Podcasts about caregiving

Caregiving is an act of love but it also comes with a kind of grief few people talk about.In this episode, I sit down with Ty Lewis, a special education teacher, reading specialist, and full-time caregiver to her mom living with dementia. Ty shares what it's like to slowly watch a parent change, how grief can begin long before goodbye, and why caregivers often feel invisible while carrying so much responsibility.This honest conversation explores:Recognizing when memory loss is more than agingNavigating anticipatory griefBalancing caregiving, work, and emotional healthWhy sharing real caregiving moments online mattersIf you're caring for someone with dementia or loving someone who is, this episode will help you feel seen, understood, and less alone.

Barry J. Jacobs, Psy.D. and Julia L. Mayer are married psychologists and coauthors of three self-help books for family caregivers, including The AARP Caregiver Answer Book.

In this episode of the Brain and Life podcast, hosts Dr. Daniel Correa and Dr. Katy Peters answer your listener questions, touching on caregiving for Alzheimer's, staying motivated with Parkinson's, and the role of supplements in managing MS.   Additional Resources Why Advanced Care Planning Is Essential for Caregivers How to Avoid Caregiver Burnout by Taking Care of Yourself How Peer Mentors Can Help Patients Navigate Life with Neurologic Disease The Gut-Brain Connection: Why a Healthy Microbiome Is Key to Disease Prevention Exploring the Link Between Gut and Brain Health     Brain & Life Podcast Episodes on These Topics Actress Yvette Nicole Brown Discusses the Caregiving Journey The Future of Caregiving with Kat McGowan Ed Begley Jr. on Utilizing a Healthy Lifestyle to Thrive with Parkinson's Disease World's Toughest Row with Brendan Cusick and Pat Morrissey: Part Two   We want to hear from you! Have a question or want to hear a topic featured on the Brain & Life Podcast? ·       Record a voicemail at 612-928-6206 ·       Email us at BLpodcast@brainandlife.org   Social Media:   Hosts: Dr. Daniel Correa @neurodrcorrea; Dr. Katy Peters @KatyPetersMDPh

In this special New Year's Eve solo episode, Dr. Mark Bonta steps away from the guest format to reflect on a landmark year for Ditch the Labcoat and to share where the show is headed next.After surpassing 50 episodes and approaching episode 100, Dr. Bonta looks back on how the podcast evolved in 2025. What started as a more traditional interview-style medical show has grown into deeper, more philosophical conversations about performance, longevity, mental health, neuroplastic symptoms, and the human side of healthcare.Using a surprising year-end analytics insight from his recording platform, he explores why the word “athlete” became one of the most frequently used terms on the show, and what that reveals about how healthcare, high performance, parenting, and recovery intersect. He also shares a candid and self-aware resolution for 2026, including how small environmental changes can shape better habits both personally and professionally.Looking ahead, Dr. Bonta outlines meaningful shifts for the podcast in 2026. Expect fewer episodes, greater depth, clearer thematic focus, and more intentional preparation to better honor guests and their work. He also highlights future areas of exploration, including neuroplastic and invisible illnesses, long COVID, chronic fatigue, high-performance mindsets, and the role of technology and AI in improving care.The episode closes with a deeply personal reflection on caregiving. A simple moment at home caring for his daughter leads to a broader meditation on touch, nursing, administrative burden, burnout, and why “caring” remains the most essential and fragile element of modern healthcare.This episode is both a thank-you to listeners and a statement of purpose for the year ahead.Mark Bonta's Links : https://ditchthelabcoat.com/ https://www.linkedin.com/in/mark-bonta-/ Episode Takeaway 1. Healthcare as Performance: Why the Athlete Mindset Keeps Appearing — Recovery, sleep, nutrition, and training principles apply far beyond elite sports.2. Filler Words Reveal Thinking: What “So” Says About Deep Conversation — Pauses often signal reflection, curiosity, and cognitive processing, not incompetence.3. Behavior Change Starts at Home: Environment Shapes Outcomes — The easiest habits are the ones your surroundings make unavoidable.4. Longevity Is Not Biohacking: It's Consistency Over Intensity — Sustainable routines outperform extreme interventions every time.5. Quality Over Quantity: Fewer Episodes, Deeper Impact — Better preparation and focus create more meaningful learning for listeners.6. Invisible Illnesses Are Real: When Scans Don't Explain Suffering — Neuroplastic symptoms demand credibility, nuance, and evidence-based care.7. Administrative Burden Erodes Care: Documentation Steals Time From Healing — Systems often pull clinicians away from the bedside.8. Burnout's Red Flag: When Caring Disappears — Loss of empathy is a warning sign that support and reflection are urgently needed.Episode Timestamps05:08 – Why “Athlete” Became One of the Most Used Words on the Show07:27 – The Most Commonly Used Word on Ditch the Labcoat (And Why It Matters)09:44 – Setting Yourself Up for Success: Habits, Environment, and Behavior Change11:39 – Longevity Lessons from Athletes and Everyday Life14:02 – Quality Over Quantity: How the Podcast Evolves in 202617:25 – Neuroplastic and Invisible Illnesses: What Medicine Still Misses19:25 – Caregiving, Touch, and the Administrative Burden of Modern Medicine24:15 – Burnout, Red Flags, and the Importance of Never Stopping CaringDISCLAMER >>>>>>    The Ditch Lab Coat podcast serves solely for general informational purposes and does not serve as a substitute for professional medical services such as medicine or nursing. It does not establish a doctor/patient relationship, and the use of information from the podcast or linked materials is at the user's own risk. The content does not aim to replace professional medical advice, diagnosis, or treatment, and users should promptly seek guidance from healthcare professionals for any medical conditions.   >>>>>> The expressed opinions belong solely to the hosts and guests, and they do not necessarily reflect the views or opinions of the Hospitals, Clinics, Universities, or any other organization associated with the host or guests.    Disclosures: Ditch The Lab Coat podcast is produced by (soundsdebatable.com) and is independent of Dr. Bonta's teaching and research roles at McMaster University, Temerty Faculty of Medicine and Queens University. 

Fluent Fiction - Serbian: Navigating Family Ties: A New Year's Eve Resolution Find the full episode transcript, vocabulary words, and more:fluentfiction.com/sr/episode/2025-12-31-23-34-01-sr Story Transcript:Sr: Снег је тихо падао уочи Нове године, покривајући улице Новог Сада белим покривачем.En: The snow quietly fell on New Year's Eve, covering the streets of Novi Sad with a white blanket.Sr: У малом кафићу, осветљеном топлим сјајем, Милан, Јована и Петар седели су за округлим столом.En: In a small café, lit with a warm glow, Milan, Jovana, and Petar sat around a round table.Sr: Ваздух је био испуњен мирисом свеже печеница и звуковима празничне музике.En: The air was filled with the smell of freshly cooked pork and the sounds of holiday music.Sr: Милан, најстарији од браће и сестара, често је преузимао одговорност за породичне ствари.En: Milan, the oldest of the siblings, often took on the responsibility for family matters.Sr: Наслонивши се на столицу, прошао је кроз уобичајени ритуал започињања разговора.En: Leaning on his chair, he went through the usual ritual of starting a conversation.Sr: "Време је да одлучимо како да се бринемо о баки", рекао је, погледајући у Јовану и Петра.En: "It's time to decide how to care for grandma," he said, looking at Jovana and Petar.Sr: Јована, практична и чврстог става, гледала је према прозору, испуњена осећањем да жели више слободе од обавеза које су често пратиле породични живот.En: Jovana, practical and steadfast, gazed toward the window, filled with a desire for more freedom from the obligations that often came with family life.Sr: "Мислим да би професионална нега била најбоља. Али знам да је скупо."En: "I think professional care would be best. But I know it's expensive."Sr: Петар, најмлађи и идеалистички настројен, није одмах одговорио.En: Petar, the youngest and idealistic, did not respond immediately.Sr: У његовом срцу се бурила мешавина емоција док је размишљао.En: A mix of emotions swirled in his heart as he pondered.Sr: "Можда можемо сами", рекао је тихо.En: "Maybe we can do it ourselves," he said quietly.Sr: "Бака је увек говорила да је породица најважнија."En: "Grandma always said that family is the most important."Sr: Напетост између њих се могла сећи ножем.En: The tension between them was palpable.Sr: Милан је осетио тежину одлуке која га је изједала.En: Milan felt the weight of the decision eating away at him.Sr: "Знам да се сви трудимо... али потребна ми је ваша подршка", рекао је, напокон откривајући своју рањивост.En: "I know we're all trying... but I need your support," he said, finally revealing his vulnerability.Sr: "Не могу сам."En: "I can't do it alone."Sr: Ћутање је за тренутак обгрлило сто, пре него што Јована усмјери поглед према Милану, њене очи пуне разумевања.En: Silence enveloped the table for a moment before Jovana directed her gaze toward Milan, her eyes full of understanding.Sr: "Поделићемо одговорности", предложила је, добронамерно.En: "We will share the responsibilities," she proposed kindly.Sr: Петар се насмешио, сада са више самопоуздања.En: Petar smiled, now with more confidence.Sr: "Видећемо шта можемо да урадимо заједно", додао је, стиснувши руку Милану.En: "We'll see what we can do together," he added, squeezing Milan's hand.Sr: Док су утичали кафом, планирали су распоред посета баки.En: As they sipped their coffee, they planned a schedule for visiting grandma.Sr: Договорили су се да свако од њих преузме по део обавеза, а у међувремену ће потражити и јефтиније професионалне опције.En: They agreed that each of them would take on a portion of the duties, and in the meantime, they would search for more affordable professional options.Sr: Нова година је била на прагу, али право славље било је у том малом кафићу.En: The New Year was imminent, but the true celebration was in that small café.Sr: Схватили су да је подршка једни другима највећи дар који могу пружити.En: They realized that supporting each other was the greatest gift they could offer.Sr: Милан је осетио олакшање.En: Milan felt relief.Sr: Научио је да не мора сам носити терет.En: He learned that he didn't have to carry the burden alone.Sr: Вере у своју породицу враћале су му снагу и наду.En: Faith in his family restored his strength and hope.Sr: Кафић је остао топло и пријатељско место у хладној ноћи, приближавајући празничне тренутке ближе срцу породице.En: The café remained a warm and friendly place on a cold night, bringing the holiday moments closer to the family's heart. Vocabulary Words:blanket: покривачsiblings: браћа и сестреresponsibility: одговорностsteadfast: чврстог ставаobligations: обавезеprofessional care: професионална негаidealistic: идеалистички настројенpondered: размишљаоtension: напетостpalpable: могла се сећи ножемvulnerability: рањивостrevealing: откривајућиgaze: погледunderstanding: разумевањеconfident: самопоуздањеschedule: распоредvisiting: посетаaffordable: јефтинијеimminent: на прагуcelebration: слављеrelief: олакшањеburden: теретfaith: вереstrength: снагаhope: надаenveloped: обгрлилоsupporting: подршкаshared: поделићемоsmile: насмешиоrestored: враћале

On January 1, 2026, Minnesota will become the thirteenth state to offer Paid Family Leave. In this episode, Allison and Justin talk with Cathy McLeer from AARP about how this new law benefits caregivers, how we can support other states in adopting this law, and other ways AARP supports caregivers of all ages. --- PFML for caregivers in Minnesota PFML for employers in Minnesota MN Caregiver Resource Guide Minnesota Paid Leave Toni's Story: Why Paid Leave Matters What States offer Paid Leave for Caregiving? --- Join us for an online support group related to this episode on Monday, January 5, from 6:00-7:15pm CT. Register Here!

Avoiding one elder care crisis after another is possible when younger generations initiate conversations with aging parents about family caregiving expectations and support. Younger generations can miss noticing the aging and health issues of grandparents or aging parents while focused on their own lives. Yet a single elder care crisis—such as a fall resulting in a hip fracture, hospitalization, and a nursing home stay—can quickly overwhelm an adult child who is balancing caregiving responsibility with work and family. This episode provides essential intergenerational caregiver advice and strategies. Younger generations will understand the complexities of caregiving, coordinating care, and accessing caregiver support resources and information by being proactive. Older adults will understand how changes in health or an unexpected event can impact their well-being and learn about the effect of managing care on their adult children. Caregiving expert Pamela D. Wilson draws on her 25 years of experience to share an insightful elder care example, along with practical tips for family caregivers. She emphasizes that honest conversations about aging, health care, finances, and legal planning are critical so younger generations do not feel their lives will be derailed by caregiving responsibilities for aging parents.Accordingly, aging parents who engage in information exchanges with their adult children about health care, legal issues, money, and care expectations can apply what they learn to improve health and well-being, thereby delaying an elder-care crisis.Tune in to this valuable expert guidance on managing caregiving demands, fostering compassion in caregiving, and preparing for the challenges ahead on your caregiving journey.  To find show transcripts and links mentioned in Episode 235 and other The Caring Generation podcasts, click here to visit Pamela's website: https://pameladwilson.com/caregiver-radio-programs-the-caring-generation/   If you enjoy this podcast, please comment, follow, like, and share it to help grow the audience and extend support to podcast listeners worldwide seeking information about health, aging, elder care, and caregiving.Check out all episodes and show transcripts with additional information on Pamela's Website https://pameladwilson.com/caregiver-radio-programs-the-caring-generation/For more caregiving, aging, and elder care tips, visit Pamela's website at https://www.PamelaDWilson.com Learn about Pamela D Wilson, her professional background, and her 25 years of experience helping aging adults and their caregivers navigate health, health care, legal, financial, and family dynamics around caregiving:  https://pameladwilson.com/pamela-d-wilson-story/Schedule a 1:1 or family elder care consultation by telephone or video call with Pamela. https://pameladwilson.com/elder-care-consultant-aging-parent-consultation-managing-senior-care-needs-meet-with-pamela-d-wilson/Sign up for Pamela's newsletter here: https://pameladwilson.com/contact/Join Pamela's Online Caregiver Support Group on Facebook https://www.facebook.com/groups/thecaregivingtrap Follow Pamela on Social Media:Facebook: https://www.facebook.com/pameladwilsoncaregivingexpert/LinkedIn: https://www.linkedin.com/in/pameladwilsoncaregiverexpert/ Twitter: https://x.com/CaregivingSpeakPamela D Wilson | Caregiver, Elderly Care & Caregiving Expert provides caregiver tips, support for caregivers, and resources for aging and elder care. Caregiving and aging for parents doesn't have to be challenging with expert caregiver advice, solutions, and strategies based on Pamela's 25 years of experience in care management, dementia care, and as an expert witness. Visit Pamela's website www.PamelaDWilson.com to access online caregiver programs, advice and tips to support caregivers and aging adults.©2018, 2025 Pamela D Wilson. All Rights Reserved

As millions of people tick into their 80's, many of you are going to realize your loved ones may need more than a weekly phone call. And as dementia attacks younger brains, they don't have to be elderly to require your attention. the work is there if you want it.

How should we live until Christ returns?1.   Worship God!2.   Focus on Jesus!3.   Anchor in the truth!4.   Live expectantly! --------DAILY DEVOTIONAL WITH RON MOOREGet Ron's Daily Devotional to your inbox each morning; visit biblechapel.org/devo.CAREGIVINGDo you have a need we can pray for? Do you need someone to walk alongside you? Do you know of another person who needs care? Let us know at caregiving@biblechapel.org.GROWTH TRACKWe all have a next step - what's yours? To learn more about our Growth Track and to take your next step, biblechapel.org/connect.

I sat down with Ken and Mary Sue Grein knowing their story would be heavy. I didn't expect it to steady me the way it did. They were just 22 years old when their son Jacob was born with severe medical complications. Within days, doctors told them he wouldn't live long and encouraged them to let him die. Ken and Mary Sue refused. They chose life, even though no one could tell them what that life would require. Jacob lived 37 years. (READ HIS STORY HERE) In our conversation, they speak candidly about what those decades held: long hospital stays, countless surgeries, daily caregiving, isolation, anger, and exhaustion. They don't sanitize any of it. But they also don't frame Jacob's life as a tragedy. What comes through instead is clarity, gratitude, and a hard-won conviction that a difficult life does not have to be a bad one. They talk about how caregiving reshaped their marriage, formed their other children, and rewired their own hearts. Disability didn't fracture their family. It refined it. Their children grew up compassionate, responsible, and unafraid of suffering. Jacob himself, despite profound limitations, lived with joy, affection, and gratitude, fully present in the life of his family. As a longtime caregiver myself, much of what they shared felt familiar: the loneliness, the way support fades, the daily choice between bitterness and gratitude. But what stayed with me most was their quiet insistence that every life is worth living, even when it arrives wrapped in fear, limitation, and unanswered questions. This is not a conversation about pretending suffering is good. It's about refusing to let suffering be the final word. Ken and Mary Sue didn't just care for their son. They learned how to live faithfully in the middle of what could not be fixed, and that is a lesson every caregiver needs. ___________________ Caregiving's Hard. Don't Do Alone! Get the New Book: A Caregiver's Companion - Scriptures, Hymns, and Forty Years of Insights for Life's Toughest Role

In this episode of Time to Care Like Caregivers, Isabel Melgarejo sits down with psychologist, author, and podcast host Dr. Mara Karpel to explore the hidden impact of ageism in healthcare and caregiving. From her personal journey advocating for her mother to her upcoming book on navigating an ageist system, Dr. Karpel shares insights, tools, and hope for caregivers who often feel unheard. A powerful conversation about dignity, advocacy, and finding passion at any age

Balance in caregiving is often talked about, but what does it really look like in everyday life? In this episode, Jerri McElroy, primary caregiver, entrepreneur, and author, shares her caregiving journey and how caregiving touches every part of our lives. From managing overwhelming medical responsibilities and advocating for a loved one, to caring for a parent with whom you may have had a complicated relationship, Jerri speaks candidly about the emotional and practical realities caregivers face. She also reflects on empathy, boundaries, and the importance of caring for yourself while caring for others. If you are a family caregiver or supporting an aging parent, you may see yourself in Jerri's story and gain insight into finding your own sense of balance along the caregiving journey. TRANSCRIPT Jerri's Linktree https://linktr.ee/jerrynjerri Daughterhood

Most weeks on Total Michigan, Cliff DuVernois sits down with dreamers and doers who are making our state brighter.This week, the spotlight turns inward.In this deeply personal year-in-review episode, Cliff reflects on 2025—a year defined by creative growth, unexpected limitations, and the heavy, sacred work of caregiving. As his mother's dementia progressed, the life he had carefully built was slowly reshaped by responsibility, sacrifice, and hard decisions no one prepares you for.What emerged from that pressure wasn't the end of Total Michigan, but a clearer purpose, stronger storytelling, and a deeper understanding of what it means to slow down, let go, and trust God with what you cannot control.This is a story about love, loss, resilience, and learning when to stop being the caregiver—and start being the son.

Summary In this conversation, Debbie Weiss shares her profound journey as a caregiver, starting from her teenage years when she took on the responsibility of caring for her father after his stroke. She discusses the emotional challenges and the evolution of her caregiving roles, including caring for her son with autism and her husband with terminal cancer. Throughout the conversation, Debbie emphasizes the importance of hope, self-discovery, and empowerment in the face of adversity. She also highlights her journey of writing books as a therapeutic outlet and her aspirations to inspire others through her experiences.TakeawaysDebbie became her father's full-time caregiver at a young age.Navigating healthcare systems can be overwhelming for young caregivers.Caregiving can lead to a shift in family dynamics and relationships.The emotional toll of caregiving can lead to feelings of grief and loss.Finding hope amidst struggles is crucial for caregivers.Self-discovery often comes from challenging experiences.Shifting from a victim mentality to empowerment is transformative.Writing can serve as a therapeutic outlet for caregivers.Creating a positive mindset is essential for personal growth.Debbie aims to inspire others through her journey and future projects.Sound bites"I lost my father. He wasn't the same person.""I had to take away the victim mentality.""I discovered I love creating."Chapters00:00 Introduction and Background00:58 The Caregiving Journey Begins03:47 Navigating Different Caregiving Scenarios06:46 The Impact of Caregiving on Relationships10:10 Finding Hope Amidst Challenges12:54 Personal Growth Through Caregiving15:46 Transforming Victimhood into Empowerment24:02 Rediscovering Identity at 5027:26 Shifting from Victim Mentality to Empowerment28:46 Tackling Weight and Self-Worth33:51 Mindset Changes and Long-Term Success36:31 The Journey to Writing a Book42:08 Finding Purpose Through Writing47:47 Embracing Creativity and Future Aspirations51:55 Podcast Intro Music Project (MASTER BOUNCE - OUTRO).mp3Keywordscaregiving, personal growth, resilience, mental health, hope, self-discovery, empowerment, writing, inspiration, supportConnect with Debbie: ⁠⁠Website⁠⁠The Sprinkle Effect Book The Sprinkle Effect WorkbookThe Sprinkle Effect Card DeckOn Second Thought Maybe I can - Inspired Caring is THE family support & education program that helps families feel calm and confident to make better decisions faster. Inspired Caring is offered as an annual membership tobusinesses to provide for the families they work with.Connect with Michele Magner:Website: www.InspiredCaring.comE-mail: hello@inspiredcaring.com Instagram: https://www.instagram.com/inspiredcaring/Facebook: https://www.facebook.com/michele.magner.90LinkedIn: https://www.linkedin.com/in/michele-magner-60a99089/YouTube: https://www.youtube.com/@inspiredcaringwithmichelem3138Custom podcast music written and produced by Colin Roberts. He does custom songs for any occasion.

This week's episode of Seekers of Meaning features Rabbi Address interviewing Barry Jacobs and Julia Meyer, authors of the AARP Caregiver Answer Book. They discuss the challenges caregivers face, including emotional, financial, and spiritual aspects, while providing guidance on planning, support systems, and coping strategies essential for caregivers. [Read more...] The post ENCORE: Seekers of Meaning 6/6/2025: Navigating the Complexities of Caregiving appeared first on Jewish Sacred Aging.

Your loved one is diagnosed with dementia. While you focus on symptoms, tasks and decisions, a long-standing pattern from your childhood is being triggered. That pattern will shape your caregiving style.  That childhood pattern is also being triggered in your loved one. Understanding the pattern can help you understand your loved one's behavior. Understanding can lead to compassion for your loved one and for yourself. From her book, Dementia, Caregiving & Personal History: How to Help, Cope, Connect, and Heal, author Tami Anastasia writes: "Our earliest relationships influence how we connect with others: our need for closeness, our ability to trust, and how we respond to life cirumstanes."  In this first of several interviews, Tami talks about the bonds we formed with the people who cared for us when we were children and how those deep-rooted attachment styles influence our relationships as adults, especially in times of stress or crisis. She sheds light on these four attachment styles:  Secure Attachment: Living with Confidence Anxious Attachment: Seeking Validation Through Caregiving Avoidant Attachment: Struggling with Emotional Closeness Disorganized Attachment: Being Caught Between Love and Fear Tami Anastasia holds a masters in counseling with more than 30 years of experience supporting family and professional caregivers. To learn more about Tami and her book, please go to her website

This show is a highlight of KET's ongoing aging series called The Next Chapter, which explores the rewards and challenges of growing older.

In-home elder care costs are rising more than three times faster than inflation.AARP estimates that caregivers in the U.S. spend an average of $7,242 out of pocket each year.Cuts to federal spending have gutted programs that support them. And amidst the longest government shutdown in history, what little help was left is quickly drying up.Why is the cost of care going up? What can be done to combat those costs?Find more of our programs online. Listen to 1A sponsor-free by signing up for 1A+ at plus.npr.org/the1a.Learn more about sponsor message choices: podcastchoices.com/adchoicesNPR Privacy Policy

Conscious Caregiving with L & L is "Tackling the Tough Conversations."   The topic of this episode is "Holiday Traditions & Seniors" featuring hosts Lori La Bey and Lance A. Slatton.   About Lori La Bey:   Lori La Bey is the founder of Alzheimer's Speaks and is co-founder of Dementia Map global resource directory and the co-host of Conscious Caregiving with L & L. Lori's mother who lived with dementia for 30 years.   Her goal has always been to shift dementia care from crisis to comfort around the world. She offers a variety of free resources to educate, empower, connect, and decrease stigmas; helping families and professionals live graciously alongside dementia.   Lori is an international speaker known for her multiple platforms and training programs.   About Lance A. Slatton - known as "The Senior Care Influencer"":   Known as "The Senior Care Influencer" Lance is a Writer, Author, Influencer, and Healthcare professional with over 20 years in the healthcare industry.   Lance A. Slatton is a senior case manager at Enriched Life Home Care Services in Livonia, MI. He is also host of the award winning podcast & YouTube channel All Home Care Matters and Co-Host of Conscious Caregiving with L & L with Lori La Bey along with The Care Advocates and The Caregiver's Journal.   Lance's book, "The All Home Care Matters Official Family Caregivers' Guide" was the recent recipient of the 2024 International Impact Book Awards.   Connect with Lori La Bey:   Official Website:  https://alzheimersspeaks.com/   Official Dementia Map Website: https://www.dementiamap.com/      Connect with Lance A. Slatton - "The Senior Care Influencer":   Official Website: https://www.lanceaslatton.com   Official Website for All Home Care Matters: https://www.allhomecarematters.com   Lance A. Slatton and Lori La Bey Co-Host and Produce Conscious Caregiving with L & L. Visit their website at:  https://consciouscaregivingll.com/   To learn more about Lance A. Slatton and Lori La Bey you can visit their websites.

“Sun of Righteousness” (Malachi 4:2)“the Anointed One” (Daniel 9:26)“my Redeemer” (Job 19:25)“Wonderful Counselor, Mighty God, Everlasting Father, Prince of Peace.” (Isaiah 9:6)Jesus – “Yahweh Saves”ImmanuelJESUS IS GOD (DIETY) WITH US (HUMANITY)Have you repented of your sin and trusted in Jesus Christ alone as your Lord and Savior? --------DAILY DEVOTIONAL WITH RON MOOREGet Ron's Daily Devotional to your inbox each morning; visit biblechapel.org/devo.CAREGIVINGDo you have a need we can pray for? Do you need someone to walk alongside you? Do you know of another person who needs care? Let us know at caregiving@biblechapel.org.GROWTH TRACKWe all have a next step - what's yours? To learn more about our Growth Track and to take your next step, biblechapel.org/connect.

In this episode of SHE MD, Mary Alice Haney sits down with Emma Heming Willis, mother, stepmother, wife, advocate, and co-founder of Make Time Wellness, a brand dedicated to women's brain health. Emma shares her journey navigating her husband Bruce Willis' diagnosis of frontotemporal dementia (FTD) and the challenges of caregiving.Emma opens up about recognizing the early warning signs, managing the complexities of a blended family, and building a support system that sustains both the caregiver and their loved one. She also discusses the concept of ambiguous loss and how relationships evolve when a partner's cognitive abilities change.Beyond caregiving, Emma dives into practical strategies for women to maintain brain health, including sleep, nutrition, mental stimulation, and social connection. She highlights the importance of self-care, setting boundaries, and seeking expert support.Through her new book, The Unexpected Journey, and her work with Make Time Wellness, Emma provides actionable insights for caregivers and women prioritizing their brain health, emphasizing resilience, love, and community.Subscribe to SHE MD Podcast for expert tips on PCOS, Endometriosis, fertility, and hormonal balance. Share with friends and visit SHE MD website and Ovii for research-backed resources, holistic health strategies, and expert guidance on women's health and well-being.Sponsors: Cymbiotika: Go to Cymbiotika.com/Shemd for 20% off plus free shippingRocket Money: Cancel your unwanted subscriptions and reach your financial goals faster with Rocket Money. Go to RocketMoney.com/shemd today.Nutrafol: Nutrafol is offering our listeners ten dollars off your first month's subscription and free shipping when you go to Nutrafol.com and enter promo code SHEMD. Vibrant Wellness: Ask your provider for the Hormone Zoomer by Vibrant Wellness — or find a Vibrant-certified provider today at vibrant-wellness.com/SheMDWhat You'll LearnStrategies for women caregivers to maintain mental and physical healthUnderstanding frontotemporal dementia (FTD) and early warning signsHow to build a caregiving support system and engage blended familiesLifestyle approaches for women's brain health, including sleep, nutrition, and mental stimulationTools to navigate ambiguous loss and adapt to changing relationshipsKey Timestamps00:00 Introduction with Mary Alice Haney and Emma Heming Willis03:50 Emma meets Bruce Willis and navigates their blended family dynamics14:50 Recognizing early signs of frontotemporal dementia and seeking diagnosis22:40 Coping with the lack of caregiving resources and support24:30 Prioritizing mental and physical health as a caregiver31:40 Building a caregiving support system with experts and family involvement35:20 Founding Make Time Wellness and creating actionable solutions for brain health38:45 The impact of caregiving on relationships and navigating ambiguous loss40:42 Closing thoughts on resilience, community support, and resources for caregiversKey TakeawaysFrontotemporal dementia (FTD) affects personality, behavior, and communication, often presenting differently than Alzheimer's.Caregiving is a family-wide challenge; support systems are essential to sustain caregivers' health.Ambiguous loss requires adaptive strategies to maintain relationships and emotional resilience.Women can prioritize brain health through lifestyle habits: sleep, nutrition, exercise, mental stimulation, and social connection.Sharing knowledge and resources helps caregivers feel supported and validated.Guest BioEmma Heming Willis is a mother, stepmother, wife, advocate, and co-founder of Make Time Wellness, a brand dedicated to women's brain health. Following her husband Bruce Willis' diagnosis with frontotemporal dementia (FTD), Emma became a passionate voice for caregiving families and authored The Unexpected Journey, highlighting resilience, love, and the practical realities of supporting a loved one with dementia.Links & ResourcesEmma Heming Willis: Make Time WellnessEmma Instagram: https://www.instagram.com/emmahemingwillisEmma Facebook: https://www.facebook.com/EmmaHemingWillisBook: The Unexpected Journey by Emma Heming Willis5% of Make Time Wellness proceeds support Hilarity for CharitySee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Have you noticed yourself feeling sad when your loved one can't remember their phone number? Do you find yourself withdrawing from friends or losing patience more easily? These feelings might be grief—and you may not even realize it's happening. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned that grief doesn't only come after our loved one passes away. It's present throughout our entire caregiving journey, from the moment of diagnosis through each individual change along the way. The good news is that understanding grief—recognizing it, honoring it, and learning to move through it without getting stuck—can transform how we experience our caregiving journey. Today we're sharing six essential tips to help you navigate grief with grace and compassion. Connect with us and share your tips: Website: https://thecaregiversjourney.org/Donate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/thecaregiversjourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.org, nancy@thecaregiversjourney.org Full Show Notes https://thecaregiversjourney.org/47-navigating-grief-throughout-caregiving-six-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned Guide: Navigating Dementia Caregiving Roadmap: https://thecaregiversjourney.org/guides/Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Read More in This Blog here

In this episode, Isabel invites listeners to pause, reflect, and imagine their future as caregivers—or as care receivers. Drawing from her experience leading her first Planning Lab for Caregivers and Retirees, she shares how planning for care can be just as meaningful and intentional as planning a trip, a new home, or retirement dreams. Through a guided journaling and reflection exercise, Isabel encourages listeners to: Explore their expectations and emotions around caregiving.Identify the mix of feelings that come with this life stage—honor, sadness, guilt, joy, or overwhelm.Recognize which emotions they may want to shift, and understand why those emotions are present.Practice self-kindness and curiosity instead of judgment. She emphasizes that caregiving is not just about challenges—it can be a season of connection, self-discovery, and love. By reframing emotions and making small changes today, we can create a more compassionate, intentional future for ourselves and those we care for. Isabel closes by reminding listeners that they deserve love, care, joy, and abundance—and that even small mindset shifts can transform the caregiving journey.

Are you struggling to pull your family together to create a working support system for someone living with dementia? Do you find family members disagreeing on what needs to be done or how to help? You're not alone, and there's a path forward. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned that transforming family dynamics into effective teamwork is one of the most challenging—yet most rewarding—aspects of the caregiving journey. In this episode, we spoke with Dr. Barry Jacobs, a clinical psychologist and family therapist who brings both professional expertise and personal caregiving experience to this conversation. Barry cared for his mother with vascular dementia and his stepfather with Alzheimer's disease for seven years, and he co-authored the AARP Caregiver Answer Book with his wife, psychologist Julia Mayer. This content aligns with Step 8 of our Navigating Dementia Caregiving Roadmap: Start Planning for the Next Stage of Care, particularly when building your personal support network of family and friends. Connect with us and share your tips: Website: https://thecaregiversjourney.org/Donate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/thecaregiversjourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.org, nancy@thecaregiversjourney.org Full Show Notes https://thecaregiversjourney.org/50-family-dynamics-in-caregiving-four-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned Barry's website www.caregiveranswerbook.comBuy the Caregiver Answer Book on Amazon https://amzn.to/4i9V9ZLNavigating Dementia Caregiving Roadmap guide https://thecaregiversjourney.org/guides/#guidesSupport the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Transforming your family into an effective caregiving team isn't easy. It's worth the effort — not just for your loved one with dementia — but for every member of your family. These four tips provide a framework: Create consensus (everyone on the same page).Define an ongoing format for decision making (regular meetings with clear rhythm).Build a family caregiving plan (who does what and when).Plan to deal with conflict (don't let disagreements become disrespectful).

Send us a textOn this episode of The Get Ready Money Podcast, I spoke with Merridith Gonzalez, the Midlife Concierge, about how we can all reimagine midlife with honesty, curiosity, and connection—while preparing for the caregiving and financial realities that come with it.

Memoirist and professor Maggie Andersen on turning a Chicago theater coming of age into No Stars in Jefferson Park, translating performance craft to the page, writing honestly about love, loss, and disability with care and permission, and trusting the long arc of a creative life.  You'll learn:Why writing “for others” can be generous without self-erasure (and how to tell the difference). What theater can teach memoirists about scene movement, including emotional marks, entrances, and exits. How to borrow “page-turner” pacing without sacrificing literary depth. What to cut or keep when you're thinking like a live audience rather than a solitary reader. How to shape a memoir around friendship and time, even when you're learning the form as you write. What “truth with care” can look like in memoir, including permission, restraint, and choosing what must be faced on the page. Ways to involve the people you're writing about early, so the work stays accountable to real humans. Why your definition of “making it” may change, and how timing, fit, and rejection can still lead to publication.  Resources and Links:No Stars in Jefferson Park About Maggie AndersenMaggie Andersen has published fiction and nonfiction in magazines such as Salt Hill, Blood Orange, the Los Angeles Review, Creative Nonfiction, Grain, Cutbank, and DIAGRAM. She has been a finalist for the Montana Prize for Nonfiction and has been nominated twice for the Pushcart Prize. She is an Associate Professor of English at Dominican University and an ensemble member at the Gift Theatre. Her debut memoir, No Stars in Jefferson Park, was published by Northwestern University Press in October 2025.   For show notes, transcripts and to attend our live podcasts visit: podcast.londonwriterssalon.com.For free writing sessions, join free Writers' Hours: writershour.com.*FOLLOW LONDON WRITERS' SALONTwitter: twitter.com/​​WritersSalonInstagram: instagram.com/londonwriterssalonFacebook: facebook.com/LondonWritersSalonIf you're enjoying this show, please rate and review this show!

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 beat by beat through the real dilemma: when to use the walker versus the wheelchair and how a gait belt and a one‑rep deadlift salvaged the transfer. We get transparent about the doubt and we also get honest about the grace that kept us moving. A stylist waited, cleared the room, and turned a noisy salon into a quiet sanctuary. Shampoo, color, cut, and something rarer: the look on my mom's face when she recognized herself again in the mirror. That smile said we chose right.Caregiving spares no one, but we always persevere.  If you're navigating Alzheimer's, mobility challenges, or just the daily logistics of being a caregiver, you'll leave with practical takeaways on the kind of patience that keeps everyone safer and well groomed.If this story made you feel seen, subscribe, share it with your village, and leave a review so other caregivers can find us. Tell me your small win this week—I'm cheering for every single one.Executive Producer/Host: J Smiles ComedyProducer: Mia HallEditor: Annelise Udoye Support the show"Alzheimer's is heavy but we ain't gotta be!"IG: https://www.instagram.com/parentingupFB: https://www.facebook.com/parentingupYT: https://www.youtube.com/@parentingupTEXT 'PODCAST" to +1 404 737 1449 - to give J topic ideas, feedback, say hi!Be sure to leave us a review!

At Christmas, we celebrate that Jesus was born in order to die and rise again!John 1:29, Genesis 22:7-8, Leviticus 5:5-6, Hebrews 10:3-4, Isaiah 53:5-7, 1 Corinthians 5:7, 1 Peter 1:18-19, Luke 22:15, 2 Corinthians 5:21, John 19:30 At Christmas, we proclaim that Jesus was born in order to die and rise again!1 Corinthians 11:26, John 1:29, John 1:35-37 --------DAILY DEVOTIONAL WITH RON MOOREGet Ron's Daily Devotional to your inbox each morning; visit biblechapel.org/devo.CAREGIVINGDo you have a need we can pray for? Do you need someone to walk alongside you? Do you know of another person who needs care? Let us know at caregiving@biblechapel.org.GROWTH TRACKWe all have a next step - what's yours? To learn more about our Growth Track and to take your next step, biblechapel.org/connect.

When you visit your ill or aging parents over the holidays, you might be in for a surprise. Maybe your mom seems confused or your dad is having trouble with driving. Maybe you're not sure if the changes you're seeing are something to worry about or are just normal aging. What should you look for? What should you worry about? What changes are not actually concerning?In this episode of The Integrative Palliative Podcast, Dr. Delia Chiaramonte discusses what to look for when you visit your aging parents and when you should worry.Do you know someone with an aging parent? Send them this episode.Knowledge is power.Happy holidays!Dr. DeliaDelia Chiaramonte, MDhttps://www.doctordelia.comCoping Courageously: A Heart-Centered Guide for Navigating a Loved One's Illness Without Losing Yourself is available here: www.copingcourageously.com Please review this podcast wherever you listen and forward your favorite episode to a friend! And be sure to subscribe!Sign up to stay connected and learn about upcoming programs:https://trainings.integrativepalliative.com/IPI-stay-in-touchI'm thrilled to be listed in Feedspot's top 15 palliative podcasts!https://blog.feedspot.com/palliative_care_podcasts/

Join Dr. Pinkston as she welcomes Erica Bacchus, author of the deeply personal book, A Promise Kept. Erica shares the extraordinary and heartbreaking story of her late husband, John, and his battle with early cognitive impairment consistent with Alzheimer's disease. This conversation delves into a highly controversial and often-unspoken topic: end-of-life choices in the face of neurodegenerative disease. Erica describes the difficulty of John's diagnosis, his profound desire to maintain agency and dignity, and the intense emotional journey she undertook as his caregiver. They discuss: The challenge of Alzheimer's and end-of-life options, particularly the catch-22 regarding mental capacity and current U.S. laws like Medical Assistance in Dying. The couple's decision to seek assistance at Dignitas in Switzerland and the seven-month, complex application process. The overwhelming emotional toll of caregiving, the isolation, and the importance of honoring a spouse's deeply held, personal beliefs about life, purpose, and death. Erica's story is a testament to unwavering love, shared independence, and the courage it takes to support a loved one's choice to have a peaceful, dignified end on their own terms.See omnystudio.com/listener for privacy information.

Recent data shows one out of every four American adults are providing some sort of unpaid caregiving for a loved one, be it a parent, child, or someone else they know with a chronic illness or disability. Caregiving can require a lot of physical, emotional and mental energy, but there's a lot of love there, too - and there is assistance out there to ensure you don't burn out. Nichole talks with Kate Granigan, CEO of Alder in Newton, about the balance that's needed to ensure caregivers can take care of themselves, and resources that can help lighten the load.See omnystudio.com/listener for privacy information.

Dementia, aging, and loss can reshape what the holidays means for our families when the people who created our most cherished traditions can no longer lead them.In this episode, learn how to adapt long-held traditions when aging parents move to retirement homes, experience cognitive decline, or are simply no longer able to host the holidays as they once did. Remember, the heart of the holidays isn't perfection—it's belonging. https://bit.ly/44yXd8iIn this Episode:00:16 - How Christmas Traditions Change When A Family Member Has Dementia04:34 - S3E50 Rebroadcast Intro, What Does it Take to Care for a Partner With Dementia?06:10 - Recipe of the Week, Funeral Raisin Pie11:55 - How Becoming a Caregiver Changes the Relationship14:51 - Interview with Michael Porter: Caregiving for a Partner with Huntington's Disease52:16 - OutroSupport the showGet show notes and resources at our website: every1dies.org. Facebook | Instagram | YouTube | mail@every1dies.org

In this special film festival episode celebrating the 10th anniversary of AlzAuthors, hosts Marianne Sciucco and Christy Byrne Yates welcome filmmaker Frank Silverstein for an intimate discussion about his documentary, “Lousy: Love in the Time of Dementia.” Frank shares his journey capturing the realities of caring for both parents with dementia, offering raw insight, practical wisdom, and hope for caregivers and families living with this disease. Featured Guest: Frank Silverstein – Veteran TV producer, author, and filmmaker. Creator of “Lousy: Love in the Time of Dementia”, a deeply personal iPhone-shot documentary chronicling his parents' decline and the challenges of caregiving. Key Discussion Topics: Behind the Film: Frank reveals how his career in news documentaries shaped his approach to filming, and why he began documenting the “real” moments with his parents as their dementia progressed. Caregiving Realities: The episode explores the confusion, unpredictability, and emotional complexity of caring for loved ones with dementia—including dealing with repeated questions, behavioral changes, and sibling dynamics. Honoring the Person: Frank shares poignant memories of his parents' lives before dementia, and discusses how core personality traits can persist even as the disease changes so much else. Sibling Care Teams: An honest look at family caregiving logistics, relationships, and the value of supporting one another—not just the person with dementia, but also fellow caregivers. Film Festival Details: For those registered for the AlzAuthors Film Festival, they can watch “Lousy: Love in the Time of Dementia” and other festival films through the end of the year. Memorable Quote: “It's very isolating when you're taking care of your parents. There's nobody really that's going to help you... you have to figure out your path out of there.” —Frank Silverstein Resources: Contact Frank Silverstein: www.franksilverstein.com AlzAuthors Podcast, “Caring for Two Parents with Dementia at the Same Time” Next Up: Join the next film festival discussion on Wine, Women, & Dementia by Kitty Norton — details and links on the AlzAuthors website Learn about the Moderators Marianne Sciucco  Christy Byrne Yates About the Podcast AlzAuthors is the global community of authors writing about Alzheimer's and dementia from personal experience to light the way for others. Our podcast introduces you to our authors who share their stories and insights to provide knowledge, comfort, and support. Please subscribe so you don't miss a word. If our authors' stories move you, please leave a review. And don't forget to share our podcast with family and friends on their own dementia journeys. We are a 501(c)(3) charitable organization. Our ongoing work supports our mission to lift the silence and stigma of Alzheimer's and other dementias. Ideas and opinions expressed in this podcast belong to the speakers and not AlzAuthors. Always consult your healthcare provider and legal and financial consultants for advice on any of the topics covered here. Thanks for listening. We are a Whole Care Network Featured Podcast Proud to be on The Health Podcast Network Find us on The World Podcast Network and babyboomer.org Want to be on the podcast? Here's what you need to know    We've got merch! Shop our Store

Family caregivers in the United States are increasingly under mental and financial stress. Elizabeth Miller, founder of the caregiver resource platform Happy Healthy Caregiver, is here to help. On today's show, Miller joins Kimberly to talk about prioritizing self-care and how you start caregiving conversations with family. Plus, we'll get in the holiday spirit with a round of This or That!Here's everything we talked about today:"New Report Reveals Crisis Point for America's 63 million Family Caregivers" from AARP "How To Prepare To Be A Caregiver And Manage The Costs" from Today "5 Powerful Tips to kick off “the Talk” with Your Loved Ones" from Happy Healthy Caregiver"How to Make a Caregiving Plan (So It's Ready When You Need It)" from The New York TimesIf our reporting has been valuable to you in 2025, consider becoming a Marketplace Investor. Give now: https://support.marketplace.org/smart-sn

Family caregivers in the United States are increasingly under mental and financial stress. Elizabeth Miller, founder of the caregiver resource platform Happy Healthy Caregiver, is here to help. On today's show, Miller joins Kimberly to talk about prioritizing self-care and how you start caregiving conversations with family. Plus, we'll get in the holiday spirit with a round of This or That!Here's everything we talked about today:"New Report Reveals Crisis Point for America's 63 million Family Caregivers" from AARP "How To Prepare To Be A Caregiver And Manage The Costs" from Today "5 Powerful Tips to kick off “the Talk” with Your Loved Ones" from Happy Healthy Caregiver"How to Make a Caregiving Plan (So It's Ready When You Need It)" from The New York TimesIf our reporting has been valuable to you in 2025, consider becoming a Marketplace Investor. Give now: https://support.marketplace.org/smart-sn

Caregiving touches every family, yet caregivers often remain unseen. In this conversation from HLTH in Las Vegas, StartUp Health co-founder Unity Stoakes sits down with Richard Lui, award-winning journalist, filmmaker, and Chief Impact Officer for StartUp Health's Caregiving Moonshot. Richard shares the personal story that sparked his mission to transform the global care economy and explains why caregiving is one of the largest and most meaningful opportunities in health. Together, they explore how innovators, investors, and leaders can build solutions that support the people holding our health system together. In this episode • Why caregiving must become a core pillar of every product and service in health• What Richard learned caring for his father with Alzheimer's• How storytelling and culture change are fueling new momentum• Where founders can find opportunity in the rapidly growing care economy• Why community and staying power are essential for caregiving innovators Join the Caregiving Moonshot If you are building solutions that support caregivers or strengthen the care economy, learn how to join our global community of Health Transformers. Meet in Person Join us at Apollo House at JPM Healthcare Week in January. Are you ready to tell YOUR story? Members of our Health Moonshot Communities are leading startups with breakthrough technology-driven solutions for the world's biggest health challenges. Exposure in StartUp Health Media to our global audience of investors and partners – including our podcast, newsletters, magazine, and YouTube channel – is a benefit of our Health Moonshot PRO Membership. To schedule a call and see if you qualify to join and increase brand awareness through our multi-media storytelling efforts, submit our three-minute application. If you're mission-driven, collaborative, and ready to contribute as much as you gain, you might be the perfect fit. » Learn more and apply today. Want more content like this? Sign up for StartUp Health Insider™ to get funding insights, news, and special updates delivered to your inbox.

Our guest is Barry J. Jacobs — he's a clinical psychologist and author based just outside of Philly who has a real heart for supporting family caregivers. And that passion is personal. Barry's caregiving journey started young — when he was just 14, his dad was diagnosed with brain cancer and sadly passed away the following year. That experience shaped the direction of his life and career. Later, from 2010 to 2017, Barry stepped into the caregiving role again — this time for his stepfather, who had Alzheimer's, and his mom, who was living with vascular dementia. He truly understands the emotional rollercoaster that comes with caregiving and has spent his career helping others navigate it with more support and less guilt.  In this episode, we discuss two of his books, co-written with his wife, one on love and relationships after 50, and one focused on addressing common family caregiving questions. We delve deeper into the topics of guilt, family dynamics, and self-care. Barry has much personal and professional wisdom to share, especially when it comes to self-kindness, using more honey and less vinegar, balancing ‘me time' and ‘we time,' and spreading ‘You Got This' confidence throughout the caregiving community. Show notes with product and resource links: https://bit.ly/HHCPod213 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjournal For podcast sponsorship opportunities contact Elizabeth: https://happyhealthycaregiver.com/contact-us/ The Happy Healthy Caregiver podcast is part of the Whole Care Network. Rate and Review the podcast: https://bit.ly/HHCPODREVIEW

Dr Shoshana Ungerleider, is a board-certified internal medicine physician, science journalist, and passionate advocate for compassionate end-of-life care.  She hosts and produces TED Health and the NY Radio Award–winning podcast Before We Go, and founded the End Well Foundation to make end of life a part of life. Shoshana regularly appears as a medical expert on CNN, MSNBC, and CBS News, with bylines in TIME, USA Today, Scientific American, and more. She executive produced the Oscar-nominated Netflix film End Game, funded the Emmy-winning Extremis, and produced Robin's Wish, about the final years of Robin Williams.  In this episode, we explore how popular culture and healthcare meet—how film, media, and storytelling shape the way we see end-of-life, grief, loss, and caregiving—and we'll hear Shoshana's story of caring for her father through cancer. From documentaries to news headlines, including EndWell's part in consulting on HBO's Emmy winning drama The Pitt, these cultural moments guide how we talk about death, support those we love, and face our own final chapters. TRANSCRIPT with resources Daughterhood

In this illuminating episode, host Darleen Mahoney welcomes Rita Shula, Senior Director of Caregiving at the AARP Public Policy Institute, for an in-depth discussion about the dramatic rise in family caregivers across America—a trend revealed by AARP's latest research. Together, they unpack the staggering statistic that one in four adults now provides some form of caregiving, exploring the forces driving this increase: a rapidly aging population, evolving care needs, and the shortage of affordable professional support.Rita Shula shares insights from the study, revealing that caregiving isn't limited to retired or older adults—most caregivers are actually employed, with a growing number balancing careers, child-rearing, and demanding care roles. Through personal stories and data, the episode dives into the emotional, physical, and financial toll caregiving takes, from invisible stressors and “sandwich generation” pressures to the impacts of loneliness and strained health.The episode also turns to solutions, as Rita Shula explains AARP's advocacy for practical policy changes such as tax credits, improved healthcare navigation, flexible savings accounts, and workplace support. Listeners will discover free resources, expert guides, and vibrant online support groups.SeniorLivingGuide.com Podcast sponsored by TerraBella Senior Living & Tom Marks, Best Selling Author on RetirementAARP 2025 Report LinkAARP Caregiving Resources The background music is written, performed, and produced exclusively by purple-planet.com.https://www.purple-planet.com/SeniorLivingGuide.com Webinars and Podcast represents the opinions and expertise of our guests. The content here is for informational and educational purposes. It does not necessarily represent the views, recommendations, opinions or advice of Fairfax 

Actor Carol Kane, known for her roles in Unbreakable Kimmy Schmidt, the Princess Bride and Taxi, lives with her 98 year old mother in Manhattan. A new documentary short called "Carol & Joy" spotlights a day in the life of two singular talents as well as touches on the demands of caregiving. Carol and Joy Kane discuss their lives together, along with director Nathan Silver.

This time on Code WACK! Suddenly, with little notice, you may find yourself having to step into a caregiving role for a friend or family member. Maybe you already have. It could be an aging parent, an ailing partner or an injured child. What does it really cost—emotionally, physically, and financially—to care for someone you love? To find out, we recently spoke with Mary-Elizabeth Harmon, a scientist turned storyteller and caregiver whose life changed in an instant. What she thought would be a brief visit to her father ultimately became a years' long caregiving journey that nearly pushed her to the brink—and ultimately inspired her vision for “vertical villages,” where neighbors foster caring communities and economies to support one another through life's toughest moments. As the founder of Village Company 360 and the caregiver of her mother in Virgina, Mary-Elizabeth reveals just how unprepared our systems are for the caregiving crisis—and why all of us need to pay attention. This is the first episode in a two-part series. Check out the Transcript and Show Notes for more! And please keep Code WACK! on the air with a tax-deductible donation.

Caring for elderly parents with dementia presents unique challenges for family caregivers, especially as memory loss progresses and decision-making becomes more complex. In this episode, caregiving expert Pamela D. Wilson shares vital caregiver tips and support strategies to help you navigate difficult choices when your aging loved ones can no longer fully understand or evaluate the consequences of decisions.Learn how to balance compassion in caregiving with the need for safety, including when to intervene in situations such as driving or living arrangements when caring for adult parents. Explore real dementia caregiver experiences and gain practical caregiver advice for managing caregiving challenges as memory loss advances with empathy and confidence.Pamela's extensive background as a home care agency owner, care manager, guardian, medical power of attorney, and expert witness provides valuable insights into eldercare solutions and offers proven and practical family caregiving support.Whether you are a new family caregiver of a person with dementia or seeking guidance on challenging family dynamics that can occur during dementia care, this episode offers eldercare solutions and actionable tips to support your caregiving journey. You'll find solutions to complex dementia caregiving challenges on this episode of The Caring Generation to share with your family members.Find podcast show transcripts and links mentioned in Episode 234 https://pameladwilson.com/caregiver-radio-programs-the-caring-generation/ For more caregiving, aging, and elder care tips for your caregiving journey, visit Pamela's website at https://www.PamelaDWilson.comLearn about Pamela D Wilson, her professional background, and her experience: https://pameladwilson.com/pamela-d-wilson-story/Schedule a 1:1 elder care consultation by telephone or video call with Pamela: https://pameladwilson.com/elder-care-consultant-aging-parent-consultation-managing-senior-care-needs-meet-with-pamela-d-wilson/Sign up for Pamela's newsletter here: https://pameladwilson.com/contact/Join Pamela's Online Caregiver Support Group on Facebook https://www.facebook.com/groups/thecaregivingtrap Follow Pamela on Social Media:Facebook: https://www.facebook.com/pameladwilsoncaregivingexpert/LinkedIn: https://www.linkedin.com/in/pameladwilsoncaregiverexpert/ X: https://www.x.com/CaregivingSpeakPamela D Wilson | Caregiver, Elderly Care & Caregiving Expert provides caregiver tips, support for caregivers, and resources for aging and elder care. Caregiving and aging for parents doesn't have to be challenging with expert caregiver advice, solutions, and strategies based on Pamela's 25 years of experience in care management, dementia care, and as an expert witness. Visit Pamela's website www.PamelaDWilson.com to access online caregiver programs, advice and tips to support caregivers and aging adults.©2018, 2025 Pamela D Wilson. All Rights Reserved

In this episode, Carolyn Dowdy shares her deeply personal journey into caregiving and the life-changing experiences that led her to found Caregiver Mental Wellness. She opens up about how many people become caregivers without realizing it, why caregiver burnout often goes unnoticed, and how long-term stress can quietly impact mental, physical, and emotional health. This episode offers insight, validation, and practical support for caregivers, parents, and anyone caring for someone they love.We explore:How Carolyn became a caregiver and what sparked her missionWhy many caregivers don't identify themselves as caregiversThe early and long-term signs of caregiver burnoutHow caregiving affects mental, emotional, and physical well-beingWhy self-care is necessary, not selfishThe impact of long-term chronic stress on healthSupport and free resources available through Caregiver Mental WellnessThe importance of recognizing and supporting youth caregiversHow non-caregivers can help and support the caregiving communityTune in to gain awareness, reassurance, and practical tools to better understand caregiving and prevent burnout. Share this episode with anyone who may be caring for a loved one—or supporting someone who is.Connect with CarolynWebsite: https://www.caregivermentalwellness.comInstagram: https://www.instagram.com/caregivermentalwellnessFacebook: https://www.facebook.com/caregivermentalwellnessLinkedIn: https://www.linkedin.com/company/caregivermentalwellnessConnect with meInstagram: https://www.instagram.com/dalitalksFacebook: https://www.facebook.com/dalitalksWebsite: https://www.dalitalks.com

Roughly 1 in 4 Americans now identifies as a family caregiver. That share has risen dramatically over the past decade. With more people needing care and limited options for affordable long-term care services in the United States, caregivers are strained—often mentally and financially. On today's show, Debra Whitman, chief public policy officer of AARP, joins Kimberly to unpack how this “invisible workforce” fits into the broader economy and how we can make caregiving more sustainable for families.Here's everything we talked about today:"Caregiving in the US 2025" from AARP"The number of “sandwich generation” caregivers is growing" from Marketplace "If Americans Were Paid For Their Caregiving, They Would Make More Than $1.1 Trillion" from the National Partnership for Women and Families"Returning to the Workforce After Being a Caregiver" from Harvard Business Review"Invisible crisis: America's caregivers and the $600 billion unpaid cost of their labor" from ABC News"Caregiving in the US 2025: Caring Across States" from AARPWe love hearing from you. Leave us a voicemail at 508-U-B-SMART or email makemesmart@marketplace.org.

Conscious Caregiving with L & L is "Tackling the Tough Conversations."   The topic of this episode is "Holiday Gifts for Seniors" featuring hosts Lori La Bey and Lance A. Slatton.   About Lori La Bey:   Lori La Bey is the founder of Alzheimer's Speaks and is co-founder of Dementia Map global resource directory and the co-host of Conscious Caregiving with L & L.   Lori's mother who lived with dementia for 30 years. Her goal has always been to shift dementia care from crisis to comfort around the world.   She offers a variety of free resources to educate, empower, connect, and decrease stigmas; helping families and professionals live graciously alongside dementia.   Lori is an international speaker known for her multiple platforms and training programs.   Connect with Lori La Bey: Official Website:  https://alzheimersspeaks.com/   Official Dementia Map Website: https://www.dementiamap.com/    About Lance A. Slatton - known as "The Senior Care Influencer"":   Known as "The Senior Care Influencer" Lance is a Writer, Author, Influencer, and Healthcare professional with over 20 years in the healthcare industry.   Lance A. Slatton is a senior case manager at Enriched Life Home Care Services in Livonia, MI. He is also host of the award winning podcast & YouTube channel All Home Care Matters and Co-Host of Conscious Caregiving with L & L with Lori La Bey along with The Care Advocates and The Caregiver's Journal.   Lance's book, "The All Home Care Matters Official Family Caregivers' Guide" was the recent recipient of the 2024 International Impact Book Awards.   Connect with Lance A. Slatton - "The Senior Care Influencer":   Official Website: https://www.lanceaslatton.com   Official Website for All Home Care Matters: https://www.allhomecarematters.com   Lance A. Slatton and Lori La Bey Co-Host and Produce Conscious Caregiving with L & L.   Visit their website at: https://consciouscaregivingll.com/ 

Roughly 1 in 4 Americans now identifies as a family caregiver. That share has risen dramatically over the past decade. With more people needing care and limited options for affordable long-term care services in the United States, caregivers are strained—often mentally and financially. On today's show, Debra Whitman, chief public policy officer of AARP, joins Kimberly to unpack how this “invisible workforce” fits into the broader economy and how we can make caregiving more sustainable for families.Here's everything we talked about today:"Caregiving in the US 2025" from AARP"The number of “sandwich generation” caregivers is growing" from Marketplace "If Americans Were Paid For Their Caregiving, They Would Make More Than $1.1 Trillion" from the National Partnership for Women and Families"Returning to the Workforce After Being a Caregiver" from Harvard Business Review"Invisible crisis: America's caregivers and the $600 billion unpaid cost of their labor" from ABC News"Caregiving in the US 2025: Caring Across States" from AARPWe love hearing from you. Leave us a voicemail at 508-U-B-SMART or email makemesmart@marketplace.org.

What does it really look like to raise a child when doctors say he won't survive?In this episode of Your Biggest Breakthrough, Ken and Mary Sue Grein share the deeply personal story of raising their son, Jacob Grein, over the course of 37 years. Born six weeks premature, Jacob faced severe medical complications, physical disabilities, deafness, and ongoing health challenges that required constant care from the day he entered the world.Ken and Mary Sue open up about the realities of parenting a medically fragile child—the fear, exhaustion, faith struggles, marriage pressures, and the daily decisions to keep going when answers didn't come easily. They reflect on the moments when they had to surrender outcomes to God, redefine what healing and success truly meant, and learn to live with hope amidst long-term caregiving.This episode isn't about a quick miracle. It's about faith lived out over decades, love that never wavers, and a son whose life profoundly shaped his family in lasting ways.If you're a parent walking a difficult road, a caregiver feeling unseen, or someone wrestling with unanswered prayers, Jacob's story—and his parents' journey—will encourage you to keep going, one day at a time.Chapters:[00:00] Podcast Preview[01:30] Topic and Guest Introduction[03:25] Jacob Grein's Traumatic Premature Birth[04:35] Surrendering Jacob's Life to God[06:54] Doctors Give Jacob Six Months to Live[09:50] Learning to Live Moment by Moment[11:40] Bringing Jacob Home After 137 Days in NICU[13:50] Discovering That Jacob is Deaf[15:14] How Jacob's Illness Tested Their Marriage[18:21] Years of Surgeries and Setbacks[20:32] Raising Other Children While Caring for Jacob[22:00] Accepting Jacob's Disabilities[23:53] Caregiving as a Lifelong Calling[26:14] How Jacob Became Their Greatest Teacher[27:53] New Definition of Success and Purpose[28:30] Jacob's Joy Despite Suffering[33:04] Losing Jacob After 37 Years[36:44] Healing After Caregiving Ends[39:13] Why Jacob's Story Brings Hope to Others[40:50] Where to Find Jacob's Story BookResources mentioned:Get Your Copy of Jacob's StoryWebsiteYouTubeInstagramFacebookGuest's bio and social handles:Kenneth and Mary Sue Grein have been married for over four decades and are the parents of four children: Jacob, Hannah, Luke, and Grace. Their love story began at Rockmont College in Denver, Colorado, where they met during freshman orientation in 1977.
Ken, a former college basketball player and lifelong contractor, grew up on his family's farm in Brighton, Colorado, where he learned the values of hard work and perseverance that would serve him throughout Jacob's medical journey. Mary Sue, a gifted pianist and devoted mother, became Jacob's primary caregiver and fiercest advocate, developing an expertise in medical terminology and special needs care that few parents possess.Together, they navigated 37 years of medical challenges, hospital stays, and daily caregiving while raising three other children and maintaining their faith through the darkest moments. Their experience as parents of a child with multiple disabilities taught them profound lessons about love, resilience, and finding joy in the smallest victories. The...

A Weaver's Journey of Art, Advocacy, and Belonging — from WEAVE: The Social Fabric Project In this edition of our special Weavers series, we sit down with Nikki Harris—fiber artist, mother, advocate, and community connector from Baltimore, Maryland. Through art and action, Nikki embodies what it means to weave the social fabric. She shares her journey from self-taught fiber artist to founding HGE Designs, and from 911 dispatcher to autism advocate with Pathfinders for Autism. This conversation delves into what it truly means to create space—for healing, for connection, and for community. Nikki opens up about raising her son Roman, navigating systems as a caregiver, and the spiritual resilience it takes to serve while healing herself. Calls to Action ✅ TELL A FRIEND ABOUT TP&R!!! Help spread the message of meaningful conversation. ✅ Subscribe to Talkin' Politics & Religion Without Killin' Each Other on your favorite podcast platform. ✅ Leave a review on Apple Podcasts, Spotify, or anywhere you listen ✅ Join the community on Substack: coreysnathan.substack.com ✅ Watch & subscribe on YouTube: youtube.com/@politicsandreligion Timestamps & Highlights [00:01:00] –

In this episode, Sarah and Miranda Rake kick things off with some Mariah Carey karaoke and a rundown of their favorite “laundry folding films.” Then journalist Courtney Martin joins to talk about the messy, tender, and often overwhelming realities of caring for aging parents while raising kids—the ultimate sandwich generation hustle. Courtney shares what it's been like to relocate her whole family, the heartbreak and beauty of moving her dad into memory care, and how communal living and worker-owned elder care centers have shaped her journey. Grab a mug of tea, add another bag (Sarah's jam), and settle in for a conversation that's equal parts comfort and reality check.Other Links:* Learning in Public: Lessons for a Racially Divided America from My Daughter's School by Courtney Martin * What Our Intergenerational Household Taught All of Us About Care (Greater Good Science Center)* Opinion: Whoever needs to hear this: It's OK to put your loved one with dementia in residential care (SF Chronicle)* Elder Care (Courtney's Substack)* On Vanishing: Mortality, Dementia, and What It Means to Disappear by Lynn Castiel Harper* Creative Care: A Revolutionary Approach to Dementia and Elder Care by Anne Basting * Travelers to Unimaginable Lands: Dementia, Caregiving, and the Hidden Humanity of Memory by Dasha Kiper * Wise Unknown Podcast * Slate's How-To Podcast * the examined family (Courtney's Substack)* Mother of It All Bookshop (Bookshop.org)* Caring Across Generations (Ai-jen Poo)* Doulagivers Elder Care Doula Directory (Doulagivers: Find a Doula)* Home Care Cooperatives* Holiday Movies We Love (Or Don't)* Mariah Carey's Christmas Specials * A Merry Scottish Christmas * A Merry Little Ex-mas * White Christmas * Christmas in Connecticut * Desk Set* A Very Murray Christmas (Netflix)* Freakier Friday* Sarah's Letterboxd If you love the work we do on Mother Of It All, please consider becoming a paid subscriber. Paid subscribers get access to everything behind the paywall, like subscriber-only episodes, book reviews and more. If you subscribe at the founding member level, we'll send you one of our awesome tote bags. And it's always free and helpful to follow, share, rate and review our show here and everywhere else you listen to podcasts you love. Thank you!* Visit our Bookshop storefront to find all the books we've mentioned here and in previous episodes. When you shop there, we get a small affiliate fee (yay, thank you!).* Visit motherofitall.com to send us ideas for a future episode or learn more about the show.* Follow the podcast on Instagram (@themotherofitall) or Bluesky (@motherofitallpod.bsky.social) This is a public episode. If you'd like to discuss this with other subscribers or get access to bonus episodes, visit motherofitall.substack.com/subscribe

166 Rachel Waters' Journey: From Care Giving Tragedy to Legal Advocacy In this episode of Hospice Explained, host Marie Betcher RN interviews Rachel Waters. Rachel shares her harrowing journey that began when she was indicted for the death of her mother while she was acting as her caregiver during hospice. Prosecutors alleged she had administered a lethal dose of morphine, leading to charges of murder and the possibility of the death penalty. Rachel describes the 19-month legal and emotional ordeal, the eventual dropping of charges, and how she is now channeling her experience into advocating for Marsha's Law — aimed at protecting family caregivers administering end-of-life medications. Rachel's story highlights the urgent need for compassionate policy reform and systematic change in hospice care protocols. 00:00 Introduction and Disclaimer  00:28 Meet the Host: Marie Betcher RN 00:43 Introducing Rachel Waters 02:23 Rachel's Story Begins 03:48 Early Signs of Trouble 05:30 A Rapid Decline 06:28 Entering Hospice Care 09:02 The Final Days 09:58 A Shocking Turn of Events 15:34 Legal Nightmare Begins 20:53 Facing Charges and Seeking Help 22:38 Turning Herself In Rachel go fund me:  https://gofund.me/77e3e7ad9   If you want to help, you can donate to help support Hospice Explained at the Buy me a Coffee link   https://www.buymeacoffee.com/Hospice  Hospice Explained Affiliates & Contact Information Buying from these Affilite links will help support this Podcast.  Maire introduces a partnership with Suzanne Mayer RN inventor of the  cloud9caresystem.com,  When patients remain in the same position for extended periods, they are at high risk of developing pressure injuries, commonly known as bedsores. One of the biggest challenges caregivers face is the tendency for pillows and repositioning inserts to easily dislodge during care.(Suzanne is a former guest on Episode #119) When you order with Cloud 9 care system, please tell them you heard about them from Hospice Explained.(Thank You)  If you would, you can donate to help support Hospice Explained at the Buy me a Coffee link  https://www.buymeacoffee.com/Hospice Marie's Contact Marie@HospiceExplained.com www.HospiceExplained.com   Finding a Hospice Agency 1. You can use Medicare.gov to help find a hospice agency, 2. choose Find provider 3. Choose Hospice 4. then add your zip code This should be a list of Hospice Agencies local to you or your loved one.