Podcasts about caregivers

In 1971, the National Cancer Act transformed cancer into a national research priority. More than 50 years later, the next frontier is no longer defined solely by scientific discovery, but by how quickly knowledge, lived experience, and patient voices can reshape healthcare itself.The concluding chapter of The Cancer Mavericks: A History of Survivorship explores how the cancer advocacy movement continues to evolve in an era of digital communities, social media, precision medicine, and grassroots activism. Building on the work of pioneers such as Mary Lasker, Rose Kushner, and the generations of survivors who followed, today's advocates are expanding the movement beyond awareness to demand health equity, trusted information, patient-centered research, and meaningful representation in healthcare decision-making.The episode examines how technology has transformed advocacy from local support groups into global communities capable of organizing in real time. Researchers, policymakers, nonprofit leaders, and survivors reflect on the growing influence of digital storytelling, online education, and peer-to-peer networks that connect patients across diagnoses, generations, and geographic boundaries. At the same time, they acknowledge new responsibilities: ensuring accurate medical information, combating misinformation, protecting trust, and keeping patients at the center of innovation.The story also looks ahead to the next generation of advocates. Young leaders are applying lessons learned from decades of cancer activism while drawing inspiration from broader movements for social justice, public health, and community organizing. Their work reflects a simple but enduring truth: meaningful change rarely begins inside institutions. It begins when ordinary people refuse to accept that the system cannot improve.Cancer survivorship has never been a finished story. Every generation inherits the progress achieved by those who came before while confronting challenges uniquely its own. The future of survivorship will be shaped not only by scientific breakthroughs, but by those willing to listen, organize, educate, and ensure that every patient's voice helps define what comes next.RELATED LINKSNational Cancer Institute⁠Cancer Moonshot⁠Centers for Disease Control and Prevention | Division of Cancer Prevention and Control⁠HopeLab⁠Tigerlily Foundation⁠Stupid Cancer⁠FEEDBACKLike this episode? Rate and review The Cancer Mavericks: A History of Survivorship on your favorite podcast platform. For more information, visit CancerMavericks.com. Please send any questions to podcasts@matthewzachary.com.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Dr. Toby Cosgrove is the former President and CEO of Cleveland Clinic, where he now serves as Executive Advisor. A cardiac surgeon and inventor, he is a member of the Cleveland Medical Hall of Fame and the Cleveland Business Hall of Fame, and has addressed the World Economic Forum at Davos and the Senate HELP Committee. In this episode of DGTL Voices, Toby tells Edward Marx about nearly flunking out of Williams College before anyone discovered he was dyslexic, running a hundred-bed casualty staging flight in Vietnam at 28, and the two decisions he's proudest of from his tenure at Cleveland Clinic, both about purpose and language rather than buildings. Plus: the three problems he thinks AI has to solve in healthcare, and his advice for people who want the C-suite. Connect with Marx Advisory at https://bio.marxadvisory.com/

Welcome to Episode 323 of Autism Parenting Secrets. This week, I'm joined by returning guest Beth Lambert, Executive Director of Documenting Hope and author of A Compromised Generation. After more than two decades immersed in children's health, Beth is more hopeful than ever. Why? The science has changed. Our understanding of the microbiome, nervous system, metabolism, environmental stressors, and other contributors to chronic childhood conditions has exploded. More practitioners are applying this knowledge clinically. And more parents are sharing stories of children making remarkable progress. But having more information and more options doesn't necessarily make a parent's job easier. In fact, it can make discernment even more important. Your child is unique. There is no universal roadmap, perfect practitioner, or silver bullet. The opportunity is to gather good information and support while becoming increasingly clear about what makes sense for your child. We also explore something parents can easily overlook: you are part of your child's environment. Your nervous system, energy, decisions, consistency, and ability to regulate matter. Supporting yourself isn't taking attention away from your child. It can be foundational to helping your child feel safe and thrive. Beth also shares why in-person community can be so powerful and what she's most excited about at Documenting Hope's upcoming Health & Healing Expo in Orlando, November 21-22. The future is changing quickly. There are more reasons for hope, more tools available, and more possibilities opening up for families. The secret this week is… Healing Is More Possible Than You Think You'll Discover: Why there's more reason for hope than ever before (1:26) Why YOU are your child's most important decision-maker (7:00) Why commitment beats chasing the next intervention (15:42) How community can create unexpected breakthroughs (23:05) Why the future of children's health could look radically different (32:48) About Our Guest: Beth Lambert is a former healthcare consultant and teacher. As a consultant, she worked with pharmaceutical, medical device, diagnostic, and other healthcare companies to evaluate industry trends. She is the author of A Compromised Generation: The Epidemic of Chronic Illness in America's Children and co-author of Brain Under Attack: A Resource for Parents and Caregivers of Children with PANS, PANDAS, and Autoimmune Encephalitis. Beth founded Epidemic Answers in 2009 and currently serves as Executive Director of Documenting Hope. She attended Oxford University, graduated from Williams College, and holds a Master's Degree in American Studies from Fairfield University. www.beth-lambert.com/documenting-hope References in this Episode: Health & Healing Expo by Documenting Hope, November 21–22, 2026 | Orlando, Florida + Virtual Healing Together by Documenting Hope A Compromised Generation by Beth Lambert Brain Under Attack by Beth Lambert Additional Resources: To learn more about personalized 1:1 support go to www.elevatehowyounavigate.com If you enjoyed this episode, share it with your friends.

Sometimes grief begins long before someone dies. It begins when the person you love is still beside you, but the life you knew together is already changing.In this episode, Teresa Reiniger sits down with Suzy McNamara for an honest conversation about caregiving, anticipatory grief, identity, faith, and carrying more than one devastating loss at once.Suzy spent five years as the primary in-home caregiver for her husband, Bob, after he was diagnosed with posterior cortical atrophy, a rare form of early-onset Alzheimer's. She shares what it was like watching changes begin in his early 50s, protecting his dignity as his world became smaller, and slowly realizing that she was no longer only his wife, she had become his caregiver, advocate, and protector.Then, while Bob was entering the final stage of his illness, Suzy's sister and best friend, Elizabeth, died. Suzy reflects on what happens when there is barely room to grieve because someone still depends on you.This conversation offers validation for caregivers who feel unseen, people experiencing anticipatory grief, and anyone carrying layered losses.About our guest: Suzy McNamara is a widow, mother of four adult children, former primary caregiver to her husband Bob, and author of The Silkworm, the Magician, and the Sister Tree: A Tale of Love and Loss.In This Episode● How early-onset Alzheimer's changed Bob's identity, career, relationships, and independence.● Why grief can begin while the person you love is still physically present.● How Suzy's identity shifted from wife to caregiver, advocate, and protector.● Protecting a loved one's dignity when others do not understand their limitations.● Grieving Suzy's sister Elizabeth while continuing full-time caregiving.● How faith, writing, friendship, and a smaller support circle helped Suzy keep going.What You'll Take Away● Anticipatory grief is real grief.● Caregivers can lose parts of their identity, too.● Protecting someone may require disappointing other people.● Surviving one difficult day deserves recognition.● You do not need a large circle—you need people who can truly stay.MEMORABLE QUOTESSuzy: “There are so many little tragedies in the big tragedy of Alzheimer's.”Suzy: “That's when the grieving really begins.”Suzy: “The caregiver loses their identity for sure.”Suzy: “You do have to build sort of a wall around your heart.”Suzy: “Getting through one day is a huge, huge accomplishment.”Teresa: “Grief does not always wait for one loss to end before another one begins.”EPISODE CHAPTERS00:00 — When Grief Begins Before Death03:33 — Bob's Early-Onset Alzheimer's Story08:26 — The Fear and Shame Before Diagnosis13:28 — When Alzheimer's Arrives in Midlife18:00 — Losing the Identity of Wife and Becoming Caregiver19:48 — Protecting Bob's Dignity and Safety24:59 — Grieving a Sister While Caring for a Husband28:16 — When Caregiving Leaves No Room to Grieve29:26 — The Story Behind Suzy's Memoir33:30 — Finding the People Who Can Truly Stay35:48 — Getting Through One Day Is an Accomplishment39:32 — Suzy's Book and Audiobook42:19 — A Reminder for Caregivers Who Feel Unseen

This week Sarah sits down with Dr. Tony Nader, a physician, neuroscientist, and leader in the Transcendental Meditation movement, to explore one of the biggest mysteries of our existence: consciousness. Together, they explore the relationship between the mind and body, science and spirituality, meditation and creativity, and what it means to access a deeper sense of self. On this episode of Moonbeaming you'll hear: How Dr. Tony Nader went from physician and neuroscientist to studying consciousness and Transcendental Meditation What consciousness actually is and why Dr. Nader believes it extends far beyond human consciousness How meditation can create a state of inner silence while maintaining deep alertness and awareness Why stress and fear narrow our consciousness and limit the possibilities we can see How calming the nervous system can create more space for creativity, intuition, and clearer decision-making The connection between meditation, the brain, creativity, and the default mode network How Transcendental Meditation can help us reconnect with what Dr. Nader describes as our deeper, truer self What it means to live from a place of greater consciousness, connection, and care --- Dr. Tony Nader is a physician, neuroscientist, Vedic scholar, and leader of the Transcendental Meditation movement. A Harvard- and MIT-trained scientist, he is the author of Consciousness Is All There Is and his newest book, The Power of Caring, which explores how caring is rooted in consciousness and how we can cultivate deeper, more fulfilling connections with ourselves and others. https://drtonynader.com/ --- Join Our Community: Join the Moon Studio Patreon: https://www.patreon.com/themoonstudio Buy the 2026 Many Moons Lunar Planner: https://moon-studio.co/products/many-moons-2026?srsltid=AfmBOopThx1yrmKl0tMjecc_EFeeN5DAiIafqPqvQ4Uke1WEi5droeam Subscribe to our newsletter: https://moon-studio.co/pages/newsletter Find Sarah on Instagram: https://www.instagram.com/gottesss/

Before school. After school. In the middle of the night when something goes wrong. Liz, Kasen, and Audrey have all learned to carry weight most of their peers never have to think about. They show up and care for a family member who needs them, again and again, in ways that rarely get noticed and even more rarely get thanked. They're not alone: an estimated 3.4-5.4 million youth provide essential caregiving in the U.S., and yet there's no national system in place at schools, hospitals, or doctor's offices to even recognize a child as a caregiver. In this episode, these three incredible young people open up about what that invisible work actually looks like day to day: the responsibility that arrives too early, the exhaustion that goes unspoken, and just how rare it was to feel truly understood — until they found other kids living the same reality. They talk about what changed when they found each other at MCEC, and what it means to finally feel seen and heard by people who simply get it. Julie Coffey, who helps lead the Caregiving Youth Student Leadership Program, joins the conversation to share how the program gives these young caregivers something they didn't know they were missing — a peer community built around the kind of service no one sees, but everyone needs.   SHOW NOTES Guests:  Liz. Kasen. Audrey. Julie Coffey: our beloved Student Well-Being Manager at MCEC. Julie manages the Caregiving Youth Student Leadership Program, as well as many of our other student initiatives, like Student-2-Student (s2s) and the Frances Hesselbein Leadership Program. As a former educator, counselor, and a military-connected Caregiving Youth herself, Julie dedicates herself to helping military-connected students recognize their place of belonging in this world. Resources: https://militarychild.org   Information about the Caregiving Youth Student Leadership Program: https://militarychild.org/programs-and-initiatives/caregiving-youth-student-leadership-program/   Citations: Armstrong-Carter E, Siskowski C, Cornish NR, Olson E. Adolescents' caregiving for family: Associations with mental health and academic performance. J Res Adolesc. 2025 Sep;35(3):e70045. doi: 10.1111/jora.70045. PMID: 40586181; PMCID: PMC12221208.   Miller KEM, Hart JL, Useche Rosania M, Coe NB. Youth Caregivers of Adults in the United States: Prevalence and the Association Between Caregiving and Education. Demography. 2024 Jun 1;61(3):829-847. doi: 10.1215/00703370-11383976. PMID: 38785364; PMCID: PMC11539003.   Mixed and mastered by Concentus Media, Inc., Temple, Texas, USA.   This episode is made possible by generous funding from the USAA Foundation.   Related MCEC Podcast Episodes: Military Kids as Caregivers published 4.29.25 S2S: Students Supporting Students published 5.25.25 S2S: Helping Students Succeed published 8.20.24  

In 1987, Mary P. Lovato, a member of Kewa Pueblo in New Mexico, was diagnosed with acute leukemia. To receive a bone marrow transplant, she had to travel more than 800 miles from home because specialized cancer care was unavailable through the Indian Health Service. When she returned, she discovered another obstacle: many in her community feared cancer so deeply that they avoided speaking about it altogether.This episode examines how cancer survivorship exposed profound inequities in the American healthcare system. Long before health equity became a national priority, advocates from underserved communities were confronting disparities rooted in geography, poverty, racism, language, underfunded healthcare systems, and historical mistrust of medical institutions. Their work demonstrated that scientific advances alone cannot improve survival if patients cannot reach, afford, or trust the care available to them.The story follows pioneers including Mary P. Lovato, who built the first national Native-led cancer support and education program for Indigenous communities, and Maimah Karmo, founder of the Tigerlily Foundation, whose breast cancer diagnosis inspired a movement to improve early detection, clinical trial participation, and representation for Black women. Their advocacy challenged longstanding barriers to culturally competent care while highlighting persistent inequities in access to screening, fertility preservation, navigation, and innovative treatments.The episode also explores why diversity in clinical research matters. For decades, many cancer clinical trials disproportionately enrolled White patients, limiting both access to promising therapies and the scientific understanding of how treatments perform across different populations. Researchers, patient advocates, and community leaders responded by redesigning outreach, improving patient navigation, reducing logistical barriers, and insisting that affected communities help shape the research itself.Cancer survivorship cannot be measured solely by scientific breakthroughs. It also depends on whether every patient has a meaningful opportunity to benefit from them. The pursuit of health equity remains one of the defining challenges and enduring responsibilities of modern oncology.RELATED LINKSNational Cancer Institute | Cancer Health Disparities⁠Indian Health Service⁠Tigerlily Foundation⁠National Cancer Institute | Cancer Clinical Trials⁠American Indian Cancer Foundation⁠Abramson Cancer Center | University of Pennsylvania⁠FEEDBACKLike this episode? Rate and review The Cancer Mavericks: A History of Survivorship on your favorite podcast platform. For more information, visit CancerMavericks.com. Please send any questions to podcasts@matthewzachary.com.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

What happens when taking care of someone else slowly requires you to disappear from your own life?Family caregiving rarely arrives according to plan. A diagnosis changes. A parent declines. A spouse becomes dependent. Roles reverse, schedules collapse, and someone quietly becomes responsible for another human being twenty-four hours a day.Amy and Monica Vest Wheeler explore the realities behind caregiver burnout, unpaid caregiving responsibilities, and the pressure to keep performing at work while privately carrying grief, medical decisions, and exhaustion. For many working caregivers, the strain is not only emotional. It can affect income, career stability, health, and the ability to remain in the workforce at all.Monica challenges the assumption that families should simply absorb this responsibility without consequence. The conversation turns toward workplace support for caregivers, the limitations of rigid bereavement and leave policies, and why flexible work for caregivers can be an act of both humanity and good leadership.Support can also begin closer to home. Another family member learns the care routine. Someone finally says what is really happening. A caregiver stops answering “fine” and allows another person to help carry the weight.Caregiving can be an expression of extraordinary love. But love does not make a person limitless. Sustainable care requires us to protect the life of the person receiving care without sacrificing the life of the person providing it.Moments That Create Momentum:When the Caregiver Becomes Invisible – Explore how responsibility for another person can consume so much emotional and physical energy that the caregiver's own needs quietly disappear.The Workplace Mask Caregivers Learn to Wear – Understand why employees may appear composed and productive while privately managing grief, medical crises, and round-the-clock caregiving responsibilities.Why Flexibility Is More Than an Employee Perk – Discover how small adjustments to schedules or work location can help organizations retain experienced employees instead of losing them to caregiving demands.The Cost of Keeping Caregiving a Family Secret – See how shame, privacy, and poor communication can leave one person carrying responsibilities that could be shared across family, friends, and community.Your Life Is Just as Worthy as the Person You're Caring For – Hear why caregiving cannot require complete self-erasure, and how protecting the caregiver may ultimately protect the person receiving care too.About the Guest:Monica Vest Wheeler speaks with heart, humor, and hard-earned wisdom, helping caregivers, families, and communities navigate some of life's most difficult moments. Her work is rooted in lived experience, including hundreds of interviews, volunteer work at more than 180 stroke and brain injury camps nationwide, facilitating hundreds of support and discussion groups, personal caregiving journeys, and her own openness about mental health. She has written more than a dozen books on Peoria, Illinois, history, along with five books exploring health, grief, and the emotional realities families face during catastrophic life events.As a writer and presenter, Monica is unafraid to address the questions many people avoid. She brings truth, warmth, humor, and practical clarity to conversations about caregiving, grief, communication, and emotional survival. Her work gives caregivers permission to ask for help without shame, encourages patients and survivors to express what they are experiencing, and reinforces one of the lessons she has seen repeatedly: families who communicate are more likely to stay connected through crisis rather than fall apart.https://www.monicavestwheeler.comhttps://www.facebook.com/monicavestwheelerhttps://www.linkedin.com/in/monicavestwheeler/About Amy:Amy Lynn Durham, known by her clients as the Corporate Mystic, is the founder of the Executive Coaching Firm, Create Magic At Work®, where they help leaders build workplaces rooted in creativity, collaboration, and fulfillment. A former corporate executive turned Executive Coach, Amy blends practical leadership strategies with spiritual intelligence to unlock human potential at work.She's a certified Executive Coach through UC Berkeley & the International Coaching Federation (ICF) In addition, Amy holds coaching certifications in Spiritual Intelligence (SQ21), the Edgewalker Profile, and the Archetypes of Change . In addition to being the host of the Create Magic At Work® podcast, Amy is the author of Create Magic At Work®, Creating Career Magic: A Daily Prompt Journal and the founder of Magic Thread Media™. Through her work, she inspires intentional leadership for thriving workplaces and lives where “magic” becomes reality.Connect with Amy:https://createmagicatwork.net/https://www.linkedin.com/company/create-magic-at-workhttps://www.facebook.com/112951637095427https://www.instagram.com/createmagicatworkhttps://www.youtube.com/channel/UCnEm4h3fUgaq8qgvZpz6dGgThanks for listening!Thanks so much for listening to our podcast! If you enjoyed this episode and think that others could benefit from listening, please share it using the social media buttons on this page.Do you have some feedback or questions about this episode? Leave a comment in the section below!Subscribe to the podcastIf you would like to get automatic updates of new podcast episodes, you can follow the podcast on Apple Podcasts or your favorite podcast app.Leave us an Apple Podcasts reviewRatings and reviews from our listeners are extremely valuable to us and greatly appreciated. They help our podcast rank higher on Apple Podcasts, which exposes our show to more awesome listeners like you. If you are enjoying the show, please leave us a review on Apple Podcasts.Mentioned in this episode:This show was brought to you in part by the Magic Thread Media Network. To learn more visit: https://magicthreadmedia.com/

Do you ever feel lost in the maze of court dates, school meetings, and sleepless nights, forced into a role you never expected? Are you a grandparent who has become the last line of defense for your family, while the system treats your love and sacrifice as just another case number? Maybe you find yourself grieving not just the loss of a peaceful retirement, but the heartbreak of watching your own child struggle, all while building a new life for your grandchildren.I'm Laura, and like you, my life was rewritten the day my grandson was removed from his mother with no warning, a reality no grandparent imagines. Navigating a system that hides its decisions behind a “black box,” my husband and I fought for months to keep our family together, relying on sheer determination and the kindness of a good attorney.Welcome to 'Grandparents Raising Grandchildren.' Here, our focus is on real stories that cut through the silence—stories shaped not only by resilience, but by the cold, hard data that reveals how deeply flawed the system is. You'll hear conversations with experts like this week's episode with Dr. Jill Bryant, a counseling professor and grandmother, who is building the research—and the case—for a future where the well-being of kinship families is not ignored. Complete Dr. Bryant's survey here to help us get the data we need! We'll discuss what it truly means to parent a second time, the grief that goes unspoken, and the shame that lingers in our quiet moments. We'll dig into the nuanced challenges of trauma, the gaps in support, and the power of speaking up—because your experience deserves recognition and your story can drive real change.Join me and a community of 2.7 million strong. Together, we will gather the voices and the data needed to transform the laws and support networks for grandparents raising grandchildren—proving that we are more than a safety net; we are the force for change our families desperately need.Send us Fan MailI want to know how you're doing. Is the podcast giving you what you need? What support are you missing most right now? Send me a Direct Message on Facebook or Instagram or email me directly at laurabrazan@grandparents-raising-grandchildren.org. I read and reply to every message because this community is built on supporting each other! States save billions by leaving children with relatives while giving us zero financial aid, zero legal aid, and zero respite. Leave a comment and let us know your name, state and what support you've been denied? We need to let our lawmakers know what we really need! A listener wrote in after reading this week's newsletter. She commented on how I shared about my husbands grief over the estrangement of his own son. Sign up to receive our weekly newsletters to read the latest stories and share with someone who needs to hear!Thank you for tuning into today's episode. It's been a journey of shared stories, insights, and invaluable advice from the heart of a community that knows the beauty and challenges of raising grandchildren. Your presence and engagement mean the world to us and to grandparents everywhere stepping up in ways they never imagined.Remember, you're not alone on this journey. For more resources, support, and stories, visit our website and follow us on our social media channels. If today's episode moved you, consider sharing it with someone who might find comfort and connection in our shared experiences.We look forward to bringing more stories and expert advice your way next week. Until then, take care of yourselves and each other.Want to be a guest on Grandparents Raising Grandchildren: Nurturing Through Adversity? Send Laura Brazan a message on PodMatch, here: https://www.podmatch.com/hostdetailpreview/grgLiked this episode? Share it and tag us on Facebook @GrandparentsRaisingGrandchilden Love the show? Leave a review and let us know!CONNECT WITH US: Website | Facebook 

Show SummaryOn today's episode, we're having a conversation with Registered Nurse, Military Spouse, and Workforce Development Advocate Tracy Steele, founder of Community Cultivator, an organization dedicated to strengthening well-being, belonging, and career stability for military spouses through community connection and professional developmentEpisode Partner:Our sponsor this week is Aetna, a trusted health care company, committed to serving Veterans, military families, and caregivers through meaningful, community-centered care. 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 GuestCommunity Cultivator was founded by Tracy Steele, SPHR, CPRW — a longtime military spouse, workforce development leader, and advocate for military spouse employment and community connection.​After more than two decades navigating military life, Tracy experienced firsthand the challenge of constantly rebuilding career momentum, professional networks, and community with every move. Through strategic volunteering, networking, and workforce development leadership, she became passionate about helping military spouses recognize their value and confidently pursue meaningful opportunities.But she realized military spouses needed more than job resources alone. They needed connection, belonging, and access to opportunities that could grow with them wherever military life led next.​So she built Community Cultivator.​What started as a vision in San Diego is growing into a nationwide movement helping military spouses build stronger careers, deeper connections, and lasting opportunities together.Links Mentioned During the EpisodeCommunity Cultivator WebsiteForeign Born Military Spouse NetworkSugar Bear Foundation WebsitePsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week is the PsychArmor course 15 Reasons to Hire a Military Spouse. As an employer, you are looking for untapped talent pools. One talent pool that can be overlooked is the diverse and highly educated group of military spouses. Take this course to learn the top 15 Reasons to Hire a Military Spouse. You can find the resource here: https://learn.psycharmor.org/courses/15-Reasons-to-Hire-a-Military-Spouse 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:)You never imagined you'd become the scheduler, medication manager, nurse, insurance expert, researcher, or advocate for someone you love.But here you are.In this episode of The Caregiver Cup Podcast, we explore how caregiving quietly changes us—not just through the roles we take on, but through the confidence, resilience, and strength we build along the way.Through personal stories, reflections, and encouragement, you'll discover that every appointment, every question, every mistake, and every act of love has been shaping you into someone more capable than you ever imagined.In this episode you'll discover: ☕ Why none of us truly signs up to become a caregiver ☕ The unexpected roles caregivers learn to navigate ☕ How mistakes often become our greatest teachers ☕ Why advocacy looks different with every doctor and care team ☕ The surprising ways caregiving helps us growReflection Question: Who am I becoming through this?Because maybe...instead of simply surviving...you're becoming.Support the show

BrainStorm wants to hear from you! Send us a text.Caregivers of people with dementia know the toll of repetitive, anxiety-driven phone calls — sometimes dozens or even a hundred a day. On this episode of BrainStorm, host Meryl Comer talks with Kirstin Thomas, co-founder of KindredMind, about the personal crisis and pivotal moment that led her to build a voice-companion app that answers those calls in the caregiver's own cloned voice. They dig into dementia separation anxiety, validation therapy, privacy safeguards, and why Thomas insists the technology is meant to be a bridge for caregivers — never a replacement. You don't want to miss this informative episode of linking caregiving and technology. Support for BrainStorm by UsAgainstAlzheimer's comes from Genentech. Genentech is committed to pushing the boundaries of scientific discovery in Alzheimer's disease by researching and developing treatments to preserve what makes us who we are.Support the show

Send us Fan MailA Father's LoveHello and welcome to Spiritual Warriors, the Caregivers. This is Episode 16 in our series on Spiritual Warfare. If you are a caregiver, you are a spiritual warrior. We want to encourage you in your walk with God and remind you that he is with you, for he said, I will never leave you nor forsake you. Hebrews 13. Verse 5, part b.My name is Dr. Stephanie Wright, and today's episode is about a father who was an amazing caregiver. It is entitled “A Father's Love.” Our scripture reading is from Mark 9:20-29.20 And they brought the young man to Jesus: and when He saw him, straightway the spirit tare him; and he fell on the ground, and wallowed foaming.21 And he asked his father, How long is it ago since this came unto him? And he said, Of a child.22 And ofttimes it hath cast him into the fire, and into the waters, to destroy him: but if thou canst do any thing, have compassion on us, and help us.23 Jesus said unto him, If thou canst believe, all things are possible to him that believeth.24 And straightway the father of the child cried out, and said with tears, Lord, I believe; help thou mine unbelief.25 When Jesus saw that the people came running together, he rebuked the foul spirit, saying unto him, Thou dumb and deaf spirit, I charge thee, come out of him, and enter no more into him.26 And the spirit cried, and rent him sore, and came out of him: and he was as one dead; insomuch that many said, He is dead.27 But Jesus took him by the hand, and lifted him up; and he arose.28 And when he was come into the house, his disciples asked him privately, Why could not we cast him out?29 And he said unto them, This kind can come forth by nothing, but by prayer and fasting. We don't know how old the son was in this scripture, but verse 21 tells us he was tormentedfrom childhood. Then verses 25 and 26 tell us he was tormented by an evil spirit. So, it appearsthat for a number of years this father was a caregiver to this young man who had been throwinghimself into fire and into water. He also witnessed his son foaming at the mouth and gnashing his teeth, and witnessed other attacks on his son's body. This is a father with a profound amount of love as a caregiver. That love is what we want to focus on today because only love can sustain a caregiver through the ravages waged against their loved ones' bodies, minds, and souls. Yes, every caregiver must pray, fast, and have faith that their loved one can be miraculously delivered like the young man in our scripture. But love is key to continuing the fight for those we care for until they are delivered, no matter what we see and hear. Continue in the caregiving work that you do. Those who are not in this daily fight don't fully understand what you are going through. So be kind to yourself while you extend kindness to those you care for. It will all work in your favor one day. Thank you for joining us today. We hope that this series will be a blessing to you, especially if you are a caregiver. And we will see you next time. Now stay tuned for Dr. Apostle Charles, as he tells you how you may contact us and listen to past podcasts on fasting, prayer, and other topics.If you want to contact us or comment on this podcast, please visit our website and select www.cgmissions.com/podcasts, where all episodes are available by category in series format. You can see some video and audio podcasts at: www.youtube.com/@cgmissionsinc then select from the video or podcast"Playlist."   CGM is a 501(c)(3) nonprofit. Donations may be made on our website:https://www.cgmissions.com/donate-here-general-and-wecare/

Caregivers live with questions that medicine cannot answer. Where is God in this? Can He be trusted? Does suffering have meaning? How long can I keep doing this? In this episode, Peter Rosenberger explains why theology is not merely an academic subject for pastors and professors. It belongs at the hospital bedside, in the waiting room, and in the kitchen at two in the morning. What we believe about God shapes what we believe about ourselves, what we attempt to carry, and where we stand when everything around us changes. The episode closes with an unexpected story and a deeply personal musical reflection on grief, faith, and offering the best of what we have.

Multiomics: The Next Frontier In Precision Medicine And Diagnostics Standard blood tests aren't giving you the most accurate picture of your health. Our expert examines the critical blind spots in standard medical testing and reveals emerging technology that catches disease at the cellular level. Guest: Dr. Adrijana Kekic, CEO & founder, Futurome Host and Producer: Kristen Farrah   Closing The Info Gap: A New App That's Empowering Patients And Caregivers Patients routinely forget up to 80 percent of the information shared during a doctor's appointment. Thankfully, a new app puts control directly back into the hands of patients by bridging this critical information gap and eliminating the stress of lost instructions. Our expert explores how empowering individuals with clear, accessible records of their care can transform the patient experience and relieve burnout for healthcare providers. Guests: Dr. Arpan Parikh, psychiatrist, CEO & co-founder, Kin Health Host: Greg Johnson Producer: Kristen Farrah Facebook: ingoodhealthpodX: @ ingoodhealthpodIG: @ingoodhealthpodYouTube: @ingoodhealthpodSpotify Apple Podcast In Good Health PodcastSubscribed to the newsletterFull ArchiveContact UsBecome an Affiliate Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Crónica de Francisco desde la selva del Yucatán sobre sus animales, ecosistema y el impacto de las personas en ese delicado entorno.

Closing The Info Gap: A New App That's Empowering Patients And Caregivers Patients routinely forget up to 80 percent of the information shared during a doctor's appointment. Thankfully, a new app puts control directly back into the hands of patients by bridging this critical information gap and eliminating the stress of lost instructions. Our expert explores how empowering individuals with clear, accessible records of their care can transform the patient experience and relieve burnout for healthcare providers. Guests: Dr. Arpan Parikh, psychiatrist, CEO & co-founder, KIN Health Host: Greg Johnson Producer: Kristen Farrah   Facebook: ingoodhealthpodX: @ ingoodhealthpodIG: @ingoodhealthpodYouTube: @ingoodhealthpodSpotify Apple Podcast In Good Health PodcastSubscribed to the newsletterFull ArchiveContact UsBecome an Affiliate Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Send us Fan MailOWNERSHIP - TAX LIENS - REAL ESTATE INVESTING. Millionaires In A Bad Economy❤️️Ai Business Help. Information & Tools: https://www.leskolovesai.com/business❤️️Grants from states and local governments: https://findhelp.org/❤️️Caregivers, Mental Health: https://www.211.org❤️️Get Your .crypto domain name here. Web 3 Unstoppable Domains and FREE Minting on Polygon. No Annual Domain Name Fees. Could be the future: https://unstoppabledomains.com/?ref=c6af699e6d94459

Get the latest activities schedules on this weeks Raider Scoreboard Gary Greenland, Head Coach of the Nortfield Bowling team kicks off the program with an invitiation to those looking for a fall activity to come join the bowling team. Regardless of skill level, Gary and his team will make it a fun experience. For more […]

Patrick Regan OBE is author of Sunday Times bestseller "Small Steps for Big Change", Director of Brighter Days, and a wellbeing advocate. Patrick shares meaningful experiences in his life that helped him understand how to manage overwhelm. He describes the importance of setting boundaries and living our values during today's ongoing changes. Patrick explains how self-awareness helps people take small steps, make intentional choices and lead differently. He advocates for compassionate leaders who emphasise human connection and psychological safety, while addressing systemic causes of burnout. Patrick highlights his practices of creating space and thinking differently.     KEY TAKEAWAYS   [01:10] Patrick's life is impacted when facing a school incident as a youth worker during his gap year.   [01:56] Patrick helps at the school and discovers how trauma and violence shape young people's lives.   [02:55] Trying to solve unfixable problems leads to Patrick absorbing others' pain.   [04:22] Comparing suffering can prevent people from recognising and addressing their own needs.   [05:12] Multiple family health crises compound Patrick's stress.    [06:04] Patrick has to face his own health crisis.   [07:21] Health is Patrick's Achilles heel; his knee pain fuels unresolved anxiety.   [08:02] Everyone bears the burden as Patrick wants to feel useful, but his capacity is limited.   [08:46] Embracing limitations is a sign of maturity that ultimately supports flourishing.   [09:58] Boundaries allow people to care for themselves and others at the same time.   [10:46] Caregivers can suffer "secondhand smoke" supporting someone through serious difficulties.   [11:31] Effective boundaries are personal, evolving, and shaped by individual needs and situations.   [13:23] Men's mental health requires more attention, conversation, and accepting vulnerability.   [14:51] Being courageous requires vulnerability to enable connection and recognise you're not alone.   [15:40] Suppressed emotions eventually surface, making human connection vital to deal with issues.   [18:10] Belonging matters more than fitting in, particularly when people need meaningful support.   [18:55] Regular check-ins with trusted friends create a valuable personal support network.   [18:47] Asking for "eight minutes" can signal an urgent need to feel heard and shift perspective.   [20:11] Honest conversations are important especially where role models are missing.   [21:08] Small changes reduce stress responses, enabling sustainable habits for long-term transformation.   [23:38] Compassionate leaders create psychological safety so people feel able to speak up and contribute.   [24:16] Patrick explains compassion as a fierce and courageous word.   [24:28] Wellbeing tools cannot change organizational cultures that burn people out.   [25:16] Questions for workplaces to address to improve culture, behaviours, and reduce burnout.    [27:29] Organizational values are meaningful when they actively guide decisions and daily actions.   [28:10] Patrick and his wife practice their belief that success is living up to your personal values.   [31:30] Different experiences shape values, confront biases, and deepen understanding of humanity.   [32:56] Listening to understand, not respond, helps people connect across different perspectives.   [35:12] Caring for others needs to coexist with self-compassion and managing the inner critic.   [37:00] Patrick comes up with "Start small, create space, think differently" when totally exhausted.   [38:23] Gratitude shifts attention toward good experiences without denying that difficulties exist.   [38:46] Creating mental space allows questioning of inner critique and listening to more constructive voices.   [39:17] Self-awareness is a fundamental characteristic of effective leadership.   [39:27] Power can be used with and for people rather than being exercised over them.   [41:53] Social media echo chambers weaken abilities to debate, disagree and understand other's views.   [43:39] Patrick seeks critical soft skills, valuing character and chemistry more than competence.   [44:00] Younger generations seek 'JOMO' (Joy of Missing Out) not sacrificing wellbeing and family.   [44:40] Connecting young people with their passions to unlock energy, creativity, and contribution.   [45:41] Creative problem-solving requires intentional space away from constant overwhelm and competing demands.       RESOURCES     Patrick Regan OBE on LinkedIn   Patrick's book "Small Steps for Big Change"   Patrick's book "Brighter Days"   Brighter Days website       QUOTES     "I think success is actually living true to your values."     "How do we use our power 'with' and our power 'for', rather than our power 'over', which is the traditional use of power."   "My favourite definition on boundaries is 'boundaries are how I love you and love me simultaneously."    "So you want to create that psychological safety within your organisation because that actually leads to more creativity and innovation and people feeling seen, valued and heard."   "Compassion? That's quite a weak word? Well, actually, it's a fierce word, it's a courageous word."    "Embracing your limitations is a sign of maturity. And actually helps you flourish ultimately."   "Let's think differently. Let's think creatively. For that, you need space."

In 2000, Katie Couric underwent a live colonoscopy on national television following the death of her husband, Jay Monahan, from colorectal cancer at age 42. The broadcast demystified a procedure many Americans feared, led to an estimated 20% increase in colonoscopy screenings, and became one of the clearest examples of how public storytelling can change healthcare behavior.This episode examines how celebrities, journalists, filmmakers, and entertainers helped reshape the public conversation about cancer during a period when survivorship was becoming increasingly visible. As breakthroughs in targeted therapies, immunotherapy, and early detection allowed more people to live beyond cancer, public figures used their platforms to encourage screening, reduce stigma, and accelerate research. Their influence extended far beyond awareness campaigns, helping transform cancer from a private diagnosis into a national public health conversation.Central to this story is Laura Ziskin, the Hollywood producer behind Pretty Woman and the Spider-Man films, whose metastatic breast cancer diagnosis inspired the creation of Stand Up To Cancer. Working alongside Couric and leaders from entertainment, journalism, and biomedical research, Ziskin championed a new funding model that required multidisciplinary scientific collaboration, helping accelerate discoveries that contributed to multiple FDA-approved cancer therapies. The episode also highlights the advocacy of actor Patrick Dempsey, whose family's experience with ovarian cancer led to the creation of the Dempsey Center, expanding support for patients and caregivers beyond medical treatment.The story also asks what celebrity advocacy often leaves unsaid. Financial toxicity, caregiver burden, chronic pain, mental health, and the long-term effects of treatment rarely receive the same attention as dramatic diagnoses or breakthrough cures. As cancer survivorship continues to evolve, the greatest challenge may not be convincing people to care about cancer, but helping them understand what it truly means to live with and beyond it.RELATED LINKSStand Up To Cancer⁠Katie Couric Media⁠Dempsey Center⁠American Association for Cancer Research⁠National Cancer Institute⁠Dana-Farber Cancer Institute | Adult Survivorship Program⁠FEEDBACKLike this episode? Rate and review The Cancer Mavericks: A History of Survivorship on your favorite podcast platform. For more information, visit CancerMavericks.com. Please send any questions to podcasts@matthewzachary.com.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Show SummaryOn today's episode, we're having a conversation with Navy Veteran Dr. Erik Won, President and Chief Medical Officer of Wave Neuroscience, an organization utilizing advanced neuroimaging and magnetic resonance therapy to help veterans recover from post-traumatic stress. DisclaimerThis podcast is for informational and educational purposes only and does not establish a doctor-patient relationship. The views and opinions expressed by the guest are entirely his own and do not reflect the views, policies, or official positions of his employer or company. Content is not intended to substitute for professional medical advice, diagnosis, or treatment.  Wave supplies MeRT to licensed clinics who provide treatment to patients. Talk to your physician to see if MeRT is right for you. Episode Partner:Our sponsor this week is Aetna, a trusted health care company, committed to serving Veterans, military families, and caregivers through meaningful, community-centered care. 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 GuestDr. Erik Won is President and Chief Medical Officer of Wave Neuroscience, Inc; a biotechnology company that has innovated breakthrough technologies called Magnetic e-Resonance Therapy (MeRT) and Synchronized Transcranial Magnetic Stimulation (sTMS). MeRT recently received FDA Breakthrough Technology designation and FDA clearance for Post-Traumatic Stress Disorders. These approaches utilize computational neuroanalytics and brain imaging to customize treatment protocols with the aim of restoring optimal neurological function.These modalities represent a form of precision-guided medicine that has been researched or is currently being used by premier institutions such as US Special Operations Command, Stanford University School of Medicine, Duke University - Human Performance Opti-Lab, University of Southern California (USC) Center for Neurorestoration, the University of California Los Angeles (UCLA) - David Geffen School of Medicine, University of Pennsylvania, Brown University, Air Force Research Laboratory, and the Texas A&M Institute for Bioscience and Technology.Erik joined Wave Neuroscience after serving as the Chief Physician and Chief Technology Officer (Health Services) for the Boeing Company. He also served as a US Navy Flight Surgeon for Marine Medium Helicopter Squadron 268, and received the distinction of serving as the ACE Flight Surgeon for the 11th Marine Expeditionary Unit, 1st Marine Expeditionary Force. Dr. Won has been published in numerous peer-reviewed journals, textbooks, and presented in numerous academic conferences. He completed his residency at the Harvard OEM combined residency program and was appointed Chief Resident. He received a Masters in Public Health (MPH) from the Harvard School of Public Health and Masters in Business Administrations (MBA) from the University of Southern California, Marshall School of BusinessLinks Mentioned During the EpisodeWave Neuroscience WebsiteBrain Treatment Center WebsitePsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week is the PsychArmor course Brain Health & Wellness Learning Series – PTSD. Nearly everyone goes through a traumatic event at least once during their lifetime. Military service members and Veterans are especially vulnerable to the lasting effects of post-traumatic stress due to the nature of their duties and experiences. While this can be a difficult diagnosis to navigate, it is treatable, and social support is one of the leading factors for lasting recovery. Having someone to trust and confide in while feeling heard and validated is a vital part of the healing process. This series on post-traumatic stress disorder explores the presentation and diagnosis of PTSD, its impact on both the Veterans you support and the lives of those around them, and effective treatment modalities, so you'll be better equipped to provide meaningful support. You can find the resource here: https://learn.psycharmor.org/courses/WWP-BHW-PTSD Contact Us and Join Us on Social Media Email PsychArmorPsychArmor on XPsychArmor on FacebookPsychArmor on YouTubePsychArmor on LinkedInPsychArmor on InstagramTheme MusicOur theme music Don't Kill the Messenger was written and performed by Navy Veteran Jerry Maniscalco, in cooperation with Operation Encore, a non profit committed to supporting singer/songwriter and musicians across the military and Veteran communities.Producer and Host Duane France is a retired Army Noncommissioned Officer, combat veteran, and clinical mental health counselor for service members, veterans, and their families.  You can find more about the work that he is doing at www.veteranmentalhealth.com  

In this episode of Women Connected in Wisdom, Christine Gautreaux is joined by guest co-host Lailona Holloway to welcome the visionary Rhea Lana Riner. Rhea Lana is the CEO and founder of Rhea Lana's Children's Consignment Events, a national franchising company with over 120 locations. What started in her living room in 1997 has grown into a multi-million-dollar enterprise that keeps the values of motherhood and community at its core. We'll explore the Financial Wellness dimension, focusing on the intersection of profitability and deep purpose. Rhea Lana shares how she has empowered thousands of moms by providing a flexible path to entrepreneurship. Connect with Rhea Lana Riner: Website: rhealana.com  Instagram: @rhealanas LinkedIn: Rhea Lana Riner More resources from today's show~ Franchising for Dummies https://www.lailonaholloway.com/ https://www.creategwinnett.org/  

After nearly six decades of quadriplegia and chronic pain, Joni Eareckson Tada speaks with uncommon clarity about suffering, hope, caregiving, and the daily grace that sustains when life does not get easier. In this conversation about her new book, Keeping Faith When Life Hurts, Joni explains why Christian hope sustains us when normal is not returning and why, despite her weariness, she refuses to retire.   You can watch the video of this interview at Caregiver.Substack.com

Perinatal mental health is often a misunderstood landscape shaped by stigma, cultural expectations, and invisible struggles that touch entire families. In this replay episode, Dr. Rebecca Dekker sits down with Dr. Kat Kaeni, perinatal mental health certified psychologist, author of The Pregnancy Workbook, and host of the Mom & Mind podcast, to break the silence around postpartum anxiety, depression, OCD, and psychosis. Drawing on her professional expertise and personal experience, Dr. Kat reveals why shame and isolation are so common, how symptoms really show up for new parents, and what makes perinatal mental health distinct from other forms of mental illness. They discuss the myths that keep parents suffering in silence, the real impact of mental health on babies and families, and how therapy and support groups, including free resources from Postpartum Support International, can empower families on the path to healing. Content Warning: This episode includes discussions of perinatal mental health disorders, including postpartum depression, anxiety, OCD, and psychosis. Sensitive topics such as intrusive thoughts, stigma, feelings of guilt and shame, and the potential for harm to self or others are addressed. Listener discretion is advised, and we encourage anyone who may be affected by these topics to reach out for support through Postpartum Support International or a trusted healthcare provider. (00:07:28) Unique Challenges in Perinatal Mental Health (00:11:05) Caregivers' Mental Health and Bonding Challenges (00:16:32) Parental Isolation Stemming from Anxiety and Depression (00:21:53) Emergent Postpartum Psychosis Symptoms (00:27:08) Overcoming Stigma in Perinatal Mental Health (00:31:54) Thought and Behavior Change Therapy for Depression (00:36:56) Perinatal Mental Health Challenges and Support Resoureces EBB 197 – Addressing Perinatal Mental Health for Communities of Color with the Co-Founders of the Perinatal Mental Health Alliance for People of Color, Divya Kumar, Jabina Coleman, and Desirée Israel Postpartum Support International The Mom & Mind Podcast The Pregnancy Workbook: Manage Anxiety and Worry with CBT and Mindfulness Techniques   For more information about Evidence Based Birth and a crash course on evidence based care, visit www.ebbirth.com. Follow us on Instagram and YouTube! Ready to learn more? Read Dr. Dekker's book, "Babies Are Not Pizzas: They're Born, Not Delivered!" If you want to get involved at EBB, join our Professional membership (scholarship options available) and get on the wait list for our EBB Instructor program. Find an EBB Instructor here, and click here to learn more about the EBB Childbirth Class.

How do families navigate a serious childhood diagnosis while still focusing on hope, quality of life, and the everyday moments that matter most? In this episode of Inside the Children's Hospital Podcast, Katie Taylor sits down with Dr. Korie Leigh, PhD, CCLS, a child life specialist, psychologist, thanatologist, author, educator, and pediatric palliative care advocate. Drawing on more than two decades of supporting children and families, Dr. Leigh shares what pediatric palliative care really is—and why it is so much more than many families believe. Together, they explore how pediatric palliative care supports children living with serious or complex medical conditions from the time of diagnosis, helping families manage not only medical needs, but also emotional, psychosocial, and spiritual well-being. Dr. Leigh discusses how parents can advocate for palliative care services, even if they are not offered at their local hospital, and explains why caregiver support and respite care are essential parts of caring for the whole family. The conversation also dives into resilience, grief, and the power of creativity. Dr. Leigh shares how writing can become a meaningful tool for processing difficult experiences, why preparing children for life's hardest moments matters, and how her books were created to help families navigate conversations surrounding illness, hospitalization, and loss with confidence and compassion. Whether you're navigating a new diagnosis, caring for a child with a complex medical condition, supporting a family through hospitalization, or you're a healthcare professional looking to better understand pediatric palliative care, this episode offers practical insights, encouragement, and hope. In This Episode, We Discuss: What pediatric palliative care really means The difference between palliative care and hospice Why palliative care should begin at diagnosis How parents can advocate for pediatric palliative care Finding support when services aren't available locally Caregiver burnout and the importance of respite care Building resilience during a child's medical journey Talking with children about illness, grief, and loss Using writing and creativity as tools for healing Improving access to pediatric palliative care through advocacy   Episode Timestamps 00:00 Meet Dr. Korie Leigh 02:33 A career in child life and palliative care 05:25 What is pediatric palliative care? 08:00 How parents can advocate for support 10:59 Insurance and access to care 12:05 Why respite care matters 14:18 Supporting families beyond the hospital 15:07 Building resilience through crisis 19:13 Writing through grief and healing 22:26 Creativity as a coping tool 27:29 Books, music, and final reflections Resources Mentioned When Everything Changes: Parenting through Loss and Grief by Dr. Korie Leigh Hero's Path Palliative Dr. Korie Leigh's Website Leigh Moody (music) George Mark Children's House The Artist's Way by Julia Cameron Medical information shared in this episode is not a substitute for professional medical advice. Please consult your healthcare team for guidance specific to your child and family.  

Motherhood has a way of rewriting the plans we were so sure we had figured out.For Susanna Peace Lovell, that meant becoming a mother to her daughter, Arizona, who is neurodivergent and has autism, ADHD, anxiety, and significant allergies. For Jacqueline, it meant infertility, loss, a 24-week premature birth, a four-month NICU stay, and eventually learning that her oldest son has autism and ADHD, and her younger son also has ADHD and sensory processing disorder.In this deeply personal conversation, Jacqueline and Susanna talk about what happens when motherhood looks nothing like the version you imagined—and how you learn to find yourself within it.They open up about receiving a child's diagnosis, the instinct to immediately jump into "fix it" mode, the fear of what the world will think of your child, and the invisible mental load of raising a child with additional needs. They also talk about something caregivers don't hear nearly enough: you are allowed to have needs, joy, interests, dreams, and an identity outside of caring for everyone else.Susanna shares the importance of compassion—for our children, for other mothers, and especially for ourselves—and why finding people who simply get it can change everything.In this episode:When motherhood doesn't look the way you imaginedProcessing an autism or ADHD diagnosisThe invisible work of parenting a neurodivergent childWhy gratitude and overwhelm can exist at the same timeLetting go of the pressure to "fix" everythingWhat other people don't understand about raising a child with additional needsBuilding a village when you can't do it aloneRediscovering joy and identity outside of caregivingWhat Susanna would tell a mom who just received her child's diagnosisWhy your child is still the exact same child they were before the labelSusanna also shares her work with We Are Brave Together, a community supporting the mental health and wellness of caregiving moms, and the anthology Suddenly Brave Together, featuring letters from experienced caregiving mothers to moms who are just beginning this journey.If you've ever wondered where you went while taking care of everyone else—or you're navigating a motherhood story you never saw coming—this conversation is for you.Connect with Susanna:SusannaPeaceLovell.comInstagram: @mamapeaceLearn more about We Are Brave Together:WeAreBraveTogether.orgSupport the show__________________________________________________________________________________Her Village is more than a podcast—it's a space for real connection, honest conversations, and meaningful friendships in the places we live.If you want to go deeper and stay connected beyond the podcast, you can join us here: joinhervillage.co

Managing up family caregiving starts with a conversation your aging parents rarely initiate—and most adult children delay until crisis hits. Pamela D. Wilson, caregiving expert, reveals how to use the idea of managing up to initiate that first caregiving discussion, navigate family dynamics, and set aging parents up for lasting independence. Learn caregiver advice and tips for managing complex family relationships, reducing sibling conflict, discussing financial and legal care concerns, making health decisions, and supporting aging parents before health care, legal, or financial care emergencies force your hand.To find show transcripts and educational links on the topic mentioned in Episode 252 and other The Caring Generation podcasts, click here to visit Pamela's website: https://pameladwilson.com/caregiver-radio-programs-the-caring-generation/ For more caregiving, aging, and elder care tips for your caregiving journey, visit Pamela's website at https://www.PamelaDWilson.comLearn about Pamela D Wilson as a caregiving expert, her professional background, and her 25 years of professional caregiving and elder care experience: https://pameladwilson.com/pamela-d-wilson-story/Schedule a 1:1 elder care consultation by telephone or video call with Pamela: https://pameladwilson.com/elder-care-consultant-aging-parent-consultation-managing-senior-care-needs-meet-with-pamela-d-wilson/Learn about private family elder care mediation offered by Pamela: https://pameladwilson.com/elder-care-mediator/Learn about Pamela D Wilson as an expert witness in caregiving, guardianship, fiduciary litigation, power of attorney, care management, and non-medical in-home care: https://pameladwilson.com/conservatorship-guardianship-expert-witness/https://pameladwilson.com/expert-witness-caregiving-home-care-guardianship/Check out Pamela's online course Caring for Aging Parents: https://pameladwilson.com/support-caring-for-elderly-parents-overwhelmed-caregiver-support-online-course/ Sign up for Pamela's newsletter here: https://pameladwilson.com/contact/Join Pamela's Online Caregiver Support Group on Facebook https://www.facebook.com/groups/thecaregivingtrapFollow Pamela on Social Media:Facebook: https://www.facebook.com/pameladwilsoncaregivingexpert/LinkedIn: https://www.linkedin.com/in/pameladwilsoncaregiverexpert/X: https://www.x.com/CaregivingSpeakPamela D. Wilson is a professional family caregiving and eldercare expert. As a caregiving consultant, expert witness, eldercare mediator and speaker, she provides caregiver advice and tips, individual and family caregiver support, and resources for aging and elder care decision-making. Pamela's 25 years of professional experience inform caregiving discussions, eldercare strategies, and care plans that encompass health, healthcare, financial, and legal aspects, as well as family dynamics. Visit Pamela's website at www.PamelaDWilson.com to access caregiver resources, online courses, her caregiving blog, library, book, videos, and podcast transcripts, offering practical advice and tips for aging adults and family caregivers providing elder care support. ©2018, 2026 Pamela D Wilson. All Rights Reserved

All Home Care Matters and our host, Lance A. Slatton were honored to welcome Katrina Love Prescott back to the show as our guest.   About Katrina Love Prescott, Writer/Director/Producer:   Katrina Love Prescott is a caregiver advocate, coach, and media producer based in Vancouver. She spent a decade in commercial TV production in New York before returning to Vancouver, where caregiving for her mother pulled her into a new line of work. She co-founded Care Nation Society, a nonprofit supporting caregivers, and Sunny Love Productions, and created Things Not to Say to a Caregiver and Therapeutic Fibbing to give caregivers real tools instead of platitudes. She advises organizations such as UBC, Vancouver Coastal Health, Providence Health Care, York University, and the BC Office of the Seniors Advocate.   In 2023 she won the Caregiver Advocacy Award from the Canadian Centre for Caregiving Excellence. Through Care Nation, she's building healthcare systems and community that actually work for people with chronic illness and the caregivers holding it together.    About Sunny Love Productions:   Change the Story. Change the World.    Jess and Katrina bring decades of experience in scripted, unscripted, and commercial production. We're impact creators — our expertise is listening to people, understanding complex issues, and turning them into stories that resonate and move people to act.   Every frame, every word is built to make the invisible visible — because the truth, told well, is more powerful than any campaign.    About "Things Not to Say to a Caregiver":   When someone says the wrong thing to a caregiver, a no-nonsense Care-y Godmother freezes the scene, educates the unintentional offender, and rewrites the moment — one caregiving crisis at a time.   Things Not to Say to a Caregiver is a comedic web series that tackles the awkward, misguided things people say to caregivers — and how we can do better. Each episode, a no-nonsense Care-y Godmother freezes the offender mid-fumble, delivers the reality check they didn't know they needed, and rewrites the moment into something actually helpful. Blending sketch comedy with real caregiving insight, TNTS turns cringeworthy into teachable moments — and reminds us that the right words can change everything

In 2006, a landmark report titled Closing the Gap: Research and Care Imperatives for Adolescents and Young Adults with Cancer confirmed what young survivors had been saying for years. While survival rates for children and older adults had steadily improved, adolescents and young adults had experienced decades of stalled progress. They had become cancer's lost generation.This episode explores how young adult survivors transformed their shared isolation into one of the most influential grassroots movements in cancer advocacy. Diagnosed during the years typically devoted to education, careers, relationships, and starting families, patients between the ages of 15 and 39 confronted challenges that extended far beyond treatment. Fertility preservation, sexual health, employment, financial toxicity, insurance, and long-term quality of life were rarely discussed in oncology clinics, leaving many to navigate survivorship alone.The episode follows advocates including Tamika Felder, Lindsay Avner, Heidi Adams, Doug Ulman, and Dr. Archie Bleyer, whose research and advocacy fundamentally changed how medicine understands adolescent and young adult cancer. Through organizations including Planet Cancer, Fertile Hope, the Lance Armstrong Foundation, and later Stupid Cancer, survivors built online communities, educational resources, conferences, and national partnerships that challenged long-standing assumptions about cancer care. Their work helped establish fertility preservation as a standard discussion before treatment, expanded research dedicated to adolescent and young adult oncology, and elevated quality of life as a critical clinical outcome alongside survival.The movement also demonstrated the power of lived experience to reshape medicine. Survivors became researchers, educators, nonprofit founders, and policy advocates, insisting that cancer care account not only for years of life saved, but for the lives patients hoped to build afterward.What began as a search for peers evolved into a national movement that permanently transformed adolescent and young adult oncology. Today, dedicated research programs, clinical fellowships, survivorship resources, and patient advocacy organizations continue to build on the foundation these young cancer mavericks created.RELATED LINKSNational Cancer Institute | Adolescent and Young Adult (AYA) Cancer Program⁠Closing the Gap: Research and Care Imperatives for Adolescents and Young Adults with Cancer⁠American Society of Clinical Oncology | Fertility Preservation Guidelines⁠Stupid Cancer⁠Livestrong Foundation⁠Journal of Adolescent and Young Adult Oncology⁠FEEDBACKLike this episode? Rate and review The Cancer Mavericks: A History of Survivorship on your favorite podcast platform. For more information, visit CancerMavericks.com. Please send any questions to podcasts@matthewzachary.com.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Self-regulation is the ability to recognize and manage our emotional, mental and physical responses to stress so we can think clearly, make sound decisions, and engage effectively with others. In healthcare and other high-pressure environments, self-regulation helps individuals move beyond instinctive "fight, flight or freeze" reactions and respond with intention, empathy and professionalism. In this episode of Caring Greatly, Jennifer Luer, DNP, RN, CPPS, CPHQ, System Director of Employee Safety and Wellbeing at SSM Health, explores the powerful role of self-regulation in healthcare leadership and workplace safety. Drawing on her journey from critical care nurse to system leader, Jennifer shares how personal experience, patient safety work, and a passion for supporting care team members shaped her approach to building a healthier, safer work environment at SSM.Jennifer also discusses why employee wellbeing deserves dedicated focus, how self-regulation helps individuals stay grounded under pressure, and why creating a culture of safety requires both personal skills and system-level support. From workplace violence (WPV) prevention to leadership communication, self-regulation techniques allow individuals to regain balance during challenging moments, reduce burnout, improve communication, strengthen relationships, and maintain the capacity to provide safe, high-quality care and effective leadership.Jennifer is a registered nurse and system leader specializing in healthcare safety and quality through evidence-based best practices and continuous improvement. Her work centers on advancing emotional, physical and psychological safety for care team members and patients alike. Pursing her passion and purpose as a nurse, she joined SSM Health in 2007. Jennifer also has than 11 years of experience in process improvement, event investigation and root cause analysis. In June 2021, she transitioned into her role as System Director of Employee Safety, following leadership of Regulatory, Infection Prevention, Risk, Quality and Patient Safety. Jennifer has been instrumental in designing and implementing the Care for Caregivers program, including systemwide education on the second-victim phenomenon. She has also helped lead key initiatives such as the rollout of WPV prevention training, simplified single-icon WPV reporting, proactive EHR workflows for violence risk, and standardized tools that support a holistic approach to care team safety. Dr. Jennifer Luer is a leader who cares greatly.Related links:Article: Built on safety, powered by peopleJennifer Luer on LinkedInThe views and opinions expressed in this podcast are those of the speakers and do not necessarily reflect the views or positions of Stryker. The provided resources may contain links to external websites or third-party content. We do not endorse, control or assume any responsibility for the accuracy, relevance, legality or quality of the information found on these external sites. Stryker Corporation or its divisions or other corporate affiliated entities own, use or have applied for the following trademarks or service marks: Caring Greatly, Stryker. All other trademarks are trademarks of their respective owners or holders.

Join Sophie and Chloe as they discuss camping with diapers, the true fanbase of FFXIV, and—as the title accurately suggests—which Disney villain would make the best caregiver!  Make sure to join the SubscribeStar to vote on this week's bet and get exclusive mini-episodes!Find us on BlueSky @theusualbet.bsky.socialEmail us at theusualmailbox@gmail.comSupport us at www.subscribestar.adult/sophieandpudding ★ Support this podcast on Patreon ★

Send Cathy a text:)What if caregiving has been changing you in ways you haven't even noticed?Welcome to Season 4 of The Caregiver Cup Podcast: Cup by Cup: Growing Through Caregiving. This season isn't about becoming the perfect caregiver. It's about discovering the strength, wisdom, compassion, and confidence that can quietly grow through caregiving—one day, one choice, and one cup at a time.In this special season preview, Cathy shares what's ahead over the next 12 weeks and introduces one powerful question that will guide every episode:Who am I becoming through this?If you've ever wondered whether you're doing enough, this season will gently shift your focus from simply surviving caregiving to recognizing the remarkable person you're becoming along the way.Support the show

Episode Summary: In this episode of the Work at Home Rockstar Podcast, Tim Melanson chats with Dr. Rob Yonover, founder and CEO of Sea Rescue Corporation, who has worked from home for over 30 years inventing survival gear for military and civilian use. What started as him "screwing around with a piece of plastic" on his patio became the SeeRescueStreamer, a signaling device he says is now military-approved worldwide and has even flown on SpaceX missions. Rob gets candid about what it actually takes to make working from home sustainable: brutal self-discipline, a simple math equation for building a passion project around a day job, and a thick skin built from years of rejection, including five no's on Shark Tank. He walks through the relentless, old-school media hustle that got his product into outlets like the Miami Herald, Outside Magazine, and Playboy, and explains why he still believes trade shows and face-to-face relationships beat digital marketing for building trust. The conversation also covers how a 15-year licensing deal with guaranteed royalties gave him the cash flow to keep inventing, what's exciting him now with a new pocket desalinator project and his published books, and his strong personal views on keeping kids off phones and social media. Who is Dr. Rob Yonover? Dr. Robert Yonover is a Ph.D. geochemist/volcanologist with a history of innovative scientific contributions and technologies that have been awarded U.S. Military/DARPA funding and U.S. Patents. The military-approved/adopted SeeRescueStreamer has saved lives on land and in water. A North Shore big wave surfer and Molokai Channel rough-water fisherman, Dr. Yonover uses the ocean as his laboratory. He's the founder and CEO of Sea Rescue Corporation and has worked from home in Hawaii for over 30 years, describing himself as a third-generation work-at-home entrepreneur following his grandmother, who ran an early medical practice out of her Chicago home, and his father, who built a mail-order business in the 1960s. The SeeRescueStreamer earned Navy approval and has since been adopted across military branches, including the Canadian Air Force. He's also the author of four books, Hardcore Inventing, Caregiver's Survival Guide, Hardcore Health, and Brainstorm Islands, and is currently working on a pocket desalinator that converts saltwater to freshwater. Connect with Dr. Rob Yonover: Website: SeeRescueStreamer.com Host Contact Details: Website: https://workathomerockstar.com Facebook: https://www.facebook.com/workathomerockstar Instagram: https://www.instagram.com/workathomerockstar LinkedIn: https://www.linkedin.com/in/timmelanson YouTube: https://www.youtube.com/@WorkAtHomeRockStarPodcast X / Twitter: https://twitter.com/workathomestar Email: tim@workathomerockstar.com In this Episode: 00:00 — Welcome and Guest Intro 00:30 — From Patio Idea to Lifesaver 01:30 — Discipline for Remote Work 03:18 — Side Hustle Time Math 04:53 — Avoiding Desperation Deals 05:52 — Handling Rejection and Doubt 08:32 — Protect Ideas Before Sharing 09:29 — Finding Your First Yes 13:42 — Old School Media Hustle 16:01 — Marketing in the Internet Age 19:50 — Work Ethic Beats the Odds 20:43 — Passion and Ownership Matter 21:55 — Tools That Still Work 22:31 — Trade Shows and Niches 24:32 — Longevity and Low Overhead 25:51 — Relationships Beat Automation 27:53 — Licensing and Cash Flow 30:28 — Thick Skin and Trolls 32:10 — Phones Without Guardrails 35:16 — What Excites Him Now 35:57 — Desalinator and Storytelling 40:00 — No Electricity Grandpa 40:58 — Where to Find Rob 41:50 — Desert Island Albums General Business Advice Disclaimer The strategies and experiences shared in this episode are based on our guest's personal journey and are for inspiration and education, not a guarantee of results. What worked for them may not work the same way for everyone. Guest Claims & Product Disclaimer Any claims made about products, approvals, or outcomes in this episode reflect our guest's own statements about their business and have not been independently verified by Work at Home RockStar. Personal Opinions Disclaimer Our guests share their own opinions and life philosophies, on technology, parenting, or anything else, which don't necessarily reflect the views of this show. 45:24 — Final Thanks and Signoff

Caregiving can feel like a private struggle, but the numbers and the lived reality say it's a hidden crisis. We sit down with Diane, a nurse with 53 years of experience and the founder of CaregiverRelief.com, to talk about what dementia caregiving really does to families and why so many caregivers feel like they're carrying the whole load alone.Diane traces her “why” back to her grandmother's Alzheimer's journey and the kind of moment every family hopes for: connection that still breaks through the fog. From there, we get honest about the long arc of caregiving, including how early grief and responsibility shape a caregiver's life, why burnout is more than “being tired,” and how relationships can wither when your world becomes meds, meals, safety, and constant vigilance.Then we go straight at the system. Diane explains the gaps she sees in dementia care support, why navigating hospitals, rehab, and long-term care can overwhelm anyone without a medical background, and what scares her about cost-sharing and Medicare Advantage co-pays tied to skilled nursing and rehab. Most importantly, she gives practical tools you can use right now: build a caregiver relief group, assign people to check on the caregiver, and put a family caregiver contract in place so time off and support are clear and fair.If you're caring for a parent with Alzheimer's or supporting someone who is, hit play, share this with your village, and then subscribe, leave a review, and tell us what kind of help would actually make your week easier.Make sure to visit caregivingrelief.com to learn more about Diane and listen to her podcast. Exec. Producer/Host: J Smiles Comedy Producer: Mia Hall Editor: Annelise Udoye Support the show"Alzheimer's is heavy but we ain't gotta be!"IG: https://www.instagram.com/parentingupFB: https://www.facebook.com/parentingupYT: https://www.youtube.com/@parentingupTEXT  'PODCAST"  to  +1 404 737 1449  - to give J topic ideas, feedback, say hi!Be sure to leave us a review! 

Our culture often treats aging as something to resist. Judaism sees it differently: years are not merely something that happen to us; they can become a source of wisdom, purpose, and depth. Drawing on the mitzvah of shiluach hakein in Parshat Ki Teitzei, the Torah's promise of long life, the mitzvah of honoring parents, and the Rebbe's teachings about aging, Rabbi Yisroel Bernath explores what it really means to “lengthen our days.”As Elul invites us to look back over another year, the deeper question is not simply, “How much older did I become?” but “How much deeper did I become?”Through the moving example of Brahm and Ilana Shiller, the sermon becomes a meditation on courage, resilience, love, and living fully even when life does not unfold as we would choose. Perhaps a long life is measured not only by how many days we receive, but by how much life we put into each day.Key PointsJudaism does not see aging as decline. Long life is a blessing, and lived experience itself carries dignity and holiness.You can retire from a career, but never from purpose. As our stage of life changes, our mission may change with it, but our ability to matter does not disappear.Ki Teitzei teaches us not to exploit devotion. Both shiluach hakein and honoring parents remind us to recognize and honor those whose love causes them to keep giving.Elul is not merely about another year passing. Growing older happens automatically. Growing deeper requires choice.Difficulty can reveal character. Real positivity is not denying pain; it is being able to say, “This is hard, and I am still going to live today.”Courage also belongs to the person standing beside the struggle. Caregivers and spouses carry their own quiet burden of love, worry, strength, and hope.Arichut yamim, long life, can also mean full days. A day filled with love, laughter, generosity, presence, and an open heart contains an extraordinary amount of life.The Elul question: We cannot always choose what happens to us, but we participate in choosing who we become within what happens.#ParshatKiTeitzei #KiTeitzei #Judaism #Jewish #Torah #Bible #BibleStudy #Elul #chabad #Rabbi #JewishWisdom #AgingWithPurpose #LongLife #purpose #resilience #Courage #ShiluachHakein #chassidus #therebbe #LivingFully #gratitude #JewishInspiration #RabbiBernath Rabbi Yisroel Bernath's New Book The Forgiveness Experiment is Available now:Paperback: https://www.amazon.com/Forgiveness-Experiment-What-Would-Your/dp/1069217638Kindle: https://www.amazon.com/dp/B0FR2QNJL6Audiobook: https://bit.ly/4tPFZhVSupport the showGot your own question for Rabbi Bernath? He can be reached at rabbi@jewishndg.com or http://www.theloverabbi.comSingle? You can make a profile on www.JMontreal.com and Rabbi Bernath will help you find that special someone.Donate and support Rabbi Bernath's work http://www.jewishndg.com/donateFollow Rabbi Bernath's YouTube Channel https://www.youtube.com/user/ybernathAccess Rabbi Bernath's Articles on Relationships https://medium.com/@loverabbi

Caregiving changes the economy of your life, and therefore it can change what good financial decision-making and your money rules looks like.When time, sleep, freedom, play, energy and attention become scarce, spending can start doing more than buying things. It can buy relief, convenience, novelty, comfort, or a tiny reminder that you still matter.In this episode, we're talking about why caregivers may need different financial rules, how to understand what your spending is actually trying to do for you, and how to care for yourself without disappearing from your own life.I dedicate this episode to Parents, people supporting sick partners, people with elderly pets or sick pets, adult children helping parents, people in temporary crisis who are constantly asking themselves: What happens to my money when my life suddenly requires much more from me?Enjoy the show! ⭐️ Book Your Introductory SessionIf you're tired of wondering why money feels harder than it should, I invite you to book a 1:1 Financial Wellness Session.Together, we'll explore the emotional, behavioral, and nervous system patterns driving your financial decisions, identify what's getting in the way, and create a practical path forward that actually works for your real life.Because I BET you don't need more financial advice... you need help understanding why you're struggling to do what you already know would help.You can book your session here. ⭐️⭐️⭐️⭐️⭐️ If this episode made you think, gave you a new perspective, or helped you feel a little less alone, would you do me a favor?Leave a 5-star review on Spotify or Apple Podcasts and email me a screenshot. Reviews help this little podcast reach more go-getters who need it. And because I appreciate you, I'll send you a special thank-you gift in return ♥️~Podcast theme song by The Jilted Irony

Send us Fan MailUSA DOUBLED DEFICIT LAST 10yrs. We Are In Trouble. Solutions. Don't Wait

Richard Brendan joins us to talk about a part of caregiving that does not get nearly enough attention: what happens when caregiving ends. Then, we turn the tables on Richard with a few questions from The Death Deck, including who he would invite to one last meal, what song he would want played at his celebration of life, and whether he would want to know the exact day he is going to die. We also look ahead to the upcoming Death Café and what people can expect if they join us.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Send a Text to the Moms - please include your contact info if you want a response. thanks!Technology is changing the way we think about mental health care—but what does that mean for families living with schizophrenia and other serious mental illnesses? Can technology actually make life easier for the people in the trenches—and how can families separate the genuinely useful tools from the hype?Nicole Gillen knows what it means to be a mom navigating the complicated world of serious mental illness. In her new book, Connected Care, she explores how technology—from apps and telehealth to AI and other digital tools—can become part of the care journey. But with so many new tools appearing every day, how do we know what is actually helpful, what is safe, and what might simply add to the overwhelm? Today, Nicole joins us to talk about the possibilities of connected care—and what families need to know before they click, download, or sign up.Nicole Drapeau Gillen is a mother, advocate, and author who translates the fast-moving landscape of technology in serious mental illness care into guidance families and clinicians can use. When she found herself thrust into caregiving for a loved one with serious mental illness, with no direction on how to help, she turned that into a mission, writing two books and building an ongoing effort to bring families and clinicians into the conversation.Her first book, Schizophrenia and Related Disorders: A Handbook for Caregivers, is a reference for every stage of caregiving, endorsed by Dr. E. Fuller Torrey as a must-read for SMI caregivers. Her second, Connected Care: A Practical Guide to Technology for Serious Mental Illness, maps apps, AI tools, telepsychiatry, and brain-based treatments for a field moving faster than anyone can track — work Dr. Akira Sawa, Director of the Johns Hopkins Schizophrenia Center, has said "directly addresses" a significant gap.Links"Connected Care: A Practical Guide to Technology for Serious Mental Illness""Schizophrenia and Other Related Disorders. A Handbook for Caregivers" WebsiteThanks for liking and sharing the podcast! Mindy and her book: https://mindygreiling.com/Randye and her book: https://randyekaye.com/Miriam and her book: https://www.miriam-feldman.com/Support the showPlease share and support the podcast so we can reach more people who need the info and support.Want to know more?Join our facebook page  Our websites:Randye KayeMindy Greiling Miriam (Mimi) Feldman

Go to todaysautisticmoment.com for the complete transcripts.Are you an Autistic Adult who found yourself as a caregiver for someone you love? Whether you were planning to be someone else's caregiver or were suddenly thrust into it because someone you are close to suddenly got ill and needed extra care; your routines are totally disrupted. You are having to arrange doctor appointments, help with medications, communicating with health professionals. It is overwhelming and maximizing your nervous system's windowof tolerance. Cheryl Cowen is Autistic, a nurse, a professional and personal caregiver.  Cheryl and Philip will discussstrategies for Autistic caregivers, share personal stories, how to manage triggers, set boundaries and seek help when needed.

Text Us!In this episode of Raising Disabled, we talked to the girls of Caffeinated Caregivers, Alyssa Nutile and Erica Stearns.  In part 1 of this 2 part episode, we talk about Alyssa and Erica's disabilities that they themselves have and they both share about their own children's disabilities and unique struggles.They are a MUST FOLLOW on Instagram at @caffeinated_caregivers because they are the queens of hilarious disability parenting memes. In part 2 of this episode, we are going to continue our conversation and talk about all four of our experiences with requesting a hospital transfer while inpatient and the highs and lows that come with being transferred.  We also share how we advocated for ourselves and why you need to know your rights as a parent or patient. Please subscribe, leave a review, and follow us on social media to know about upcoming episodes and to participate in this podcast.Instagram - @raisingdisabledpodcastFacebook - Raising Disabled Podcast

Episode SummaryIn this episode of The Yoga Therapy Hour, Amy sits down with Danielle Burke, a certified yoga therapist and licensed professional counselor, to explore what happens when traditional talk therapy meets embodied practice.Danielle shares her journey from mental health counseling into integrative wellness, where she now blends yoga therapy, somatic awareness, and lived experience to support clients in reconnecting with themselves. Together, they explore what it means to feel “stuck in your story,” how breath and body awareness interrupt that pattern, and why self-awareness is not just insight—but a skill that must be practiced.This conversation offers a steady and honest look at anxiety, burnout, overgiving, and the quiet work of learning to trust yourself again. Through the lens of the yamas and niyamas, Danielle brings forward a practical framework for navigating uncertainty, building inner stability, and reducing unnecessary suffering.Key Themes Explored1. When Talk Therapy Isn't EnoughDanielle reflects on her work as a licensed counselor and the moment she recognized something was missing—clients could process their experiences cognitively, but often remained disconnected from their bodies. Yoga therapy offered a way to integrate both.2. The Body as the Entry PointClients often arrive stuck in patterns of thinking, or unable to access their thoughts at all due to overwhelm. Danielle highlights a simple but profound observation: many people stop breathing when recounting difficult experiences. Reconnecting to breath becomes the doorway back to regulation and presence. 3. Self-Awareness as a Practice, Not a TraitAwareness is not assumed—it is cultivated. Through consistent practice, clients begin to recognize their internal states, expand their capacity for choice, and shift from automatic reaction toward intentional response.4. Working with Anxiety Without Trying to Eliminate ItRather than attempting to “fix” anxiety, Danielle reframes the work:Can you recognize it?Can you stay with it?Can you also notice what else is present?This introduces the possibility of holding multiple truths at once, rather than being defined by a single state.5. The Yamas and Niyamas as a Regulatory FrameworkEthical principles such as ahiṃsā (non-harming/kindness) and svādhyāya (self-study) become practical tools for daily living. They support clients in discerning how they want to show up—for themselves and in relationship with others.6. Caregivers, Overachievers, and the Cost of Self-AbandonmentDanielle's primary clients are often women who have spent years supporting others while losing connection to their own needs. The work becomes one of reclaiming worth, voice, and internal alignment.7. Letting Go of Control (Īśvara Praṇidhāna in Practice)Through simple, real-life moments—like dogs barking during a podcast—Danielle illustrates how acceptance reduces suffering. The shift is subtle but powerful:From “this shouldn't be happening” → to “this is happening, and I can still be here.”8. Change Requires Doing Something DifferentInsight alone is not enough. Sustainable change comes through practice, patience, and a willingness to step outside familiar patterns—even when those patterns are uncomfortable.What a Session with Danielle Looks LikeSessions are adaptive and client-centered, typically including:Reflective conversation and active listeningGentle inquiry and pattern recognitionBreath awareness and regulation practicesMovement or physical practice (when appropriate)Yoga Nidra or guided meditationPersonalized tools such as journaling prompts or recorded practicesThe process remains grounded in yoga philosophy while accessible to clients regardless of their familiarity with yoga.Notable Reflections“Awareness gives us choice. And choice gives us power.” “The only way to change is to do something different.” “We can hold more than one experience at the same time.” About Danielle BurkeDanielle Burke is a certified yoga therapist and licensed professional counselor with over a decade of experience in mental health. She now works through an integrative wellness model, combining yoga therapy, somatic practices, and psychological insight to support clients in reconnecting with their bodies, their values, and their sense of self.Based in interior Alaska, Danielle works with clients both in person and online.Connect with Danielle BurkeWebsite: www.inlightandlovewellness.comInstagram: @inlightandloveytLinkedIn: Danielle BurkeClosing ReflectionThis conversation invites a steady reconsideration of how we relate to ourselves. Not through force or perfection, but through awareness, practice, and a willingness to meet what is here—one moment at a time.

Our guest this week is Rick Corbett of Loganville, GA who worked in the electrical industry for 25 yeara before becoming a full-time caregiver. Rick is father of two boys including one with Hydrocephaly and a caregiver to a young woman with special needs. Rick and his x-wife, Mary, were married for 29 years and are the proud parents of two boys: Sean (30), who lives with his mom and Richard (36) who has Hydrocephalus, a rare, complex, and chronic illness.  Rick is also caregiver to Morgan (32) who is wheelchair bound due to a brain injury suffered at birth.  We learn about how Richard was warmly embraced by his high school classmates where he was known as "Touchdown Richard" becuase of his enthusiam for and involvment with the high school football team.  We also learn about the impact the Tim Tebow Foundation 'Night To Shine' program has had.It's an uplifting story about a father's devotion to his children and others all on this episode of the SFN Dad to Dad Podcast.Thius episode was recorded at St. John Neumann Church in Lilburn, GA on day #18 and stop #37 of the SFN U.S. Tour,  Special thanks to SFN Mentor Father Scott Sowers, who was featured in episode #9, for organizing the gathering at St. John Neumann Church.  Show Notes - Phone – (404) 578-5259Email – rjcorbett79@yahoo.comSpecial thanks to all those who supported the SFN U.S. Tour, a month-long, 50-state, 60+ stop tour that took place from May 21 to June 21, 2026: to strengthen and grow the Special Fathers Network and distribute 1,000+ complimentary copies of our new book: Dads Raising Children With Special Needs & Disabilities: A Guide For 21st Century Dads. Special Fathers Network –SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 900+ SFN Mentor Fathers, who are raising kids with special needs, have said: “I wish there was something like this when we first received our child's diagnosis. I felt so isolated.  There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through.”SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videosPlease support the SFN. Click here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/  

Send us Fan MailWhy can giving feel easy, but receiving feel uncomfortable?In this Spiritual Spotlight Series Quick Tip, Rachel Garrett explores why empaths, healers, caregivers, space holders, and chronic givers often struggle to accept help, rest, compliments, support, or care without guilt.For many people, the nervous system has learned that love, worth, or belonging comes from being useful. So when someone offers support, the body may immediately brace and questions appear: What do they want in return? Am I being selfish? Do I deserve this?Rachel shares why receiving is a spiritual practice, not a weakness. When we constantly give without allowing ourselves to receive, we can become depleted, disconnected, resentful, and less able to hear our intuition clearly.You'll learn how to notice resistance to receiving without judging yourself, how nervous system patterns influence your ability to accept support, and a simple body-based practice using the affirmation:“I am allowed to receive.”You'll also discover practical ways to begin receiving today—accepting a compliment without deflecting, resting before exhaustion takes over, allowing someone to help you, and choosing relationships and spaces where you don't always have to be the strong one.If you're always the person everyone turns to but struggle to let others show up for you, this episode is your reminder that healing isn't only about what you give.Sometimes healing is learning how to let yourself receive.Support the showSpiritual Spotlight Series is hosted by Rachel Garrett, RN, CCH — Akashic Records Practitioner, Master Energy Healer, and Certified Crystal Healer.Conversations about the things we almost don't say out loud. For the ones who feel everything — but question it.Each episode features real stories of spiritual awakening, healing, and transformation from guests across all walks of life, alongside solo teachings on Akashic Records, crystal healing, nervous system support, and intuitive development.Healing doesn't have to be heavy.New: Join the monthly live Akashic reading → YouTube membership at $4.99/month → youtube.com/@rachelgarrett/membership✨ Explore More Spiritual Wisdom & Stay Connected

In 2006, the Institute of Medicine published From Cancer Patient to Cancer Survivor: Lost in Transition, concluding that millions of Americans were surviving cancer only to find themselves navigating a healthcare system unprepared for life after treatment. The report challenged oncology to recognize that curing cancer was not the end of care, but the beginning of survivorship.This episode explores how the growing cancer survivorship movement exposed the long-term consequences of cancer treatment that medicine had largely overlooked. As survival rates improved following the National Cancer Act of 1971, millions of survivors faced chronic fatigue, neuropathy, infertility, cognitive impairment, financial hardship, employment discrimination, anxiety, depression, and post-traumatic stress. These were not rare complications. They became defining features of survivorship for many patients.Drawing on the work of oncologist Dr. Patricia Ganz, survivor advocate Ellen Stovall, and researchers, clinicians, and survivors across the country, the episode examines how survivorship research expanded beyond recurrence and mortality to include quality of life, psychosocial care, rehabilitation, and long-term follow-up. Their efforts helped establish survivorship care plans, multidisciplinary survivorship clinics, and a broader understanding that cancer affects every aspect of a person's life long after treatment ends.The episode also confronts persistent inequities in survivorship care. Insurance coverage often ends when treatment stops, supportive services remain inconsistent, financial toxicity continues to drive medical hardship, and racial, geographic, and socioeconomic disparities still influence who receives comprehensive follow-up care. For many survivors, finishing treatment simply marks the beginning of another struggle.Modern oncology increasingly recognizes that surviving cancer is measured by more than years of life. It is also measured by quality of life, dignity, access to care, and the ability to rebuild a future after treatment. That evolution remains one of the most significant legacies of the cancer survivorship movement.RELATED LINKSNational Academy of Medicine | ⁠From Cancer Patient to Cancer Survivor: Lost in Transition⁠National Cancer Institute Office of Cancer Survivorship⁠American Society of Clinical Oncology | Survivorship Compendium⁠CancerCare⁠HopeWell Cancer Support⁠National Coalition for Cancer Survivorship⁠FEEDBACKLike this episode? Rate and review The Cancer Mavericks: A History of Survivorship on your favorite podcast platform. For more information, visit CancerMavericks.com. Please send any questions to podcasts@matthewzachary.com.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Are you exhausted from constantly taking care of everyone else while putting your own needs on the back burner?In this powerful episode of Empowered in Health, Erin sits down with Dr. Lisa Muehlenbein. Dr. Lisa is a nationally recognized expert on physician burnout, helping both medical families and healthcare organizations foster resilience, connection, and aculture of well-being through her MedLife Matrix™ methodology.In our conversation, we talk about midlife burnout, the invisible load women carry, the importance of self-care, marriage, relationships and what really happens when your own needs are continually pushed aside!Lisa also shares her deeply personal journey of realizing that she was burned out - even when she didn't recognize it herself. Her experience led her to study burnout and eventually research how professional burnout can affect spouses, families, and relationships - especially for physician families.Lisa teaches us incredible lessons that apply to so many women who feel like they are carrying the emotional weight of their families.If you've ever thought:• "I'll take care of myself when things calm down."• "Everyone else needs me more than I need me."• "I don't have the right to complain."• "Life will be better when the kids are older."• "I'll have time for myself someday."This conversation is for you.Lisa introduces the idea of "Someday Syndrome" - the belief that life will finally get better after the next milestone, only to discover that "someday" keeps moving further away.You'll also hear why the invisible load can create loneliness, resentment, emotional exhaustion and disconnection in relationships. And why communication is essential for reconnecting with your partner!If you're a woman navigating midlife, motherhood, marriage, burnout, or the overwhelming responsibility of caring for everyone else, this episode is a reminder that your needs matter too.You don't have to wait for someday to start taking care of yourself.Connect More with Lisa here:Website: https://www.themedlifematrix.comMastering the MedLife Matrix Course: https://www.themedlifematrix.com/mastermedlifePodcast: The MedLife Support Podcasthttps://podcasts.apple.com/us/podcast/the-medlife-support-podcast/id1867028871?i=1000744036887Dissertation Research: Physician Burnout and the Marital Relationship: Spouse Perspective https://www.themedlifematrix.com/resourcesInstagram: https://www.instagram.com/themedlifematrixLinkedIn: https://www.linkedin.com/in/lisa-muehlenbein-phd-3088b73a/Facebook: https://www.facebook.com/themedlifematrixIf this episode resonated with you, please subscribe and leave a review on your favorite podcast platform. Sharing this episode with a friend can also help us reach more incredible women on their journey to better health.Thank you for being a part of our community and investing in your wellness journey!

Parent. Partner. Employee. Caregiver. The strong one. The reliable one. The one who holds it all together. Most of us have been living inside our roles for so long that we've started to mistake them for our identity. In today's episode Celeste draws a clear line between the roles you play and who you actually are — and explains why knowing the difference is one of the most liberating realizations a person can have. If you've ever felt lost when a role was taken away — when the kids grew up, the relationship ended, the job changed — this one will explain why and show you the way back to yourself. Today's shift: Name one role you've been living inside — and ask yourself honestly, who am I outside of this? Classes Store Follow Celeste podcast page on tick tock , facebook and instagram Follow STWYT Wellness center on tick tock , facebook and instagram

In 1967, breast surgeon Dr. Harold P. Freeman arrived at Harlem Hospital expecting to treat cancer. Instead, he confronted a healthcare system where poverty, racism, lack of insurance, and institutional barriers often determined who lived long enough to receive treatment. Patients frequently arrived with advanced disease, not because medicine lacked answers, but because access to care had failed them.This episode explores how cancer survivorship expanded beyond medical breakthroughs to include healthcare access, health equity, and organized advocacy. Building on the early work of the National Coalition for Cancer Survivorship (NCCS), it examines the recognition that surviving cancer depended not only on research, but also on whether patients could navigate a fragmented healthcare system.Freeman responded by creating one of the nation's first patient navigation programs at Harlem Hospital in 1990. Community-based navigators helped patients overcome practical barriers including insurance, transportation, appointments, communication, and fear. The model dramatically improved timely diagnosis and treatment, increased breast cancer survival in Harlem, and ultimately inspired the Patient Navigator Outreach and Chronic Disease Prevention Act of 2005, establishing navigation as a cornerstone of modern oncology care.The episode also follows cancer survivor Ellen Stovall, whose leadership transformed survivorship into a national policy movement. Through the NCCS, she united advocates across cancer types, fought for insurance protections, expanded access to clinical trials, helped shape the creation of the Office of Cancer Survivorship at the National Cancer Institute, and organized the landmark 1998 National March for Cancer Survivorship in Washington, D.C. Her work reframed survivorship as a public policy issue rather than a personal experience.Together, Freeman and Stovall demonstrated that scientific progress alone could not eliminate disparities in cancer outcomes. Their work established two enduring principles that continue to shape oncology today: patients need someone to help them navigate care, and survivors must have a voice in the policies that govern it. Modern cancer survivorship depends on both.RELATED LINKSNational Coalition for Cancer Survivorship⁠Harold P. Freeman Patient Navigation Institute⁠National Cancer Institute Office of Cancer Survivorship⁠Patient Navigator Outreach and Chronic Disease Prevention Act of 2005⁠American Cancer Society⁠Tuskegee Study Timeline | Centers for Disease Control and Prevention⁠FEEDBACKLike this episode? Rate and review The Cancer Mavericks: A History of Survivorship on your favorite podcast platform. For more information, visit CancerMavericks.com. Please send any questions to podcasts@matthewzachary.com.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Welcome to a very, very, very special bonus episode of Out of Patients, and one unlike anything published on this feed before. For nearly 20 years, Matthew Zachary has handed these microphones to patients, caregivers, doctors, advocates, troublemakers, and people with something worth saying. This time, he handed them to his daughter. Hannah Greenzweig grew up around this show, and now she has commandeered the studio with 3 of her wonderfully creative high school friends to talk about something they built entirely themselves. There is an enormous amount of Dad Pride baked into this episode, along with the strange and wonderful realization that sometimes your kid grows up, takes your chair, takes your microphone, and produces a better show without you.Hannah Greenzweig, Michael Aidinov, Gwendolyn Baldini, and Astronomy are student artists from the Roundabout Youth Ensemble at James Madison High School in Brooklyn. Working alongside teaching artists from Roundabout Theatre Company, they spent a school year creating an original play from the ground up, writing every scene, developing every character, and producing the performance themselves.Instead of discussing a Broadway production, they dissect one they invented.Their play, Subject Matter, began with a room full of improbable ideas. Murderous bounce houses, pirate family sagas, underwater adventures, courtroom dance battles, and birthday parties at math museums all competed before the group settled on an absurd rivalry between New York's fictional History Museum and Math Museum. From there, they built a fully staged comedy about institutional competition, sabotage, oversized personalities, and the unexpected discovery that history and mathematics need each other more than either side wants to admit.The conversation pulls back the curtain on a creative process most audiences never see. The students explain how scenes evolved through constant rewrites, how characters emerged from improvisation, how costumes came together with last minute ingenuity, and how rehearsals often collapsed into uncontrollable laughter. They recount cutting favorite ideas, solving production problems with limited resources, and trusting each other enough to keep rewriting until the story worked.The episode also captures something harder to script: teenagers speaking honestly about collaboration without adults translating their experience. They celebrate classmates who stepped into unexpected roles, teachers who quietly held the production together, and the strange joy of creating something that exists only because everyone showed up.It is a conversation about theater, friendship, education, creativity, and what happens when 4 young artists get the microphones and the adults get out of the way.RELATED LINKSRoundabout Theatre CompanyRoundabout Youth EnsembleJames Madison High SchoolFEEDBACKLike this bonus 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.