Podcasts about caregivers

Lana Wilhelm is a nurse, case manager, and caregiver advocate. After her husband suffered a stroke in 2021, Lana found herself on the other side of the healthcare system and discovered how little support exists for those caring for the people they love. Now, as the founder of CarePower Connect and host of the Both Sides of the Bed podcast, she helps caregivers feel seen, supported, and less alone. Today, Lana shares how her husband's stroke transformed their marriage, why caregivers must allow themselves to be vulnerable, and how even the smallest acts of kindness can provide meaningful relief. She opens up about grieving the husband she once knew while learning to love and accept who he is now, and offers practical ways friends, family members, and communities can better support caregivers. My friends, if you or someone you love is caring for others, walking through an unexpected change, or struggling to ask for help, this conversation is for you. You'll be reminded that vulnerability is a sign of strength, difficult moments can coexist with hope, and none of us are meant to carry life's heaviest burdens alone.

Trish Yonker, LCPC, explores how foster care, family separation, instability, and disrupted relationships can affect children and the people who care for them. She offers practical guidance for pacing trauma treatment, building emotional and physiological safety, supporting overwhelmed caregivers, responding to behavioral and developmental needs, and creating flexible, relationship-centered care for foster and adoptive families. Interview with Elizabeth Irias, LMFT.Earn CE credit for listening to this episode by joining our low-cost membership for unlimited podcast CE credits for an entire year, with some of the strongest CE approvals in the country (APA, NBCC, ASWB, and more). Learn, grow, and shine with Clearly Clinical Continuing Ed by visiting https://ClearlyClinical.com. Hosted on Acast. See acast.com/privacy for more information.

Vasanta Pundarika built her career inside healthcare investment banking before launching Lotuspring, an advisory firm focused on women's health and behavioral health. She spent nearly 20 years advising healthcare systems, treatment providers, and growth stage companies on mergers, financing, and operational strategy while watching the industry repeatedly misunderstand the people it claimed to serve.The conversation starts unexpectedly with anthropology, bread, and language. Vasanta explains how she spent years changing the pronunciation of her own name to make other people comfortable before eventually reclaiming it. That thread opens into a much larger discussion about adaptation, identity, and what institutions quietly train people to tolerate.From there, the discussion moves into behavioral health, women delaying care, and the invisible labor that healthcare business models routinely ignore. During COVID, Vasanta noticed men's behavioral health units refilled faster than women's units. The reason had nothing to do with demand. Women were still home managing caregiving responsibilities, children, aging parents, and households while their own mental health collapsed in the background.The episode examines what happens when healthcare companies become “snazzy big brands” before building real clinical substance underneath. Vasanta describes the tension between mission and margin inside healthcare startups, private equity backed care models, and behavioral health expansion. The conversation pushes on who benefits when healthcare scales aggressively, who absorbs the operational pressure, and how patient trust erodes long before executives notice it on a dashboard.They also discuss patient advocacy culture, anthropology as systems analysis, healthcare capitalism, prior authorization, investor language, and why some clinically excellent companies never survive long enough to scale.RELATED LINKSVasanta PundarikaLotuspringWomen's Health HorizonsSakhi for South Asian SurvivorsNACDPrinceton University Anthropology DepartmentFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

In this episode of Next Steps for Seniors, host Wendy Jones welcomes Lynn Breuer and Beth Seelbach from Jewish Family Services to discuss two valuable programs: the Caring Connections Neighborhood Hub and Retirement Reimagined. Lynn and Beth share resources to support family caregivers and help retirees create purposeful next chapters. Caring Connections Neighborhood Hub: Located at the J in West Bloomfield (open to all faiths) Monthly Memory Cafes with music, art, and activities for caregivers and loved ones with dementia Caregiver support groups, workshops, and respite services Evidence-based cognitive training classes (Mind Aerobics) Retirement Reimagined: Nine-week workshop series helping recent retirees rediscover purpose, set goals, and build meaningful lives after work Addresses isolation, loss of structure, and finding new fulfillment For more information, call 248-592-2313. Podcast Schedule: Tune in to Next Steps for Seniors with new episodes dropping twice a week at 7:00 AM! Every Tuesday: Educational and insightful content to help you navigate the practical steps of aging. Every Friday: Spiritual and emotional support to encourage your heart and mind. Be sure to subscribe on Apple, Spotify, IHeart Podcasts so you never miss an episode, and if you enjoyed today's show, please leave us a rating and review!Learn more : https://omny.fm/shows/next-steps-4-seniors-with-wendy-jonesSee omnystudio.com/listener for privacy information.

In this episode of the award-winning Caregiver S.O.S. On Air, hosts Ron Aaron and Carol Zernial sit down with Dr. Grace Macalino, a public health researcher and the founder and CEO of CAPWA AllCare. Drawing from her personal experience navigating the complex journey of caring for her aging parents, Dr. Macalino discusses a critical yet often overlooked aspect of caregiving: the massive shift in personal identity.

This podcast was created using NotebookLM.This podcast highlights the critical role of caregivers in managing the oral hygiene of both children and the elderly, particularly for those in the "sandwich generation" who support both age groups simultaneously.

Home care agencies are hitting an operational wall as they grow, and the fix isn't what you'd expect. Discover why offshore remote recruiters and coordinators are helping franchises cut labor costs by up to 60% while building resilient, proactive teams. Find more info at https://smartscale360.com/blogs/news/why-homecare-agencies-across-the-u-s-are-adding-remote-recruiters-and-coordinators SmartScale 360 City: Tampa Address: 1209 E Cumberland Ave Website: https://smartscale360.com/

In this episode, Cedric Bertelli reminds us that we don't have to carry emotional pain forever. discusses the Emotional Resolution (MRES) methodology, its applications for emotional health, and practical techniques for managing emotional difficulties like anxiety and trauma. Discover how this innovative approach can help you resolve emotional patterns and improve mental well-being."Close your eyes peacefully and feel the emotion."Chapters:00:00 Introduction to Emotional Techniques and Emotional Awareness00:29 Feeling Emotions Through Physical Sensations00:58 The Practice of Interoception in Emotional Resolution01:54 The Emotional Health Institute and MRES Methodology03:04 Goals of Making Emotional Resolution Accessible04:11 Common Signs of Emotional Difficulties05:13 Understanding the Brain's Construction of Emotional Difficulties06:09 How MRES Addresses Outdated Brain Predictions07:08 The Technique of Feeling Sensations Without Breathing08:37 Feeling Sensations and the Role of Interoception09:18 Testing the Effectiveness of Emotional Resolution11:04 Next Steps and International Collaboration for MRES12:11 Advice for Those Struggling with Emotional Pain13:10 How to Connect with the Emotional Health Institute"Your brain recognizes past trauma in your current environment."Key Topics and Takeaways:*Managing emotional difficulties like anxiety and PTSD*The role of interoception in emotional health*Techniques for feeling and releasing emotions*The importance of feeling sensations without interference*Clinical studies validating MRES effectiveness*Global and multilingual approach to emotional healing*Steps to start resolving emotional painBe sure to follow his journey with his 1st episode here in 2024 here! Support the showEnjoy the show and thank you for being here. Please subscribe to stay current and share with a friend who could use this episode. Want to Support the Show:Leave a five-star review on Apple Podcasts or Spotify to help others find usJoin our monthly support groups and community support initiativesAll questions for the host or guests: Email PodcastsByLanci@gmail.com.Show Partner: Living Proof TBI Coaching specializes in recovery for Traumatic Brain Injury Survivors, Families, and Caregivers. Book a free call here.CRISIS LINE: DIAL 988

For forty years I've said that healthy caregivers make better caregivers—and this week that truth became personal in a new way. In this episode, I share an update following my recent cancer treatment and explain why caregivers must be willing to care for themselves if they hope to care well for others. Then I tell a story that could only happen in Montana. Two strangers drove up our mountain road looking for a man named "Don," leading to an unforgettable conversation with a sheriff's deputy that challenged the way I think about responsibility, self-reliance, and being a good neighbor. Along the way, we'll laugh about a small-town post office, reflect on the lessons hidden in everyday life, and revisit Andraé Crouch's timeless hymn, "Bless the Lord, O My Soul," and why it has meant so much to Gracie and me through decades of caregiving. Whether you're caring for a spouse, parent, child, or friend—or simply trying to live faithfully where God has planted you—I hope this conversation encourages you to prepare well, shoulder your responsibilities with grace, and remember that hope is never far away. Healthy caregivers make better caregivers. And healthy caregivers help make stronger families.  There's more at Caregiver.substack.com

El grupo investigador en el proyecto en internet de Latino Northfield visita el programa y compartimos las canciones de sabios cantores que cantaron en el evento de lanzamiento del sitio web, una iniciativa estupenda.

In this episode of the award-winning Caregiver S.O.S. On Air, hosts Ron Aaron and Carol Zernial sit down with Dr. Grace Macalino, a public health researcher and the founder and CEO of CAPWA AllCare. Drawing from her personal experience navigating the complex journey of caring for her aging parents, Dr. Macalino discusses a critical yet often overlooked aspect of caregiving: the massive shift in personal identity. When we become caregivers, we easily get swallowed up by "the doing"—the endless list of daily tasks, doctor appointments, and logistics. But what happens to who we are? Dr. Macalino introduces her Evidence-Informed Caregiver Identity Framework, offering listeners a much-needed language to understand the emotional evolution, isolation, and unspoken guilt that comes with stepping into a caregiving role. Whether you are balancing a career, managing long-distance care, or learning how to transition a loved one into memory care, this episode offers a compassionate roadmap to finding agency, setting boundaries, and reclaiming moments of joy. Key Takeaways The Distinction Between 'The Doing' and 'The Being': Caregiver burnout and isolation often don't stem from the physical tasks themselves, but from the unaddressed emotional toll of an eroding personal identity. The 'Deafening Silence' of Caregiving: Unlike becoming a parent, society rarely acknowledges or celebrates the massive identity shift of becoming a caregiver, leaving many to feel entirely alone. Reclaiming Your Original Role: When the scale tips and you forget you are a daughter, son, or spouse because you are only acting as a caregiver, it is a sign of trouble. Transitioning a loved one to professional care (like memory care) can painfully but beautifully allow family members to step back into their original roles as husbands, wives, or children. The Power of Bahala Na: Embracing a cultural mindset of letting go of control—acknowledging that you have done your absolute best and accepting that "it is what it is"—is essential for releasing caregiving guilt and shame. Moving from Survival to Agency: By understanding the stages of the caregiver identity, individuals can move past mere survival and gain the agency to keep themselves in control of their own journey. About Dr. Schauf Dr. Grace Macalino Schauf, PhD, MPH, is the Founder and CEO of Kapwa AllCare. Drawing on her background in public health and her personal caregiving experiences, she developed the Caregiver Identity Framework, an evidence-informed approach that helps caregivers better understand their journey, reclaim agency, and build sustainable support systems for themselves and their loved ones. Hosts Ron Aaron and Carol Zernial, and their guests talk about Caregiving and how to best cope with the stresses associated with it. Learn about "Caregiver SOS" and the "Teleconnection Hotline" programs. Caregiver SOS On Air is a presentation of the WellMed Charitable Foundation. For more resources, tips, and past episodes, visit caregiversos.org or email your questions to radio@wellmed.net.See omnystudio.com/listener for privacy information.

Learn more : https://omny.fm/shows/next-steps-4-seniors-with-wendy-jonesSee omnystudio.com/listener for privacy information.

Children pick up on caregiver stress in ways we often miss: tired voices, missed routines, hushed conversations. Discover how faith-based, age-appropriate stories help families reconnect and create safe spaces for honest dialogue during illness, aging, or caregiving challenges. Kids Caregiver Collection/Series City: Frisco Address: 8700 STONEBROOK PKWY PO BOX 309 Website: https://kidscaregivercollection.com/

When my 90-year-old mother-in-law moved into our home earlier this year, caregiving became deeply personal. Seeing the stairs, stubborn jar lids, fear of falling and loss of independence through her eyes changed how I understood aging, dignity and love—and inspired this conversation. Millions of people in the middle of their own lives suddenly become caregivers. Most arrive untrained, unprepared and too often unsupported, yet they keep showing up because love asks them to. Few understand that journey more deeply than Amy Coupal, CEO of the Ontario Caregiver Organization. As a child, Amy helped care for her brother, who lived with cerebral palsy. Years later, she walked beside her mother through cancer and palliative care. Today, she helps her father navigate life in his late eighties, holding their ordinary moments close because she knows their time together is not unlimited. Amy gives voice to the exhaustion, guilt, anticipatory grief and invisible mental load carried by caregivers. Leanne Kaufman, President and CEO of RBC Royal Trust, then explains how honest conversations and thoughtful planning can answer some of caregiving's hardest questions before a crisis makes them urgent. This is a deeply personal story—but it is also one that may profoundly affect any of us as our lives, and the lives of those we love, unfold.

What if your loved one in spirit could tell you that you did everything right? In this deeply emotional episode of Radio Medium, internationally renowned psychic medium Laura Lee connects with Anne from California for a remarkable psychic reading filled with healing, validation, and comforting spirit messages from loved ones in the afterlife. As Laura tunes in to spirit, Anne's mother and grandmother step forward together, offering unmistakable evidence of their continued presence through a cherished family ring, meaningful memories, and the spirit of a child connected to their lineage. Most importantly, Anne receives the message she has desperately needed to hear: the difficult end-of-life decisions she made as her mother's devoted caregiver were made with love, compassion, and courage. Spirit lovingly asks her to release the guilt, stop second-guessing herself, and trust that her mother is at peace, surrounded by family in heaven. This powerful mediumship reading explores grief healing, caregiver guilt, family love, forgiveness, and the enduring connection between this life and the next. If you've ever questioned a difficult decision, cared for someone through illness, or longed for reassurance from a loved one in spirit, this heartfelt episode offers profound spiritual guidance, hope, and the reminder that love never dies.

Burn scars around Utah at high risk of mud flows, flooding Caregiver charged in death of three men with disabilities has court appearance State senator named to lead conservative think-tank U.S. House passes bipartisan bill to make Daylight Saving Time permanent Todd Blanche faces Congressional hearing to become new U.S. Attorney General Tough Conversations with Kids: How parents can assist in stopping and preventing bullying ...and more!

The man charged in the death of three men with disabilities in February is in court this morning, as lawyers work to convince a judge to send the case to trial. Prosecutors say that Isaiah Vaughn Pulu left three of his "Safe and Sound Services" clients in a running car for at least 3.5 hours. The three men died due to carbon monoxide poisoning. KSL Legal Analyst Greg Skordas explains why this wouldn't be a death penalty case.

**Women Connected in Wisdom on YouTube** Resources & What we are up to Don't drown in the demands of caregiving. Veronica Pulido shares how to stay Aflote and protect your mental & emotional wellness while supporting a loved one through serious illness. In this episode of Women Connected in Wisdom, my guest co-host Cynthia Phelps and I, Christine Gautreaux, are joined by Veronica Pulido, the Founder and CEO of Aflote (formerly Good Grief). Veronica's mission was born from her personal journey of caring for her father during a rare form of cancer. She realized that the medical journey is often as exhausting for the caregiver as it is for the patient, and she created Aflote to ensure no one has to navigate that path alone. We focus on the Mental and Emotional Wellness dimensions, specifically addressing the heavy load of supporting someone through a serious illness. Veronica explains how Aflote provides the community, tools and resources needed to manage the complex logistics and emotional strain of caregiving. If you are currently feeling overwhelmed by a medical crisis or the responsibilities of being a caregiver, this whole-self conversation offers the clarity and support you need to keep going. Connect with Veronica Pulido: Website: https://aflote.com/ Instagram: @joingoodgrief / @vero.pulido LinkedIn: Veronica Pulido More resources from today's show cynthia@innerally.com  emberlightway.org  

In this episode of the award-winning Caregiver SOS On Air podcast, hosts Ron Aaron and Carol Zernial sit down with board-certified geriatric psychiatrist Dr. Thomas Weiss to tackle one of the most challenging chapters in caregiving: identifying and managing early-onset dementia.

Brad Power spent years advising major corporations on systems design, process engineering, and decision making before lymphoma shoved him into the patient side of American healthcare. Instead of accepting the experience at face value, he started reverse engineering the machinery around cancer itself. Brad is the founder of Cancer Patient Lab and Open Cancer AI, two projects built around a blunt reality most patients discover too late: the healthcare system rewards people who know how to navigate it. Everyone else risks getting steamrolled by information asymmetry, insurance barriers, administrative friction, and institutional incentives designed around efficiency instead of human survival.The conversation starts with Harvard Business Review and Tumblr blogs before moving directly into the darker architecture underneath modern cancer care. Power explains how hospitals optimize for throughput, how insurance companies reward operational consistency over personalized medicine, and why many patients quietly end up needing a crash course in oncology, reimbursement policy, and behavioral psychology while fighting for their lives.The discussion digs into CAR-T therapy, functional testing, AI assisted decision support, and the growing collision between personalized medicine and standardized care pathways. Power argues that engaged patients often get better outcomes because they learn how to push for off guideline treatments, contest denials, and ask smarter questions. The counterpoint lands hard: patients should never have needed to become experts in the first place.The episode also explores the cultural consequences of AI entering cancer care. OpenAI advertising, data privacy, trust erosion, pharmaceutical influence, and “agentic AI” all collide inside a healthcare economy already drowning in distrust. Power sees artificial intelligence as a force multiplier for patient literacy and access. The larger system still decides who gets approved, who gets delayed, and who gets left behind.By the end, the conversation lands exactly where modern healthcare keeps forcing people to land: survival increasingly depends on learning how the machine works before the machine works on you.RELATED LINKSBrad PowerCancer Patient LabOpen Cancer AIHarvard Business ReviewResearch to the PeopleCAR T Cell TherapyFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Alzheimer's can make yesterday disappear, but it can also make love get very specific, very fast. I'm talking with Dan Phillips from the Georgia Chapter of the Alzheimer's Association, and his story hits on every level: a grandmother diagnosed, a career pivot into advocacy, and then the brutal reality that multiple people he loves are living with the disease. We keep it real about what families actually face, including denial, confusion, and those moments when you realize you're hearing heartbreaking news for the “first time” over and over again.We break down what “redirecting” really means in dementia caregiving and why picking your battles isn't giving up, it's protecting someone's nervous system. Dan shares how humor can be a lifeline, from a perfectly timed joke to what we call the “lie of love,” the kind, creative story that calms fear when the truth would only reopen the wound. We also talk caregiver stress, why caregivers can go down first, and why getting help doesn't mean you love your person any less. Sometimes it's the only way to get back to mother-daughter time instead of patient-caregiver time.Then we zoom out to hope and action: early warning signs people miss, why early diagnosis matters more than ever, and how Alzheimer's research is changing fast, including biomarker blood tests and treatments that can slow progression for some. Dan also explains the Alzheimer's Association's Do What You Love program, where dinner parties, pickleball, golf, church cookouts, and community events turn into funding for research, care, and support.If this conversation makes you feel seen, share it with someone who's carrying this quietly. Subscribe, leave a review, and tell us what part of caregiving you want to hear about next.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! 

Are you a grandparent shouldering the daily stress of raising your grandchildren while quietly navigating your own chronic pain or health challenges? Is the health of the kinship caregiver your top priority? Have you found yourself getting up at 3am to manage family needs, only to realize your own body is running on empty? Do you feel guilty for putting your medical needs last while caring for kids who have experienced trauma—kids who might be battling their own struggles with body image or eating? In this space, we tackle these heavy realities head-on, focusing deeply on the vital connection between Eating Disorders and Kinship Caregiver Health.You're doing the heart-work. We're here to help you lead with love—without losing yourself in the process.After becoming a kinship caregiver, I learned how easy it is to sacrifice your health for the sake of stability at home. In our community, we rarely talk about how stress, medical trauma, and the demands of caregiving can lead to disordered eating, body image struggles, or emotional burnout. But ignoring our own well-being puts our families at risk—if the kinship CEO crashes, the whole organization feels the fallout.In this episode, Tamie Gangloff, unpacks how chronic illness and eating disorders intersect—both for grandparents and the kids in our care. We'll share practical steps for self-advocacy with medical providers, tips for re-centering your health in the midst of chaos, and gentle daily reminders that nurture compassion for yourself. For more information about Tamie visit her website and don't forget to download her "medical appointment planning worksheet" here!Send us Fan MailAs a grandmother raising two grandchildren, one of my favorite things is watching them connect with the world around them. That's why I'm so in love with Dr. Dale Atkins new children's book "Dear Deer". Purchase directly through her website, Amazon or Barnes and Noble. Help our kids log off the screeens and tune back into the world! A grandmother raising grandchildren leaves a review and share her story and how every listener encourages her in her role as a kinship caregiver, one podcast at a time.Thank you for tuning into today's episode. It's been a journey of shared stories, insights, and invaluable advice from the heart of a community that knows the beauty and challenges of raising grandchildren. Your presence and engagement mean the world to us and to grandparents everywhere stepping up in ways they never imagined.Remember, you're not alone on this journey. For more resources, support, and stories, visit our website and follow us on our social media channels. If today's episode moved you, consider sharing it with someone who might find comfort and connection in our shared experiences.We look forward to bringing more stories and expert advice your way next week. Until then, take care of yourselves and each other.Want to be a guest on Grandparents Raising Grandchildren: Nurturing Through Adversity? Send Laura Brazan a message on PodMatch, here: https://www.podmatch.com/hostdetailpreview/grgLiked this episode? Share it and tag us on Facebook @GrandparentsRaisingGrandchilden Love the show? Leave a review and let us know!CONNECT WITH US: Website | Facebook 

In this episode, we explore the journey of schizophrenia diagnosis and treatment, the importance of community support, and how to reduce stigma around mental health. Nicole and Erin share personal stories, professional insights, and resources to empower those affected."You're not alone and there is always hope."Chapters:00:58 Nicole shares her journey as a care partner for her daughter with schizophrenia03:33 The importance of advocacy and normalizing mental health issues04:04 Erin discusses the diagnosis and treatment journey for schizophrenia10:09 Nicole recounts her family's experience with diagnosis and misinformation14:06 Introduction to Homeground and its role in reducing stigma16:09 What makes Homeground different from other resources18:02 The importance of community and accessible resources19:24 Words of support for those struggling with mental health issues21:39 Closing remarks and contact information for Nicole and Erin"Mental illness is a brain illness, not a personal failing."Key Topics and Takeaways:*Stigma and misinformation in mental health*Sharing personal stories helps reduce stigma and provides hope.*Community platforms like Homeground connect patients and caregivers.*Diagnosis of schizophrenia can be complex and delayed.*Understanding brain illnesses as physical health issues reduces stigma.*Advocacy and open conversations are vital for mental health awareness. Support the showEnjoy the show and thank you for being here. Please subscribe to stay current and share with a friend who could use this episode. Want to Support the Show:Leave a five-star review on Apple Podcasts or Spotify to help others find usJoin our monthly support groups and community support initiativesAll questions for the host or guests: Email PodcastsByLanci@gmail.com.Show Partner: Living Proof TBI Coaching specializes in recovery for Traumatic Brain Injury Survivors, Families, and Caregivers. Book a free call here.CRISIS LINE: DIAL 988

Summary In this episode, Tara Jenkins, a board-certified music therapist, shares her insights on how music can be a powerful tool in dementia care, emotional connection, and caregiver support. Discover practical tips, scientific insights, and personal stories that highlight the transformative power of music. keywordsmusic therapy, dementia care, emotional connection, caregiver support, neuroplasticity, music and memory, mental health, therapeutic music, neurodiversity, holistic health key topicsMusic activates multiple brain areas including memory and emotionMusic can evoke positive and negative emotional responsesPersonalized music choices are crucial for meaningful engagementOverstimulation and environment impact music therapy effectivenessMusic can be used for relaxation, motivation, and emotional releaseThe importance of knowing individual music preferences and historyMusic therapy supports both people with dementia and caregiversCreating playlists and using music for self-care and stress reliefFull circle moments and personal stories highlight music's impactGuidelines for safe and effective music use in care settings sound bites"Music activates many areas of our brain at once""Music connects us emotionally to a time and place""Music can impact us both positively and negatively"Chapters00:00 Audio Setup Challenges00:58 Introduction to Music Therapy06:25 The Science of Music and Memory12:28 Emotional Connections to Music16:06 Navigating Music's Impact on Emotions20:19 Understanding Individual Preferences in Music Therapy23:26 Creating a Calm Environment for Dementia Care24:53 The Importance of Choice in Music Therapy28:30 Using Music for Different Therapeutic Outcomes33:51 Incorporating Music Preferences in Care Plans37:41 Exploring New Music and Emotional Connections43:01 The Emotional Spectrum of Music and Caregiving45:52 Building Community Through Music Therapy50:18 Encouragement for Caregivers and Personal Playlists53:04 Podcast Intro Music Project (MASTER BOUNCE - OUTRO).mp3 resourcesCheck out Tara's Link TreeInstagramLinkedInWebsiteHilarity for CharityWhat's Tara listening to?Olivia Dean and Led Zeplin

All Home Care Matters and our host, Lance A. Slatton were honored to welcome Deidra Jackson as guest to the show.   About Deidra Jackson, 2026 Dole Caregiver Fellow, Illinois:   Deidra Jackson has served as a healthcare executive for the last 25 years leading product and business development efforts across national and regional payer organizations as well as digital health platforms. Her decades of experience developing healthcare resources revealed what she now sees in her own family—that sick and aging veterans are not the ones tracking appointments, managing medications, or translating clinical instructions into daily living. It is their caregivers.   Deidra's father Leroy Avery, Jr. served four years on active duty in the U.S. Air Force. As an Airman, he served with the Military Police during the Vietnam War. Leroy was exposed to Agent Orange, which has triggered or complicated a list of debilitating health conditions, including diabetes, heart failure, kidney failure, gastroparesis, and recurring blood clots.   Leroy's dependence on his daughter has grown over the years. Deidra's role as a caregiver began with smaller, episodic acts of care before evolving into daily oversight of his basic needs and safety. Deidra managed his care during extended hospital stays and attempts at living alone, before moving him into an independent living facility. She soon realized that he needed more support and care, so she moved him into her family home.   Before becoming a Dole Caregiver Fellow, Deidra was already building connections between other veteran caregivers. She published a memoir and companion journal about her caregiving journey to bring awareness to the experience and assure her fellow caregivers that they are not alone. Deidra also speaks at events about her caregiving experience, including her keynote address at the Military Caregiver Breakfast at the 2025 Military World Expo.   As she continues her advocacy, Deidra is eager to use her professional and personal experience to champion the idea of formalizing the role of the caregiver within healthcare delivery. She says, "When caregivers are recognized, supported, and integrated into care planning, outcomes improve for veterans, costs are reduced, and communities are strengthened nationwide." Her passion is ensuring people are seen, heard, and supported.   About the Dole Caregiver Fellowship:   The Elizabeth Dole Foundation Dole Caregiver Fellows Program is a selective leadership and advocacy fellowship for individuals who provide care and support to wounded, ill, or injured service members and veterans of all generations. Participants—spouses, parents, adult children, friends, or other loved ones—are chosen from across the United States to represent caregivers across their communities and nationally.   During a two-year term, Fellows receive training, build networks, and work with policymakers, organizations, and the public to raise awareness of the value of caregivers and the challenges they face. They advocate for improved support and resources and advise the Foundation on programs and policy priorities affecting military and veteran families. In addition, by sharing their stories and experiences, they help other caregivers recognize themselves as caregivers, connect to resources, and feel welcomed in a community where every caregiving journey is valued.

More than one in five Americans are family caregivers. And this work, even under the most supportive conditions, can be really intense. This week, Kelli's offering strategies for family caregiving, in community. Because wherever you're at—in a waiting room, on hold with the insurance company, or making another pot of coffee after another night of lost sleep—you don't have to tackle this responsibility alone.Cared For is executive produced and hosted by Kelli Dunham.It's executive produced by Erica Getto and Myrriah Gossett for Good Get, in collaboration with PRX.For more resources, and to join the conversation, head to kellidunham.substack.com or @caredforpodcast on Instagram.Need to set up your Slate Plus feed? If you subscribed through Slate.com, check out our FAQ at slate.com/podcastfaqs for easy instructions. Members subscribed via Apple Podcasts get automatic access—no setup required. Hosted on Acast. See acast.com/privacy for more information.

More than one in five Americans are family caregivers. And this work, even under the most supportive conditions, can be really intense. This week, Kelli's offering strategies for family caregiving, in community. Because wherever you're at—in a waiting room, on hold with the insurance company, or making another pot of coffee after another night of lost sleep—you don't have to tackle this responsibility alone.Cared For is executive produced and hosted by Kelli Dunham.It's executive produced by Erica Getto and Myrriah Gossett for Good Get, in collaboration with PRX.For more resources, and to join the conversation, head to kellidunham.substack.com or @caredforpodcast on Instagram. Hosted on Acast. See acast.com/privacy for more information.

Tardive dyskinesia (TD) is often misunderstood, misdiagnosed, or simply ignored — leaving many people feeling isolated, frustrated, and afraid to speak up. In this episode, we share the deeply personal story of Sherland Peterson, a woman living with tardive dyskinesia, while exploring the physical, emotional, and social impact of this complex movement disorder. Whether you are living with TD yourself, caring for someone who is, or simply trying to better understand the realities of long-term mental health treatment, this episode offers insight, validation, and practical understanding. Our guest discusses what it was like to first notice the symptoms, the challenges of getting answers, and how TD affected confidence, relationships, communication, and daily life. Listeners will learn: the emotional toll of living with visible involuntary movements  how psychiatric medication side effects can create complicated treatment decisions  what caregivers and loved ones should know about supporting someone  how stigma and shame can prevent people from seeking help  If you've ever wondered what TD actually feels like beyond the clinical definition — or if you're searching for hope, support, and real-world perspective — this episode delivers an authentic and compassionate look at life with TD.We would like to thank Teva Pharmaceuticals for providing educational support for this episode. “In my case, my mouth was so affected by TD (tardive dyskinesia), my jaw would quiver, my speech would be slurred.” ~Sherland Peterson Our guest, Sherland Peterson, is a vocal advocate for mental health awareness and has appeared in numerous podcasts, TV, and radio interviews in which she shares her mental health journey. Ms. Peterson attended Hunter College and City College of NYC. She has taught English at LaGuardia Community College, City College of NYC, and DeVry Institute in NYC. She has also served as a Schedule C in the Obama administration's Administrative Conference of the US. Our host, Gabe Howard, is an award-winning writer and speaker who lives with bipolar disorder. He is the author of the popular book, "Mental Illness is an Asshole and other Observations," available from Amazon; signed copies are also available directly from the author. Gabe is also the host of the "Inside Bipolar" podcast with Dr. Nicole Washington. Gabe makes his home in the suburbs of Columbus, Ohio. He lives with his supportive wife, Kendall, and a Miniature Schnauzer dog that he never wanted, but now can't imagine life without. To book Gabe for your next event or learn more about him, please visit gabehoward.com.

By the time the paper hit version 71, Dr. Nirosha Murugan had already done the hard part. The data were real. The experiment had worked. A team of researchers had used a wearable bioreactor to trigger limb regeneration in frogs, a result with obvious implications for regenerative medicine. But the science still wasn't getting over the line. The problem wasn't the work. It was the translation.On this episode of Standard Deviation, host Oliver Bogler talks with Dr. Nirosha Murugan, a biophysicist and Tier II Canada Research Chair in Tissue Biophysics at Wilfrid Laurier University, about what happens when a scientist working at the edges of quantum biology, bioelectricity, and tissue regeneration runs headfirst into the unwritten rules of academic publishing. Murugan's research asks biologists to think beyond molecules and chemistry alone, and to consider the physical signals, electromagnetic fields, and invisible forces that shape development and healing. It is ambitious science. It is also exactly the kind of work that can make gatekeepers nervous.Bogler follows Murugan through the less glamorous part of discovery: the hidden curriculum of getting a paper published, securing scientific credibility, and learning that data do not simply “speak for themselves.” Murugan describes how jargon buried the pitch of her own work, how a lack of editorial support left her at a disadvantage, and how the JEDI program at the Life Science Editors Foundation paired her with a former journal editor who taught her how to structure a manuscript, write a cover letter, and survive peer review.The result was publication in Science Advances, but the larger story is about power. Who gets taught the rules of biomedical research. Who has access to grant writers, editors, and institutional polish. Who is left to brute-force their way through the maze. And how one scientist, having finally found the map, now makes sure her own trainees do not have to learn it the hard way.RELATED LINKSDr. Nirosha Murugan⁠Wilfrid Laurier University⁠Life Science Editors Foundation⁠JEDI Program⁠Science Advances paper on limb regeneration⁠FEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Dementia caregiving asks you to carry things nobody prepares you for, and some of the hardest parts are never said out loud. This video isn't based on research. It's based on what I've learned from working with thousands of caregivers over the past 17 years as a geropsychologist. If caregiving still hurts even though you're doing everything right, if people question your decisions, if you can't stop replaying every hard moment in your head, I want you to hear this first: none of that means you're failing. In this episode I walk you through five truths about dementia caregiving I wish every caregiver knew, the ones that can make this whole journey feel a little more possible to live.  If you'd like to see this episode on video, you can hop on over to my YouTube channel here. → Join the Care Collective: https://tinyurl.com/podcast-cc  → Get free weekly tools and tips in my newsletter, The Dementia Dose: https://tinyurl.com/dementiadose-podcast  ⏱ CHAPTERS 0:00 - Why this caregiving journey always involves pain 2:40 - Why you can't control how others feel about your caregiving decisions 5:00 - Why you can't take away your loved one's emotional pain 6:50 - Catching the harsh things you say to yourself 7:49 - Why no caregiver has all the answers, and why that's okay #dementia #dementiacaregiver #dementiacaregiving #caregiversupport #alzheimers   --- Hi, I'm Dr. Natali Edmonds, a board-certified geropsychologist specializing in dementia care. Whether your loved one has Alzheimer's, frontotemporal, Lewy body, vascular, or mixed dementia, we believe that to create a dementia-friendly world, we must first create a caregiver-friendly world. This content is for educational purposes only and is not a substitute for professional medical advice. Always consult with a healthcare provider for medical guidance.

Send us Fan MailJoin 5-Minute Parenting with special guest, Diana Derringer, as she shares her compelling story as the caregiver of her husband for the past twenty years. Diana shares candidly about the miracles, hard times, and blessings of being his caregiver. Her husband's health diagnosis 21 years ago launched Diana on a roller coaster ride, with many ups and downs. But in the midst of it all, Diana chooses joy daily, and is on the show today to share encouragement for riding the challenges and sometimes chaotic circumstances of caring for someone with a serious health diagnosis. Although Diana's story is one of a spouse, her wisdom and practical tips apply to anyone in a caregiving situation. Parents are the ultimate caregivers, of course, and many are in that tough life stage called "The Sandwich Generation." Caring for kids and aging parents. Is that you? Listen in and be encouraged! Diana is an award-winning writer and author who shares hope and joy through devotions, articles, dramas, Bible studies, planning guides, and poems in more than 70 publications, including The Upper Room, Guidepost, The Secret Place, and Missions Mosaic. She also writes radio dramas and television programs for Christ to the World Ministries and shares weekly blog posts on Words, Wit, and Wisdom. Her adventures as a social worker, adjunct professor, youth Bible study teacher, friendship family for international university students, and caregiver for her husband supply a constant flow of writing ideas. 

This week's short & sweet edition of the Summer Practice Tip series is for the parents and caregivers supporting a young music student in their life!  Join the Musical Nest Community for Teachers - a supportive space for teachers so they feel connected and have resources to support the students and families they work with run by Christine & Frequent guest on the podcast Barbie Wong   Sign up for the Monthly Newsletter: SuzukiTriangle.com/Newsletter Resources at SuzukiTriangle.com Connect with Christine on Instagram Email: Christine@SuzukiTriangle.com  TRANSCRIPT 

Do your loved ones in spirit hear your prayers? Can they guide you through life's most difficult seasons? In this heartfelt episode of Radio Medium, internationally known psychic medium Laura Lee connects with Tia from Michigan for an evidential psychic reading filled with powerful spirit messages, emotional validation, and hope. During this moving mediumship session, Laura connects with Tia's father, Russ, in spirit, who lovingly confirms he remains close, watching over the family as they navigate caregiving responsibilities after her mother's serious health crisis. Through unmistakable validations, spirit acknowledges Tia's unwavering strength, encourages her to trust an upcoming career opportunity, and reminds her that divine timing is unfolding—even when life feels uncertain. This touching reading explores grief healing, faith, resilience, caregiving, and the enduring connection between loved ones on Earth and in the afterlife. Whether you're caring for aging parents, grieving someone you love, seeking spiritual guidance, or wondering whether your loved ones still walk beside you, this episode offers comfort, reassurance, and an inspiring reminder that love never ends. Tune in for a powerful intuitive reading that will strengthen your faith and renew your hope.

A Breakthrough for Caregivers & When the Postal Service Mailed ChildrenSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

All Home Care Matters and our host, Lance A. Slatton were honored to welcome Shannon Tuimalealiifano as guest to the show.   About Shannon Tuimalealiifano, 2014 Dole Caregiver Fellow, Florida:   Shannon and her husband, Sualauvi "Sua" Tuimalealiifano, are both Army veterans who met while serving at Fort Bragg. As a military child herself, Shannon understood the strength, camaraderie, and sacrifice that come with military life. After enlisting two years after high school, she served as a trained lab tech and combat medic, later working at Womack Army Medical Center.   But nothing could have fully prepared Shannon for the life-changing journey that began after Sua was injured in combat while serving with Army Special Operations in Afghanistan. A paratrooper, jumpmaster, and Special Operations soldier, Sua sustained a severe spinal cord injury that eventually left him quadriplegic.   At the time, Shannon was raising three young children, ages 6, 4, and 9 months. Within a week of Sua's medevac from Afghanistan, she joined him at Walter Reed National Military Medical Center, followed by rehabilitation at James A. Haley VA Hospital in Tampa. What followed was a long and difficult road through hospital stays, rehabilitation, military transition challenges, and the daily realities of full-time caregiving.   After nearly two years in hospitals and rehab, Shannon and Sua returned to Fort Bragg without the support or accessibility their family needed. Their home was not wheelchair accessible, and Sua's wheelchair could not fit through the doors. Eventually, the family relocated to Hawaii through a compassionate reassignment so they could be closer to Sua's family and support system.   Even with family help, Shannon faced overwhelming exhaustion, sleep deprivation, and the emotional weight of caregiving around the clock. She later found healing through an equine therapy program with other military caregivers, describing it as "lifesaving and life-giving."   Through community, connection, and support from organizations including the Elizabeth Dole Foundation's Hidden Heroes program, The Rosie Network, the VA, and Wounded Warrior Project's Independence Program, Shannon found strength, purpose, and a deeper understanding of the importance of supporting military and veteran caregivers.   Shannon's story is one of service, sacrifice, resilience, and the power of caregiver community.     About the Dole Caregiver Fellowship:   The Elizabeth Dole Foundation Dole Caregiver Fellows Program is a selective leadership and advocacy fellowship for individuals who provide care and support to wounded, ill, or injured service members and veterans of all generations. Participants—spouses, parents, adult children, friends, or other loved ones—are chosen from across the United States to represent caregivers across their communities and nationally.   During a two-year term, Fellows receive training, build networks, and work with policymakers, organizations, and the public to raise awareness of the value of caregivers and the challenges they face. They advocate for improved support and resources and advise the Foundation on programs and policy priorities affecting military and veteran families. In addition, by sharing their stories and experiences, they help other caregivers recognize themselves as caregivers, connect to resources, and feel welcomed in a community where every caregiving journey is valued.

Today we're talking about the power of community, resilience, and what it really means to show up bravely in the caregiver parenting journey. My guest is fellow community builder and mom on a mission Jessica Patay, the founder of We Are Brave Together, a global community supporting moms raising children with disabilities and other unique needs. Jessica's work is deeply rooted in her own experience as a caregiving mom to her son Ryan, who was diagnosed with Prader-Willi syndrome, and her mission is all about making sure no parent has to walk this path alone. In our conversation, Jessica shares her story and the inspiration behind building such a powerful, life-giving community for mothers. We talk about the isolation so many caregivers experience, the importance of connection and support, and what it looks like to cultivate resilience in the midst of ongoing challenges. Jessica also offers practical, compassionate insights for parents who are feeling overwhelmed, reminding us that even in the hardest seasons, we are not alone—and we were never meant to do this by ourselves. About Jessica Patay  Jessica Patay is passionate about serving caregiving moms and creating authentic communities.  She has always fostered deep, life-giving friendships and has been intentional about her community of girlfriends.  As a caregiving mom herself, this passion carries on as she gathers women to encourage them, mentor them, inspire them, and validate their intense and precious journeys. Her own story as a mom to a child with a disability, began in 2003 when her second son, Ryan, was born and diagnosed with a rare, genetic disorder, called Prader-Willi syndrome. Within two days of receiving this diagnosis, she received a phone call from a mentor mom from the Prader-Willi California Foundation.  Immediately she felt relief and comfort knowing she was NOT ALONE. Thankfully, Ryan is sandwiched in the middle of siblings Luke and Kate, both fierce and loving cheerleaders and helpers to Ryan. Jessica is the founder of The We Are Brave Together organization, a supportive community for moms of children with disabilities and all unique needs, which has grown into an international community of over 4200 moms. She has helped launch over 25 support groups all over the United States, and in New Zealand and Australia, in the last five years. She is the host of the Brave Together Podcast. Things you'll learn from this episode  Why community is a critical foundation for healing, resilience, and feeling less alone as a caregiver How distinguishing between caregiving and motherhood can help parents better understand their experience How We Are Brave Together creates connection through circles, retreats, and shared storytelling Why bravery often shows up in small, everyday moments rather than big, visible acts How Jessica's work, including Suddenly Brave Together, reflects and validates the lived experience of caregivers Why systemic challenges can leave caregivers isolated—and how taking small, practical steps can help them find support now Resources mentioned  We Are Brave Together Brave Together Podcast Becoming Brave Together: Heroic, Extraordinary Caregiving Stories from Mothers Hidden in Plain Sight by Jessica Patay Suddenly Brave Together: Letters to Caregiving Moms in a Defining Moment of Their Lives by Jessica Patay We Are Brave Together Facebook Group Demystifying Disability: What to Know, What to Say, and How to be an Ally by Emily Ladau Emily Ladau on Demystifying Disability: What to Know, What to Say, and How to be an Ally (Tilt Parenting Podcast) Kelley Coleman on Everything No One Tells You About Parenting a Disabled Child (Tilt Parenting Podcast) Margaret Webb Parent Coaching Learn more about your ad choices. Visit podcastchoices.com/adchoices

Dr. Jess Peatross trained in conventional medicine and worked as a hospitalist before she started questioning why so many chronically ill patients kept getting worse inside the healthcare system she trusted. Her perspective carries weight because she spent years following every protocol exactly as taught before walking away from hospital medicine entirely.Raised in Huntington, West Virginia during the opioid crisis, she entered medicine believing the system existed to heal people. Instead, she found hospitals driven by billing codes, liability management, and pharmaceutical dependence while patients with chronic illness, autoimmune disease, mold exposure, and chronic pain cycled endlessly through appointments and prescriptions.Dr. Peatross explains what pushed her toward functional medicine, cannabis therapy, and prevention focused care after watching patients improve only after leaving conventional treatment pipelines behind. The conversation tackles physician burnout, chronic illness stigma, healthcare incentives, and the growing collapse of trust between patients and institutions.The discussion also moves into supplements, environmental toxins, ultra processed food, and the uncomfortable economics behind keeping people permanently sick but continuously billable. Dr. Peatross describes the professional backlash that comes with challenging medical orthodoxy while Matthew connects her experience to the broader erosion of public trust across American healthcare.Together they unpack what happens when patients stop believing the system can help them and start searching elsewhere for answers.RELATED LINKSDr. Jess PeatrossInstagramMarshall UniversityBrave New WeedFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Are you a grandparent raising grandchildren, carrying the silent weight of anger, resentment, or shame from a family crisis? Have you been told to “just forgive” but found that advice hollow, leaving you alone with pain that keeps resurfacing? Does your anger feel like a protective shield—yet you secretly yearn for true relief, clearer connection, and more energy to nurture those in your care?I'm Laura Brazan, and like you, I've wrestled with the burdens of kinship caregiving, often mistaking fury for healthy boundaries—until it clouded even the brightest moments with my grandchildren. Through raw honesty and real-world practice, I discovered that forgiveness isn't about excusing harm, but reclaiming personal peace and power.Welcome to 'Grandparents Raising Grandchildren: Nurturing Through Adversity.' In this episode, forgiveness expert Katherine Giovanni reveals a groundbreaking, practical path for kinship caregivers. Together, we'll dismantle the myth that you have to rush forgiveness, and instead, gently learn to process hurt through a proven step-by-step system. You'll hear how releasing anger—starting with the “easy” daily irritations—can lift the fog not only from your mind but from generations to come.For more information about Katharine and her work, I encourage you to visit her website. Download her free foregiveness audit worksheet here!Through expert guidance and lived experience, we'll explore authentic strategies for healing emotional wounds, teaching forgiveness to grandchildren, and ending the cycle of intergenerational trauma. If you're ready to stop passing down the burden and begin leading your family with renewed clarity, compassion, and resilience, you belong here.Join our supportive community and take the next step toward a brighter legacy—for yourself and those you love.Send us Fan MailAs a grandmother raising two grandchildren, one of my favorite things is watching them connect with the world around them. That's why I'm so in love with Dr. Dale Atkins new children's book "Dear Deer". Purchase directly through her website, Amazon or Barnes and Noble. Help our kids log off the screeens and tune back into the world! A grandmother raising grandchildren leaves a review and share her story and how every listener encourages her in her role as a kinship caregiver, one podcast at a time.Thank you for tuning into today's episode. It's been a journey of shared stories, insights, and invaluable advice from the heart of a community that knows the beauty and challenges of raising grandchildren. Your presence and engagement mean the world to us and to grandparents everywhere stepping up in ways they never imagined.Remember, you're not alone on this journey. For more resources, support, and stories, visit our website and follow us on our social media channels. If today's episode moved you, consider sharing it with someone who might find comfort and connection in our shared experiences.We look forward to bringing more stories and expert advice your way next week. Until then, take care of yourselves and each other.Want to be a guest on Grandparents Raising Grandchildren: Nurturing Through Adversity? Send Laura Brazan a message on PodMatch, here: https://www.podmatch.com/hostdetailpreview/grgLiked this episode? Share it and tag us on Facebook @GrandparentsRaisingGrandchilden Love the show? Leave a review and let us know!CONNECT WITH US: Website | Facebook 

You can't rewrite a blueprint you've never let yourself look at, and that goes for your relationships too.Buckle up, because we're kicking off the High Self-Worth Summer series with the foundational piece nobody wants to touch: the relational trauma you carry from your relationship with your parents. And before you say "but Dr. Morgan, my parents and I are great now", that's exactly why you need this one. This isn't about blame. There are ways your parents failed you, and they were doing the best they could with what they had. Both are true. In this episode I'm walking you through why avoiding this work quietly runs your love life, your friendships, and even your career and how to finally examine, process, and release what you've been carrying so you can stop recreating that familiar (not safe) emotional home.Inside the episode:The Mother & Father Wounds: Explores how early caregiving shapes self-worth ("Am I too much?") and external relationship patterns (trusting steady love, proving worth).Repetition compulsion in plain terms — why your nervous system chases familiar over healthy, and how that keeps you dating the same emotionally unavailable person in a new outfit until you look at the blueprint.Becoming the love scientist — the exact practice for noticing your patterns in real time: who you're attracted to, what triggers you, what you tolerate, and how you talk to yourself.Ready to do the work?The pattern isn't your fault, but the healing is your responsibility, and I've made it easy. Grab the Identity Reset ($47), my go-to course with a daily journal, rewiring prompts, and self-soothing strategies. It's 10 minutes a day and it's the one thing over a thousand people tell me changed everything.

Navigating the care of our aging parents is one of the most profound, yet least talked about, transitions we face as adults. This is really common—we rarely sit down to discuss end-of-life wishes or logistics until a sudden medical crisis throws us into an emotional whirlwind. When you are managing this transition from a distance—whether due to life circumstances or the unique demands of military deployment and relocation—the weight can easily ripple into your marriage, leading to invisible strain and emotional disconnection. In this episode, I sit down with gerontologist Janice Goldmintz to explore how couples can navigate these heavy role reversals, manage complex family dynamics, and protect their relationship bond while honoring their parents' autonomy. What this really means is that you don't have to carry this heavy weight alone. You'll walk away with small, practical tools to stay on the same team with your partner, lean on external resources safely, and build your own emotional resilience toolkit so you can thrive, not just survive. >>>Make sure to like, review, and subscribe to get all the future episodes and help the podcast be found by others who would benefit the most.  Read the show notes for this episode here.    Free Relationship Pattern Assessment Are you having the same conversation over and over? Many couples assume they have a communication problem when they're actually stuck in a relationship pattern that keeps creating the same conflict. Take the free Relationship Pattern Assessment to identify the pattern that may be keeping you disconnected and learn what to focus on next.

I thoroughly enjoy doing my podcasts. It's the one thing I truly miss from my television news reporting days — interviewing extraordinary people every single day. Through The Bonnell Foundation, I now host a weekly podcast, and honestly, I wish I could do them daily. Not only does it bring me so much joy, but it also gives me the opportunity to share the stories of the incredible people I meet along the way. Kate O'Donnell is one of those people. Kate was inspired by a brother she never met. Her brother Joey died from cystic fibrosis just three months before she was born. CF is a brutal disease, but the community that rises from this tragedy is filled with some of the most inspiring, compassionate, and courageous people you will ever meet. Kate's father, Joe O'Donnell, became one of the cystic fibrosis community's most influential volunteer leaders and fundraisers. Together with his wife Kathy, he founded The Joey Fund in memory of Joey. Today, Kate is helping carry that legacy forward and bringing new energy and passion to the mission. And trust me — by the end of this podcast, you're probably going to want a Joey hat of your own. You can support The Joey Fund here: https://joeyfund.org/donate-1 Kate is smart, fun, energetic, and deeply committed to making a difference in the CF community. I know you'll be inspired by everything she continues to do. Like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

Johnny Crowder is back from another lens! In this bonus episode, we stop by our host's other podcast series, That Entrepreneur Show! Johnny Crowder shares his journey from personal mental health challenges to building Cope Notes, a leading mental health texting platform. He discusses the importance of focus, sticking to your mission, and strategic scaling in entrepreneurship."Anyone building something extraordinary sticks to the plan"Chapters00:00 Johnny Crowder's Reflection on Building Focus00:53 Introduction to Johnny Crowder and his Mission02:31 Johnny's Personal Journey with Mental Health04:02 Challenges in Selling to Enterprise Clients06:58 Memorable Contracts and Scaling Milestones11:27 Upcoming Features and International Expansion13:55 Advice for New Entrepreneurs17:26 Influences and Future Inspirations18:46 Where to Find Johnny and Cope Notes"People won't always articulate what they need" Other Takeaways*How to handle rejection and build credibility*Stick to your core mission and avoid shiny object syndrome*Build infrastructure for big opportunities even before they arrive*Focus on incremental progress and celebrate small wins*Lessons learned from building and scaling Cope Notes*Persistence and focus are key to long-term success*Strategic partnerships and legal considerations are crucial in scalingSupport the showEnjoy the show and thank you for being here. Please subscribe to stay current and share with a friend who could use this episode. Want to Support the Show:Leave a five-star review on Apple Podcasts or Spotify to help others find usJoin our monthly support groups and community support initiativesAll questions for the host or guests: Email PodcastsByLanci@gmail.com.Show Partner: Living Proof TBI Coaching specializes in recovery for Traumatic Brain Injury Survivors, Families, and Caregivers. Book a free call here.CRISIS LINE: DIAL 988

Click here to receive today's free gift on the Radio Page:  For Better or Worse – Disability has a way of trying even the best of marriages. The cumulative effects of daily routines that never vary, social isolation, financial pressures, unmet expectations, and a life that is vastly different from most couples can wear on the spirits of the strongest husband and wife. Married to Joni Eareckson Tada for more than 37 years, Ken Tada shares that disability does not have to be the defining word in your marriage. Instead disability is an invitation for you and your spouse to depend on Jesus in your weakness and grow closer to each other than you ever thought possible. --------Thank you for listening! Your support of Joni and Friends helps make this show possible. Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org. Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

A student in China was at the top of her class until she became addicted to playing video games. She then became depressed and lost all interest in school, her family, or even taking care of her self. Her grandmother is a practitioner and shared Some of Master Li's teachings about video game addiction. After the seed of Dafa was planted in her heart, she was able to move forward, and she is now happily pursuing a masters degree. This and other experience-sharing from the Minghui website.Original Articles:1. [Celebrating World Falun Dafa Day] Falun Dafa Saved My Granddaughter From Depression2. [Celebrating World Falun Dafa Day] I Was a Caregiver for 18 Days To provide feedback on this podcast, please email us at feedback@minghuiradio.org

Conscious Caregiving with L & L is "Tackling the Tough Conversations."   The topic of this episode is "Memory Cafes & 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. Lori's 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 is also the new President of AlzAuthors.  Lance's book, "The All Home Care Matters Official Family Caregivers' Guide" was the recent recipient of the 2024 International Impact Book Awards.   To learn more about Lance A. Slatton and Lori La Bey you can visit their websites.

Dave Good was a District Court Judge living in Cedar Rapids. In 2003, at the age of 56, he was diagnosed with early onset Alzheimer's. His wife Kathy became his caregiver while continuing to work full time. On this episode, Kathy Good, who now guides other caregivers as the Senior Director of the Chris and Suzy DeWolf Family Innovation Center for Aging and Dementia of Mercy, shares her story. Then Good and Michael Wagler, Iowa State Director for the AARP, will talk about the resources those who care for loved ones with dementia. (This show was originally produced July 24, 2025.)

Country & Western Tuesday

Farla Efros is a senior retail executive and former CEO who built and sold companies before facing her own breast cancer diagnosis. She brings that same operational mindset into a healthcare system that expects patients to manage complexity while they are at their most vulnerable.She was on a client call in Spain when the diagnosis came through. A clear mammogram had missed it. An MRI caught it. Within hours, she was ordering binders, building a plan, and structuring her treatment like a turnaround strategy. Every appointment became a meeting. Every doctor faced an agenda with dozens of questions. She paid out of pocket for PET scans that were denied and hired a third party firm to validate her treatment path when her own doctors resisted outside input. The conversation tracks what happens when a high-functioning executive enters a system built on delay, denial, and fragmentation. Efros describes negotiating for tests, managing physician relationships, and assembling an “executive board” of advisors across conventional and alternative care. She calls the experience “the worst client I ever had,” exposing how administrative burden shifts onto patients and families.The tension sits between what worked for her and what is inaccessible to most. Her approach requires confidence, time, and fluency in navigating power. The system rewards that behavior while quietly failing patients who cannot replicate it. Insurance coverage still left her paying out of pocket. Doctors pushed standard protocols over precision medicine. Survivorship offered little support once treatment ended.This episode examines how cancer care operates as a series of incentives rather than a coordinated system, and why patients are forced to become operators just to get through it.RELATED LINKSFarla EfrosFarla Efros on LinkedInF*ck CancerF*ck Cancer on AmazonAccentureCTOAMPULL QUOTES“I treated cancer like the worst client I ever had.”“They wouldn't approve the test, so I paid for it myself.”“Every appointment was a negotiation.”FEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Caregiving is quietly breaking millions of people, and no one warns you it will break you too. I brought Roy Remer on to talk about the one thing every caregiver needs to hear—empathy without action doesn't heal anyone, it burns you alive. Roy is a meditation teacher, hospice volunteer, and author of Zen Caregiving. He's sat at the bedside of people in their final hours, and he's distilled everything he learned into a path that doesn't ask you to do more—it asks you to show up differently. This conversation will change how you see yourself, your loved ones, and what it really means to serve. If you're caring for someone—or know someone who is—this is for you.00:00 The Hidden Burden of Caregiving 03:07 Introducing Roy Remer & Defining the Caregiver 05:48 The State of Caregivers in an Aging World 09:15 Mindfulness as an Insurance Policy for Caregivers 13:29 Presence: The Core of Zen Caregiving 17:18 The Five Stages of Compassion & Empathy vs. Compassion 24:44 Empathic Distress vs. Compassion Fatigue 29:11 Helping vs. Serving: A Covenant of the Soul 33:51 Accepting Resistance & The Gift of Witnessing 36:25 Nature Loss, Grief & The Cycles of Life 41:44 What the Dying Teach Us About Living Now 47:31 Where to Find Roy's Work & Final Blessing LEARN MORE ABOUT ROY REMER:https://www.zencaregiving.org/ JOIN MY COMMUNITY In The Space Between membership, you'll get access to LIVE quarterly Ask Amy Anything meetings (not offered anywhere else!), discounts on courses, special giveaways, and a place to connect with Amy and other like-minded people. You'll also get exclusive access to other behind-the-scenes goodness when you join! Click here to find out more --> https://shorturl.at/vVrwR Stay Connected: - Instagram - https://tinyurl.com/ysvafdwc- Facebook - https://tinyurl.com/yc3z48v9- YouTube - https://tinyurl.com/ywdsc9vt- Website - https://tinyurl.com/ydj949kt Life, Death & the Space Between Dr. Amy RobbinsExploring life, death, consciousness and what it all means. Put your preconceived notions aside as we explore life, death, consciousness and what it all means on Life, Death & the Space Between.**Brought to you by:Dr. Amy Robbins | Host, Executive ProducerPodcastize.net | Audio & Video Production | Hosted on Acast. See acast.com/privacy for more information.