope

In this reposted episode of the Dementia Caregivers’ Corner Podcast, I revisit my conversation with Sharon Lukert, a retired Buddhist chaplain and author of Until My Memory Fails Me.

Sharon shares her personal experience of living with Mild Cognitive Impairment (MCI), from noticing the first changes in her memory to navigating the emotions surrounding a diagnosis. 

Drawing on more than 20 years of supporting people through illness, grief, and end-of-life care, she reflects on finding meaning and connection as her own life changes.

We explore everyday coping strategies, spirituality, mindfulness, and the importance of community. At the heart of this conversation is a person whose experiences, relationships, and voice deserve to be heard.

Whether you are experiencing memory changes, supporting someone you love, or working in care, Sharon’s reflections offer an invitation to listen with compassion.

In This Episode

• Recognising the first signs of memory changes.

• The emotional experience of Living with Mild Cognitive Impairment: Sharon Lukert’s Story of Hope

 that support independence.

• Finding grounding through spirituality and mindfulness.

• The role of family, friendship, and community.

• The inspiration behind Until My Memory Fails Me.

A Reflection to Take Away

When memory begins to change, the need for love, belonging, dignity, and meaningful connection remains. Sharon reminds us to make space for the person’s story—and to listen.

Connect with Sharon

Book: Until My Memory Fails Me

 Website: sharonlukert.com

 LinkedIn: Sharon Lukert

Related Episodes

• Living with Dementia: Dallas Dixon Reveals What Real… — USA

• C.O.R.E. C.A.R.E. Principles in Dementia Care — Australia

• Honouring Jennifer Josey (1944–2024): A Journey… — UK

Please share this episode with someone who may find comfort, understanding, or encouragement in Sharon’s story.

Dementia Caregivers’ Corner Podcast—How deep is your love?

Episode Title: When the Coffee Stops Smelling: The Overlooked Link Between Smell and Dementia 

Repost: In this episode of the Dementia Caregivers’ Corner Podcast, I’m joined by Duncan Boak, co-founder and CEO of SmellTaste, to explore the often-overlooked impact of changes to smell and taste.

Duncan shares his personal experience of losing his sense of smell following a severe head injury and how this led him into advocacy and support for people living with smell and taste disorders.

We discuss the relationship between smell, memory and dementia, and why changes in smell and taste can affect much more than enjoyment of food. They can influence appetite, emotional wellbeing, quality of life and everyday safety — including the ability to detect smoke, gas or spoiled food.

We also explore sensory experiences such as smell hallucinations and why caregivers and healthcare professionals need greater awareness of olfactory impairment in dementia care.

Duncan also discusses his contribution to A New Approach to Dementia: Examining Sensory and Perceptual Impairment, edited by Professor Andrea Tales, Professor Jan Kremláček and Dr Emma Richards.

In this episode:

• Duncan’s personal journey with smell loss

• The connection between smell, taste, memory and dementia

• How sensory changes can affect eating and everyday life

• Safety risks associated with loss of smell

• Smell hallucinations and other overlooked sensory experiences

• Support and advocacy for people affected by smell and taste disorders

• Why sensory impairment deserves greater attention in dementia care

An important conversation reminding us that dementia is about much more than memory loss.

#DementiaCare #DementiaAwareness #OlfactoryImpairment #SensoryPerception #SmellAndTaste

Episode Title: When the Eyes and Brain See Differently: Understanding Vision Changes in Dementia

Repost: Vision changes in dementia can go far beyond poor eyesight. A person may be able to see clearly, yet struggle to interpret what they are seeing.

In this episode, Juliah Ratladi is joined by Advanced Clinical Practitioner and Independent Prescribing Optometrist David Knight to explore the complex relationship between vision, perception and dementia.

Drawing on clinical expertise and real-life caregiving experiences, they discuss how different dementias can affect visual perception, whether poor eyesight may contribute to cognitive decline, challenges with vision assessments, and practical changes families can make at home to improve safety and independence.

A fascinating conversation for families, caregivers and healthcare professionals who want to understand why, in dementia, seeing isn't always as simple as what meets the eye.

Repost: What happens to the mother–daughter relationship when dementia enters the family?

In this episode of the Dementia Caregivers’ Corner Podcast, Donna Houston shares her experience as the daughter of renowned dementia activist Agnes Houston MBE, who was diagnosed with early-onset Alzheimer’s at the age of 57.

Donna reflects on the early signs before her mum’s diagnosis, the challenges they faced navigating a system that did not always provide the support they needed, and how they made a conscious decision to face dementia together.

We also explore an important question for families: Should adult children become caregivers for a parent living with dementia? Donna shares her perspective on balancing being a daughter with providing care, protecting their relationship, and what nearly two decades alongside dementia have taught her about love, family and resilience.

🎧 Tune in for an honest daughter’s perspective on what it means when dementia becomes part of family life.

Dementia care. How deep is your love?

Repost: When we talk about dementia, memory loss is often the first thing that comes to mind. But dementia can also change the way a person sees, hears, tastes, smells, touches and makes sense of the world around them.

These sensory and perceptual changes can have a profound impact on everyday life, yet they remain one of the less understood and less discussed aspects of dementia...

After listening to Agnes, think about a behaviour you have seen in someone living with dementia that you previously found difficult to understand.

Could sound, sight, touch, taste, smell or the way they perceive their surroundings have played a part?

Sometimes understanding what the person may be experiencing is the beginning of understanding the behaviour.

🎙️ Dementia Caregivers’ Corner Podcast

If you enjoyed this conversation or know someone who could benefit from understanding the sensory side of dementia, please share this episode.

And if you enjoy the podcast, please consider leaving a review. Every review and share helps us reach more families, caregivers, professionals and communities with dementia education and awareness.

Until next time, take care, and bye for now!

#DementiaCaregiversCorner #AgnesHoustonMBE #DementiaAwareness #SensoryChanges #DementiaCare

Can technology make everyday life easier for people living with dementia and those who care for them?

In this episode of the Dementia Caregivers' Corner Podcast, I speak with Allyson Schrier, caregiver, dementia advocate, and co-founder of Zinnia TV—a pioneering AgeTech platform designed to enrich the lives of people living with dementia through engaging, dementia-friendly video content.

After caring for her husband, Allyson transformed her personal experience into an innovative solution that is helping families, caregivers, and care providers around the world create more meaningful moments while reducing stress.

How Allyson's caregiving journey inspired the creation of Zinnia TV.

The role of technology in supporting people living with dementia.

Simple ways to make digital tools accessible for older adults.

Why compassionate, person-centred care should always come before technology.

The importance of culturally inclusive dementia care for diverse communities, including immigrant and African families.

The exciting future of AgeTech and how innovation is shaping dementia care.

✅ Great innovations often begin with lived experience.

✅ Technology should enhance human connection—not replace it.

✅ Compassion remains the most powerful tool in dementia care.

✅ Inclusive technology ensures every family can benefit, regardless of culture or language.

Whether you're a family caregiver, healthcare professional, dementia advocate, or simply interested in how innovation is transforming dementia care, this conversation is packed with practical insights and inspiration.

If you enjoyed this episode, please follow, rate, and review the Dementia Caregivers' Corner Podcast on your favourite podcast platform. Your support helps us reach more families and raise dementia awareness around the world.

Please share this episode with someone who could benefit from learning how technology and compassion can work together to improve the lives of people living with dementia and those who care for them.

Episode Title: The Dementia and Death Conversation: Why Waiting Can Cost Families

Death is one of the few certainties in life, yet it remains one of the conversations many of us avoid.

In this thought-provoking episode of the Dementia Caregivers Corner Podcast, Juliah Ratladi is joined by hospice social worker Lisa Pahl, who has spent nearly two decades supporting individuals and families through some of life's most challenging moments. Drawing on her experience in hospice care and emergency medicine, Lisa shares why talking about death isn't about giving up hope—it's about giving people a voice while they still have one.

The conversation explores the importance of advance care planning, particularly for people living with dementia, where the opportunity to express wishes can gradually be lost. Lisa also discusses the inspiration behind the Death Deck, the End-of-Life (EOL) Deck, and the Dementia Deck—innovative conversation tools designed to help families navigate topics that are often difficult to begin.

Together, Juliah and Lisa discuss cultural attitudes toward death, why many families avoid these conversations, how to introduce advance care planning compassionately, and why meaningful conversations today can prevent uncertainty and distress tomorrow.

Whether you're a family caregiver, healthcare professional, or simply someone who wants to prepare for the future with confidence, this episode offers practical guidance and gentle encouragement to start the conversations that matter most.

Because peace at the end often begins with conversations held long before the end.

To learn more about Lisa's End-of-Life Deck and Dementia Deck, or to purchase a copy, visit thedeathdeck.com.

Episode Summary

Designing for Dementia: How Smart Technology and Environments Support Sensory Changes | Professor Andrea Tales

Repost: In this episode, I am honoured to be joined by Professor Andrea Tales, Professor of Neuropsychology and Dementia Research at Swansea University, Fellow of the British Psychological Society, and Fellow of the Learned Society of Wales.

Together, we explore why dementia should be understood as more than a memory disorder. Drawing on research from her co-authored book, A New Approach to Dementia: Examining Sensory and Perceptual Impairment, Professor Tales explains how changes in vision, perception, and sensory processing can profoundly affect the daily lives of people living with dementia.

Using real-life caregiving experiences, we discuss how visual perception changes may explain behaviours that are often misunderstood, why thoughtful environmental design matters, and how SMART technologies such as Alexa and digital clocks can support independence, reduce distress, and improve quality of life when tailored to the individual.

Whether you are a family caregiver, healthcare professional, or simply interested in understanding dementia more deeply, this episode offers practical, evidence-based insights that could transform the way you think about dementia care.

Throughout the conversation, I also share real-life experiences from my own dementia care journey, highlighting how understanding sensory changes transformed the way I supported people living with dementia.

Episode Title: When Reality Changes: Understanding Lewy Body Dementia Through a Caregiver's Eyes | Kathy Teyler Jarrett

In this episode of the Dementia Caregivers Corner Podcast, I am joined by Kathy Teyler Jarrett, author of You Are Not Alone: Dealing with Lewy Body Dementia and a passionate advocate for Lewy Body Dementia (LBD) awareness.

Kathy shares her deeply personal journey as the primary caregiver for her husband, offering invaluable insight into a form of dementia that is often misunderstood and overlooked. We discuss the early warning signs, the challenges of obtaining a diagnosis, and the complex symptoms that make Lewy Body Dementia unique, including hallucinations, sleep disturbances, and changes in movement.

Kathy recounts the frightening incident that became a turning point in recognising that something was seriously wrong, and she reflects on the realities of navigating daily life as a caregiver. We also explore the overwhelming amount of information available to caregivers and how to identify practical support that truly makes a difference.

Finally, Kathy speaks candidly about life after caregiving, sharing how she rebuilt a sense of purpose following her husband's death and why she felt compelled to write her book to support others walking a similar path.

This is a powerful conversation about resilience, education, and the importance of ensuring that no caregiver feels alone.

1. Lewy Body Dementia is often misunderstood and difficult to recognise.

2. Caregivers need practical guidance, not just information.

3. Life after caregiving requires healing and rediscovery.

Episode Title: Dementia in Africa: The Conversations We Need to Have

In this episode, we explore the realities of living with dementia and caregiving in African communities through a heartfelt conversation with Julia Mogotsi from Gaborone, Botswana. The discussion highlights the different types of dementia, the lack of adequate support following diagnosis, and how families are often left to navigate the journey alone.

We reflect on the progression of dementia over time, especially during and after the COVID era, and the emotional impact it has on both the person living with dementia and their caregivers. The episode also examines the unique challenges dementia caregivers face — from wandering and aggression to hallucinations, emotional burnout, and balancing work responsibilities.

The conversation further focuses on the urgent need for dementia awareness across Africa, where stigma, misinformation, and cultural beliefs continue to place vulnerable older people at risk of neglect, abuse, and even death. Through real-life stories from Botswana, Namibia, and South Africa, the episode calls for communities, leaders, neighbours, employers, and health professionals to work together in creating understanding, compassion, and protection for people living with dementia.

This is an emotional but important conversation aimed at encouraging awareness, support, and honest dialogue about dementia in African communities.