Podcasts about caregivers

Long before cancer survivors organized into a movement, Hollywood had already shaped how Americans understood the disease. Films rarely used the word “cancer,” physicians often withheld diagnoses from patients, and the people who survived were almost nowhere to be found on screen.Recorded before The Cancer Mavericks: A History of Survivorship became a documentary series, this bonus conversation explores where the project first began. Matthew Zachary sits down with his mother, Roz Greenzweig, a retired educator and lifelong film enthusiast whose memories of classic cinema became an unexpected lens for understanding how cancer was portrayed throughout the twentieth century.Together, they revisit landmark films including Dark Victory, Love Story, and other iconic portrayals that reflected an era when cancer was treated as unspeakable, inevitable, and almost always fatal. Their conversation contrasts those carefully constructed Hollywood narratives with the lived reality of a family confronting a brain cancer diagnosis in 1995, revealing how popular culture both reflected and reinforced the fears surrounding the disease.The discussion also foreshadows many of the themes explored throughout the documentary series: the evolution of patient advocacy, the emergence of cancer survivorship, the role of caregivers, and the power of storytelling to influence public understanding. Before policy changed, before advocacy organizations grew into national movements, conversations like these were already challenging long-held assumptions about what cancer looked like and who had the right to tell its story.Consider this the prologue to The Cancer Mavericks. Before the movement found its history, it began with a family trying to make sense of the stories they had inherited.RELATED LINKSAmerican Cancer Society⁠National Cancer Institute⁠American Film Institute⁠ER (NBC)⁠50/50 (Official)⁠Chasing Life (ABC Family Archive)⁠FEEDBACKLike this episode? Rate and review The Cancer Mavericks: A History of Survivorship on your favorite podcast platform. For more information, visit CancerMavericks.com. Questions? Email podcasts@matthewzachary.com.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

In this episode, Lisa Ackland Carriere — founder of The Writing Well and writer at The Daily Calling on Substack — joins us to talk about the side of caregiving no one signs up for. When caregiving is forced on you by circumstance rather than chosen as a profession, compassion fatigue can quietly take root, leaving you emotionally shut down and disconnected from your own identity. Lisa shares her personal journey through years of layered crisis — parenting a son with ADD, developmental delays, and learning disabilities; a move that strained her marriage; the sudden loss of her mother; her brother's brain cancer diagnosis and death; and her husband's subsequent pancreatic cancer diagnosis. We talk about what compassion fatigue really looks like for caregivers — nurses and everyday women alike — how God reframes identity and purpose through the caregiving journey, and practical ways to support a caregiver both in the thick of crisis and in the aftermath, whatever the outcome. In This Episode: What compassion fatigue is and how it accumulates over years of caregiving for a loved one who needs ongoing, difficult care Lisa's story: a son with developmental and learning challenges, a marital rift after relocating for his schooling, and a cascade of loss — her mother, her brother, and her husband's health The difference between caregiving as a chosen profession and caregiving that's simply your life How identity gets buried under years of "just showing up," and how it can be reclaimed How God reframes purpose and identity in the middle of caregiving crisis Practical ways to support a caregiver mid-crisis Practical ways to support a caregiver after the crisis — whether their loved one survived or passed away About Lisa Ackland Carriere: Lisa Ackland Carriere is the founder and director of The Writing Well, providing writing services and collaborative partnerships to professionals. Her business grew out of her 20-year career as a college English instructor and as a writer and communicator for global ministries. She also writes for Christian women on Substack at The Daily Calling with Lisa Ackland Carriere. Connect with Lisa: Website: lisaacklandcarriere.com The Writing Well: thewritingwellconsulting.com Substack: substack.com/@lisaacklandcarriere Ready for a life-changing conversation? Book your complimentary stress assessment and get personalized tools you can use — even in the middle of a 12-hour shift. Book today! (complimentary, but spaces fill fast)  Shalom Shalom,  Xx, Shan  ……CONNECT…… The STAT Protocol: 5 min Emergency Reset Take the Free QUIZ-  Are you in burnout or just stressed?? Stress Assessment (free) - get to the root of your stress

Caregiving takes more than anyone sees.   What if the exhaustion, brain fog, and burnout you've been feeling… isn't just in your head—but your body asking for support? In this episode, I'm speaking directly to the caregiver—the one holding everything together behind the scenes. Because when someone you love is diagnosed, the focus rightfully shifts to them. But almost no one talks about what happens to your body while you're surviving it all. We talk about the physical impact of long-term stress, how caregiving affects your detox pathways, energy, and mental clarity—and why waiting until things "calm down" to take care of yourself often leads to deeper burnout. I also share the story behind the Untoxin Method and why I created it specifically for caregivers who need real support, not another overwhelming protocol. This episode is both validation and a path forward—because you deserve to feel supported, too.   LINKS:   Recommended Tools & Resources: The Untoxin Method If you've spent months caring for everyone else while putting your own health last, the Untoxin Method is created for you. This guided 21-day detox program includes a prep week, a 7-day reset, and a gradual transition back to everyday life. You'll receive: A complete detox supplement kit Simple, done-for-you meal plans A step-by-step daily protocol Live coaching and accountability A supportive community of parents and caregivers who understand the journey If you're ready to restore your energy and prioritize your own healing, learn more and register here: https://seasonjohnson.info/join-today   Community & Support Join Thrive Through Cancer Community: Join Thrive Through Cancer Community: https://biodynamicwellness.com/thrive-through-cancer  Thrive Beyond Cancer Program: https://biodynamicwellness.com/thrive-beyond-cancer Learn More About Biodynamic Wellness: https://biodynamicwellness.com Follow us on Instagram: @BiodynamicWellness   Connect with Season: Website: www.seasonjohnson.com Instagram: @seasonjohnson

Tamara Cook grew up poor in a small Texas town with eight siblings, a mother struggling to hold everything together, and a biological father who was never in the picture — and when her babysitter started abusing her at just seven years old the life she deserved was already being taken from her before she was old enough to understand what was happening. In this episode of Locked In with Ian Bick, she shares how her mother fell into addiction and began pimping her out, how her parents splitting sent everything into further chaos, how she eventually started selling drugs herself and ultimately became a pimp — the exact monster she had always been afraid of and never wanted to become. She opens up about her own addiction the relationships the multiple children she was raising in the middle of everything, and what a seven year sentence in the Texas Department of Corrections finally did to give her back the life that started being taken from her when she was seven years old. _____________________________________________ #womeninprison #TrueCrime #redemptionstory #prison _____________________________________________ Connect with Tamara Cook: YouTube: https://youtube.com/@tamarasherrell87?si=0laBG70KXTx69hZI TikTok: https://www.tiktok.com/@nobodybby87?_r=1&_t=ZP-98ZtlRlPlcc _____________________________________________ Hosted, Executive Produced & Edited By Ian Bick: https://www.instagram.com/ian_bick/?hl=en https://ianbick.com/ _____________________________________________ Timestamps: 00:00 Tamara Cook Introduction 00:21 Growing Up in Amarillo 02:02 Early Family Life & Childhood Memories 06:46 Life Changes at Age Seven 09:05 Abuse and Family Struggles 13:17 Mother's Addiction Begins 20:28 Role Reversal: Becoming the Caregiver 23:12 Trauma, Betrayal & Survival 27:01 Deeper Into Abuse and Neglect 33:32 Adolescence in Chaos 39:00 Survival and First Crimes 43:43 Turning to the Streets & Dealing 49:57 Dealing Drugs and Gang Life 58:00 Solo Survival and Criminal Hustle 01:05:30 Becoming a Dealer and a Pimp 01:14:00 Running Operations and Family Fallout 01:26:02 Violence, Survival & Self-Defense 01:35:29 From Teen Mom to Emancipation 01:46:06 Trying to Be a 'Normal' Wife & Mother 01:56:02 Losing Children and Hitting Rock Bottom 02:05:40 Falling into Addiction 02:11:00 Deep Addiction, Homelessness & Jail Time 02:24:00 Year Under Investigation & Final Arrest 02:33:50 Prison: The Breaking Point 02:46:00 Life Changing Years Inside 03:02:00 Release, Recovery & Faith 03:14:00 Domestic Violence and New Beginnings 03:18:00 Career, Ministry, and Healing 03:26:00 Mother's Redemption and Passing 03:33:00 Forgiveness, Recovery and Purpose 03:35:51 Reflection & Message of Hope _____________________________________________ To advertise on the show, contact sales@advertisecast.com or visit https://advertising.libsyn.com/LockedInWithIanBicka

Programa musical en este caluroso verano. Esperamos que disfruten de este programa musical.

Dom Kelly, Co-Founder, President, and CEO of New Disabled South, joins us for a conversation about disability justice and building systems that truly support disabled people and their families. We talk about the connection between art and activism, why awareness alone is not enough, and how community care can keep one person from carrying everything alone. Plus, our co-hosts discuss caring for senior animals and a new report showing Indiana leads the nation in the decline of children enrolled in Medicaid.See 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 Caregiver S.O.S. On Air, host Ron Aaron is joined by comedian, author, speaker, and educator Danny Klein-Modisett, founder of Laughter On Call. Danny shares her journey of navigating her mother’s Alzheimer’s diagnosis and how an unexpected moment of humor transformed her approach to caregiving, leading to the creation of an organization that brings comic relief and connection to seniors, family members, and professional caregivers nationwide. Main Topics Covered The Origin of Laughter On Call: How hiring a comedian to engage her mother led Danny to discover the profound impact of laughter on cognition, mood, and trust. The Science and Benefits of Laughter: How shared humor releases endorphins and dopamine, boosts oxygen intake, improves memory retention, and helps break down the sense of isolation often felt by those with dementia. Affiliative Humor vs. Misuse of Humor: Why inclusive, warm, and bonding humor builds psychological safety, whereas mockery or sarcasm shuts people down. Improv & Stand-Up Tools for Caregivers: How adopting a comedian’s mindset—learning to "reset" after a bad moment, letting go of rigid expectations, and avoiding argument through "Yes, and..." principles—prevents caregiver burnout. Connecting Through Virtual & Corporate Programs: How Laughter On Call expanded during the pandemic to offer interactive virtual workshops, corporate team-building, and workplace morale-boosting. Key Takeaways for Caregivers Laughter Builds Instant Trust: A single moment of shared, authentic laughter can lower defenses, build psychological safety, and foster trust between care recipients and caregivers. Practice the Art of the "Reset": Just like a stand-up comic who recovers after a joke flops, caregivers can benefit from letting go of rigid schedules and quickly resetting when things don't go according to plan. Meet Them Where They Are: "Knowing your audience" in caregiving means accepting the individual’s current reality rather than trying to correct them or pull them into yours. Showing Up Matters: Showing up with reasonable expectations and self-care directly impacts the care recipient’s well-being and helps mitigate caregiver depression. About Dani Dani Klein Modisett is the Founder/CEO of Laughter On Call. She is also a comedian/actor and author of the book, “ Take My Spouse, Please. ” a part-memoir, part how-to for creating shared laughter to keep your marriage happy and healthy. Dani taught Stand-Up at UCLA for 10 years and has coached keynote speakers, business leaders, and Congressional candidates to use more humor in their communication. She has been a speaker at CALA, ICAA, Stanford, MIT, Columbia, UCLA, Dartmouth, Fuqua and Harvard Business School where Laughter On Call is currently being used as a case study. Her TEDx talk was chosen as an Editor’s Pick, “What My Mother’s Alzheimer’s Taught Me About Alzheimer’s" Resources Mentioned Laughter On Call: laughteroncall.com Danny Klein-Modisett: kleincomedy.com 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.

After 17 years living with cardiomyopathy, Terri Cecere received a life-saving heart transplant. Moved by the generosity that saved his wife, her caregiver husband, George, decided to give back in the ultimate way—by donating a kidney to a total stranger. Kent has an inspiring conversation with George and Terri Cecere as they unpack the emotional journey of transplantation, the realities of caregiving, and how a single act of kindness can ripple out to save multiple lives. In this episode, we discuss: The Caregiver's Perspective: The unspoken emotional realities of supporting a loved one through chronic illness and organ failure. Paying It Forward: How receiving one gift of life inspired George to become a living kidney donor. Debunking Living Donation: Why altruistic kidney donation is far more doable—and needed—than most people realize. Building a Community: How George founded TCH Caregiver's Heart to ensure transplant caregivers never have to walk the path alone. For more information on kidney donation and support, reach out to Kent at Kidney Solutions or call him directly at 830-285-2140. Host: Kent Bressler Producer: Jason Nunez Remember to keep breathing, and thank you for listening to Kent's Kidney Stories!

  Caregiving can feel painfully slow. The same responsibilities, struggles, and prayers continue day after day. But slow does not mean aimless. In this episode, I draw from the careful adjustments required for Gracie's new prosthetic legs. A body shaped by decades of trauma cannot be corrected overnight. Neither can a life. God understands what has shaped us, knows exactly what He is correcting, and works with a wisdom that never hurries and never wastes time. I also celebrate eight years of Hope for the Caregiver on American Family Radio, share a small-town Montana story involving our postmaster and an urgent request for Imodium, and return to Ecclesiastes 3:11 with the caregiver hymn of the week, "In His Time." When progress seems glacial and caregiving appears endless, I keep returning to what is true: God makes all things beautiful in His time.

In this special bonus episode of the Focused Healthy Family Podcast, Don Grothoff steps into the guest chair as he's interviewed by Stewart Mada, host of Senior Care Connections and owner of Visiting Angels Lake Norman. Don shares his personal caregiving journey and explains how that experience led him to dedicate his life to helping caregivers reduce stress and emotional overwhelm through Emotional Freedom Techniques (EFT), also known as Tapping. The conversation explores the emotional challenges caregivers face every day, why it's so important to start family conversations about aging before a crisis occurs, and how simple mind-body techniques can help calm the nervous system during difficult seasons of life. Stewart and Don also discuss one of today's biggest threats to older adults—senior scams and fraud. From common telephone scams to the growing dangers of AI voice cloning, they share practical advice families can use to help protect aging loved ones. You'll also hear Don talk about: His family's personal experiences with caregiving and health challenges. How EFT helped his family through difficult times. The importance of supporting caregivers—not just the person receiving care. Why planning early makes aging decisions easier for everyone. How technology and AI are changing healthcare for both good and bad. Whether you're caring for a parent, supporting a spouse, or preparing for your family's future, this conversation offers encouragement, practical wisdom, and reminders that caregivers deserve care too. Visit FocusedHealthyFamily.com to learn more about Don's work, listen to additional podcast episodes, and discover resources designed to help caregivers reduce stress and build resilience. https://www.1350whip.com/podcasts

Many of us don't realize how deeply trauma shapes our relationships, view of God, and everyday reactions. Past wounds can leave us feeling stuck, disconnected, or unsure how to move forward—but healing is possible through Christ.In this episode, Ellen talks with pastor and licensed therapist Dr. Evan Marbury. Together, they discuss why healing often takes more than time, how lament becomes part of God's healing work, and what it means to pursue emotional healing without ignoring pain or bypassing it with easy answers.You'll learn:What trauma is—and how it's different from ordinary painWhy some wounds don't heal with time aloneHow Scripture speaks to trauma, grief, and emotional healingThe role of lament in emotional healingHow to care well for someone carrying deep emotional painWhen seeking professional counseling can be a wise next stepHow God meets us with compassion, truth, and hope. Whether you're carrying wounds of your own or walking alongside someone who is hurting, this conversation will encourage you to move toward healing, wholeness, and deeper trust in God.Understanding Trauma and Resilience: A Guide for Counselors, Caregivers, and Ministers by Evan MarburyScripture referenced:Luke 10:25-37 | John 5:1-15 | Psalm 13 | Romans 15:13Resources:EvanMarbury.com | ESV | Journal | Logos (get a free trial here!) | Blue Letter BibleSend us Fan MailGrow deeper in your love and understanding of God's word with The Courage For Life Study Bible! Discover more at CourageForLifeBible.com.Support the showYouTube channel ☕ Instagram Some of the links in this episode may be affiliate links, meaning if you click through and make a purchase, we may earn a small commission at no extra cost to you.

Send us Fan MailBeing “the strong one” sounds like praise until it starts to feel like a rule you can't break. If you're the family caregiver who keeps track of the meds, the appointments, the bills, the behavior changes, and the constant next thing, you may look capable on the outside while feeling depleted on the inside. We're naming that reality honestly, because being human is not a spiritual failure and caregiver burnout is not a character flaw.We unpack the hidden work that so many caregivers carry: the mental load of remembering, the emotional weight of watching someone you love change, and the quiet loneliness that comes when people only see the outcomes, not the cost. Then we turn to a grounding truth from Scripture through Hagar's story in Genesis: God is “the God who sees me.” That perspective matters when caregiving feels like a wilderness, because you are not overlooked, and you are not only useful, you are loved.From there, we draw a clear line between faithfulness and exhaustion. Jesus invites the weary and burdened, and he also models rest, prayer, and stepping away from constant demand. We talk about what real strength can look like right now: telling the truth before burnout tells it for you, asking for one specific kind of help, receiving support without apologizing, and building small rhythms of restoration that are realistic in everyday caregiving life.If you know someone who's tired of holding it all together, share this episode with them. Subscribe, leave a review, and help more family caregivers find hope and practical support in their season of caring.

Whether the parents or some other caregiver if you're of an unhealed heart and mind, it will affect how you parent your children. Far too many children are suffering because of their parents. It's wrong! Parents should always be the protectors, but unfortunately it's not always the case. God bless the children!Shout out ot MillionPodcastsBecome a supporter of this podcast: https://www.spreaker.com/podcast/relationships-and-relatable-life-chronicles--4126439/support.

Join us for a captivating conversation with Maria Slavin, discussing her time in BU's Post-Professional Occupational Therapy Doctoral Program. She dives into her doctoral project, developing a course for caregivers on co-regulation and the importance of regulation and attachment!

In this episode of Widow, Wisdom and Wealth™, Donna welcomes Raymond Lavine, host of Planning with Purpose and two-time EXPY award winner, for a candid conversation about long-term care planning. Rather than getting lost in policy jargon, the discussion focuses on why these conversations matter now—especially for widows, widowers, and families navigating major life transitions. Together, they explore caregiving, vulnerability, legacy, and the importance of having a plan that protects both your loved ones and your future. What You'll Learn in This Episode: Why long-term care planning is really about love, responsibility, and protection The difference between caregiving for children and caregiving for adults Why people often avoid planning for care until it becomes urgent How long-term care planning can reduce anxiety and improve decision-making Why family conversations about care, legacy, and end-of-life wishes matter How planning ahead can support both the person needing care and their family The role of estate planning in shaping care, memorial, and transition decisions Key Takeaways: Long-term care is not just a financial issue—it's an emotional and family issue. A plan gives you more control, more dignity, and more options. Avoiding the conversation can create stress for family members later. Caregivers should be treated with respect and appreciation. Planning for care, legacy, and memorial wishes can bring peace of mind. Even difficult conversations become easier when they're handled early. Memorable Moments: Donna shares her own experience of becoming a widow at 40 and thinking about who would care for her if she got hurt or became ill. Raymond explains how caregiving changes when the person needing care is an adult. The conversation turns personal as they discuss planning funerals, legacy, and how people want to be remembered. Raymond shares a story about a client whose long-term care plan helped his family through a difficult transition. About the Guest and Contact Info Raymond Levine is the host of Planning with Purpose and a two-time EXPY award winner. He helps people think through long-term care planning in a way that supports real-life transitions, caregiving needs, and family peace of mind. Co-Author of the Amazon Best-Selling Book, Empathy and Understanding in Business Podcast Host of Planning with Purpose 2 Time EXPY® Award Recipient https://fountainofvitality.com/video/long-term-care-plan-considerations-and-challenges-ep-35-fountain-of-vitality https://www.youtube.com/watch?v=S98UnoiyTrQ    

Have we always been the caretakers? I am joined by reviewer George Dunn (@georgesreads) to talk about horror stories that are centered around the giving or receiving care either professionally or for a loved one.  Movies:  Relic The Taking of Deborah Logan Insidious  The Perfection The Haunting Would You Rather? Saint Maud The Skeleton Key I Am the Pretty Thing That Lives in the House Misery Books:  A Veritable Household Pet by Viggy Parr Hampton The Caretaker by Marcus Kliewer Frost Bite by Angela Sylvaine The Vessel by Adam Nevill The Only One Left by Riley Sager Helpmeet by Naben Ruthnum The Shining by Stephen King Mary: An Awakening of Terror by Nat Cassidy Nestlings by Nat Cassidy The Haunting of Hill House by Shirley Jackson My Darling Girl by Jennifer McMahon We Spread by Iain Reid Chilling Obsession: The Ervil LaBaron Cult Final Girl Playlist:  Join our Patreon Community!  

Rebecca Bloom is a former employee benefits and executive compensation attorney who spent more than 25 years helping women navigate cancer, work, insurance, disability coverage, and financial survival. She is the founder and author of When Women Get Sick, a book built from decades inside the legal, workplace, and patient advocacy systems most people only discover after diagnosis.Bloom started in Big Law at Simpson Thacher handling employee benefits and compensation work she originally chose to pay off student loans. Then her mother was diagnosed with breast cancer. Suddenly the language she used in corporate law offices became the language of survival at home. Explanation of benefits forms. Coverage disputes. Second opinions. Disability protections. Medical leave. Bills no one could explain.That collision changed the direction of her life.In this episode, Bloom explains how serious illness quietly turns patients into unpaid administrators managing paperwork, logistics, financial risk, and emotional labor while trying to survive treatment. She breaks down how employer based health insurance shapes nearly every aspect of cancer care in America and why women often carry the invisible burden of protecting everyone else from discomfort while they themselves fall apart.The conversation digs into workplace power, the illusion of the healthcare “safety net,” caregiver exhaustion, and the class divide hiding underneath patient empowerment culture. Bloom explains why educated, insured women with resources still struggle to navigate healthcare bureaucracy and what happens to patients without those advantages.This episode explores cancer care, health insurance, employee benefits, patient advocacy, workplace protections, caregiving, and the structural incentives that force sick people to become project managers of their own survival.RELATED LINKSRebecca BloomWhen Women Get SickBay Area Cancer ConnectionsSimpson Thacher & BartlettFEEDBACKLike 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.

Caring for those with dementia represents a major public health challenge, with caregivers, especially spouses, providing long-term, largely unpaid care. With caregiving stress linked to a decline in mental and physical health, it is crucial to understand the complex burden these care partners face in order to  support them. Dr. Donna de Levante Raphael joins the podcast to shed light on the effects of caregiving on the spousal caregiver and share possible interventions and programs to support their needs.  Guest: Donna de Levante Raphael, PhD, gerontologist, director of research, Alzheimer's Foundation of America Show Notes Read Dr. Donna de Levante Raphael's newly published review, “The Impact of Dementia Caregiving on the Health of the Spousal Caregiver,” on the MDPI website.  Learn more about Dr. Donna de Levante Raphael at her profile on the Alzheimer's Foundation of America website. Learn more about ambiguous loss and anticipatory grief, mentioned by Dr. de Levante Raphael at 34:44, by listening to our past episode, “A Guide to Grief: Strategies for Navigating Loss and Dementia.”  Connect with us Find transcripts and more at our website. Email Dementia Matters: dementiamatters@medicine.wisc.edu Follow us on Facebook and Twitter. Subscribe to the Wisconsin Alzheimer's Disease Research Center's e-newsletter. Enjoy Dementia Matters? Consider making a gift to the Dementia Matters fund through the UW Initiative to End Alzheimer's. All donations go toward outreach and production. Learn about Dr. Chin's book, When Memory Fades: What to Expect at Every Stage, from Early Signs to Full Support for Alzheimer's and Dementia.

Show SummaryOn today's episode, we're having a conversation with Dr Debbie Bradbard, Military and Veteran Spouse and the inaugural director of the Boeing Center for Veteran Transition and Military Families at the Virginia Tech in Alexandria, VA. The center's goal is to harness the potential of service members, veterans and their families to thrive in tomorrow's workforce—through skills, mentorship, research, entrepreneurial support, and resources that build future-ready careers and drive economic opportunityEpisode Partner: This episode is sponsored by CareLinx by Sharecare, connecting Veterans, Service Members, and military Families with trusted home care and caregiver support.  Provide Support: Take a moment to turn your gratitude into action. For just $15, you can help provide military culture training to one person who supports veterans and their families, equipping them to respond with greater understanding, confidence, and care. GIVE HERE through our giving page at psycharmor.org. Provide FeedbackAs a dedicated member of the audience, we would like to hear from you. If you PsychArmor has helped you learn, grow, and support those who've served and those who care for them, we would appreciate hearing your story. Please follow this link to share how PsychArmor has helped you in your service journey Share PsychArmor StoriesAbout Today's GuestDeborah Bradbard is the inaugural director of the Boeing Center for Veteran Transition and Military Families at the Virginia Tech in Alexandria, VA.  As a Senior Researcher at Syracuse University's, D'Aniello Institute for Veterans and Military Families (IVMF), Bradbard spent nearly a decade publishing signature publications and shaping policy and best practices for veterans and military families.  Her work on military spouse and veteran employment have been cited by the White House, members of Congress, CNN, the Center for Deployment Psychology and utilized by national professional organizations including The American Psychological Association (APA) and The Society for Human Resource Management Foundation (SHRM) where her work has been downloaded by over 20,000 human resource professionals nationwide.  As Director of Research and Policy at Blue Star Families (BSF), she directed implementation of their national survey whose results have had an enduring influence on military family policy on spouse employment, childcare, and financial readiness. In the private sector at Booz Allen Hamilton, she developed clinical support tools that have been utilized by providers across the entire military health system of over 3 million users.  A frequent speaker for national conferences, Bradbard educates policy makers, elected officials, and employers about the evolving needs of the military community.  A psychologist by training, Dr. Bradbard received her Ph.D. from Auburn University and her MPA from Syracuse University.Links Mentioned During the EpisodeBoeing Center for Veteran Transition and Military FamiliesVirginia Tech in DC on LinkedInDr. Bradbard on LinkedInPsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week is the PsychArmor Course Understanding and Utilizing Your Educational Benefits. provides service members, Veterans and their families with a comprehensive overview of the U.S. Department of Veterans Affairs educational benefits program. You can find the resource here: https://learn.psycharmor.org/courses/Understanding-and-Utilizing-Your-Educational-Benefits Contact Us and Join Us on Social Media Email PsychArmorPsychArmor on XPsychArmor on FacebookPsychArmor on YouTubePsychArmor on LinkedInPsychArmor on InstagramTheme MusicOur theme music Don't Kill the Messenger was written and performed by Navy Veteran Jerry Maniscalco, in cooperation with Operation Encore, a non profit committed to supporting singer/songwriter and musicians across the military and Veteran communities.Producer and Host Duane France is a retired Army Noncommissioned Officer, combat veteran, and clinical mental health counselor for service members, veterans, and their families.  You can find more about the work that he is doing at www.veteranmentalhealth.com  

When aging parents face unexpected health crises, families without a financial safety net experience high stress and relationship challenges. Learn how adults of all ages can learn to develop protective aging and elder care strategies.Caregiving expert Pamela D. Wilson offers professional caregiving guidance and tips to help you learn to self-direct health care, choose a long-term care strategy, and protect yourself from Social Security-related financial risks you may be unaware of.Learn the importance of creating individual and family plans for aging that support financial security, day-to-day stability, and confidence, and that allow you to manage your health and create financial stability for yourself, your elderly parents, and future generations.For professional family caregiver support and advice about health, healthcare, financial, legal, and family dynamics around caregiving and eldercare, including private, family elder care mediation, visit Pamela's website at www.PamelaDWilson.comRequest a professional 1:1 virtual, family caregiver consultation, or private family elder mediation session with Pamela D Wilson: https://pameladwilson.com/elder-care-consultant-aging-parent-consultation-managing-senior-care-needs-meet-with-pamela-d-wilson/Learn how private family elder care mediation can preserve family relationships and create frameworks for problem-solving and decision-making: https://pameladwilson.com/elder-care-mediator/Listen to The Caring Generation podcast on Wilson's website: https://pameladwilson.com/caregiver-radio-programs-the-caring-generation/Learn about Pamela D Wilson, her professional background, and her experience: https://pameladwilson.com/pamela-d-wilson-story/Learn about Pamela D Wilson as an expert witness in caregiving, guardianship, fiduciary litigation, care management, and non-medical in-home care: https://pameladwilson.com/conservatorship-guardianship-expert-witness/ https://pameladwilson.com/expert-witness-caregiving-home-care-guardianship/ https://pameladwilson.com/power-of-attorney-advisor-or-protector/Check out Pamela's online course Caring for Aging Parents: https://pameladwilson.com/support-caring-for-elderly-parents-overwhelmed-caregiver-support-online-course/Sign up for Pamela's caregiver newsletter: https://pameladwilson.com/contact/Invite Pamela to speak to your company or group. Learn more and download a copy of her speaker's kit: https://pameladwilson.com/caregiving-speaker-aging-parents-expert-advocate-keynotes-presentations-digital-caregiver-programs/Follow Pamela on Social Media: Facebook: https://www.facebook.com/pameladwilsoncaregivingexpert/LinkedIn: https://www.linkedin.com/in/pameladwilsoncaregiverexpert/ X: https://x.com/CaregivingSpeakPamela D. Wilson is a professional family caregiving and eldercare expert. As a caregiving consultant, expert witness, eldercare mediator and speaker, she provides caregiver advice and tips, individual and family caregiver support, and resources for aging and elder care decision-making. Pamela's 25 years of professional experience inform caregiving discussions, eldercare strategies, and care plans that encompass health, healthcare, financial, and legal aspects, as well as family dynamics. Visit Pamela's website at www.PamelaDWilson.com to access caregiver resources, online courses, her caregiving blog, library, book, videos, and podcast transcripts, offering practical advice and tips for aging adults and family caregivers providing elder care support. ©2018, 2026 Pamela D Wilson. All Rights Reserved

DeAndre Safer and Jevon Hill from Helping Hands Home Management join us for a conversation about recognizing when a family needs more support and knowing where to begin. We talk about home care, Medicaid waivers, caregiving, and why finding the right resources can feel so overwhelming. They also share details about the upcoming Senior Summer Festival. Plus, our co hosts discuss Danny Glover's recent diagnosis.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Little/Caregiver dynamics often focus on what Littles need, but Caregivers are people too. They get tired, overwhelmed, and burned out just like anyone else. In this episode, we talk about what caregiver burnout can look like, why it happens, and how both partners can work together to build a dynamic that's caring, supportive, and sustainable. Because the healthiest relationships aren't built on one person giving until they're empty. They're built on care that goes both ways.Visit https://linktr.ee/pinkkinkpodcast for links to our Patreon, Pink Kink Boutique, Pink Kink Institute, social media accounts and more!Affiliates - SireDonLeather.com (use code PINKKINK to save 10% on your order)Obedienceapp.com/pinkkink for a 20% discounthttps://love-blanket.com/?ref=PINKKINKPODCAST and use code PINKKINK10 for 10% off

Hey, it's Amy Newmark with your Chicken Soup for the Soul and I'm excited about sharing stories with you from Chicken Soup for the Soul: Care for the Caregiver, which is our most recent book. The stories in this book provide support and tips and plenty of humor for people who are involved in caregiving for family members with dementia, whether Alzheimer's or one of the other kinds. These stories are incredibly helpful to someone who is starting to navigate the caregiving journey and they are also helpful and supportive for old pros. The dementia caregiving journey lasts for years, and everyone can benefit from the wise words and the humorous anecdotes shared by people who have been there, done that. Learn more about your ad choices. Visit podcastchoices.com/adchoices

When life gets messy, chaotic, or completely overwhelming, our automatic response is often to pull back, isolate, and try to bear the crushing weight of caregiving all on our own. In this episode of She Will Flourish, we are pulling back the curtain on the silent struggle millions of caregivers face every single day. Carole Leatham joins the front porch to share how a lifetime of navigating profound personal trauma, ministry, and her husband's intense mental health crisis birthed a powerful mission to support the overlooked server—proving that you don't have to be perfect to be a vessel of hope. It is one of the heaviest dynamics a woman can carry: being the one who holds everything together while silently falling apart behind closed doors. Whether you are navigating a spouse's chronic illness, a family mental health crisis, or the messy seasons of life that leave you emotionally drained, the trap of hyper-independence will tell you that taking time for yourself is selfish. But your well-being isn't a luxury—it is the very fuel for your calling. We are blowing the doors off the isolation trap. Carole Leatham, author of Are You Ready to Find Joy When Life Gets Messy? and founder of The Caretakers Journey, joins us for a raw, beautiful look at what it truly means to turn personal pain into a sanctuary for others. From finding radical faith at sixteen after surviving childhood abuse to navigating the grueling reality of long-term caregiving, Carole's life is a masterclass in kingdom resilience.We break down the profound impact of the "ministry of presence"—the simple, unpolished act of just showing up for someone without needing to have all the right answers. If you've been feeling completely inadequate to serve, running on absolute empty, or waiting until you have it all figured out to finally step into your assignment, this conversation will give your soul permission to start exactly where you are and prioritize the health of the woman behind the mission.Visit the Front Porch: Ready to stop hiding, start growing, and flourish alongside women who will encourage your God-given calling? Join the sisterhood today inside the Flourish Collective at ⁠⁠⁠www.wewillflourish.org⁠Connect with Carole Leatham : Follow Carole on Instagram at ⁠⁠ ⁠@carolesjourney and learn more about Carole HERE, for encouragement and wisdom, and grab a copy of her powerful book, Are You Ready to Find Joy in Your Messy Life?: How I'm Surviving My Husband's Struggles with Anxiety, Depression, and Suicidal Thoughts (Surviving a Loved One's Struggle with Mental Health Issues) HERE.Follow Rachel Earp: Stay connected with Rachel on Instagram at ⁠⁠⁠@iamrachelearp⁠⁠⁠ or visit ⁠⁠⁠www.rachelearp.com⁠ for daily encouragement, faith-filled inspiration, and practical resources.About the She Will Flourish Podcast: The She Will Flourish Podcast is a welcoming space where women grow in confidence, deepen their faith, and embrace God's calling. Through honest conversations, biblical wisdom, and practical encouragement, Rachel equips women to flourish in every season of life.Subscribe & Review: If this conversation encouraged you to stop playing small and step boldly into your calling, please leave a 5-star rating and review on Apple Podcasts or Spotify! Your support helps more women discover the She Will Flourish Podcast and become part of this growing community.Remember: God doesn't call the fearless—He calls the willing. Don't let fear keep you from the purpose He has already placed within you.This episode is powered by ⁠⁠⁠EARPware.

Our continuing series featuring the personal stories of dementia has revealed something: Caregiving is critical in a person's dementia journey. Miles for Memories also knows a caregiver sometimes needs help and advice.This time on Creating Dementia Solutions, Miles for Memories founder Sherii Sherban talks about a new caregiving concept under development called Caregivers for Alzheimer's and Related Dementia Support (CARDS). Sherii shares how the concept features a mentoring program, what will be a 24-hour online resource center - and the chance for anyone to be part of a dementia caregiver coalition.Episode ResourcesMiles for Memories websiteMiles for Memories technologySherii Sherban talks to Community Matters about MFM technologyMore Creating Dementia Solutions episodesABOUT MILES FOR MEMORIESMiles For Memories is a Calhoun County, Michigan organization created in 2013 to raise awareness and funds for Alzheimer's Disease. Later in 2014, the vision was expanded to include all types of dementia. MFM raises money each year through sponsorships, community events, and grants to gather funds to create local programming for both the person living with dementia and the caregiver. Along with local efforts, 20% of the funds to prevention-related dementia research. Miles for Memories is a committee of 70-plus volunteers and are always looking for more to get involved.

Ray White is joined by Zimi Mphefu, Caregiver and Fundraiser at Angel’s Baby Sanctuary t speak to us about the organization’s journey, their current projects and how South Africans can get involved. Tags: 702, Aubrey Masango show, Aubrey Masango, Bra Aubrey, South African Doing Great Things, SADGT, Ray White, Zimi Mphefu, Angel’s Baby Sanctuary, Anne Ebrahim The Aubrey Masango Show is presented by late night radio broadcaster Aubrey Masango. Aubrey hosts in-depth interviews on controversial political issues and chats to experts offering life advice and guidance in areas of psychology, personal finance and more. All Aubrey’s interviews are podcasted for you to catch-up and listen. Thank you for listening to this podcast from The Aubrey Masango Show. Listen live on weekdays between 20:00 and 24:00 (SA Time) to The Aubrey Masango Show broadcast on 702 https://buff.ly/gk3y0Kj and on CapeTalk between 20:00 and 21:00 (SA Time) https://buff.ly/NnFM3Nk Find out more about the show here https://buff.ly/lzyKCv0 and get all the catch-up podcasts https://buff.ly/rT6znsn Subscribe to the 702 and CapeTalk Daily and Weekly Newsletters https://buff.ly/v5mfet Follow us on social media: 702 on Facebook: https://www.facebook.com/TalkRadio702 702 on TikTok: https://www.tiktok.com/@talkradio702 702 on Instagram: https://www.instagram.com/talkradio702/ 702 on X: https://x.com/Radio702 702 on YouTube: https://www.youtube.com/@radio702 CapeTalk on Facebook: https://www.facebook.com/CapeTalk CapeTalk on TikTok: https://www.tiktok.com/@capetalk CapeTalk on Instagram: https://www.instagram.com/ CapeTalk on X: https://x.com/CapeTalk CapeTalk on YouTube: https://www.youtube.com/@CapeTalk567 See omnystudio.com/listener for privacy information.

Scheduling has become the top challenge for home care agencies, driving costly turnover. Discover how virtual assistants tackle last-minute gaps, reduce burnout, slash labor costs by up to sixty percent, and free owners to focus on growth instead of chaos. More info at https://smartscale360.com/blogs/news/virtual-assistant-scheduling-benefits-for-home-care-agencies SmartScale 360 City: Tampa Address: 1209 E Cumberland Ave Website: https://smartscale360.com/

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.

Host Teresa Huizar speaks with Dr. Jamie Yoder of Colorado State University about how adversity and trauma increase risk for teens' problematic sexual behaviors and how trauma-focused cognitive behavioral therapy (TF-CBT) can be leveraged to expand treatment resources and reduce punitive responses. Yoder describes her clinical background with justice-involved youth and emphasizes that trauma is a major, though not causal, risk factor linked through intermediaries like attachment disruptions, executive functioning impacts, and trauma symptoms. They discuss why trauma has been poorly integrated into PSB interventions due to adult-like assumptions and punishment-oriented systems, then review Yoder's pilot testing TF-CBT across community and residential/justice settings, highlighting feasibility, the need for agency buy-in and readiness, and the role of caregiver involvement. The conversation underscores caregiver shame, clinician bias and support needs, and calls for trauma-informed, rehabilitative approaches and broader systems change.  Time Stamps: 00:00 Episode Overview 01:58 Jamie's Path to PSB Work 05:35 How Trauma Raises Risk 09:10 Why Trauma Was Ignored 13:53 Testing TF-CBT in Settings 18:34 Caregivers and Engagement 22:48 Study Results and Meaning 26:06 Shame as Treatment Target 31:51 Clinician Bias and Support 35:53 Trauma Informed Treatment Plans 40:14 Recommendations and Systems Change 45:33 Closing and Resources Resources:Trauma Focused Cognitive Behavioral Therapy for Adolescents with Problem Sexual Behaviors: Feasibility and Acceptability for Alleviating Traumatic Stress, Regulation Problems, and Sexual Behavior Problems | Journal of Child & Adolescent Trauma | Springer Nature Link Support the showDid you like this episode? Please leave us a review on Apple Podcasts.

******Support the channel******Patreon: https://www.patreon.com/thedissenterPayPal: paypal.me/thedissenterPayPal Subscription 1 Dollar: https://tinyurl.com/yb3acuuyPayPal Subscription 3 Dollars: https://tinyurl.com/ybn6bg9lPayPal Subscription 5 Dollars: https://tinyurl.com/ycmr9gpzPayPal Subscription 10 Dollars: https://tinyurl.com/y9r3fc9mPayPal Subscription 20 Dollars: https://tinyurl.com/y95uvkao ******Follow me on******Website: https://www.thedissenter.net/The Dissenter Goodreads list: https://shorturl.at/7BMoBFacebook: https://www.facebook.com/thedissenteryt/Twitter: https://x.com/TheDissenterYT This show is sponsored by Enlites, Learning & Development done differently. Check the website here: http://enlites.com/ Dr. Stijn Vanheule is a clinical psychologist, professor at Ghent University, and psychoanalyst in private practice. He is the author of the books "The Subject of Psychosis: A Lacanianperspective" and "Diagnosis and the DSM: A Critical Review", and of multiple papers on Lacanian and Freudian psychoanalysis, psychoanalytic research into psychopathology, and clinical diagnosis. His latest book is Why Psychosis Is Not So Crazy: A Road Map to Hope and Recovery for Families and Caregivers. In this episode, we focus on Why Psychosis Is Not So Crazy. We start by discussing how psychosis is approached by mainstream clinical psychology and by psychoanalysis. We talk about what mental disease is, stigmatization, what triggers psychotic episodes, and what psychotic episodes express. Finally, we discuss how psychotic experiences should be dealt with, how people can communicate with a psychotic person, and whether anyone is really insane.--A HUGE THANK YOU TO MY PATRONS/SUPPORTERS: PER HELGE LARSEN, BERNARDO SEIXAS, ADAM KESSEL, MATTHEW WHITINGBIRD, ARNAUD WOLFF, TIM HOLLOSY, HENRIK AHLENIUS, ROBERT WINDHAGER, RUI INACIO, ZOOP, MARCO NEVES, COLIN HOLBROOK, PHIL KAVANAGH, SAMUEL ANDREEFF, FRANCIS FORDE, TIAGO NUNES, FERGAL CUSSEN, HAL HERZOG, NUNO MACHADO, JONATHAN LEIBRANT, JOÃO LINHARES, STANTON T, SAMUEL CORREA, ERIK HAINES, MARK SMITH, JOÃO EIRA, TOM HUMMEL, SARDUS FRANCE, DAVID SLOAN WILSON, YACILA DEZA-ARAUJO, ROMAIN ROCH, YANICK PUNTER, CHARLOTTE BLEASE, NICOLE BARBARO, PAWEL OSTASZEWSKI, NELLEKE BAK, GUY MADISON, GARY G HELLMANN, SAIMA AFZAL, ADRIAN JAEGGI, JOÃO BARBOSA, JULIAN PRICE, HEDIN BRØNNER, FRANCA BORTOLOTTI, GABRIEL PONS CORTÈS, URSULA LITZCKE, SCOTT, ZACHARY FISH, TIM DUFFY, SUNNY SMITH, JON WISMAN, WILLIAM BUCKNER, LUKE GLOWACKI, GEORGIOS THEOPHANOUS, CHRIS WILLIAMSON, PETER WOLOSZYN, DAVID WILLIAMS, DIOGO COSTA, ALEX CHAU, CORALIE CHEVALLIER, BANGALORE ATHEISTS, LARRY D. LEE JR., OLD HERRINGBONE, DAN SPERBER, ROBERT GRESSIS, JEFF MCMAHAN, JAKE ZUEHL, MARK CAMPBELL, TOMAS DAUBNER, LUKE NISSEN, KIMBERLY JOHNSON, JESSICA NOWICKI, LINDA BRANDIN, VALENTIN STEINMANN, ALEXANDER HUBBARD, BR, JONAS HERTNER, URSULA GOODENOUGH, DAVID PINSOF, SEAN NELSON, MIKE LAVIGNE, JOS KNECHT, LUCY, MANVIR SINGH, PETRA WEIMANN, CAROLA FEEST, MAURO JÚNIOR, TONY BARRETT, NIKOLAI VISHNEVSKY, STEVEN GANGESTAD, TED FARRIS, HUGO B., JORDAN MANSFIELD, CHARLOTTE ALLEN, PETER STOYKO, DAVID TONNER, LEE BECK, PATRICK DALTON-HOLMES, NICK KRASNEY, RACHEL ZAK, DENNIS XAVIER, CHINMAYA BHAT, RHYS, ALEX MACLEOD, HAIDAR, JULIEN PORCHER, ROBERT SUNDSTRÖM, JON STEWART, AND JENNIFER MARTIN!A SPECIAL THANKS TO MY PRODUCERS, YZAR WEHBE, JIM FRANK, ŁUKASZ STAFINIAK, TOM VANEGDOM, BERNARD HUGUENEY, CURTIS DIXON, THOMAS TRUMBLE, KATHRINE AND PATRICK TOBIN, JONCARLO MONTENEGRO, NICK GOLDEN, CHRISTINE GLASS, IGOR NIKIFOROVSKI, PER KRAULIS, ADAM HUNT, ANTHONY DI LORENZO, AND JOÃO BARBOSA!AND TO MY EXECUTIVE PRODUCERS, MATTHEW LAVENDER,SERGIU CODREANU, AND GREGORY HASTINGS!

Unpaid caregiving & the burden it places on families // AGREE TO DISAGREE: Men-only gyms seek to protect Christian men from lust // WE HEAR YOU! and WORDS TO LIVE BY

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.

Why does it feel so hard to make plans, think long term, or imagine your future when you are caring for someone with cancer? In this episode, Charlotte begins the Living Until the Next Scan series by naming the way cancer caregiving can contract time. She explores how life starts to get organized around scan cycles, results, and reprieves instead of seasons, milestones, or the long arc of your own life. She also talks about the quiet losses that come with living inside a shorter timeline, including planning hesitation, conversation avoidance, relationship strain, and the grief of losing access to the long view of your future. This episode offers a simple grounding practice to help you remember that your life is still happening now, even in the middle of uncertainty.In this episode, Charlotte explores:why cancer caregiving can make it hard to plan far into the futurehow scan cycles start to reshape your relationship with timethe loneliness of living on a different timeline from the people around youa simple practice to help you reconnect with the life that is still happening right now

Show SummaryOn today's episode, we're having a conversation with Veteran family member Chris Weedon, Founder and Executive Director of the Mentally Shredded Foundation, a nonprofit dedicated to preventing burnout and strengthening mental resilience through movement, reflection, conversation, and community.Episode Partner: This episode is sponsored by CareLinx by Sharecare, connecting Veterans, Service Members, and military Families with trusted home care and caregiver support.  Provide Support: Take a moment to turn your gratitude into action. For just $15, you can help provide military culture training to one person who supports veterans and their families, equipping them to respond with greater understanding, confidence, and care. GIVE HERE through our giving page at psycharmor.org. Provide FeedbackAs a dedicated member of the audience, we would like to hear from you. If you PsychArmor has helped you learn, grow, and support those who've served and those who care for them, we would appreciate hearing your story. Please follow this link to share how PsychArmor has helped you in your service journey Share PsychArmor StoriesAbout Today's GuestChristopher D. Weedon, MBA, is the Founder and Executive Director of the Mentally Shredded Foundation, a nonprofit dedicated to preventing burnout and strengthening mental resilience through movement, reflection, conversation, and community. A former collegiate soccer captain who also competed at the semi-professional level, and a former strength and conditioning coach, Christopher created the Mentally Shredded 3-in-1 Method after navigating his own mental health challenges and recognizing the need for proactive, accessible wellness experiences. Since 2022, the organization has served more than 2,000 participants through live programs and reached more than 10,000 people through educational content and The Mentally Shredded Show podcast. Christopher is building a scalable model that equips organizations and communities to make mental wellness a regular practice rather than a crisis response.Links Mentioned During the EpisodeMentally Shredded WebsiteChris Weedon on InstagramMentally Shredded on InstagramChris Weedon on LinkedInPsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week is the PsychArmor Course Bolstering Resilience, part of the Brain Health and Wellness Learning Series. This mini-course series on resilience, sponsored by Wounded Warrior Project, spotlights five supporting factors proven to bolster resilience among service members, veterans, their families, and caregivers: SMART goals, mental health, nutrition, sleep, and exercise. Each element builds upon a foundation of service and increases the ability to successfully cope with high levels of stress and pressure. You'll learn why these supporting pillars are so important to overall well-being, their application in daily life, and how it's never too late to make a lasting change. You can find the resource here:  https://learn.psycharmor.org/courses/WWP-BHW-bolstering-resilience Contact Us and Join Us on Social Media Email PsychArmorPsychArmor on XPsychArmor on FacebookPsychArmor on YouTubePsychArmor on LinkedInPsychArmor on InstagramTheme MusicOur theme music Don't Kill the Messenger was written and performed by Navy Veteran Jerry Maniscalco, in cooperation with Operation Encore, a non profit committed to supporting singer/songwriter and musicians across the military and Veteran communities.Producer and Host Duane France is a retired Army Noncommissioned Officer, combat veteran, and clinical mental health counselor for service members, veterans, and their families.  You can find more about the work that he is doing at www.veteranmentalhealth.com  

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.

Send us Fan MailECONOMIC DISASTER COMING. Stock Trading. New Skill Sets. Lead To Buy Assets.❤️️Grants from states and local governments: https://findhelp.org/❤️️Caregivers, Mental Health: https://www.211.org

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.

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.

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

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.

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 

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.

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.