Podcasts about caregivers

Sometimes, you are so consumed by caring for a loved one with a serious mental illness, like schizophrenia or bipolar disorder, that taking a moment for yourself feels like a betrayal. In this episode, host Gabe Howard and Dr. C. Alec Pollard reveal the hidden crisis of caregiver burnout in the world of serious mental illness. They dismantle the myth that self-care is selfish, showing how neglecting your own needs can worsen stress and strain the very relationships you cherish.   Dr. Pollard dives into the toxic beliefs that trap caregivers—those who support individuals with schizophrenia, bipolar disorder, and other severe conditions—into a cycle of resentment and exhaustion. With breakthrough strategies and compassionate advice, this episode offers a wake-up call for anyone feeling overwhelmed by the relentless demands of caregiving. Learn how nurturing yourself not only protects your well-being but also empowers you to care more effectively for your loved one. “If you can do no good, at least do no harm. A lot of the, the things that families don't understand and caregivers is that they're actually doing things that not only they know it doesn't work okay. When they're doing these things, these naggings and lectures and all that, they know it's not working. But what they may not appreciate is it's actually making things worse over time.” ~C. Alec Pollard, PhD Our guest, C. Alec Pollard, Ph.D., is Founding Director of the Center for OCD and Anxiety-Related Disorders at Saint Louis Behavioral Medicine Institute and Professor Emeritus of Family and Community Medicine at Saint Louis University School of Medicine. He is a licensed psychologist who works with a range of obsessive-compulsive and anxiety-related disorders, with a special interest in obstacles that might inhibit the pursuit of recovery or interfere with effective participation in treatment. He is on the Scientific and Clinical Advisory Board of the International OCD Foundation and chairs the organization's Training Subcommittee, including a national training initiative called the Behavior Therapy Training Institute.  Dr. Pollard is former chair of the Clinical Advisory Board of the Anxiety and Depression Association of America and has authored over 100 publications, including 3 books – “The Agoraphobia Workbook, Dying of Embarrassment: Help for Social Anxiety & Phobia,” and “When a Loved One Won't Seek Mental Health Treatment: How to Promote Recovery and Reclaim Your Family's Well-Being.” Inside Mental Health's host, Gabe Howard. lives with bipolar disorder and is a nationally recognized speaker and podcast host. He is the author of the book, Mental Illness is an Asshole and other Observations, available from Amazon; signed copies available directly from the author. To learn more about Gabe, please visit gabehoward.com. Like the Inside Mental Health podcast? Find it on your favorite podcast player or visit psychcentral.com/show! Learn more about your ad choices. Visit megaphone.fm/adchoices

In 2020, Emily Mendenhall drove from Washington, DC to Okoboji, Iowa, a town of 800 that swells to 200,000 every summer, and walked into a pandemic that looked nothing like the one dominating national headlines. Inside gas stations and bars, masks marked you as an outsider. In one stop, a man told her family they would not be served if they kept theirs on. Her 6 year old daughter cried, confused. Mendenhall, a medical anthropologist at Georgetown University, did what she always does. She started asking questions. Over months, she interviewed neighbors, former classmates, and local officials, including her own brother in law who helped lead the local COVID response. The result became Unmasked, a case study in how community identity, economics, and politics shaped public health decisions in real time. That work led directly into her latest book, Invisible Illness: A History, from Hysteria to Long COVID, where she tracks a much older problem. Patients with chronic illness, especially women, often fail to meet medicine's demand for proof. Without a clear diagnosis, they lose access to care, insurance coverage, and legitimacy. Mendenhall argues that long COVID did not create this failure. It exposed it.This conversation centers on how healthcare systems reward certainty and punish complexity. Long COVID clinics send patients to 17 specialists without resolution. Insurance structures require diagnoses that many conditions cannot provide. Medical training still struggles to integrate trauma, mental health, and chronic disease into a coherent model of care.Mendenhall brings lived experience into the conversation. After COVID, she dealt with months of fatigue and escalating anxiety that altered her baseline health. She does not claim the label of long COVID, but she understands how quickly the system becomes harder to navigate once symptoms stop fitting clean categories. The stakes are not theoretical. In the United States, access to healthcare, disability benefits, and treatment still depends on whether a condition can be measured, coded, and reimbursed. For millions living with invisible illness, the burden of proof becomes the illness itself.RELATED LINKSEmily MendenhallInvisible Illness: A History, from Hysteria to Long COVIDScience PoliticsGeorgetown UniversityFEEDBACKLike 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.

"That's my own formula — passion and compassion tempered by dedication and humor." This episode is sponsored-in-part by Maddie's Fund, OcuTrap, and Drop Traps: Beginning and Advanced Certification Workshop. After more than five decades behind the exam table, Dr. Kevin Lynch has treated thousands of pets, mentored generations of veterinary staff, and built one of Long Island's longest-running animal hospitals. His new memoir, Off the Leash: Tales From a Lifetime of Healing Pets and Wonder, traces that journey from a 13-year-old kid who talked his way into a part-time job at a local animal hospital to a veterinarian whose guiding philosophy is simple: treating the animal is only half the work, and tending to the person on the other end of the leash is the rest. Dr. Lynch and Stacy dig into one of the thorniest debates in animal welfare: the divide between "indoor-only" advocates and the realities of outdoor and community cat caregiving. Drawing on his own farm-cat memories from working summers on a dairy farm before vet school, he makes the case for listening over judging, and for meeting cat caregivers where they are instead of where a textbook says they should be. From there, the conversation turns practical: how should trappers and community cat program managers actually approach a veterinarian for the first time? Dr. Lynch's answer centers on intention, relationship-building, and showing up with a plan rather than a crisis. The episode also gets personal. Dr. Lynch opens up about compassion fatigue and burnout, a topic he says is as urgent in veterinary medicine today as it's ever been, and shares the daily habits, including a deliberately disciplined relationship with his phone, that keep him from burning out after 51 years in practice. He and Stacy also revisit one of the most harrowing chapters of his career: volunteering with search-and-rescue dogs at Ground Zero after 9/11, an experience he says revealed both the depths of tragedy and the best of human nature. Rounding out the conversation, Dr. Lynch shares a few of the stories from his book, including an unforgettable lesson in slowing down before attempting a DIY tick removal. He also talks about where listeners can find his memoir, his YouTube series The Pet Mindset Show, and the dental care device he invented for dogs and cats. Press Play Now For: How a 13-year-old's unpaid job at a Long Island animal hospital turned into a 51-year veterinary career Dr. Lynch's perspective on the indoor-only versus outdoor/community cat debate, and why he believes there's no one-size-fits-all answer His honest advice for trappers and caregivers on how to approach a veterinarian for the first time Why showing up with "a plan" rather than a crisis is the fastest way to build trust with a vet The role of compassion fatigue and burnout in veterinary medicine, and the daily habits that help him stay in the game His "physical mailbox" approach to managing phone use and protecting mental bandwidth A first-hand account of volunteering with search-and-rescue dogs at Ground Zero after 9/11 The story behind a Rottweiler named Big Shot, and the unexpected humanity he witnessed during that crisis Two unforgettable cat stories from his memoir, including a lesson in patience before attempting DIY pet care Where to find his memoir, his YouTube series, and the dental device he invented for pets Resources & Links Off the Leash: Tales From a Lifetime of Healing Pets and Wonder (Amazon) Dr. Kevin Lynch's website The Pet Mindset Show (YouTube) Plaque Be Gone dental device

Why can a quiet day feel harder than a busy one when you are caring for someone with cancer?In this episode, Charlotte continues the When Calm Feels Unsafe series by talking about what happens when the busyness finally stops and your nervous system no longer has tasks to keep it occupied.She explains why constant motion can become a form of emotional protection, why anxiety often rushes in when there is finally space to rest, and why that reaction is not a failure of rest but evidence of how much you have been carrying.Charlotte also shares a simple grounding practice to help you meet those slow moments with a little more steadiness, so your body can begin to learn that stillness does not have to be dangerous.

Show SummaryOn today's episode, we're replaying a conversation with Michael Bailey, Deputy Director of Leadership Programs for the George W. Bush Institute. We talk about some of the initiatives of the Bush Institute, including the Veteran Leadership Program, the Democracy is a Verb initiative and the Bush Institute's efforts to celebrate America 250.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 GuestMichael Bailey serves as Deputy Director, Leadership Programs, for the George W. Bush Institute. In this role, he manages the Stand-To Veteran Leadership Program, which focuses on developing the leadership skills of veterans and those who serve them and their families. Bailey also supports alumni engagement efforts for the Institute's international leadership programs.Prior to joining the George W. Bush Institute, Bailey provided operations, media, and communications support to The American Choral Directors Association, a music organization dedicated to the excellence and advancement of choral music.Bailey is a native of Arlington, Texas. He received his Bachelor of Arts in Music (Voice) from The University of Oklahoma, and he holds a Master of Business Administration with concentrations in finance and real estate from Southern Methodist University Cox School of Business. He has a passion for running and enjoys racing in half and full marathons.Links Mentioned During the EpisodeGeorge W. Bush InstituteStand-To Veteran Leadership ProgramAmerica 250Democracy is a Verb initiative  PsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week is The PsychArmor course The Myths and Facts of Military Leaders. This course identifies four of the most popular myths about military leaders and how they don't align with the reality of working alongside Veterans and Service members. You can find the resource here:  https://learn.psycharmor.org/courses/The-Myths-and-Facts-of-Military-Leaders Episode Partner: Are you an organization that engages with or supports the military affiliated community? Would you like to partner with an engaged and dynamic audience of like-minded professionals? Reach out to Inquire about Partnership Opportunities 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  

On this West Virginia Morning, our partner HealthQ explores why embracing the title of “caregiver” matters—and how recognition and support can make a difference in this phase of life. The post Caring For The Caregivers Of Aging Adults, This West Virginia Morning appeared first on West Virginia Public Broadcasting.

Send Cathy a text:)Have you ever felt like caregiving has emptied your cup... or even cracked it?You're not alone.In this episode, we're talking about what rebuilding really looks like after burnout, overwhelm, emotional exhaustion, or a difficult caregiving season.You'll discover:✨ Why rebuilding isn't about becoming the person you were before caregiving ✨ The three ways a caregiver's cup can "break" ✨ How to begin rebuilding one small step at a time ✨ Why celebrating small wins matters more than you think ✨ How to move forward with hope, compassion, and graceBecause healing doesn't happen all at once.

This time on Code WACK!   Imagine being cut off from Mom - a nursing home resident - for months. You can't bring her favorite foods, or help dress her, hug her, or even hold her hand. For thousands of families during the COVID-19 pandemic, this became a heartbreaking reality. And without new laws, advocates say, it could very well happen again. That's why they are fighting to ensure our loved ones are never again separated from those they depend on most in nursing homes and other long-term care settings Today we're speaking with Tony Chicotel, senior staff attorney with California Advocates for Nursing Home Reform, or CANHR. For decades, Tony has fought to protect the rights of nursing home residents. And he says the isolation and neglect that families experienced during COVID was one of the most painful chapters of his career. This is part two of a two-part series on the Essential Caregiver's Act.  Check out the Transcript and Show Notes for more!  And please keep Code WACK! on the air with a tax-deductible donation at heal-ca.org/donate. 

In this episode of Living in the Long-Middle, we are joined by Phil and Caitlyn Stewart, a husband-and-wife team sharing their experiences from both sides of the cancer journey—the patient perspective and the caregiver perspective. When cancer enters a relationship, it impacts more than just one person. Phil and Caitlyn offer an honest look at how they have navigated the challenges, uncertainties, and realities of ocular melanoma together. Through their conversation, they explore the unique roles of patient and caregiver, the importance of communication, and how partnership can provide strength during difficult times. Their story highlights the resilience that comes from facing adversity as a team and the lessons they have learned while living in the long-middle of cancer survivorship. Whether you are a patient, caregiver, family member, or friend, this episode offers meaningful insights into the power of support, understanding, and shared hope.

This time on Code WACK! Imagine being cut off from Mom - a nursing home resident - for months. You can't bring her favorite foods, or help dress her, hug her, or even hold her hand. For thousands of families during the COVID-19 pandemic, this became a heartbreaking reality. And without new laws, advocates say, it could very well happen again. That's why they are fighting to ensure our loved ones are never again separated from those they depend on most in nursing homes and other long-term care settings Today we're speaking with Tony Chicotel, senior staff attorney with California Advocates for Nursing Home Reform, or CANHR. For decades, Tony has fought to protect the rights of nursing home residents. And he says the isolation and neglect that families experienced during COVID was one of the most painful chapters of his career. This is part two of a two-part series on the Essential Caregiver's Act. Check out the Transcript and Show Notes for more! And please keep Code WACK! on the air with a tax-deductible donation at heal-ca.org/donate.

Family caregivers know what it feels like to fall short. In this episode, Peter Rosenberger explores the difference between failure and faithfulness, why perfection is a burden no caregiver can carry, and why your attendance record matters more than your performance record. Peter also reflects on stewardship, productivity, and the responsibility of using what God has entrusted to us—right where we are. In a special Father's Day message, he shares the moving story behind the words, "Daddy's here," from Gracie's awakening after a devastating accident to comforting his own son through a painful childhood injury. Through these experiences, Peter points listeners to the greater assurance of God's presence when explanations fail and life doesn't make sense. Topics Covered: Perfectionism and caregiving Failure versus faithfulness The caregiver's attendance record Stewardship and productivity Father's Day reflections Finding comfort in God's presence Why presence often matters more than answers More resources for family caregivers at Caregiver.Substack.com

What are personal boundaries, and why do we feel so guilty setting them? In this episode, we break down the different types of boundaries we all need to protect our time and emotional well-being—and why they are absolutely essential for family caregivers. Burnout, exhaustion, and resentment shouldn't be the price of supporting a loved one. Learn how setting clear limits is not about caring less, but about preventing caregiver burnout so you can actually provide better care. If you are feeling drained, overextended, or struggling to say no to family caregiving demands, this episode will show you exactly how to find your lines and hold them. Listen and more: https://bit.ly/4viWWRZIn this podcast, we discuss:What are personal boundaries and the different types of boundaries. How to set boundaries as a family caregiver to protect your time and emotional health. Recognizing the major signs of caregiver exhaustion and caregiver burnout. Practical strategies for setting boundaries with aging parents without the guilt. Why drawing lines isn't selfish, but actually leads to preventing caregiver burnout and delivering better care. Timestamps:00:00 - Intro: Remembering Fathers and Boundaries in Caregiving01:51 - Recipe of the Week: Dad's Pineapple Salsa02:14 - A Father and Boundaries - An Essay by Nick Dothée (Washington Post)08:42 - "Personal Boundaries" - What does that mean?13:21 - Why Boundaries are Important in Caregiving14:44 - Charlie's Stoic Aging Father - How His Family Set Boundaries with Love19:33 - Cold Chicken and Last Breaths - Remembering and Grieving a Father22:27 - Outro#howtosetboundaries #healthyboundaries #boundarysetting #mentalhealthtips #emotionalwellbeing #caregiverstress #burnoutprevention #griefsupport #fathersdaygrief #rememberingdadSupport the showConnect with Us: Email our Host: mail@every1dies.org  Website: https://every1dies.org: Find show notes, links and expanded resources Follow Us: Facebook | Instagram | YouTube  

On this special bonus episode, we sit down with filmmaker Anthony Lucero, writer and director of Paper Bag Plan, a moving film that shines a light on the realities of family caregiving, disability advocacy, and long term planning for individuals with special needs. Drawing from his own deeply personal experiences, Anthony shares how caring for his physically disabled brother and coping with the loss of his sister (who left behind a daughter with special needs) inspired the story behind Paper Bag Plan. The film serves as both a heartfelt tribute to family caregivers and an exploration of one of the most pressing questions many families face: What happens to a child with a disability when their parents or primary caregivers are no longer able to provide support? During the conversation, Anthony discusses the emotional journey of creating the film, the importance of raising awareness about caregiving challenges, and the need for families to engage in future planning for loved ones with disabilities. Show Notes/Links: www.hotflashescooltopics.com Film: Paper Bag Plan Find Out More! Website http://hotflashescooltopics.com Mail hotflashescooltopics@gmail.com Instagram https://www.instagram.com/hotflashesandcooltopics Facebook : www.facebook.com/hotflashescooltopics YouTube https://www.youtube.com/@HotFlashesCoolTopics Pinterest https://www.pinterest.com/hcooltopics/ Want to Leave a Review for Hot Flashes and Cool Topics? Here's How: For Apple Podcasts on an iPhone or iOS device: Open the Apple Podcast App on your device. Click on the “search” icon Type into the search bar “Hot Flashes and Cool Topics” and click on the show Towards the bottom, look for “Ratings and Reviews” Click on “Write a Review” and leave us your thoughts and comments! For Apple Podcasts on a computer: On the Apple Podcasts website, go to the search bar and type “Hot Flashes and Cool Topics” After clicking on the show, find the “Listen on Apple Podcasts” button and click on it The “Hot Flashes and Cool Topics” podcast should open on the Apple Podcasts application Keep scrolling on the page until you see “Ratings and Reviews” Click on “See All” If you want to give us a five-star rating, hover over the empty stars! • • If you want to leave your thoughts and comments, click on “Write a Review

AI couldn't cure his mother's stage 4 cancer. It caught three near-fatal errors, found a same-day appointment, and helped her leave on her own terms. When Pratik Desai's mother was diagnosed with stage four duodenal adenocarcinoma — a rare cancer with roughly 3,000 US cases a year — she was nearly discharged without an oncology appointment. Over the next 76 days, Desai used AI at her bedside, from 5am to 10pm, to understand each report, prepare for every appointment, and push a stretched health system to move at the pace her diagnosis demanded. This is a frank account of where AI helped, where it didn't, and the line he refuses to cross. This is a 1:1 interview in The Agentic Patient — a Faces of Digital Health series on how patients and caregivers actually use AI: which tools, which prompts, and which guardrails. GUEST Pratik Desai — New Jersey-based AI practitioner; caregiver and builder of a free, local AI tool for patients HOST Tjaša Zajc — Founder & host, Faces of Digital Health / The Agentic Patient WHAT THE CONVERSATION COVERS - Using AI to interpret a biopsy report and push for a same-day "stat" CT scan - Why AI and the doctors agreed on the care — and clashed on the speed - Finding a same-day oncology appointment through an AI-assisted network search - An error-riddled CT report the AI refused to read — and what it did to trust - Running three Claude "personas" as built-in second and third opinions - A local, open-source AI tool that keeps medical data off the cloud - How to prompt as a patient or caregiver: awareness, knowledge, advocacy — not diagnosis - Where AI failed him: prognosis, and the rule he broke under pressure - Defining quality of life when the outcome is already known CHAPTERS 0:00 How patients use AI — and the guardrails 1:20 Day one: a healthy mother, a diagnosis no one would name 3:34 The first prompt, and pushing for a stat CT scan 7:43 Using AI in the open: agreement on care, friction on speed 9:35 The counterfactual: 76 days with AI at the bedside 12:40 Finding a same-day appointment through a network search 13:40 The CT report the AI refused to read 15:50 When trust erodes: good faith, not competence 18:41 Why switching hospitals wasn't an option 21:54 Defining quality of life: her three goals 28:27 Three Claude personas, and a local private tool 35:12 How to prompt: awareness, knowledge, advocacy — not diagnosis 37:54 Where AI fell short, and the closing asks THE AGENTIC PATIENT SERIES New to the series? Start here → [PASTE PREVIOUS AGENTIC PATIENT EPISODE LINK] All episodes → https://www.facesofdigitalhealth.com/agentic-patient-blog MORE FROM FACES OF DIGITAL HEALTH

Jennie and Leeza Gibbons continue their vulnerable conversation about caregiving with practical, practice-able resources like: how to create a "sanity sanctuary," protect your relationships and how to find five minutes to move. Plus, Leeza shares her transformative "5 More Strategy" to laugh more, move more, plan more, break more and connect more. Listen for your permission slip to breathe. Follow @IChooseMewithJennieGarth on Instagram and TikTokFollow @JennieGarth on Instagram, TikTok, and Facebook See omnystudio.com/listener for privacy information.

In today's discourse, we delve into the poignant narrative of Sarah Vosburgh, whose experiences elicit profound reflections on the complexities of caregiving, particularly in the context of Alzheimer's disease. As she navigates the tumultuous waters of familial relationships, we witness a remarkable transformation in her connection with her mother, catalyzed by the latter's diagnosis, which compels Sarah to confront the intricacies of guilt, grief, and the labyrinthine healthcare system.Her candid revelations illuminate the emotional labor inherent in caregiving, as well as the subtle, yet significant, shifts in roles that often occur when a parent becomes dependent on their child. With a blend of humor and gravitas, Sarah shares insights from her memoir, "Who Will Name the Bees?", which serves as both a personal testament and a guiding light for others traversing similar paths. Join us as we explore the delicate interplay of love and loss, and the invaluable lessons learned through the lens of vulnerability and resilience. Within the contours of this episode lies a deeply resonant exploration of the caregiving experience as articulated by Sarah Vosburgh, who shares the trials and tribulations that arise when a loved one is diagnosed with Alzheimer's disease.Sarah's narrative, rich in emotion and insight, elucidates the complexities of her relationship with her mother, which, despite its historical misunderstandings, is transformed into a profound bond as she assumes the role of caregiver. The episode highlights the emotional labyrinth caregivers navigate, where guilt, grief, and love intertwine in a delicate dance, challenging the very fabric of familial relationships. As we traverse the intricacies of Sarah's journey, we are confronted with the stark realities of the healthcare system that surrounds Alzheimer's. Sarah poignantly recounts her struggles with navigating this convoluted landscape, illustrating the often unseen burdens borne by caregivers.This episode serves not only as a testament to the resilience of the human spirit but also as a clarion call for greater empathy and understanding towards those who walk the challenging path of caregiving. Sarah's reflections encourage listeners to build bridges of connection and compassion, fostering an environment where shared experiences can illuminate the darker aspects of caregiving, ultimately leading to a greater appreciation for the love and depth inherent in these relationships. In a world where Alzheimer's can feel isolating, Sarah's story is a reminder that we are not alone, and that our journeys, though fraught with difficulty, can also be filled with moments of grace and profound connection.Takeaways:The podcast episode emphasizes the profound emotional labor inherent in caregiving, particularly when navigating the complexities of Alzheimer's disease.Sarah Vosburgh's journey illustrates the intricate relationship dynamics that can evolve between a caregiver and an individual suffering from cognitive decline.The importance of presuming good intent in interpersonal relationships is a recurring theme, as exemplified by the wisdom shared by Sarah's mother.You're not alone in your caregiving experience, and seeking support is important for your mental and emotional well-being.Links referenced in this episode:SarahVosberg.comamazon.comMentioned in this episode:My friend Dr. Noah St. John calls this 'the invisible brake.' He's giving our listeners a free Revenue Ceiling Audit to help you see what's REALLY holding you back. You'll also get a FREE 30-day membership to Noah Bot, giving you access to Dr. Noah's 30 years of experience to help you reach your next level. But hurry, because there are only 50 available this month. So if you're tired of being stuck at the same revenue level and want to finally break through, get your FREE Revenue Ceiling Audit at https://www.noahvault.com?aff=d28bf6c78150c7f09896297dfe1701c1cd191ac6fc9976779212cec5d38e94d6

Jennie and Leeza Gibbons continue their vulnerable conversation about caregiving with practical, practice-able resources like: how to create a "sanity sanctuary," protect your relationships and how to find five minutes to move. Plus, Leeza shares her transformative "5 More Strategy" to laugh more, move more, plan more, break more and connect more. Listen for your permission slip to breathe. Follow @IChooseMewithJennieGarth on Instagram and TikTokFollow @JennieGarth on Instagram, TikTok, and Facebook See omnystudio.com/listener for privacy information.

Femmes, Thems, and Searching for Gems - Table Talk from a Femme/NB Perspective Episode 1: Character Creation and Caregiver Roles (we're calling the November 2025 episode of Twin Portals our FTG Pilot!) Beth, Bailey, and Laura got together again to share more femme/non-binary experiences and perspectives from years around various gaming tables. They delve into their favorite parts of character creation, one of their not-favorite parts (getting nudged into caregiver roles), and put together some rapid-fire team chemistry by assembling a team on the clock! Featuring: Bailey Fazzio (She/Her) Beth Brophy (They/She) Laura O'Brien (She/They) Producer: Scott Hebert (He/Him) --- "Twin Portals" is unofficial Fan Content permitted under the Fan Content Policy. Not approved/endorsed by Wizards. Portions of the materials used are property of Wizards of the Coast. ©Wizards of the Coast LLC. --- Thank you to the Minnesota State Arts Board, the Arrowhead Regional Arts Council, the Minnesota Legacy Amendment, and the voters of Minnesota! --- The title song, "Avernum," used with permission, and thanks to Leeland Campana of Star Wolf. --- Content Inquiries: twinportalsgame@gmail.com Business Inquiries: scootalongproductions@gmail.com

In this Pride Month episode of Shrinking it Down: Mental Health Made Simple, Gene and Khadijah are joined by Dr. Alex Keuroghlian for a wide-ranging, candid conversation about supporting LGBTQ+ youth. As Chair of the Department of Psychiatry at MaineHealth and former founding director of the MGH Psychiatry Gender Identity Program, Dr. Keuroghlian draws on nearly a decade leading the National LGBTQIA+ Health Education Center and his own published research to discuss the environments and policy climate that put LGBTQ+ young people at risk, what it actually looks like when a child comes out, and how families can repair when a conversation doesn't go as hoped. Citing research showing that strong family support is the greatest predictor of good mental health, academic performance, and housing security for youth down the road, Dr. Keuroghlian makes a compelling case for the power of family acceptance. This episode explores that power, the value of parents sharing their own stories, and the warning signs caregivers should watch for — offering insight, hope, and practical guidance for anyone who wants the LGBTQ+ kids in their life to feel loved, supported, and free to be who they are. Tune in now!Media ListDr. Alex Keuroghlian (MaineHealth)PFLAG (National advocacy group for friends and family of LGBTQIA+ people)The Trevor ProjectHuman Rights CampaignWhat to Look for, When to Worry, What to Do (MGH Clay Center) Hosted on Acast. See acast.com/privacy for more information.

Cynthia and John are hosting a new episode this week with Lynda Anderson, Ph.D. Research Associate with the Institute of Community Integration at the University of Minnesota. The episode is dedicated to discussing the 2023 Community Report of Family & Individual Needs for Disability Supports. During the show, they will be reviewing the survey findings and discussing the impact of the research on the IDD community.    Resources mentioned in the episode: Disability Scoop  FINDS Community Report 2023  Want to share stories with us? Email us at Quillopod@myquillo.com  To learn more about Quillo Connect visit MyQuillo.com 

Stop settling for "normal" lab results when you know your body can feel better. Christine and guest co-host SatiMa Ra join Dr. Aleksandra Gajer to uncover the root causes of our physical wellness. In this Episode 229 of Women Connected in Wisdom, I am delighted to be joined by guest co-host SatiMa Ra as we welcome Dr. Aleksandra Gajer to the show. Dr. Gajer is a premier medical professional who transitioned from the high-stakes world of academic emergency medicine to founding The Gajer Practice, where she focuses on investigative, whole-self care. We'll explore the Physical Wellness dimension, looking at why the standard medical model often misses the "why" behind chronic fatigue, hormonal imbalances, and inflammation. With SatiMa Ra's soulful perspective and Dr. Gajer's rigorous clinical background, we bridge the gap between science and spirit. We discuss how gut health and personalized nutrition serve as the foundation for true longevity. Whether you are navigating the complexities of aging or looking to optimize your daily energy, this conversation offers the evidence-based wisdom you need to take ownership of your physical vessel. Connect with Dr. Aleksandra Gajer Website: https://thegajerpractice.com/Instagram: @thegajerpractice YouTube: @TheGajerPractice

Some seasons of love require us to show up even when we are tired, overwhelmed, and grieving before the goodbye ever comes.In this heartfelt episode of Female Voices: Life & Loss, host Wayna Berry sits down with her mother, Laverne Hill, for a deeply personal conversation about caregiving, dementia, family responsibility, faith, and the emotional weight of caring for someone through their final chapter.Laverne shares her experience working in caregiving for over 10 years, helping families assess needs, navigate support services, and understand what it takes to care for elderly parents, dependent adults, and loved ones who can no longer fully care for themselves. She also opens up about her own family journey — caring for her father, supporting her mother through dementia, making the difficult decision to place her mother in a nursing facility, and learning how to keep going when caregiving felt physically, emotionally, and spiritually exhausting.This episode speaks directly to caregivers who are tired, adult children facing hard decisions, families navigating dementia, and anyone carrying the complicated grief that can come before loss.If you are caring for someone you love, this conversation is a reminder that you are not alone, support is available, and doing your best with love still matters.Memorable QuotesLaverne Hill: “You don't want to just talk around them. You don't want to forget them. This is their journey.”Laverne Hill: “Caregiving can be overwhelming. Sometimes families can do so much, and they do need extra help.”Laverne Hill: “You need a worker who has this heart for people, who really wants to make sure that people are okay.”Laverne Hill: “She wasn't just a client. I want the family to know that she wasn't just a number for us.”Laverne Hill: “You just have to stop, breathe, and remember why you're here.”Laverne Hill: “These are her golden years. I'm going to make sure they're golden.”Laverne Hill: “You can't help anybody when you're broken.”Laverne Hill: “Long as you're doing the best that you could do for your person that you love, you are blessed.”Wayna Berry: “Share this with somebody who's in this season.”Wayna Berry: “We're still growing until the Lord calls us home.”Topics Discussed● Assessing care needs, diagnoses, home safety, and family support● Caring for aging parents and dependent loved ones● Dementia, memory loss, and moments of clarity● The emotional and physical strain of caregiving● Making the difficult decision to choose nursing home care● Finding strength through faith, prayer, and community● Caregiving requires love, patience, support, and practical resources.● Asking for help is not a sign of failure.● Every person receiving care deserves dignity and a voice.● Nursing home care can sometimes be the safest, most loving choice.● Caregivers must also protect their own well-being.Key Takeaways● Caregiving requires love, patience, support, and practical resources.● Asking for help is not a sign of failure.● Every person receiving care deserves dignity and a voice.● Nursing home care can sometimes be the safest, most loving choice.● Caregivers must also protect their own well-being.

Families often wait too long to start hospice care, missing months of support. Learn how hospice teams and in-home caregivers work together to provide families with comfort, daily care, and peace of mind during end-of-life at https://encorecaregivers.com/home-health-care-services/ Encore Caregivers City: Houston Address: 7925 Katy Fwy Suite N Website: https://encorecaregivers.com/

This time on Code WACK! What role do family members and friends play in the lives of nursing home residents? When COVID hit, how were residents impacted when their loved ones were no longer allowed to visit them? Today, we share the story of Melody Taylor Stark, who became an advocate for the Essential Caregivers Act after her husband, a retired dentist and nursing home resident, dramatically declined, then died, after being denied her daily visits during the dark days of COVID. Melody is a founding member of Essential Caregivers Coalition, a member of Caregivers for Compromise, and San Gabriel Valley Disability Collaborative, and Facebook co-administrator for Aging Enlightened, a group that was begun by a prominent reporter for Kaiser Health News. She works diligently to advance positive system changes in disability rights and long-term care. This is part one of a two-part series on the Essential Caregiver's Act. Check out the Transcript and Show Notes for more! And please keep Code WACK! on the air with a tax-deductible donation at heal-ca.org/donate.

At 25, Jace Yawnick was building a career in health and wellness sales, chasing growth, status, and the usual young adult fantasy of getting somewhere fast. Then his body stopped cooperating. Fatigue turned into chemotherapy. The diagnosis was primary mediastinal B cell non Hodgkin lymphoma, and the rest of his life split into before and after. Now in remission, he talks about cancer the way people actually live it, not the way nonprofits package it. He gets into survivorship, mental health, young adult isolation, and the deadening absurdity of prior authorization. One of the sharpest parts of the conversation lands on a simple American insult disguised as policy: treatment innovation means very little when insurance can still deny the scan, the drug, or the next step. Jace has seen that firsthand, including during routine monitoring after active treatment. This episode tracks what happens when a young cancer patient becomes a public voice and refuses to play mascot. It covers oncology, insurance, remission, advocacy, and the long mental hangover that follows survival. It also names the part too many institutions dodge: the system works great right up until it doesn't, and when it fails, patients get handed the bill, the panic, and a camera if they want anyone to care. RELATED LINKSJace Beats CancerJace Yawnick on LinkedImConquer Cancer ArticleCURE Today ArticlePyure BrandsFEEDBACKLike 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.

Connect the dots between AAC caregiver coaching and adult learning.Guest: Daj Mitchell, MS, CCC-SLPEarn 0.10 ASHA CEUs for this episode with Speech Therapy PDWatch on YoutubeMichelle Dawson, MS, CCC-SLP, CLC, BCS-S, FNAP, is joined by Daj Mitchell for a joyful discussion on powerful AAC caregiver coaching. Together, they explore Malcolm Knowles' Principles of Adult Learning and how these concepts can help SLPs better support caregivers throughout the AAC journey. Daj breaks down the four levels of caregiver readiness for AAC implementation and shares practical strategies for meeting families where they are. Gain ideas for tailoring AAC coaching conversations, strengthening caregiver engagement, and creating more meaningful opportunities for communication success across everyday routines.About the Guest: Daj Mitchell, MS CCC-SLP, graduated from Governors State University with her Bachelor's in Speech-Language Pathology and a minor in Psychology. She received her Master's in Speech-Language Pathology and Audiology from Illinois State University and holds a variety of certifications and awards, including, but not limited to, certification as a Lingraphica Technology Specialist, Level I and Level II Sensory certified, and a recipient of two successive ASHA ACE awards.Show Notes:Contact Daj on Instagram: @yourslpdajListen to Daj's Podcast: Co-Treat Corner: Collaboration Tips for Therapists Love Money: Support Spero Stuttering

What happens when the very thing you need most... peace, quiet, a day with nothing urgent, starts to make you anxious instead of relieved? In this episode, Charlotte explains how prolonged caregiving can train the nervous system to normalize hypervigilance, mistrust calm, and brace for the next crisis even when nothing is wrong in the moment. She talks about why rest can feel unfamiliar, why quiet can trigger scanning instead of ease, and why this response is not a personal failure but an intelligent adaptation to living inside ongoing uncertainty. Charlotte also shares a simple grounding practice to help you notice when your body is waiting for something to happen and begin collecting a different kind of evidence: that sometimes quiet is just quiet.

Show Summary On today's episode, we're having a conversation with Army Veteran Ramon Salazar, Senior Manager of Learning and Experience Design for PsychArmor, as well as Executive Director for Warriors At Ease, an organization dedicated to empowering the military and veteran community with the tools and knowledge to harness the transformative power of yoga and meditation.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 GuestRamón Salazar is a US Army Veteran with a diverse background in education and wellness. Holding a Master's degree in Education and experience in instructional design, he currently serves as an instructor at the University of Arizona. As an E-RYT 500 (Experienced Registered Yoga Teacher that has completed at leased 500 hours of advanced yoga teacher training and logged a minimum of 2,00 hours of teaching experience), Ramón brings a deep understanding of yoga practice, skillfully tailoring his approach to the specific needs of the military community. He incorporates trauma-informed techniques and mindful movement to foster healing and resilience. Ramón also holds various certifications in other wellness areas. His commitment to education and holistic well-being reflects his belief in yoga's power to positively impact individuals and communities.Links Mentioned in this Episode Ramon on PsychArmorWarriors At Ease websitePsychArmor Resource of the WeekThis week's resource of the week is PsychArmor's online course library, including many courses designed and led by Ramon. PsychArmor offers trusted, expert-led training for anyone who wants to better understand and support service members, Veterans, and their families. Whether you're a health care provider, educator, employer, caregiver, or simply someone who wants to make a difference — these courses are designed for you.You can find the resource here:https://learn.psycharmor.org/collections Episode Partner: Are you an organization that engages with or supports the military affiliated community? Would you like to partner with an engaged and dynamic audience of like-minded professionals? Reach out to Inquire about Partnership Opportunities Contact Us and Join Us on Social Media Email PsychArmorPsychArmor on TwitterPsychArmor 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  

Self-hate is not a personal feeling. It is the absorbed internal voice of a critical caregiver, mistaken for the self's own thought. You have been arguing with the wrong narrator for thirty years.This video walks through what self-hate actually is, why it has resisted every affirmation and every gratitude journal, and how the voice in your head was installed by a childhood caregiver before you had words to question it. If you have been trying to be kinder to yourself and the voice still wins, this names the speaker.Kenny Weiss is the creator of the Worst Day Cycle™, the Authentic Self Cycle™, and the Emotional Authenticity Method™. This teaching maps self-hate to the Three Internal Voices, the Shame-Based Child, the emotional download, and the survival persona that has been running on a caregiver's recording.Self-hate is not a personal feeling. It is the absorbed voice of a critical childhood caregiver, mistaken for the self's own thought. The voice was installed during the theta brainwave state of the first seven years and has been running in the first person ever since.Three voices live inside every adult, the Hurt Inner Child who is still longing, the Shame-Based Child who relays the caregiver's cruel definitions in the first person, and the Authentic Adult who knows underneath it all that something is off. When a person says I hate myself, it is almost never the Authentic Adult speaking.Affirmations, gratitude journals, and self-compassion practices cannot reach self-hate because they speak to the voice without questioning the source. A person cannot heal a voice they still think is theirs. They can only heal a voice they finally hear as not theirs.The Emotional Authenticity Method™ addresses self-hate at the speaker level. Its six steps trace the voice from somatic down-regulation through earliest memory to Feelization, where the body builds a new emotional addiction to the Authentic Self instead of to the inherited narrator.Kenny Weiss is a relationship, communication, and childhood trauma recovery specialist and the creator of the Worst Day Cycle™, the Authentic Self Cycle™, and the Emotional Authenticity Method™. He is the author of Your Journey To Success and Your Journey To Being Yourself.TOPICS COVERED: why do I hate myself, how to stop hating yourself, self-hate, inner critic, absorbed voice, shame-based child, three internal voices, why affirmations do not work, emotional download, Worst Day Cycle, Authentic Self Cycle, Emotional Authenticity Method, Kenny Weiss, survival persona, childhood blueprint0:00 — The Voice You Have Been Believing Is Not Yours1:30 — The Client Who Recognized Her Mother in Her Own Mouth3:00 — The Theta Brainwave Install of the Internal Narrator6:00 — The Three Voices and Who Is Actually Speaking9:00 — The Worst Day Cycle Around the Inherited Voice11:30 — Why Affirmations and Gratitude Have Not Worked13:00 — The Authentic Self Cycle Around the Speaker15:30 — The Emotional Authenticity Method as the Identification Tool18:00 — Identity Close

Send Cathy a text:)Have you ever taken a break, gone for a walk, met a friend for coffee, or asked for help... only to feel guilty afterward?You're not alone.In this episode, we're talking about the guilt that often shows up when caregivers finally start taking care of themselves.We'll explore: ✨ Why caregiver guilt is so common ✨ The stories we tell ourselves about self-care ✨ What guilt sounds like in everyday life ✨ A simple 4-step practice to help release guilt ✨ And why taking care of yourself isn't selfish—it's necessaryIf you've ever thought:

Share this program with a friend or family member at www.joniradio.org!  --------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.

On January 17, 2026, eighty-three-year-old Gail Crane was reported missing from her home in May's Lick, Kentucky. Investigators determined her former caretaker, Rita Lang, who had been let go the day prior, was a person of interest. Crane was located a hundred miles away inside Lang's vehicle with unexplained injuries. Lang was charged with kidnapping.Sixteen days later, eighty-four-year-old Nancy Guthrie was reportedly abducted from her home in the Catalina Foothills of Tucson, Arizona.Tony Brueski and Robin Dreeke examine the structural parallels between the two cases and whether the caregiver-orbit theory applies to the Guthrie investigation. Nancy lived alone with a predictable routine and a rotating set of individuals with access to her property and schedule. Investigators have publicly stated her family has been cleared.The central evidentiary challenge to this theory is the doorbell camera footage. The individual on Nancy's porch reportedly did not know the camera was present — a reaction inconsistent with someone who had regular access to the property. Robin provides the FBI behavioral framework for evaluating whether this detail eliminates the insider theory or whether a secondary scenario — an individual inside the orbit directing a third party — remains viable.The discussion also addresses investigative methodology: how the orbit list is constructed, what “cleared” means procedurally in an active investigation, and how far publicly available information could take a stranger.Join Our SubStack For AD-FREE ADVANCE EPISODES & EXTRAS!: https://hiddenkillers.substack.com/Want to comment and watch this podcast as a video? Check out our YouTube Channel. https://www.youtube.com/channel/UC8-vxmbhTxxG10sO1izODJg?sub_confirmation=1Instagram https://www.instagram.com/hiddenkillerspod/Facebook https://www.facebook.com/hiddenkillerspod/Tik-Tok https://www.tiktok.com/@hiddenkillerspodX Twitter https://x.com/TrueCrimePodThis publication contains commentary and opinion based on publicly available information. All individuals are presumed innocent until proven guilty in a court of law. Nothing published here should be taken as a statement of fact, health or legal advice.#NancyGuthrie #SavannahGuthrie #GailCrane #RitaLang #CaregiverAbduction #FBI #PimaCounty #TrueCrimeToday #Tucson #TrueCrime

Nancy Guthrie was eighty-four, lived alone in the Catalina Foothills, and kept a routine that put a rotating cast of people inside her world on a predictable schedule. Caregivers. Service workers. Contractors. Delivery drivers. The pool route. The landscaper. People who could stand in front of that house without anyone looking twice.Investigators have publicly cleared her family. But the family is not the orbit — and the orbit is where this theory lives.Sixteen days before Nancy vanished, eighty-three-year-old Gail Crane was taken from her Kentucky home by a caregiver who'd been let go the day before. Crane was found a hundred miles away, injured, inside the caregiver's vehicle. The caregiver was charged with kidnapping. The parallel is documented. Tony Brueski and Robin Dreeke test whether it maps to Tucson.The strongest piece of evidence fighting this theory is on Nancy's porch. The man in the doorbell footage clearly didn't know the camera was there — it stopped him cold. Anyone who regularly entered her life would have seen it. Robin examines whether the theory can survive that detail, how investigators actually build and cut down the orbit list in the first forty-eight hours, and the version where the face on camera was never inside her life — but the person who sent him was.What does “cleared” actually require in a case this public? Robin explains what has to check out before that word gets attached to anyone.Join Our SubStack For AD-FREE ADVANCE EPISODES & EXTRAS!: https://hiddenkillers.substack.com/Want to comment and watch this podcast as a video? Check out our YouTube Channel. https://www.youtube.com/channel/UC8-vxmbhTxxG10sO1izODJg?sub_confirmation=1Instagram https://www.instagram.com/hiddenkillerspod/Facebook https://www.facebook.com/hiddenkillerspod/Tik-Tok https://www.tiktok.com/@hiddenkillerspodX Twitter https://x.com/TrueCrimePodThis publication contains commentary and opinion based on publicly available information. All individuals are presumed innocent until proven guilty in a court of law. Nothing published here should be taken as a statement of fact, health or legal advice.#NancyGuthrie #SavannahGuthrie #GailCrane #InsiderTheory #DoorbellCamera #PimaCounty #FBI #Tucson #HiddenKillers #TrueCrime

Text your thoughts and questions!Many women spend their lives carrying invisible responsibilities for their families without ever realizing how much energy, thought, and emotional labor those responsibilities require. Whether it's keeping the peace, anticipating needs, preserving family traditions, or caring for aging parents, daughters are often expected to do it all—and do it well. The challenge is that these expectations can become so ingrained that many women never stop to ask an important question: How much is enough?This week, in episode 318 of the Positively LivingⓇ Podcast, I sit down with Dr. Allison Alford, communication scholar, researcher, and author of Good Daughtering: The Work You've Always Done, the Credit You've Never Gotten, and How to Finally Feel Like Enough. Allison shares insights from more than a decade of research on the often-unspoken role of adult daughters, exploring the invisible labor they perform, the societal expectations they carry, and how women can redefine what it means to be a "good enough" daughter.Dr. Allison M. Alford is a communication scholar, researcher, professor at Baylor University, and leading expert on the experience of adult daughters. Through years of interviews and research, she has examined the emotional, cognitive, logistical, and identity-based labor women perform within families. Her work helps daughters recognize their contributions, challenge unrealistic expectations, and create healthier, more sustainable relationships with their families and themselves.Key Takeaways:Daughtering is more than caregiving. It includes the ongoing emotional, cognitive, logistical, and identity work daughters perform to keep families connected and functioning.Much of a daughter's labor is invisible. While tasks like visits and phone calls are visible, the planning, worrying, emotional management, and family coordination often go unnoticed.Society places unique expectations on daughters. Women are often expected not only to care for family members but to do so willingly, skillfully, and without complaint.The mental load extends beyond remembering tasks. Daughters frequently anticipate problems, navigate family dynamics, and remove obstacles before anyone else notices them.Emotional labor has a real cost. Acting as the peacemaker, confidant, or emotional "thermostat" for a family can lead to exhaustion, overwhelm, and burnout.Birth order and family structure can influence daughtering experiences. Eldest daughters and only daughters often feel heightened responsibility, though every family dynamic is unique.You have agency to redefine your role. Even long-standing family patterns can be reassessed, and it's possible to establish healthier expectations and boundaries.Being a "B+ daughter" is enough. Striving for perfection isn't sustainable. Leaving room for your own needs, relationships, and well-being allows you to show up for your family without losing yourself in the process.The invisible work you do for your family matters. But so do your needs, your capacity, and your well-being. You don't have to earn your worth through endless giving. What would change if you allowed yourself to believe that you are already enough?Thank you for listening! If you enjoyed this episode, take a screenshot of the episode to post in your stories and tag me!  And don't forget to follow, rate, and review the podcast and tell me your key takeaways!Learn more about Positively LivingⓇ and Lisa at https://positivelyproductive.com/podcast/Stop trying to fit into someone else's productivity rules! Grab my free Productivity Toolkit, a collection of workbooks designed to help you explore how you work, uncover what truly matters to you, and create your very own energy-friendly systems. Get it here: www.positivelyproductive.com/plpkitCONNECT WITH DR. ALISON ALFORD:WebsiteInstagramFacebookTikTokCONNECT WITH LISA ZAWROTNY:FacebookInstagramResourcesWork with Lisa! LINKS MENTIONED IN THIS EPISODE:Good Daughtering: The Work You've Always Done, the Credit You've Never Gotten, and How to Finally Feel Like Enough(Find links to books/gear on the Positively Productive Resources Page.)Episode 156: How to Reduce Mental Load as a Parent or Caregiver with Roxanne FerberBook a Clarity CallLibby AppDance Song Playlist V1, V2, V3Music by Ian and Jeff ZawrotnyStart your own podcast with Buzzsprout!The Self-Care to Wellness Bundle is available for 1 week only - from July 9th - July 16th

This time on Code WACK! What role do family members and friends play in the lives of nursing home residents? When COVID hit, how were residents impacted when their loved ones were no longer allowed to visit them?  Today, we share the story of Melody Taylor Stark, who became an advocate for the Essential Caregivers Act after her husband, a retired dentist and nursing home resident, dramatically declined, then died, after being denied her daily visits during the dark days of COVID.  Melody is a founding member of Essential Caregivers Coalition, a member of Caregivers for Compromise, and San Gabriel Valley Disability Collaborative, and Facebook co-administrator for Aging Enlightened, a group that was begun by a prominent reporter for Kaiser Health News. She works diligently to advance positive system changes in disability rights and long-term care. This is part one of a two-part series on the Essential Caregiver's Act.  Check out the Transcript and Show Notes for more! And please keep Code WACK! on the air with a tax-deductible donation at heal-ca.org/donate.  

Forty years ago, following the first surgery I went through with Gracie, the doctor told me to take a break. So I went to a movie. While I was gone, people questioned my commitment, my character, and whether I could handle being a caregiver at all. Decades later, another surgeon faced with one of Gracie's most complex surgeries gave me the exact same instruction: "Go see a movie." In this episode, I explore what that experience taught me about caregiver guilt, boundaries, stewardship, and learning what is—and isn't—mine to carry. I also revisit one of the most powerful load-bearing hymns ever written, It Is Well With My Soul, and explain why grieving people continue to find strength in its timeless words. If you've ever felt guilty for resting, struggled with criticism, or wondered how to stay healthy while caring for someone who isn't, this episode is for you. Healthy Caregivers Make Better Caregivers™

The “sandwich generation” is made up of people balancing the demands of raising children while caring for aging loved ones. This hour, we learn about the emotional, professional and financial realities facing this population of caregivers. Journalist Kelli María Korducki discusses her reporting on caregiving and career sacrifice, while University of Connecticut professor Laura Mauldin offers insight into the gender dynamics of care. And later, we hear from a Connecticut resident and member of the "sandwich generation.” We learn what it's like to navigate these responsibilities in everyday life and what policies could provide some relief. Guests: Kelli María Korducki: independent, New York City-based journalist and author Laura Mauldin: associate professor in the Department of Social and Critical Inquiry at the University of Connecticut and author of "In Sickness and Health: Love Stories from the Front Line of America’s Caregiving Crisis." Natalie Shurtleff: Associate State Director of Advocacy and Outreach for AARP Connecticut Support the show: http://wnpr.org/donateSee omnystudio.com/listener for privacy information.

As part of the 2026 Developmental Disabilities Conference, Tamar Heller, Director, Institute on Disability and Human Development, University of Illinois Chicago, discusses aging and aging caregivers. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 41459]

This time on Code WACK! What role do family members and friends play in the lives of nursing home residents? When COVID hit, how were residents impacted when their loved ones were no longer allowed to visit them? Today we share the story of Melody Taylor Stark, who became an advocate for the Essential Caregivers Act after her husband, a retired dentist and nursing home resident, dramatically declined, then died, after being denied her daily visits during the dark days of COVID. Melody is a founding member of Essential Caregivers Coalition; a member of Caregivers for Compromise, and San Gabriel Valley Disability Collaborative; and Facebook co-administrator for Aging Enlightened, a group that was begun by a prominent reporter for Kaiser Health News. She works diligently to advance positive system changes in disability rights and long-term care. This is part one of a two-part series on the Essential Caregiver's Act. Please keep Code WACK! on the air with a tax-deductible donation at heal-ca.org/donate.

As part of the 2026 Developmental Disabilities Conference, Tamar Heller, Director, Institute on Disability and Human Development, University of Illinois Chicago, discusses aging and aging caregivers. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 41459]

As part of the 2026 Developmental Disabilities Conference, Tamar Heller, Director, Institute on Disability and Human Development, University of Illinois Chicago, discusses aging and aging caregivers. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 41459]

Aportaciones de inmigrantes a la vida de Estados Unidos y la forma de hacer que los caballos se acostumbren poco a poco desde su nacimiento a las personas, historia narrada por Francisco desde su rancho.

Holly Hess from CICOA Aging & In-Home Solutions joins us for a helpful conversation about dementia support, Memory Cafés, Dementia Friends Indiana, and how families can take the first step when they are not sure where to turn. We talk about what a dementia friendly community looks like in everyday life and how CICOA helps older adults, people with disabilities, and caregivers find resources that fit their needs. We also look at Indianapolis' clinician led response teams and the Hoosier Heroes preparing for the National Veterans Golden Age Games.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

We wrap up the season with scores and highlights of the week on the Raider Scoreboard with Jimmy LeRue. Head Coach of the Girls track team, Janet Smith recaps the results of the State Highschool track meet. She also talks about being the commencement speaker at this years graduation and the fund raising event at […]

Who has the authority to make educational decisions for a student? In this episode, host Michelle Cannon is joined by Lozano Smith attorneys Amanda Cordova and Anna Wood to discuss the legal framework surrounding educational rights, including special education considerations. The conversation explores custody arrangements, caregiver authority, AB 495, and when students hold their own educational rights. Join us as we explore practical guidance for navigating custody orders and other common educational rights issues faced by school districts. Show Notes & References 2:30 – Overview of educational rights 4:05 – Educational rights unique to parents of students who qualify for special education 5:45 – Parents and others who qualify as educational rights holders 7:23 – Custody arrangements for divorced, separated or unmarried parents 9:53 – Disagreements between parents with joint legal custody and how school districts should respond 11:32 – The importance of asking for custody orders 12:03 – Rights of parents who do not hold custodial rights 13:25 – What school administrators should be looking for when they receive a custody order 16:30 – Stepparents and caregivers, and assigning educational rights 18:23 – Assembly Bill (AB) 495 and caregiver’s affidavit (Client News Brief 46 – November 2025) 19:12 – Adult students holding their own educational rights   For more information on the topics discussed in this podcast, please visit our website at: www.lozanosmith.com/podcast   Disclaimer: As the information contained herein is necessarily general, its application to a particular set of facts and circumstances may vary. For this reason, this podcast episode does not constitute legal advice. We recommend that you consult with your counsel prior to acting on the information contained herein.

At 20 years old, newly arrived from Puerto Rico and trying to build a future in science, Benjamin Suarez Jimenez found himself sitting in front of two senior faculty members accused of plagiarism. He knew the material. He had done the work. His mistake came from failing to cite class notes during an exam because nobody had told him that was expected. In a matter of minutes, he watched what felt like his entire career flash before him.On this episode of Standard Deviation, host Oliver Bogler examines the hidden architecture of academic science through the experiences of Dr. Benjamin Suarez Jimenez, Assistant Professor at the University of Rochester and a neuroscientist studying PTSD, anxiety, trauma, and spatial cognition through virtual reality and video game environments.Benjamin traces his path from Puerto Rico to the mainland United States, through the NIH, Columbia University, and eventually to leading his own laboratory. Along the way, he encountered a series of barriers that had little to do with scientific ability and everything to do with access to unwritten rules. From academic gatekeeping to grant writing expectations, he learned that success in biomedical research often depends on knowledge that never appears in a textbook.Oliver explores how those invisible obstacles shape careers, influence research funding, and determine who gains access to opportunity. The conversation also examines the Justice, Equity, Diversity, and Inclusion Program at the Life Science Editors Foundation, which pairs scientists from underrepresented backgrounds with experienced scientific editors. Through that mentorship, Benjamin transformed a critical grant proposal into a successful pilot award that helped launch an NIH R01 application.The discussion extends beyond one scientist's experience. Benjamin describes helping a former mentee navigate dissertation roadblocks that threatened her graduation, illustrating how institutional bureaucracy can delay careers and discourage talented researchers. Together, they explore the hidden administrative burden, cultural barriers, and bias that many scientists carry alongside their research, and what happens when someone who receives support turns around and opens the door for others.RELATED LINKSLife Science Editors FoundationBenjamin Suarez Jimenez LabDr. Benjamin Suarez JimenezBenjamin Suarez JimenezFEEDBACKLike 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.

If your loved one with Alzheimer's disease is on one of the new treatment drugs, or you have been weighing whether to try them, the headlines from this spring may have stopped you cold. A major review from one of the most respected research organizations in the world concluded these drugs show no meaningful benefit. Researchers immediately fired back. And you are in the middle of all of it, as a caregiver trying to make real decisions for a real person. Your confusion is completely warranted. This is not a simple story. One headline says breakthrough. The next says it does nothing. But the full picture is more complicated than either side is telling you. In this episode I walk you through what the Cochrane review actually found, why experts are so divided on it, and the three questions you can bring to your loved one's neurologist to make a more informed decision for your specific family. Cochrane Collaboration Review (Full Study): https://www.cochrane.org/about-us/news/anti-amyloid-alzheimers-drugs-show-no-clinically-meaningful-effect  Get free weekly tools and tips in my newsletter, The Dementia Dose: https://tinyurl.com/dementiadose-podcast  Join the Care Collective: https://tinyurl.com/podcast-cc  ⏱ CHAPTERS  0:00 - The headlines that stopped caregivers  1:46 - Who these drugs are actually designed for  2:56 - What the Cochrane review found  5:26 - Why researchers are pushing back  7:50 - 3 questions to ask your loved one's doctor #dementia #dementiacaregiver #alzheimers #caregiving #alzheimersresearch --- 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.

Dr. Sarah Matt trained as a burn surgeon, working in a field where patients arrive with catastrophic injuries and survival depends on speed, skill, and resources. She left the bedside after confronting a limit that medicine does not like to admit. One physician can only see so many people in a day. The system surrounding those patients decides the rest. She moved into health technology, held leadership roles in startups, and built global infrastructure at Oracle to scale care across populations. Then she watched billions of dollars in digital health and AI initiatives stall out when they hit real clinical environments.This episode follows that pivot from surgeon to strategist and back into direct patient care in rural New York, where she now treats uninsured patients, migrant workers, and communities pushed to the margins. The conversation centers on a persistent failure across healthcare systems. Products get built for regulators, executives, and investors instead of the people who use them. The result shows up in failed adoption, broken workflows, prior authorization delays, and rising physician burnout.The discussion cuts through health policy language and lands on lived consequence. The system rewards speed over usability, scale over trust, and compliance over care. Patients absorb the fallout. Physicians carry the liability. The incentives remain intact.RELATED LINKSDr. Sarah MattThe Borderless Healthcare RevolutionThe Clinical RealistJessica FedererSovatoFEEDBACKLike 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.

Joann returns with her daughter, Erika, to provide her perspective on why she does not want her grandfather to attend her graduation ceremony. The discussion focuses on Erika's feelings, personal concerns, and the family dynamics influencing her decision. Call 1-800-DR-LAURA / 1-800-375-2872 or make an appointment at DrLaura.com Follow me on social media: Facebook.com/DrLaura Instagram.com/DrLauraProgram YouTube.com/DrLaura Join My Family!! Receive my Weekly Newsletter + 20% off my Marriage 101 course & 25% off Merch! Sign up now, it's FREE! Each week you'll get new articles, featured emails from listeners, special event invitations, early access to my Dr. Laura Designs Store benefiting Children of Fallen Patriots, and MORE! Sign up at DrLaura.com Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

David never expected his marriage to shift from partnership to full-time caregiving. As his wife's health problems grow, he's feeling emotionally exhausted, overwhelmed, and unsure how to balance love, responsibility, and his own needs.  Call 1-800-DR-LAURA / 1-800-375-2872 or make an appointment at DrLaura.com Follow me on social media: Facebook.com/DrLaura Instagram.com/DrLauraProgram YouTube.com/DrLaura Join My Family!! Receive my Weekly Newsletter + 20% off my Marriage 101 course & 25% off Merch! Sign up now, it's FREE! Each week you'll get new articles, featured emails from listeners, special event invitations, early access to my Dr. Laura Designs Store benefiting Children of Fallen Patriots, and MORE! Sign up at DrLaura.com Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.