Podcasts about caregivers

As co-founder of Soaring Families, Mike George transformed his personal experience into impact, helping families move from survival mode to resilience and joy. He leaned on his background in AI, process improvement, and enterprise systems to develop The Soaring Families Way™, a structured yet compassionate approach that equips families with practical tools to regain control, reduce stress, and find fulfillment. https://www.seniorcareauthority.com/resources/boomers-today/

In this heartfelt interview, Martha shares her journey of resilience and faith following her husband's traumatic brain injury. Discover how community, faith, and perseverance have shaped her path of caregiving, healing, and giving back. Martha Boswell is a full time caregiver for her husband David, a traumatic brain injury survivor. She plans events and hosts Caregiver Coffees for the Brain Injury Association of Louisiana, and she is the author of four books. Her latest novel, Nothing to Lose, is a faith-based fictional account of life with a brain injury—a story of redemption and resilience—available on Amazon. She loves spending time with her family and connecting with other caregivers. Please connect on Facebook @supperontheshelf Instagram @tbiwifelife   Chapters 00:00 Introduction and Martha's Background 01:10 Perseverance and Faith in the Journey 02:06 Husband's Injury and Initial Shock 04:39 Life Before and After the Injury 09:23 The Fall and Immediate Aftermath 12:28 Medical News and Family's Response 14:05 Miracle Moment: Eyes Open in January 16:25 Early Rehabilitation and Challenges 19:43 Insurance and Financial Stress 21:28 Living with a Changed Husband 23:30 Rebuilding Marriage and Hope 26:29 Motivation and Purpose in Recovery 28:54 Living Safely and Caregiver Strategies 31:23 Support Groups and Community Resources 33:40 Faith as the Foundation 36:26 Lessons Learned and Resilience 38:37 Dark Moments and God's Use of Suffering 41:08 Creative Outlets and Healing 43:43 Self-Regulation and Spiritual Strength 45:52 Community Events and Support Initiatives 48:54 Connecting and Outreach Efforts 50:25 Recovery, Resilience, and Restoration 52:23 Hope in Eternity and Present Moments 54:20 Closing Remarks and Gratitude

From Fear to Peace: Growing Spiritually as a Dementia Caregiver by Linda Knebel Pruden Lindaknebelpruden.com https://www.amazon.com/Fear-Peace-Spiritually-Dementia-Caregiver-ebook/dp/B0F7J3DJ3F An instant #1 New Release in Dementia. This spiritual growth book explores Linda Pruden’s experience as a dementia caregiver for her husband. Inspired by his own determination to find spiritual gifts embedded in the journey, her story provides encouragement for those living with a chronic illness and the people who love them. “A powerful read for caregivers facing the journey of caring for someone with dementia. Her growth and faith over years of caring for Rob is an amazing blend of self-discovery and acceptance. An incredibly validating and relatable read.” —Lisa M. Brown, MSW, LISW, caregiver services program coordinator for Lyngblomsten Community Services When Linda’s husband, Rob, was diagnosed with dementia, he described it as a gift and an opportunity to grow spiritually. As things grew more difficult, Linda remembered these words and began her mission to live out his hopes. Offering a fresh, positive outlook on serving as a dementia caregiver, From Fear to Peace is a reassuring road map for any faith-testing journey. Linda Knebel Pruden is an author and national speaker residing in St. Paul, Minnesota. She received her master’s degree in speech/language pathology from Purdue University, and went on to write five books for teachers, as well as her award-winning memoir, Reflections on a Changing Family. Having grown through the experience of being a caretaker, it is now her passion to help others unbury their own truths and find beauty in painful times. This book covers caring for dementia, but is also an essential read for . . . people hoping for spiritual growth and peace, those looking to effectively provide caregiver support, and families needing a guide for walking in grace. During the hardest of times, Linda’s words help readers to let go of expectations and hold tight to hope . . . it’s only then that we can move from fear to peace. “Linda has created tools that will guide you through those darkest hours of transitions and fears. It is a story of empowerment and gratitude.” —Kristin Burich, healing facilitator About the author Linda Knebel Pruden is an author and national speaker residing in St. Paul, Minnesota. She received her master's degree in speech/language pathology from Purdue University, and went on to write five books for teachers, as well as her award-winning memoir, Reflections on a Changing Family. Having grown through the experience of being a caretaker, it is now her passion to help others unbury their own truths and find beauty in painful times.

Episode Summary: Caring for others is one of the most beautiful expressions of Christlike love, yet it can also be one of the most exhausting. Whether someone is caring for an aging parent, a chronically ill spouse, a child with special needs, or a friend struggling through a difficult diagnosis, caregivers often experience emotional fatigue, compassion overload, and spiritual depletion. In honor of National Caregiver’s Day, today on Your Hope-Filled Perspective we are shining a bright and honoring spotlight on caregivers who quietly pour out strength and tenderness day after day. If you are a caregiver who feels seen and unseen all at once, this conversation is for you. Quotables from the episode: In this episode we want to acknowledge the deep emotional and spiritual cost that comes with caregiving, whether it’s caring for children, spouses, parents or someone else. Many caregivers love fiercely yet carry silent burdens. They often neglect their own rest while tending to the needs of others. They juggle responsibilities, appointments, medications, medical decisions, financial pressures, and emotional strain until their own souls feel frayed. If that describes you, know that God sees every moment of sacrifice. He understands every tear cried in private. He knows how heavy this calling can feel. Whether you are in a short-term caregiving season or you have been carrying this responsibility for years, we want to help you find strength, rest, and spiritual renewal. Yet God created rest not as a luxury but as a divine necessity. He invites caregivers to receive the strength they need directly from His presence. Caregivers often do not realize how overwhelmed they are until they are already close to burnout. They believe they should be able to keep going. They think rest is selfish. They feel guilty for asking for help. But caregiving is not meant to be a one-person mission. Caregiver burnout does not happen overnight. It happens slowly and quietly, often while someone is trying to be strong for everyone else. God never intended caregiving to be an isolating burden. Galatians teaches us to carry one another’s burdens. That includes the weight of caregiving. Asking for help is not a failure. It is a biblical principle If you have begun feeling resentful or emotionally disconnected, that is a powerful signal that your soul is in need of restoration. You cannot pour out what has not been filled. I want caregivers to hear this truth. You are not responsible for outcomes. You are responsible to love well and to walk faithfully, but God holds the results. Scripture References: Isaiah 40:29 “He gives strength to the weary and increases the power of the weak.” Psalm 73:26 “My flesh and my heart may fail, but God is the strength of my heart and my portion forever.” Psalm 18:28 “You, Lord, keep my lamp burning; my God turns my darkness into light.” Jeremiah 31:25 “I will refresh the weary and satisfy the faint.” Recommended Resources: Free Caregiver Burnout Warning Sign Checklist Reframing Rejection: How Looking Through a Different Lens Changes Everything By Jessica Van Roekel Sacred Scars: Resting in God’s Promise That Your Past Is Not Wasted by Dr. Michelle Bengtson The Hem of His Garment: Reaching Out To God When Pain Overwhelms by Dr. Michelle Bengtson Today is Going to be a Good Day: 90 Promises from God to Start Your Day Off Right by Dr. Michelle Bengtson Breaking Anxiety’s Grip: How to Reclaim the Peace God Promises by Dr. Michelle Bengtson Breaking Anxiety’s Grip Free Study Guide Free PDF Resource: How to Fight Fearful/Anxious Thoughts and Win Hope Prevails: Insights from a Doctor’s Personal Journey Through Depression by Dr. Michelle Bengtson Hope Prevails Bible Study by Dr. Michelle Bengtson Free Webinar: Help for When You’re Feeling Blue Social Media Links for Host and Guest: Connect with Rev. Jessica Van Roekel: Website / Instagram / Facebook Connect with Dr. Bengtson: Order Book Sacred Scars / Order Book The Hem of His Garment / Order Book Today is Going to be a Good Day / Order Book Breaking Anxiety’s Grip / Order Book Hope Prevails / Website / Blog / Facebook / Twitter (@DrMBengtson) / LinkedIn / Instagram / Pinterest / YouTube / Podcast on Apple Co-Host: Jessica Van Roekel is a worship leader, speaker, and writer who believes that through Jesus, personal histories don’t need to define the present or determine the future. She inspires, encourages, and equips others to look at life through the lenses of hope, trust, and God’s transforming grace. Jessica lives in rural Iowa surrounded by wide open spaces which remind her of God’s expansive love. She loves fun earrings, good coffee, and connecting with others. Hosted By: Dr. Michelle Bengtson Audio Technical Support: Ashton Bengtson Discover more Christian podcasts at lifeaudio.com and inquire about advertising opportunities at lifeaudio.com/contact-us.

The most misunderstood symptoms of Alzheimer's and dementia are behavioral changes such as agitation, aggression, and social withdrawal. Author Lisa Skinner, in her book Truth, Lies & Alzheimer's: Its Secret Faces, identifies these as the "secret faces" of the disease—non-verbal communication used when a patient can no longer express physical pain or fear through words. Families often mistake these for personality flaws rather than neurological symptoms. While standard medical advice often focuses on "reality orientation"—constantly correcting a patient's confusion—Skinner advocates for an unconventional path that prioritizes emotional peace of mind over factual accuracy. This approach meets the patient in their own reality to reduce dementia-related distress, shifting the focus from clinical management to emotional validation. The "Truth vs. Lie" dynamic is a cornerstone of this compassionate care model. Skinner argues that "therapeutic fibbing" is often the kinder choice. Forcing a patient to face a painful truth, such as the death of a spouse decades ago, causes them to relive traumatic grief repeatedly. Entering their world to provide comfort is a more humane alternative than a truth that causes unnecessary psychological harm. In the realm of regenerative medicine, as highlighted in Skinner's work with Dr. Anand Srivastava, the narrative of brain diagnoses is shifting from inevitable decline toward potential cellular repair. Advances in stem cell research and cellular rejuvenation offer a future where "devastating" diagnoses are viewed through the lens of biological mitigation and neuro-regeneration rather than just symptom management. For caregivers navigating the "relentless pace" of the caregiver's gauntlet, the most immediate mental health shift is to Release the Guilt. Recognizing that "you cannot pour from an empty cup" is essential. Skinner emphasizes that accepting personal limitations and acknowledging that "good enough" care is more sustainable than perfectionist burnout is the first step toward reclaiming mental well-being. Web: https://www.mindingdementiasum... - Looking for that extra spark to level up your life? Say hello to Ash Brown—your go-to American powerhouse, motivational speaker, and the ultimate hype-woman for your personal and professional growth. Ash isn't just a voice in personal development; she's a trusted friend who brings real-talk wisdom and contagious energy to every conversation. Whether you're stuck in a rut or ready to scale your dreams, Ash is here to fuel your journey with a mix of heart and hustle.

The Silent Threat Women Face Heart disease remains the number one killer of women in America, yet nearly half of all women fail to recognize it as their greatest health threat. During a recent Community Health episode of The Valley Today, host Janet Michael talks with Dr. April Shewmake, a board-certified interventional cardiologist at Winchester Cardiology and Vascular Medicine I Valley Health, to uncover the truth about cardiovascular health. What emerged was a compelling conversation that challenges common misconceptions and empowers listeners to take control of their heart health. Understanding the Specialist's Perspective Dr. Shewmake brings a unique dual expertise to her practice. As an interventional cardiologist, she treats heart attack emergencies in the catheterization lab using minimally invasive procedures to open blocked arteries. However, she emphasizes that general cardiology—the preventive side of her work—plays an equally vital role. "Before things become an emergency or a heart attack," she explains, "that's the general cardiology piece." This preventive approach focuses on long-term care, diagnostic imaging, and medication management to stop heart disease before it starts. The Prevention Paradox Perhaps the most striking revelation from the conversation centers on prevention. According to Dr. Shewmake, between 70 and 90 percent of heart disease is entirely preventable. This statistic transforms heart health from a matter of fate into one of choice. The key lies in daily habits that many people overlook: maintaining a healthy diet, exercising regularly, controlling blood pressure, managing stress, getting adequate sleep, and remaining tobacco-free. Nevertheless, Dr. Shewmake acknowledges that genetics do play a role. Some patients develop heart disease despite doing everything right. This reality underscores why awareness and early detection remain crucial, even for those who maintain healthy lifestyles. Recognizing the Warning Signs When it comes to identifying potential heart problems, Dr. Shewmake urges people to pay attention to specific symptoms. The major warning signs include chest pressure, shortness of breath, fatigue, dizziness, nausea, and pain radiating to the jaw, arms, or back. Critically, symptoms that appear during physical exertion and improve with rest signal early-stage heart disease. Furthermore, Dr. Shewmake dispels the Hollywood myth that distinguishes heart attacks from indigestion. In reality, many people—particularly young adults and women—delay seeking treatment because they assume their symptoms indicate simple indigestion. Women especially tend to experience atypical presentations, manifesting nausea and shortness of breath rather than classic chest pain. "Don't delay," she insists. "If you think something's wrong, come to the hospital." The 911 Rule Dr. Shewmake reinforces a critical safety message: never drive yourself to the hospital if you suspect a heart attack. Instead, call 911 immediately. Emergency medical services can begin life-saving treatment en route, significantly improving outcomes. This advice echoes the guidance of other cardiologists and represents a consensus among heart specialists. Women's Unique Risk Profile The conversation takes a deeper dive into the specific challenges women face regarding heart disease. Dr. Shewmake reveals that nearly 45 percent of women over age 20 have cardiovascular disease, yet less than half recognize this reality. Heart disease kills more women than all cancers—including breast cancer—combined, claiming one in three female lives. Moreover, women face distinct risk factors that men do not encounter. Hormonal changes during menopause, pregnancy-related complications, and autoimmune conditions all contribute to cardiovascular risk. Additionally, women often present with symptoms later in life but develop more complex disease. The medical community sometimes dismisses women's symptoms, compounding the problem. The Caregiver's Dilemma Janet raises an important point about women's tendency to prioritize others' health over their own. Women rush their husbands and children to the doctor at the first sign of trouble, yet they dismiss their own symptoms as minor inconveniences. Dr. Shewmake validates this observation and emphasizes the need to close the gap in how heart disease gets recognized and treated in women. She advocates for reframing primary care visits as self-care—an hour dedicated to one's own wellbeing. Using the airplane oxygen mask analogy, she reminds women that they must take care of themselves first to remain available for their families.  The Rising Threat to Young Adults Alarmingly, cardiovascular disease increasingly affects younger populations. Dr. Shewmake shares that her youngest female heart attack patient was 38, while her youngest male patient was just 30. Janet recounts the tragic story of her son's two high school friends—both in their early thirties—who died from heart attacks within three months. This trend stems from rising cardiovascular risk factors among young people, including diabetes, high blood pressure, and high cholesterol appearing at earlier ages. Additionally, genetics likely play a stronger role in these younger cases. Young adults often assume they're invincible, delaying treatment when symptoms appear. This dangerous mindset can prove fatal. Know Your Numbers Throughout the conversation, Dr. Shewmake repeatedly emphasizes the importance of knowing four critical numbers: cholesterol, blood pressure, BMI, and blood sugar. These metrics serve as early warning indicators for heart disease risk. She encourages everyone to discuss these numbers with their primary care physician and take action when they fall outside healthy ranges. Importantly, all these risk factors respond to treatment. Modern medicine offers excellent options for managing weight, cholesterol, and blood sugar. Some newer weight-loss medications not only help patients shed pounds and lower A1C levels but also provide cardiovascular benefits. These treatments represent powerful tools in the fight against heart disease. The Technology Trap When Janet mentions the false sense of security that fitness trackers provide, Dr. Shewmake agrees wholeheartedly. While devices like the Apple Watch offer some benefits, they cannot replace a comprehensive medical evaluation. No wearable technology can measure cholesterol levels, assess blood glucose, or provide the nuanced analysis that comes from a conversation with a healthcare provider. The Path Forward Dr. Shewmake welcomes referrals from primary care physicians when patients need specialized cardiovascular assessment. She sees many patients who request consultations even when their primary care doctors deem it unnecessary, and she views these visits as valuable opportunities for in-depth risk evaluation. Cardiologists can order specialized tests and provide individualized guidance that goes beyond population-level statistics. Breaking the Biggest Myth As the conversation concludes, Dr. Shewmake tackles the most dangerous misconception about heart disease: that it primarily affects men. While society recognizes heart attacks as the leading killer of men, this awareness doesn't extend to women. This gap in understanding costs lives. Her final message centers on empowerment. She urges everyone—especially women—to listen to their bodies, take symptoms seriously, and advocate for themselves when they know something feels wrong. Heart disease may be common, but it remains both preventable and treatable. Early action saves lives, and awareness changes everything. The Simple Truth Ultimately, Dr. Shewmake's message boils down to simple, actionable steps: eat well, move more, manage stress, get enough sleep, know your numbers, and remain tobacco-free. These everyday habits make a profound difference in cardiovascular health. Combined with regular medical care and self-advocacy, they form a powerful defense against America's leading cause of death. The conversation serves as both a wake-up call and a roadmap. Heart disease doesn't discriminate, but knowledge and action provide protection. By recognizing symptoms early, understanding personal risk factors, and prioritizing preventive care, individuals can take control of their heart health and potentially add years to their lives.

Rosanne Corcoran knows caregiving from the inside. When her mother moved in with vascular dementia, Rosanne became her primary caregiver for years, navigating the daily realities, emotional toll, and quiet endurance that so often go unseen. Today, she channels that lived experience into advocacy as a support-circle leader and podcast host with Daughterhood, a community built to reduce isolation and provide support to caregivers. With an estimated 63 million caregivers in the U.S., and 44% of them providing high levels of care, this conversation matters more than most of us realize. As Rosanne puts it: “Caregivers at the core are isolated, overwhelmed, carrying guilt, and living with grief, and almost no one recognizes any of that.” If you are a caregiver – or know someone who is – listen in, share this episode, and help make the invisible labor of caregiving visible.

Sarah Gromko and Matthew Zachary go back to SUNY Binghamton in the early 1990s, when they were barely 19 and living inside rehearsal rooms. She starred in campus musical theater productions. He served as pianist and music director for many of those shows and played rehearsal piano for the THEA101 repertory company. This episode reunites two former theater nerds who grew up and took very different paths through art, illness, and work that still circles the same truth.Gromko trained as a singer and composer, studied film scoring at Berklee College of Music, worked in New York and New Orleans, then moved into healthcare as a speech language pathologist and recognized vocologist. She explains aphasia, apraxia, dysarthria, and dysphagia with clarity earned from the clinic. She recounts helping a 16 year old gunshot survivor in New Orleans speak again using Melodic Intonation Therapy. The conversation covers voice banking for ALS, gender affirming voice care, and the damage caused when medicine confuses speech loss with intelligence loss. The result feels like an epic reunion powered by 1990s nostalgia and sharpened by decades of lived consequence.RELATED LINKSSarah GromkoGramco VoiceMelodic Intonation 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.

You brought them home from the hospital. Everyone celebrated.But instead of relief, you felt dread.In this first episode of our four-part series, The Things You Don't Say Out Loud, we're naming something many cancer caregivers experience but rarely admit:Loneliness.Not the kind that comes from being physically alone.The kind that settles behind your ribs.The kind that shows up at 2:00 AM.The kind that grows when everyone calls you “strong.”Caregiver loneliness is complicated. You're surrounded by people—doctors, texts, meal trains, family. And still, you can feel completely unseen.In this episode, we talk about:Why hospital discharge can bring dread instead of reliefThe loneliness of being “the strong one”The quiet erosion of friendships during caregivingThe weight of making medical decisions aloneWhy well-meaning support sometimes misses the markThe difference between solitude and lonelinessWhat it actually means to be witnessedAnd most importantly, you'll walk away with a simple nightly practice you can do in less than 2 minutes to begin seeing yourself again.Because the goal isn't to fix you.It's to help you feel seen.

Show SummaryOn this episode, we have a conversation Today we're having a conversation with Michael Witt, Community & State Outreach Manager for the DirectEmployers Association. DirectEmployers is a non-profit member association built by employers, for employers, and we talked about how they support their member employers to better serve the military and veteran population as well as how DirectEmployers has worked to become a PsychArmor Veteran Ready OrganizationProvide 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 Witt is the Community & State Outreach Manager for DirectEmployers Association (DE). DE is a non-profit member association built by employers, for employers. After 21 years of service with Iowa Workforce Development, including Division Administrator of Field Operations, oversight of WIOA federal programs and state workforce programs, he works closely with DE's 1k+ Member companies to implement strategies for improved recruitment and retention of skilled talent across the country.Links Mentioned During the EpisodeDirectEmployers Association WebsiteDirectEmployers VetCentral Webpage PsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week is the Behind the Mission Podcast episode with Lori Adams, in episode 122. During this conversation, Lori and I talk about the National Association of State Workforce Agencies, the national organization representing all 50 state workforce agencies, D.C. and U.S. territories. These agencies deliver training, employment, career, business and wage and hour services, in addition to administering the unemployment insurance, veteran reemployment and labor market information programs. You can find the resource here:  https://psycharmor.org/podcast/lori-adams  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  

Send Cathy a text:)We're about two-thirds of the way through Season 2, and before we move forward, I felt a pull to slow down.No new framework. No new acronym. No fresh hack to master.Just you and me.Because underneath rhythm, boundaries, resets, time management, and emotional protection… there's one core truth:You can't pour from a cup that's quietly leaking.In this bonus episode, we gently explore what an “energy leak” really is — and why so many caregivers feel exhausted even when they haven't “done that much.”Energy leaks aren't always dramatic. They often look like:The conversation you replay in your head The guilt you carry for resting The constant explaining and justifying Doom scrolling that leaves you heavier The tension in your shoulders The “what if” thoughts at 2amNot all exhaustion is physical. Some of it is emotional leakage.In this episode, I guide you through reflective journaling prompts (that you can write, walk with, or simply sit with) to help you notice where your energy may be quietly draining.✍️ The 4 Journaling Prompts:Where do I feel most drained right now? Is it a person, a responsibility, a pattern, or my own thoughts?What do I keep saying yes to that leaves me resentful? (Resentment is often a boundary leak.)What input could I reduce? News, social media, constant researching, self-criticism?When do I feel most steady or peaceful? The opposite of the leak often shows us the solution.I also share powerful messages from caregivers in this community — because when one caregiver speaks up, it helps another feel less alone.We talk about: Why awareness is the first step How small adjustments can close big leaks Why you don't need to “fix the whole pipe” — just tighten one place And how protecting your energy is sacred workIf you've been wondering why you feel so tired… This episode is your gentle reset.Because awareness is not weakness. It's wisdom. And you are wiser than you think.

A caregiver in Utah, tasked with supervising three men with special needs, allegedly left them in a running van parked in his cramped garage, resulting in their tragic deaths as he spent over four hours eating and watching anime, according to police reports. Nicole Partin reporting.See omnystudio.com/listener for privacy information.

Guest: Dr. Mona Amin Board-Certified Pediatrician, IBCLC   CEU objectives for this episode: Identify three common contributors to burnout among NICU nurses and healthcare professionals. Describe the role of mentorship and professional support systems in promoting resilience, retention, and career longevity. List three actionable strategies NICU nurses and other healthcare professionals can use to advocate for themselves and promote whole-life sustainability while maintaining high-quality patient- and family-centered care. This episode is eligible for CEUs. Visit https://handtohold.org/resources/podcasts/nicu-heroes/ to complete the questionnaire. It is the sole responsibility of the individual to verify if this credit is valid and eligible for use in your State and/or for your discipline for licensure or certification renewal.

Host Kosmo Esplan talks with President Teddy Roosevelt, as impersonated by Adam Lindquist.

Kari Berit joins host Ron Aaron and co-host Carol Zernail to talk about how to remain S.A.N.E. as a caregiver on this edition of Caregiver SOS.

When Insurance Gets Between Doctors and PatientsDr. Elizabeth Ames and Dr. Caleb Bupp are deeply committed to their patients. But like so many clinicians today, they're spending an extraordinary amount of time battling insurance companies instead of practicing medicine.Between prior authorizations, step therapy requirements, and outright coverage denials, physicians and their teams are buried in paperwork, often at the direct expense of patient care. Time that should be spent listening, diagnosing, and treating is instead consumed by forms, phone calls, and appeals.Boston Globe reporter Jonathan Saltzman raised the concern and Dr. Ames brought it to my attention. The reporter talks about, a new program rolled out by Blue Cross Blue Shield of Massachusetts. The insurer says the initiative is designed to control rising healthcare costs for its 3 million members, noting that costs have increased by 30 percent since 2021. But, the program specifically targets physicians who bill for the most expensive visits. The reason for the increased expense, which is discussed in our podcast, is because doctors are choosing to spend more time with rare disease patients who have complicated health issues. They need to spend more time with complex medical needs patients than say, someone with a sore throat.Drs. Ames and Bupp warn that this approach fundamentally misunderstands patient care, particularly for those with complex or rare conditions. “These patients don't need less time; they need more” says Dr. Ames. Physicians argue that policies like this risk rushed appointments, strained doctor/patient relationships, and poorer outcomes. Nowhere is this more concerning than in the rare disease community, where delays and denials can be devastating.Dr. Elizabeth Ames and Dr. Caleb Bupp talk about what this looks like in real life. As pediatric geneticists, they see firsthand how insurance barriers impact families already navigating diagnostic odysseys, uncertainty, and fear. Their work sits at the intersection of cutting-edge science and deeply human stories, and insurance interference often disrupts both. Dr. Ames, “Usually we get faxes saying, this has been denied and we start working on it. But the family gets a letter that the drug they need, the process is delayed by a “no”. We try and have good communication and say, “hey, we got this denial,” we're working on it. But I think it's deaths by a thousand cuts for the family. Families take the denial as, “I'm not worth of coverage, and that's really hard”. Dr. Bupp says they have had to hire genetic counselors, a job that didn't exist even 5 years ago, “We have a job description in our organization for it now because of the complexities that come with trying to unravel these insurance situations”.We should also note that Dr. Ames, Dr. Bupp, and I all serve on the Rare Disease Advisory Council (RDAC) in Michigan. “I think rare disease advocacy, there is power in numbers. One person can be a huge difference maker, but it's not one plus one equals two. It really exponentially grows, and I think with things like rare disease advisory councils, that gives you a better connection within your state, for state government and for advocacy. And I also think, or I hope, that it gives a place for an individual to plug in and that can then magnify and amplify. their voice so that they're not alone”. Many states have RDAC's, You can see if your state has an RDAC. For more on the Michigan RDACIn this article and in the podcast we are not speaking on behalf of the council, but it's important to understand why bodies like RDAC exist in the first place. Michigan is home to approximately one million people living with rare diseases, and the RDAC was created to ensure their voices, and experiences help shape policy. RDAC meetings are open to the public, and anyone in Michigan can participate and offer public comment. We hope you join our meetings via zoom (sometimes hybrid).This conversation isn't just about insurance policies. It's about time, trust, and whether our healthcare system truly serves patients, especially those with the most complex needs. Speak up, share your story. Advocate. Make a difference, Mold the future, for future generations.To look at the Everylife Diagnosis Odyssey https://everylifefoundation.org/delayed-diagnosis-study/ discussed in the podcast.  Everylife impact of diagnosis: https://everylifefoundation.org/burden-study/ Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

According to AARP estimates, 26% of NYC residents are caregivers to a spouse, family member, or other loved one. Ahead of National Caregivers Day on February 20, our guest is Aisha Picott, social work care manager at Elderplan/HomeFirst, part of the not-for-profit MJHS Health System to talk about self-care for caregivers. MJHS has many free resources on their website, and bite-sized videos on their YouTube Page, covering on a wide range of questions and topics for caregivers.

In this conversation, Sandra Magsamen discusses her approach to creating children's literature that emphasizes connection, love, and emotional intelligence. She shares insights into her creative process, the importance of feedback from readers, and how her work aims to foster self-love and connection between caregivers and children. Magsamen also reflects on her artistic journey, the role of perseverance, and the significance of storytelling in shaping lives. Takeaways Connection is at the heart of children's literature. Love is an action that caregivers can demonstrate. Books can provide comfort and emotional support to children. Feedback from readers is validating and inspires future work. Objects like books and blankets can hold deep emotional significance. Stories can change lives and shape worldviews. Curiosity fuels creativity and artistic expression. Perseverance is essential in the creative process. Every project is an opportunity to connect hearts. The act of reading together fosters intimacy and connection.   Chapters 00:00 The Heart of Connection in Children's Literature 02:48 Love as an Action: The Role of Caregivers 05:34 Impactful Feedback: Stories from Readers 08:31 The Power of Objects and Books in Shaping Lives 11:06 Curiosity and Creativity: Fueling the Artistic Journey Learn more about our special guest: https://www.sandramagsamen.com/ Learn more with Jeff and Tricia https://www.shiftingschools.com/ Our show is produced by Sagheer M. Learn more: https://www.upwork.com/freelancers/~01a20f0c0c32996d55  

Termina Metro Surge pero no la presencia de agentes federales. Mensaje de unidad de Bad Bunny en la Superbowl.

In this special Valentine's Day episode of Hope for the Caregiver, I share what it means to carry love when the person you cherish can no longer carry it back in the same way. I talk about relaunching our local caregiver support group after a long pause, about sitting alone in an empty room before anyone showed up, and why caregivers need a place where they are understood. I reflect on decorating Gracie's hospital bed through one holiday after another, and why sometimes it's okay to buy your own Valentine's card as a tribute to a love that is still very real. I also address the shallow theology that collapses under the weight of suffering and remind fellow caregivers that our hope must be anchored in Scripture, not sentiment. I close by singing "I Will Sing of My Redeemer," because even when our hearts are breaking, we can still sing — and that song carries us.

Get up to date with all the scores and highlights of the week with the Raider Scoreboard with Liz Campbell. Head Coach of the Girl’s Hockey team, Jeff LaPanta, recaps the section final game and the seasons successes. Mari Cruz, Captain of the the Nordic Ski team joins the program to talk about the State […]

In today's episode, Laurie and George discuss how improving caretaking in your relationship can lead to better sex. If you've felt bogged down by the mental load or have heard your partner make complaints about it this is a must listen episode. Join us as we guide you through 'four ways to be a better caregiver.' Learn how recognizing your partner's needs, taking action before asking, and making the little things important will increase and improve your sexual connection. Make sure to check out our NEW website www.bravelovegreatsex.com for updates on our upcoming book release and other ways you can support your relationship. We're on a mission to help our brave lovers have great sex! Check out this episode's sponsor (and help the pod!): Uberlube.com -- Laurie's long-time favorite personal lubricant! Learn more about your ad choices. Visit megaphone.fm/adchoices

When someone we care about is living with chronic illness, we often want to help, but we are often unsure of how. We may worry about saying the wrong thing, doing too much, or not doing enough. And in that uncertainty, support can sometimes turn into advice, reassurance, or attempts to fix.Learn what it means to show up without fixing. We will explore what meaningful support can look like for people living with chronic illnesses, support rooted in listening, respect, and consistency rather than solutions. This conversation is for anyone who wants to show up and care, even when there are no easy answers. Show Notes and Resources: https://bit.ly/3Mxexo5#ChronicIllnessSupport #ShowingUp #ChronicIllness #Caregiving #EveryoneDiesPodcast #SupportSystem #detroitstyle #SupportWithoutFixing #SeriousIllness #SpoonTheoryIn this Episode:00:00 - Intro, Showing Up Without "Fixing"02:14 - What's Your Favorite Chocolate? From classic name brands to boutique NYC confectionaries06:46 - An Eastside Legend: The $5,000 helicopter "money drop" in Detroit08:18 - Recipe of the Week: Detroit-Style Pizza Dip09:27 - How to Help a Friend with Chronic Illness: Support, Listening & Oreos18:34 - Discussion: What Experiences Have You Had Supporting Someone with Chronic Illness?23:51 - Excerpt from "Grief is Like Glitter" by Erin Hanson26:25 - OutroRelated Podcasts:S5E3: Grief Groceries – Practical advice on how to provide tangible help without placing the burden of “choosing” on the person you are supporting.S5E1: How to Help Someone Feel Seen, Heard and Understood – A deeper dive into the psychology of communication and how to move past the diagnosis to connect with the person.S1E15: What People with Serious Illness Want (Part 2) – Firsthand insights from those living with serious illness about which gestures of support were truly meaningful.S6E24: Grounding Techniques “Life Hack” – Tools to help both the caregiver and the patient stay present and calm during the “uncomfortable moments” of chronic illness.S3E10: Understanding and Managing Fatigue – Essential listening for supporters to understand why “just getting more sleep” doesn't fix chronic fatigue and how to respect a loved one's limited energy.Support the showGet show notes and resources at our website: every1dies.org. Facebook | Instagram | YouTube | mail@every1dies.org

When One Parent Plans Ahead for Care — and the Other Doesn'tIn this thoughtful conversation, Betsy Wurzel speaks with Suzanne Scheer, J.D., Certified Long-Term Care® specialist, about how personal caregiving experiences shaped her passion for helping families prepare for the future. Suzanne explains when to consider long-term care insurance, what it covers, and why early planning can ease emotional and financial stress.The discussion also explores disability insurance, caregiving challenges, and essential planning steps such as updating wills, creating medical directives, and assigning power of attorney.Thank you for being part of Passionate World Talk Radio Network. Please follow, share, and help us continue meaningful conversations that support and inform our community. ❤️Become a supporter of this podcast: https://www.spreaker.com/podcast/chatting-with-betsy--4211847/support.

Stefan Barta, MD, MS Cutaneous T‑cell lymphoma (CTCL) is a rare condition that often raises important questions for patients and families. In this episode, we sit down with Dr. Stefan Barta, of the University of Pennsylvania, to bring clarity to what CTCL is, how it's diagnosed, and what patients can expect from staging and treatment. Dr. Barta breaks down the differences between CTCL subtypes, explains why diagnosing someone can take time, and shares the most up-to-date therapies, including skin directed treatments, immunotherapies, and emerging clinical trial options. Most importantly, he offers reassurance for those newly diagnosed: “The future is absolutely bright… there is a lot of hope for our patients with CTCL.” DOWNLOAD TRANSCRIPT CLICK HERE to participate in our episode survey. Mentioned on this episode: Cutaneous T-cell lymphoma Cutaneous Lymphoma Foundation Clinical Trial Support Center Additional Blood Cancer United Support Resources: Free Nutrition Consultations Information Specialists Financial support Online Chat Free telephone/web patient programs Free booklets Young Adult Resources Support groups Caregiver support Caregiver Workbook Survivorship Workbook Advocacy and Public Policy Patient Community Mental Health Resources Episode supported by Kyowa Kirin, Inc. and Cutaneous Lymphoma Foundation.The post Cutaneous T-Cell Lymphoma (CTCL): Illuminating a Brighter Path Forward first appeared on The Bloodline with Blood Cancer United Podcast.

Feeling exhausted while caring for others? You're not alone. In this episode, certified health coach Lauren Fisher shares practical strategies for caregiver wellness, including nutrition, movement, sleep, and stress management. We explore the 80/20 rule for eating, small manageable changes, and tools for self-compassion when you're running on empty. Lauren Fisher Health Coaching Daughterhood Circle with Lauren  TRANSCRIPT DAUGHTERHOOD

Send a textGrowth stalls when great clients arrive and caregiver applications vanish. We tackle that crunch head-on with a practical, fast-moving playbook to recruit exceptional caregivers in a competitive market—and to keep them after day one. We start by naming the seasonal dip few talk about: tax refunds and school breaks reduce both applications and availability every spring. The fix is to prepare early and compress the entire hiring cycle, so motivated candidates choose your agency within days, not weeks.We walk through a two-day job fair strategy designed less for foot traffic and more for urgency. Promoting on job boards, social, and text lists with “interviews on site” sparks immediate requests to interview now. Pair that momentum with a text-first workflow: a short form screens deal breakers, candidates self-book interviews 24/7, and you run a thorough phone interview without forcing duplicate applications. If they're a fit, invite them to a single in-person orientation where you complete paperwork, run a quick drug screen and background check, teach core skills, and—crucially—hand them initial hours before they leave the building.You'll also get the interview frameworks and ad tactics that separate you from the crowd. We break down open-ended, behavioral, and situational questions that reveal values, reliability, and judgment. Then we show how to write caregiver ads that convert by leading with benefits, not rules: flexible schedules, earned wage access, holiday differentials, paid training, and real 24/7 support. Use our headline formula and include pay ranges to increase clicks, then refresh weekly to stay visible. Finally, plan your funnel with clear math: to hire five, target forty applicants, twenty interviews, and ten orientations.Retention ties it all together. The first 90 days make or break loyalty, so commit to weekly, human check-ins that ask about their experience and solve problems fast. Add meaningful recognition, a simple caregiver newsletter, and mentor support to build community that lasts. Subscribe, share this with an owner who needs a recruiting reset, and leave a quick review telling us which tactic you'll implement this week.Continuum Mastery Circle IntroVisit our website at https://asnhomecaremarketing.comGet Your 11 Free Home Care Marketing Guides: https://bit.ly/homecarerev

Join us in community:  Women Connected in Wisdom Community Listen to past episodes: https://womenconnectedinwisdompodcast.com/ Glo from head to toe by joining the shealo glo glo club at www.shealoglo.com ! Stillpoint: A Self-Care Playbook for Caregivers Join Christine at an event! Book a free coaching consult with Christine here: https://christinegautreaux.com Like & Subscribe to get notifications of when we are live: Women Connected in Wisdom Instagram Women Connected in Wisdom on Facebook Podcast Resources:   Ready to feel strong and vibrant at every stage of life? Desi Bartlett shares how to transform your physical wellness through joyful movement and strength after 35. In this episode of Women Connected in Wisdom, we are joined by the incredible Desi Bartlett, MS, CPT E-RYT. With over 25 years of experience and a client list that includes Hollywood's biggest stars, Desi brings a wealth of knowledge on how to care for our bodies through yoga, strength, and mindful transitions. We explore the Physical Wellness dimension, specifically focusing on how women can navigate the changes that come with motherhood and aging. Desi will share insights from her book, "Total Body Beautiful", and explain how a whole-self approach to fitness can lead to lasting vitality. Whether you are a new mom or navigating life after 35, this conversation will help you reconnect with the joy of movement. Women Connected in Wisdom is a community-driven podcast hosted by Christine and Shannon, where we explore the 8 Dimensions of Wellness to help you live a more balanced, purposeful life. Connect with Desi Bartlett: Website: https://www.desibartlett.com/ Instagram: https://www.instagram.com/mothersintolivingfit/ Facebook: https://www.facebook.com/DesiBodyMind/ LinkedIn: https://www.linkedin.com/in/desi-bartlett-ms-cpt-eryt-a4457b6/ Resources talked about in the show: Meet Charm La'Donna, the Black choreographer behind Bad Bunny, Kendrick Lamar & Beyoncé's halftime shows - TheGrio Charm La'Donna (@charmladonna) • Instagram photos and videos

Send a textPodcast 3: Teaching Strategies and Education TipsDNP Website Link: https://amrossi359.wixsite.com/mysitePost-Survey Link: https://ufl.qualtrics.com/jfe/form/SV_3XjGBKEzMxll6HcThis is part three of a three-part podcast series. In this episode, we will discuss teaching strategies and education tips. ReferencesMuijsenberg, A. J., Houben-Wilke, S., Zeng, Y., Spruit, M. A., & Janssen, D. J. (2022). Methods to Assess Adults' Learning Styles and Factors Affecting Learning in Health Education: A Scoping Review. Patient Education and Counseling, 107, 107588. https://doi.org/10.1016/j.pec.2022.107588 Wong, C. I., Desrochers, M. D., Conway, M., Stuver, S. O., Mahan, R. M., & Billett, A. L. (2023). Improving Home Caregiver Independence with Central Line Care for Pediatric Cancer Patients. PEDIATRICS, 151(4). https://doi.org/10.1542/peds.2022-056617 

Send a textPodcast Episode 2: Home Care and FAQsDNP Website Link: https://amrossi359.wixsite.com/mysitePost-Survey Link: https://ufl.qualtrics.com/jfe/form/SV_3XjGBKEzMxll6HcThis is part two of a three-part podcast series. In this episode, we will discuss caregiver central line home care and FAQs.  ReferencesAims Vascular Access. (2021). IV Update. In a Review of Vascular Access & IV Infusion Topics. https://aimsvascularaccess.com/wp-content/uploads/2021/09/IVUpdateMarch2021-1.pdf Burkhart, S. (2022, March). Central Line Care. Cincinnati Children's Hospital. https://www.cincinnatichildrens.org/health/c/central-line-careCenters for Disease Control and Prevention. (2024, February 28). Guidelines for the Prevention of Intravascular Catheter-Related Infections. https://www.cdc.gov/infection-control/hcp/intravascular-catheter-related-infections/summary-recommendations.html Children's Minnesota. (n.d.). Care at Home: Central Lines. https://www.childrensmn.org/references/pfs/homecare/central-line-care-at-home-booklet.pdf Children's Oncology Group. (2011). COG family handbook (2nd ed.). https://childrensoncologygroup.org/docs/default-source/pdf/COG_Family_Handbook_2nd_Ed_English_HighRes.pdf

Send a textDNP Podcast: Improving Nurse Confidence in Caregiver EducationPodcast Episode 1: The importance of Caregiver TeachingDNP Website Link: https://amrossi359.wixsite.com/mysitePost-Survey Link: https://ufl.qualtrics.com/jfe/form/SV_3XjGBKEzMxll6HcThis is part one of a three-part podcast series. In this episode, we will discuss the importance of caregiver teaching in the post-BMT caregiver population. We will also discuss the types of central lines and the common complications associated with them.  ReferencesDavis, M. B. H. (2013). Pediatric Central Venous Catheter Management: A Review of Current Practice. Journal of the Association for Vascular Access, 18(2), 93–98. https://doi.org/10.1016/j.java.2013.04.002 Firstenberg, M., Kornbau, C., Lee, K., & Hughes, G. (2015). Central line complications. International Journal of Critical Illness and Injury Science, 5(3), 170. https://doi.org/10.4103/2229-5151.164940 Hanisch, B. R., Cohen, W., Jacobsohn, D., & Song, X. (2020). Impact of Hospital-Acquired Infections on Post-Transplant One Year Mortality in Pediatric Bone Marrow Transplant Patients. American Journal of Infection Control, 49(2), 179–183. https://doi.org/10.1016/j.ajic.2020.07.020 Sridhar, D. C., Abou-Ismail, M. Y., & Ahuja, S. P. (2020). Central venous catheter-related thrombosis in children and adults. Thrombosis Research, 187, 103–112. https://doi.org/10.1016/j.thromres.2020.01.017

Elana Cohen is an occupational therapist who has two decades experience working with children of all ages and abilities - and their families. She's Nelson based - working for Health NZ's Child Development Service, as well as in private practice. Elana says parents and caregivers need lots of support to help neurodivergent children flourish.Go to this episode on rnz.co.nz for more details

Lana Wilhelm from the Stroke Caregiver's Connection is here, and some baseball analysis!- h2 full 2200 Wed, 11 Feb 2026 22:09:20 +0000 WB4MoCXUKpdIWqSB1gn1h1uPFJ41Q5RI comedy,religion & spirituality,society & culture,news,government The Dave Glover Show comedy,religion & spirituality,society & culture,news,government Lana Wilhelm from the Stroke Caregiver's Connection is here, and some baseball analysis!- h2 The Dave Glover Show has been driving St. Louis home for over 20 years. Unafraid to discuss virtually any topic, you'll hear Dave and crew's unique perspective on current events, news and politics, and anything and everything in between. © 2025 Audacy, Inc. Comedy Religion & Spirituality Society & Culture News Government False

* Request A copy of the Free Financial Caregivers Resource Guide: LINK   We don't talk enough about the financial toll of caregiving.   Many caregivers are not just dealing with a loved one's emotional and physical needs, but financial needs as well.   In today's new episode, we are sharing expert advice from Certified Financial Planner, Beth Pinsker.  Beth's new book, My Mother's Money: A Guide to Financial Caregiving is a comprehensive resource to help navigate the financial difficulties in caring for aging parents.   From proactive measures (Power of Attorney and health proxies) to the final IRS tax return, she explains in great detail what we should be doing now and in the future for our loved ones.   Show Notes/Links: www.hotflashescooltopics.com   FOLLOW IG: @hotflashesandcooltopics for all things women 50+.   SUBSCRIBE to Hot Flashes & Cool Topics podcast for free wherever you find podcasts.   CHECK OUT our website hotflashescooltopics.com to learn more.

Send us a text (Note: we are not able to respond but LOVE to hear from you!!)Ethics educator and special needs mom, Anika Atkins, joins me for a conversation about medical mistakes, ethical repair, and what it looks like to rebuild trust after hard experiences in the healthcare system. We talk about apologies, advocacy, and how caregivers can communicate clearly without losing themselves in the process.Read the full show notes here.Join the WAITLIST for the Pathway to Peace Coaching CommunityIf you are looking for more: Sign up for The Pathway to Peace Coaching Community Waitlist Get The Special Needs Mom Survival Pack free resource Connect with Kara, host of The Special Needs Mom Podcast:Instagram: https://www.instagram.com/thespecialneedsmompodcast/Website: https://www.kararyska.com/

If you've ever felt stuck in your body, overwhelmed by responsibility, or unsure how to choose yourself without guilt — this episode will hit home.In this conversation, Ryan Kassim sits down with his client Tommy, who shares his deeply personal journey through weight loss, emotional eating, mental health, and self-acceptance. What starts as a desire to improve his health becomes a powerful story of identity, resilience, and learning how to trust himself again.Tommy opens up about growing up as a caretaker, struggling with confidence and self-worth, and navigating the emotional weight of caring for family during illness and loss. He reflects on how food became both comfort and control — and how fitness, especially running, helped him reconnect with his body in a way that felt freeing instead of punishing.This episode isn't about perfection or extreme discipline. It's about taking small steps, setting boundaries, releasing guilt, and learning that self-care isn't selfish — it's necessary.⏱️ Episode Chapters00:00 – Tommy's Journey Begins02:28 – Weight Struggles & the Caretaker Role05:42 – Mindset, Confidence, and Self-Identity08:09 – Family Challenges & Emotional Weight11:01 – Loss, Grief, and Control13:24 – Setting Boundaries & Rebuilding Confidence15:50 – Food Anxiety & Emotional Eating18:56 – Embracing Change & Personal Growth21:37 – Small Steps Toward Independence24:11 – Finding Joy in Fitness & Running27:03 – Reflecting on Progress29:17 – A Major Weight Loss Milestone32:18 – Letting Go & Healing Through Loss35:31 – Honoring Strength & Memories39:09 – Stepping Outside Comfort Zones43:25 – Trusting Yourself & the Process

Parents and caregivers need lots of support to help neurodivergent children flourish, an Occupational Therapist says.

Matt Hampton and Dr Tom Ingegno came into my world the way the best guests always do. They found me first. They pulled me onto their Irreverent Health Podcast, a show that blends medicine, curiosity, and unapologetic nonsense the same way Gen X kids blended Saturday morning cartoons with nuclear-war anxiety. We recorded together, we went off the rails together, and by the end I told them the rule. If you ever come to New York, you sit in my studio. No exceptions.They showed up. They took the hot seat. They told Alexa to shut up. They joked about Postmates. They compared bifocals before I even hit record. From there it turned into a full blown eighties time machine powered by weed policy, AI diagnostics, acupuncture philosophy, art school trauma, cannabis data science, paranormal detours, and the kind of deep cut pop culture references only Gen X survivors can decode.Matt builds AI systems. Tom heals people with needles and a lifetime of East Asian medicine. Together they make healthcare funny without pretending it works. They remind you that curiosity carries weight when the system collapses under its own stupidity.This episode is a reunion of three loudmouths raised on Atari, late night cable, and the hard lesson that you either tell the truth or get flattened by it. Go subscribe to Irreverent Health. These guys earned it.RELATED LINKS• Irreverent Health Podcast• Matt Hampton – Consilium Institute• Envoy Design• Dr. Tom Ingegno – Charm City Integrative Health• The Cupping Book• You Got Sick—Now What?• Matt Hampton on LinkedIn• Dr. Tom Ingegno on LinkedInFEEDBACKLike 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.

Show SummaryOn this episode, we have a conversation Today we're having a conversation with Jesse Gould, founder of the Heroic Hearts Project and a former Army Ranger, about what it means for veterans to heal when traditional systems don't have all the answers. Heroic Hearts works with leading medical researchers to improve veterans access to psychedelic programs for the treatment of PTSD.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 GuestJesse Gould is Founder and President of the Heroic Hearts Project, a 501(c)(3) nonprofit pioneering psychedelic therapies for military veterans. After being deployed as an Army Ranger in Afghanistan three times, he founded the Heroic Hearts Project in 2017 to spearhead the acceptance and use of ayahuasca therapy as a means of addressing the current mental health crisis among veterans. The Heroic Hearts Project has raised over $350,000 in scholarships from donors including Dr. Bronner's and partnered with the world's leading ayahuasca treatment centers, as well as sponsoring psychiatric applications with the University of Colorado Boulder and the University of Georgia.  Jesse helps shape treatment programs and spreads awareness of plant medicine as a therapeutic method. He has spoken globally about psychedelics and mental health, and received accolades including being recognized as one of the Social Entrepreneurs To Watch For In 2020 by Cause Artist. Driven by a mission to help military veterans struggling with mental trauma, he is best known for his own inspiring battle with PTSD and his recovery through ayahuasca therapy. Jesse's work can be seen and heard at NY Times, Breaking Convention, San Francisco Psychedelic Liberty Summit, People of Purchase, The Freq, Psychedelics Today Podcast, Kyle Kingsbury Podcast, Cause Artist, and The GrowthOp. Links Mentioned During the EpisodeHeroic Hearts Project WebsiteThe Veterans Guide to Psychedelics on AmazonThe Veteran's Field Manual for Psychedelics on Amazon PsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week the PsychArmor Veteran Ready program. This program offers a short, self-paced online training experience that builds foundational understanding of military culture and practical skills for supporting Veterans, service members, and their families with respect and confidence. Large organizations like the Coast Guard Chief Petty Officers Association can partner with PsychArmor to provide this military-cultural education to their members, helping teams, departments, and entire workforces become more Veteran Ready and better connected to the military-connected community.. You can find the resource here: https://learn.psycharmor.org/pages/veteran-ready 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  

Larry Lee shares about the challenges of taking care of his aging parents.

Receive caregiver advice and tips focused on family caregiving relationships for aging parents and elderly loved ones with dementia who might need nursing home care. Learn why home care for aging parents often outshines nursing home care, especially when family caregivers provide extensive personalized 1:1 support. Caregiving expert Pamela D. Wilson discusses the differences between family caregivers and hired caregivers, shares practical tips, outlines circumstances when nursing home care might be necessary, and addresses the associated risks for elderly parents and family members. Learn the steps family caregivers can take to advocate for loved ones with dementia who live in nursing homes. Gain insights into the challenges of elder care and discover why family caregiving discussions, caregiver support, and care planning are crucial to ensure the health and well-being of aging loved ones in this episode of The Caring Generation podcast. To find show transcripts and links mentioned in Episode 238 and other The Caring Generation podcasts, click here to visit Pamela's website: https://pameladwilson.com/caregiver-radio-programs-the-caring-generation/Check out show transcripts, videos, and caregiver support resources for over 200 episodes of The Caring Generation podcast here: https://pameladwilson.com/caregiver-radio-programs-the-caring-generation/For more caregiving, aging, and elder care tips, visit Pamela's website at www.PamelaDWilson.comLearn about Pamela D Wilson, her professional background, and her experience as a caregiving expert: https://pameladwilson.com/pamela-d-wilson-story/Schedule a 1:1 caregiver consultation with Pamela D Wilson: https://pameladwilson.com/elder-care-consultant-aging-parent-consultation-managing-senior-care-needs-meet-with-pamela-d-wilson/Learn about Pamela D Wilson as an expert witness in caregiving, guardianship, power of attorney 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/Sign up for Pamela's newsletter here: https://pameladwilson.com/contact/Follow Pamela on Social Media:Facebook: https://www.facebook.com/pameladwilsoncaregivingexpert/LinkedIn: https://www.linkedin.com/in/pameladwilsoncaregiverexpert/Twitter: https://x.com/CaregivingSpeakPamela D. Wilson, a caregiving expert, expert witness, educator, and caregiver consultant, provides caregiver advice, practical tips, support, and resources for aging and elder care decision-making. Developing caregiving, aging, and eldercare strategies is easier with expert caregiver advice and solutions founded on Pamela's 25 years of professional experience. Visit Pamela's website www.PamelaDWilson.com to access online caregiver resources, courses on care management, power of attorney, and guardianship, plus practical advice and tips for aging adults and family caregivers providing elder care support. ©2018, 2026 Pamela D Wilson. All Rights Reserved

Send a textFEBRUARY 2026 STOCK MARKET RECORDS. Any Questions? Wealth BuildBancus Crypto Debit Card Presentation

Send Cathy a text:)Caregiving isn't just physical work — it's emotional and mental work, too.We plan for appointments, treatments, schedules, and tasks… but most caregivers never create a plan for their mental and emotional health.In this episode of The Caregiver Cup Podcast, we're talking about how to protect your mental and emotional space — so you can show up more fully, without feeling drained, resentful, or overwhelmed.We explore:what mental and emotional space really ishow draining people and constant advocacy can quietly exhaust youwhy comparison is one of the biggest (and sneakiest) energy drainshow to protect your emotional bandwidth without guiltsimple, practical tools to create space that feels calm, personal, and even sacredThis episode isn't about shutting people out or caring less. It's about caring sustainably — and remembering that you matter, too.Because finding peace doesn't come from big changes. It comes from small steps, reflection, and choosing to protect what keeps you grounded.And when you protect your inner space, everything you give comes from a healthier place.Support the show

Cancer, Motherhood & the Choice to Rise. In her 30s, juggling a blossoming career and an 18-month-old baby while dealing with COVID shutdowns and the death of a best friend, Amanda heard the words "stage 2 triple-positive breast cancer - 2 tumors." And into the darkness she went.  But a few weeks into her diagnosis and depression, she knew a mindset shift had to be made—for her, her daughter, and her world. Tune in to discover how she shifted from despair to finding joy, humor, and wisdom in this deeply human and relatable podcast episode featuring Amanda Gunville.  We also discuss her debut memoir and guidebook: Finding Hope & Joy in Cancer: Wisdom for Patients, Caregivers, Family & Friends. Part memoir, part guidebook, and part pep talk. It offers an honest, uplifting, and empowering look at navigating life after a cancer diagnosis. You can buy it here and download her free patient care guidebook, filled with small joys that make a big difference!   Ready to discover hope and joy in unexpected places? Listen to this podcast episode! P.S. Mindset shifts paired with Probiotic Support are a match made in healing heaven because probiotics lead to a strong gut that produces the serotonin (your happy hormone) needed to keep moving forward. Your gut microbiome can also influence how well chemotherapy, hormone therapy, and immunotherapy work. So make sure to give it the fuel it needs through our Probiotic Support supplement. To learn more surprising truths about your gut and breast cancer, please review this blog post.

When you're parenting on high alert for years, your nervous system eventually tries to protect you. Sometimes that protection looks like numbness, irritability, shutdown, or going through the motions. In this episode, Jeff Noble sits down with Michael Harris, known online as FASD Elephant, to break down the science of blocked care and the small, realistic ways caregivers can find their way back to connection.In this episode you'll hear • What blocked care is and why it happens when stress stays too high for too long • How the stress response can shut down your social engagement system and make you feel emotionally flat • Why anxiety keeps pulling you into worst case futures and how to come back to the present moment • The difference between self regulation and auto regulation and why auto regulation is the real level up • A one minute grounding tool you can practice anywhere even when life is loud • How to use “the gap and the gain” to track real progress when it feels like nothing is changing • Why grief and ambiguous loss often hide underneath anger and resentment • How to avoid toxic positivity and build something steadier and more sustainableStart here first Caregiver Kickstart Workshop (free): https://www.fasdsuccess.com/fasdworkshop2026Watch the full episode on YouTube https://youtu.be/2jcTNnkMfR0Listen on Apple Podcasts https://podcasts.apple.com/ca/podcast/the-fasd-success-show/id1492499195Listen on Spotify https://open.spotify.com/show/6ntB51glqYnRPmXCh6lOGqResources mentioned FASD Elephant (Michael Harris): https://www.facebook.com/fasdelephant Michael's email: michael@fasdelephant.com Medium (Michael's writing hub): https://medium.com Praise for Change: https://praiseforchange.comFind FASD Success Website: https://www.fasdsuccess.com Free Facebook group: https://www.facebook.com/groups/FASDforever Instagram: https://www.instagram.com/FASDSuccess Facebook page: https://www.facebook.com/FASDSuccess YouTube: https://www.youtube.com/@FASDSUCCESSThe biggest free training for families is back. We start with a new brain-body approach to aggression that stops the blame. Then, we tackle Advocacy in Action—giving you the tools to talk to professionals and teachers who just don't get this hidden disability. Finally, we build your blueprint for long-term stability and support.Register: fasdsuccess.com/fasdworkshop2026Support the show

In today's episode, you will hear all that went on for Alzheimer's Advocacy at the Georgia State Capital in Atlanta. We showed up with facts, handwritten notes, and a clear ask: allocate $2 million for caregiver support programs that keep families afloat and reduce avoidable health costs. That number might seem small until you compare it to what families already contribute—775 million hours of unpaid care in Georgia, valued at $13 billion. When you see that gap, the request becomes a refund on dignity.What brought the day to life were the people behind the statistics. Meet Ross: two years into an Alzheimer's diagnosis, a former long-term care insurance pro who now leans on the very coverage he once sold. He can't work in the same way, but he's found a new job—advocating, educating, and showing up for others who wake to the same reality. We walked offices, delivered fact sheets, and invited representatives to a simple lunch. We also learned a powerful truth repeated on both sides of the aisle: lawmakers want to hear from us. They need the lived details—how mornings fall apart without rest, how training prevents injuries, how a navigator can keep a family from burning out. Data sets the stage, but stories decide the scene. Many thanks to the Alzheimer's Association of Georgia for inviting us. Visit Alz.org for more information. If you're caring, cared for, or simply care, your voice can shift policy. Share the episode, bring a friend into the conversation, and tell your representative what support would change your week. Subscribe, leave a review, and send this to someone who needs strength today.Executive Producer/Host: J SmilesProducer/Videographer: Mia HallEditor: Annelise UdoyeSupport 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!

In this episode, Dr. Shelby Blankenship PT, DPT discusses the multifaceted support needed for caregivers, focusing on physical, mental, and social aspects. She emphasizes the importance of self-care routines, acknowledging burnout, and seeking community support to enhance the wellbeing of caregivers. Want to make sure you stay up to date in all things Geriatrics in less than 3 minutes every other week? Join thousands of others in our free MMOA Digest email list - https://institute-of-clinical-excellence.kit.com/a3837f54b7

Certified coach and medical educator Kathleen Muldoon discusses her article "AI moderation of online health communities." Kathleen shares the harrowing personal story of having her social media account disabled when an algorithm mistook compassion for abuse. She explores how online support groups act as critical public health infrastructure for families navigating chronic illness and rare diseases. The conversation highlights the danger of allowing automated systems to police complex medical conversations without understanding nuance or context. Kathleen argues that instead of relying on censorship, health care providers must actively engage in these digital spaces to foster trust. Listen to learn why preserving human connection in digital spaces is essential for patient healing. Partner with me on the KevinMD platform. With over three million monthly readers and half a million social media followers, I give you direct access to the doctors and patients who matter most. Whether you need a sponsored article, email campaign, video interview, or a spot right here on the podcast, I offer the trusted space your brand deserves to be heard. Let's work together to tell your story. PARTNER WITH KEVINMD → https://kevinmd.com/influencer SUBSCRIBE TO THE PODCAST → https://www.kevinmd.com/podcast RECOMMENDED BY KEVINMD → https://www.kevinmd.com/recommended

In a world of shifting policies and "Wild West" internet searches, how do you find the truth? This episode dives into the recent major changes in the caregiver support world, including the transition of AlzAuthors under the leadership of All Home Care Matters. We move past the industry headlines to focus on the human element: why community is the only thing that keeps a caregiver sane when the ground is shifting. Inside the Conversation: Vetting the Noise: Why "human-filtered" information is the best defense against the costly misinformation and false promises targeting caregivers today. The Power of Storytelling: How memoirs and fiction provide the "me too" moments and emotional escape that medical manuals simply cannot offer. The "First 48" Strategy: Lance shares his personal journey of being "new to the wheel" and why professional healthcare often misses the human needs of the family. Bridging the Gap for 2026: As the "Silver Tsunami" peaks, we discuss how veterans can support the massive new wave of caregivers entering the trenches this year. Our Guest: Lance A. Slatton Lance A. Slatton, CSCM The Senior Care Influencer & President of AlzAuthors Lance A. Slatton is a healthcare professional with over 20 years of experience and is widely recognized as "The Senior Care Influencer." He is a Senior Case Manager at Enriched Life Home Care Services and the host of the award-winning podcast and YouTube channel, All Home Care Matters. Lance's leadership in the industry was solidified in early 2026 when he was named President of AlzAuthors, a global community of over 400 authors sharing authentic dementia stories. A prolific writer and advocate, Lance is a monthly columnist for McKnight's Home Care News and the author of the All Home Care Matters' Official Family Caregivers Guide. Notable Achievements: 2024 & 2025: Named Top Healthcare Influencer of the Year. YouTube Silver Creator Award: Recognizing excellence in healthcare media. Academy of Interactive Visual Arts: Juror (2023–2025). "50 Under 50": Recognized by the New York City Journal.

Visit www.joniradio.org for more inspiration and encouragement! --------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.