Podcasts about caregivers

Gigi Robinson grew up with Ehlers-Danlos syndrome, a disease that turns your joints into overcooked spaghetti. Instead of letting it sideline her, she built a career out of telling the truth about invisible illness. We talk about what it takes to grow up faster than you should, why chronic illness is the worst unpaid internship, and how she turned her story into a business. You'll hear about her days schlepping to physical therapy before sunrise, documenting the sterile absurdity of waiting rooms, and finding purpose in the mess. Gigi's not interested in pity or polished narratives. She wants you to see what resilience really looks like, even when it's ugly. If you think you know what an influencer does, think again. This conversation will challenge your assumptions about work, health, and what it means to be seen.RELATED LINKSGigi Robinson Website: https://www.gigirobinson.comLinkedIn: https://www.linkedin.com/in/gigirobinsonInstagram: https://www.instagram.com/itsgigirobinsonTikTok: @itsgigirobinsonA Kids Book About Chronic Illness: https://akidsco.com/products/a-kids-book-about-chronic-illnessFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship inquiries, email podcast@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Learn about a helpful book with resources for dementia caregivers. My guest Dr. Beverly Thorn is dual trained in the neurosciences and clinical psychology. She is the author of hundreds of articles, two books, and four workbooks on coping with chronic illness. She has also been trained as an end-of-life doula and served as her… Continue reading Ep. 508 Navigating Life as a Dementia Caregiver with Beverly Thorn PhD

Welcome to the Sustainable Clinical Medicine Podcast! In this episode, Dr. Sarah Smith sits down with Dr. Jessi Gold, psychiatrist, author, and Chief Wellness Officer for the University of Tennessee system. Together, they delve into Dr. Gold's fascinating journey through medicine—from her early days resisting the pull of psychiatry, despite her father's influence, to finding her true calling in supporting healthcare workers and college students through mental health challenges. Dr. Gold shares candid stories about her own mental health struggles, the barriers to seeking help in medicine, and how the COVID-19 pandemic reshaped her clinical focus to frontline healthcare workers. She opens up about recognizing burnout in herself, the subtlety of its symptoms, and the lessons she learned about self-care, connection, and setting boundaries. Along the way, Dr. Gold offers practical strategies for identifying burnout early, building resilience, and creating sustainable ways to care for ourselves and each other in healthcare. If you've ever wondered how to stay well while caring for others—or found yourself feeling isolated in your own struggles—this episode is for you. Join us as Dr. Gold brings wisdom, vulnerability, and humor to the vital conversation about humanity in medicine, and learn simple, actionable steps you can take to support your own mental health. Let's dive in! Here are 3 key takeaways from this episode: Burnout Creeps in Subtly: It's rarely one big event. The signs can include relentless fatigue, irritability with routine work tasks (like inbox overload!), and gradual withdrawal from friends and family. Often, they go unnoticed until things become critical. Check in With Yourself—Intentionally: Gold emphasizes the importance of pausing after tough clinical interactions to genuinely ask yourself, “How am I doing?” This simple self-awareness practice is more powerful than it sounds and is a foundational skill in building emotional resilience. Connection is Medicine, Too: Vulnerability among colleagues and strong social connections are not just “nice to have”—they're protective against burnout. Sharing how you're really doing creates a culture of support and reduces feelings of isolation in tough times. Meet Dr. Jessi Gold: Jessi Gold, MD, MS is the Chief Wellness Officer of the University of Tennessee System and an Associate Professor in the Department of Psychiatry at the University of Tennessee Health Science Center. This inaugural leadership position encompasses all five University of Tennessee campuses, UT Knoxville, UT Chattanooga, UT Southern, UT Martin, and UT Health Science Center, and includes over 62,200 students and 19,0000 faculty and staff. In her clinical practice, she sees healthcare workers, trainees, and young adults in college. Dr. Gold is also a fierce mental health advocate and highly sought-after expert in the media on everything from burnout to celebrity self-disclosure. She has written widely for the popular press, including for The New York Times, The Atlantic, InStyle, Slate, and Self. Her first book, HOW DO YOU FEEL? One Doctor's Search for Humanity in Medicine came out in October 2024 from Simon Element and is a national bestseller. Dr. Gold is a graduate of the University of Pennsylvania with a B.A. and M.S in Anthropology, the Yale School of Medicine, and Stanford University Department of Psychiatry, where she served as Chief Resident. You can find her book at https://www.simonandschuster.com/books/How-Do-You-Feel/Jessi-Gold/9781982199777 -------------- Would you like to view a transcript of this episode? Click here **** Charting Champions is a premiere, lifetime access Physician only program that is helping Physicians get home with today's work done. All the proven tools, support and community you need to create time for your life outside of medicine. Learn more at https://www.chartingcoach.ca **** Enjoying this podcast? Please share it with someone who would benefit. Also, don't forget to hit “follow” so you get all the new episodes as soon as they are released. **** Come hang out with me on Facebook or Instagram. Follow me @chartingcoach to get more practical tools to help you create sustainable clinical medicine in your life. **** Questions? Comments? Want to share how this podcast has helped you? Shoot me an email at admin@reachcareercoaching.ca. I would love to hear from you.

Happy Anniversary to Joni and Ken Tada – 43 years of marriage! Listen in as Joni talks about why she and Ken lean so hard on the Lord as a married couple. -------- Thank you for listening! Your support of Joni and Friends helps make this show possible.   Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org.   Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

About this episode: Caregivers—both paid and unpaid—are the silent backbone of the nation's workforce, providing crucial support to America's young, aging, and disabled populations. But 24 states stand on the precipice of crisis with looming threats to caregiver stipends, salaries, and other resources. In this episode: what led to this tipping point, how proposed cuts to Medicaid could make it worse, and how to build a more supportive system for caregivers, patients, and loved ones. Guest: Stacey B. Lee, JD is a professor of Law and Ethics at Johns Hopkins University's Carey Business School, with a joint appointment at the Bloomberg School of Public Health, where she specializes in business law, health law, and negotiations. Host: Stephanie Desmon, MA, is a former journalist, author, and the director of public relations and communications for the Johns Hopkins Center for Communication Programs at the Johns Hopkins Bloomberg School of Public Health. Show links and related content: Despite Political Divisions, U.S. Adults Across Parties Back Affordable Care, Support for Caregivers—Johns Hopkins Bloomberg School of Public Health Department of Health Policy and Management These Are The States On The Brink Of A Caregiver Crisis — And Trump Medicaid Cuts Could Make It Worse—HuffPost America's Unseen Workforce: The State of Family Caregiving—Columbia University Mailman School of Public Health The Forgotten Youths Who Are Caregivers For Their Families—Public Health On Call (April 2024) Transcript information: Looking for episode transcripts? Open our podcast on the Apple Podcasts app (desktop or mobile) or the Spotify mobile app to access an auto-generated transcript of any episode. Closed captioning is also available for every episode on our YouTube channel. Contact us: Have a question about something you heard? Looking for a transcript? Want to suggest a topic or guest? Contact us via email or visit our website. Follow us: @‌PublicHealthPod on Bluesky @‌JohnsHopkinsSPH on Instagram @‌JohnsHopkinsSPH on Facebook @‌PublicHealthOnCall on YouTube Here's our RSS feed Note: These podcasts are a conversation between the participants, and do not represent the position of Johns Hopkins University.

Episode 105 - Rachel Shapiro shares her journey of caregiving after her daughter's stroke, balancing family, work, and hope as she navigates life's unexpected challenges. Disclaimer: Please note that all information and content on the UK Health Radio Network, all its radio broadcasts and podcasts are provided by the authors, producers, presenters and companies themselves and is only intended as additional information to your general knowledge. As a service to our listeners/readers our programs/content are for general information and entertainment only.  The UK Health Radio Network does not recommend, endorse, or object to the views, products or topics expressed or discussed by show hosts or their guests, authors and interviewees.  We suggest you always consult with your own professional – personal, medical, financial or legal advisor. So please do not delay or disregard any professional – personal, medical, financial or legal advice received due to something you have heard or read on the UK Health Radio Network.

Samira and guest Chris Schuler delve into the emotional and practical challenges faced during the cancer diagnosis and treatment process. Chris shares his personal experiences as a caregiver for his father diagnosed with glioblastoma, highlighting the confusion and fear that accompany such news. The conversation explores the importance of understanding treatment options, the role of family in caregiving, and the complex emotions of grief that arise during this journey. Chris emphasizes the need for clear communication and advocacy in healthcare, as well as the disconnect between the information provided and the emotional realities faced by families. About our Guest:Chris is a staunch brain cancer awareness advocate. He was the primary caregiver to his late Dad, Donald Schuler, who was diagnosed with GBM in July 2021. He works closely with organizations across the globe, amplifying their critical work and building key relationships to further improve outcomes for patients.His career has spanned almost two decades through philanthropic roles in a variety of industries including non-profit, public and private higher education, and healthcare. He's currently working with Cure Brain Cancer Foundation, an Australian non-profit dedicated to improving outcomes in brain cancer. He's a Venture Partner with Varia Ventures, working to raise awareness for emerging venture funds dedicated to uncovering and funding innovative discoveries to improve brain health. He also works closely with SageMedic, a precision oncology start-up supporting patients looking for the most effective treatment for cancer. TakeawaysChris felt a sense of responsibility to support his parents after the diagnosis.The emotional impact of a terminal diagnosis can be overwhelming.Understanding treatment options is crucial for caregivers.Grief can manifest differently in family members during a health crisis.Clear communication from healthcare providers is essential.Many caregivers feel lost in the healthcare system.The binder provided by the hospital was not helpful for Chris or his mom.Caregiving involves navigating complex emotions and responsibilities.Patients and families need to advocate for themselves in medical settings.The experience of receiving a terminal diagnosis is traumatic and disorienting. The feeling of helplessness is a common struggle for caregivers.Chris's mother chose not to Google her husband's condition, living in the moment instead.Chris believes there are hidden joys in caregiving, despite the challenges.Chapters00:00 Introduction and Context of Caregiving02:54 Navigating the Diagnosis Process05:54 The Emotional Impact of a Terminal Diagnosis08:50 Understanding Treatment Options and Next Steps11:53 The Role of Family in Caregiving15:07 Grief and Its Manifestations in Caregiving17:56 The Disconnect Between Information and Understanding25:00 Navigating Cancer: A Personal Journey31:48 The Search for Answers: Clinical Trials and Second Opinions39:51 The Emotional Toll: Grief, Faith, and Resilience46:49 The Caregiver's Perspective: Finding Joy Amidst SorrowConnect with Us:Enjoyed this episode? Make sure to subscribe, rate, and review! Follow us on Instagram, Facebook, or Linkedin @MantaCares and visit our website at MantaCares.com for more episodes and updates. Disclaimer:All content and information provided in connection with Manta Cares is solely intended for informational and educational purposes only. This content and information is not intended to be a substitute for medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.

All Home Care Matters and our host, Lance A. Slatton were honored to welcome Kimberly Anderson Director of Business Development at UI Medical & QuickChange Wrap.   About Kimberly Anderson:   Kimberly Anderson is the Director of Business Development at UI Medical, makers of the QuickChange® Wrap—a urine management device for men. With over 20 years in the medical field, she spent the last eight traveling nationwide to educate healthcare providers on QuickChange, previously serving as UI Medical's Director of Clinical Education.   Kimberly is passionate about restoring dignity for men with incontinence and supporting caregivers through education on alternatives to traditional devices, helping to prevent UTIs, dermatitis, and pressure injuries.   About UI Medical & QuickChange Wrap:   UI Medical LLC is a California-based company dedicated to improving the lives of less mobile individuals through innovative, easy-to-use solutions. We manufacture the QuickChange® Wrap, a Class I medical device designed specifically for men who are wheelchair users, bed-bound, or have unique incontinence needs.   Proudly made in the USA, the QuickChange Wrap is available through major distributors like Medline Industries, as well as online retailers including Amazon and Walmart. Our patented design serves a distinct yet underserved population—approximately 15% of incontinent men—and we're committed to supporting both users and caregivers with a product that brings comfort, dignity, and convenience.   UI Medical holds international patents and complies with CE and UKCA standards. We are registered in the U.S., EU, UK, Australia, and many other countries. Our ISO 13485–certified manufacturing facility in California ensures high-quality production and minimizes supply chain risks. A list of our institutional clients can be found on our website at www.quickchange.com.   Connect with QuickChange Wrap: Official Website:  https://www.QuickChange.com 

Episode Description:If you've ever wondered what happens when a Bronx-born pediatric nurse with stage 4 colon cancer survives, raises a kid, becomes a policy shark, and fights like hell for the ignored, meet Vanessa Ghigliotty. She's not inspirational. She's a bulldozer. We go way back—like pre-Stupid Cancer back—when there was no “young adult cancer movement,” just a handful of pissed-off survivors building something out of nothing. This episode is personal. Vanessa and I built the plane while flying it. She fought to be heard, showed up in chemo dragging her kid to IEP meetings, and never stopped screaming for the rest of us to get what we needed. We talk war stories, progress, side-eyeing advocacy fads, TikTok activism, gatekeeping, policy wins, and why being loud is still necessary. And yeah—she's a damn good mom. Probably a better one than you. You'll laugh. You'll cry. You'll want to scream into a pillow. Come for the nostalgia. Stay for the righteous anger and iced coffee.RELATED LINKSVanessa on LinkedInColorectal Cancer Alliance: Vanessa's StoryZenOnco Interview with VanessaFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship inquiries, email podcast@matthewzachary.com.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Jessica Kim was the primary caregiver for her mother with pancreatic cancer and later her father with congestive heart failure, both of whom lived their final years in her home. In this conversation, Jessica shares how these two caregiving scenarios impacted her life, family, and home, how she managed her relationship with her siblings throughout, and how this role inspired her to create ianacare. --- ianacare.com --- Join us for an online support group related to this episode on Monday July 7 from 6:00-7:15om CT. Register Here!

What would happen if you were suddenly thrust into the role of caregiver for someone you love? Would you have any idea what to do or how to do it? It's estimated that as many as 50 million people in the United States are caregivers, a job that virtually none of them trained for. We all know someone who became a caregiver and had to learn on the fly. Unfortunately, there are precious few resources that can help. Sue Ryan and Nancy Treaster experienced it first-hand. These inspiring women worked together in the software industry before finding themselves facing a similar life challenge: becoming caregivers for their husbands, both of whom were battling dementia. There was plenty of information about their husbands' diagnoses. Doctors were happy to provide them with hordes of information about what to expect as the disease progressed, but nobody was there with practical information about how to be a caregiver for someone with dementia. Their lived caregiving experience gave Sue and Nancy all the training they needed to make sure nobody else would have to figure it out on their own. That's when they founded the sensationally popular podcast, The Caregiver's Journey. Each episode features truly practical advice about how to manage as a caregiver. Topics range from self-care to advice for clipping your loved one's fingernails. They truly cover it all. The Caregiver's Journey has since grown to a powerhouse brand that fills a hugely meaningful gap for anyone who finds themselves having to be a caregiver. The organization was recently granted nonprofit status. In this episode, Sue and Nancy discuss their former careers, their friendship, and their own personal journeys. It's at times compelling, heart wrenching and funny, but it's entirely inspirational and helpful. To learn more about The Caregiver's Journey, visit them at thecaregiversjourney.org. And look up “The Caregiver's Journey” on any podcast app. ******* If you enjoy Second Act Stories, please leave us a review here. We may read your review on a future episode! Subscribe to the Second Act stories Substack. Check out the Second Act Stories YouTube channel. Follow Second Act Stories on social media: Facebook LinkedIn Instagram Second Act Stories theme music: "Between 1 and 3 am" by Echoes.

What would happen if you were suddenly thrust into the role of caregiver for someone you love? Would you have any idea what to do or how to do it? It's estimated that as many as 50 million people in the United States are caregivers, a job that virtually none of them trained for. We all know someone who became a caregiver and had to learn on the fly. Unfortunately, there are precious few resources that can help. Sue Ryan and Nancy Treaster experienced it first-hand. These inspiring women worked together in the software industry before finding themselves facing a similar life challenge: becoming caregivers for their husbands, both of whom were battling dementia. There was plenty of information about their husbands' diagnoses. Doctors were happy to provide them with hordes of information about what to expect as the disease progressed, but nobody was there with practical information about how to be a caregiver for someone with dementia. Their lived caregiving experience gave Sue and Nancy all the training they needed to make sure nobody else would have to figure it out on their own. That's when they founded the sensationally popular podcast, The Caregiver's Journey. Each episode features truly practical advice about how to manage as a caregiver. Topics range from self-care to advice for clipping your loved one's fingernails. They truly cover it all. The Caregiver's Journey has since grown to a powerhouse brand that fills a hugely meaningful gap for anyone who finds themselves having to be a caregiver. The organization was recently granted nonprofit status. In this episode, Sue and Nancy discuss their former careers, their friendship, and their own personal journeys. It's at times compelling, heart wrenching and funny, but it's entirely inspirational and helpful. To learn more about The Caregiver's Journey, visit them at thecaregiversjourney.org. And look up “The Caregiver's Journey” on any podcast app. ******* If you enjoy Second Act Stories, please leave us a review here. We may read your review on a future episode! Subscribe to the Second Act stories Substack. Check out the Second Act Stories YouTube channel. Follow Second Act Stories on social media: Facebook LinkedIn Instagram Second Act Stories theme music: "Between 1 and 3 am" by Echoes.

Rose Aguilar is the host of KALW's “Your Call.” She shared some of her personal caregiving experiences, along with some advice for the event participants, on how to navigate their own journeys with caregiving.

What makes a city feel like home as we age? In this conversation with Indianapolis City-County Councilor Nick Roberts, we explore how public spaces, transportation, and even neighborhood design can impact daily life for older adults. As one of the youngest council members in the country, Nick shares what he's learning from older residents who show up, speak up, and care deeply about the communities they call home. We talk about the importance of being seen, the vision behind reimagining areas like Castleton, and how thoughtful leadership can help create cities that work for every generation.Show notes:www.Joyshouse.orghttps://www.indy.gov/activity/councilor-nick-robertshttps://visitcaregiverway.com/See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Who says you need a Caregiver to enjoy Littlespace? In this episode, we're busting the myth that Littles need a Daddy, Mommy, or CG to feel valid. We explore the beauty of peer-based Littlespaces—where Littles support each other through creativity, connection, and care, without formal power exchange. From craft nights and snack rotations to setting healthy boundaries and avoiding burnout, this episode is packed with ideas, emotional insights, and real talk for Littles looking to build their own village.Because Littlespace isn't about who's in charge. It's about who makes you feel safe, seen, and silly.Visit us at pinkkinkpodcast.comAffiliates - SireDonLeather.com (use code PINKKINK to save 10% on your order) Obedienceapp.com/pinkkink for a 20% discountVisit https://linktr.ee/pinkkinkpodcast for links to our Patreon, Pink Kink Boutique, Pink Kink Institute, social media accounts and more!

FRIDAY HR 2 RRR Trivia - Scientists have figured out how to this from plastics. What is it? Caregivers. We play whats on the Monsters Calander. Amber wants to design the next promo shoot. Russ talkes to A.I.

Editor's Summary by Kirsten Bibbins-Domingo, PhD, MD, MAS, Editor in Chief, and Linda Brubaker, MD, Deputy Editor of JAMA, Deputy Editor of JAMA, the Journal of the American Medical Association, for articles published from June 21-27, 2025.

Executive Director of Northfield Shares Carrie Carroll goes over the now open grant application process, a current open position with the organization, and more.

Wayne Quist and Cliff Reynolds from Veterans Empowered discuss their organization, their book Veterans in Crisis, and the affects of PTSD in veterans.

Send us a textCaregiving isn't just about love. It's about expectations, exhaustion, and the quiet unraveling that happens when your needs are always last.In this episode, Anna and Tim crack open the emotional reality of caregiving; the roles we take on, the ones we're handed, and how they can feel good until they don't. Join them as they name what rarely gets said: the burnout, the self-erasure, and the resentment that builds when care turns into obligation.This Episode Covers:Why saying “I don't want to” can feel impossibleThe tension between love and emotional depletionHow caregiving identities can slowly consume youPerforming capacity vs actually having itFeeling like it's never your turnRage, withdrawal, and the need to be witnessedWhy resentment doesn't make you unlovingLetting go of the fantasy of being the “good one”Until next time, here's to deeper connections and personal growth.Mad love!The podcast is now on YouTube! If you prefer to watch, head over to https://www.youtube.com/playlist?list=PLw3CabcJueib20U_L3WeaR-lNG_B3zYqu__________________________________________Don't forget to subscribe to the Badass Confidence Coach podcast on your favorite podcast platform!CONNECT WITH ANNA:Instagram https://www.instagram.com/askannamarcolin/TikTok https://www.tiktok.com/tag/askannamarcolinEmail hello@annamarcolin.comWebsite https://www.annamarcolin.com__________________________________________And for all your nutritional supplement needs, go to https://www.DrinkAG1.com/ANNA for five free travel packs and a free one-year supply of Vitamin D/K2

What does it mean to age with dignity in today’s healthcare system? What will it take to truly transform how we care for older adults in America? In this episode, the first of a six-part series, we explored the documentary Aging in America: Survive or Thrive, created by the John A. Hartford Foundation. We spoke with Terry Fulmer, PhD, RN, FAAN, president of The John A. Hartford Foundation, to explore the legacy of Dr. Robert Butler and how hospitals are utilizing the “4 Ms” framework (What Matters, Medication, Mentation, Mobility) to enhance care for older adults. We dive into the stark disparities based on income, race, and geography, and highlight programs working to close those gaps. From dementia care models to creative workforce solutions and caregiver support, this conversation offers a hopeful, practical look at reimagining aging in America. Visit johnahartford.org/agefriendly for information about the 4Ms of age-friendly care. Helpful articles and videos can also be found here. Additional resources: Harvard Business Review article on how employers can support family caregivers of older adults The RUSH University Medical Center Caring for Caregivers program My Health Checklist The Reframing Aging Initiative The UCLA Alzheimer's and Dementia Care programSee omnystudio.com/listener for privacy information.

Send us a textYour loved one's behavior isn't the source of your stress—your reaction to it is." This powerful insight forms the foundation of Rick Henkin's transformative approach to dementia caregiving, which he shares in this deeply moving episode.When Rick's wife Sonia was diagnosed with Alzheimer's at 65, their world shifted dramatically. From her developing Capgras syndrome (believing Rick was an imposter) to the heartbreak of seeing her relationship with their granddaughters deteriorate, Rick faced the crushing weight that so many caregivers experience. The turning point came not from changing his circumstances, but from changing his mindset.Rick takes us through his journey of discovery—how he went from anger and frustration to finding what he calls his "heaven on earth" state of peace and acceptance. He shares candid stories that will resonate with anyone who's cared for someone with dementia, from Sonia putting toothpaste in her hair to "borrowing" pancakes from strangers in restaurants. Rather than sources of stress, these moments became cherished memories through Rick's transformed perspective.Most powerfully, Rick reveals how his relationship with Sonia evolved to where spending time with her became his source of respite rather than stress. "Caregivers have the ability to make the rest of their loved one's life miserable or joyful," he notes—a profound responsibility and opportunity.Whether you're caring for someone with dementia or facing any caregiving challenges, Rick's practical wisdom offers a path forward. By focusing on what you can control—your own thoughts and reactions—rather than what you can't, you'll discover how to lift the burden of caregiving stress while providing better care for both your loved one and yourself.

Northfield Police Chief Jeff Schroepfer discusses upcoming traffic laws about to be implemented, the upcoming Picnic in the Park event on July 28th, and more.

Mox, Lindsay, & Ryan return for the second episode of Pride Spill the Beans: Proud & Restless. Listen in as they cover drag in our current culture, allyship, pop culture representation, and movie theater snacks! Special guest Steve Mooney provides our sponsor introduction!

Craig Wasner, Maren Wasner, Casey Wasner, and Rob Ryden discuss their music backgrounds and the Wazaroo Music Fest at the Wasner Barn this Saturday, June 28th.

All Home Care Matters and our host, Lance A. Slatton were honored to welcome Michael Herrington & Kevin Hansen as guests to the show.   About Michael Herrington:   Michael Herrington is a passionate advocate for senior well-being and caregiver support. As President and Co-Founder of Ways 2 Wellness, he leads initiatives that combat loneliness and cognitive decline through engaging activity books and resources that keep seniors mentally sharp and emotionally connected.   With a strong background in publishing and marketing, Michael previously led large-scale sales and distribution efforts for major brands like Time Inc. and Comag Marketing Group. Now, he channels that expertise into Ways 2 Wellness, helping organizations create impactful, customized materials that enhance cognitive well-being and strengthen community connections.   About Ways 2 Wellness:   Ways 2 Wellness creates engaging, custom-branded activity books designed to reduce loneliness and enhance cognitive health in seniors. By combining mental stimulation with meaningful branding, these resources not only promote well-being but also support organizations in strengthening their presence and outreach.   About Kevin Hansen:   Kevin has helped hundreds of businesses with their branding/logo development, website presence, and digital marketing. For the last 8 years, he's worked with home care agencies throughout the country in satisfaction management and, more recently, in business development. He's the author or Branded by Design: Home Care / Home Health Edition, which serves as a guide to agencies creating a new brand, redesigning an existing brand, or striving to improve their brand messaging.   About Home Care Ops:   Home Care Ops offers resources, templates, operational methodologies, and training for every leadership level. Through easy-to-follow courses, information-packed webinars, and Summits with some of the greatest minds across any industry, owners and operators can stop the cycle of reaction and start taking true control over their business's success. Our team strives to help home care owners solve more problems at every level - Build | Grow | Scale.

Episode 104 - Stacy Ryan's powerful journey through cancer, loss and love - from caregiving to finding joy again, proving life can bloom after heartbreak. Disclaimer: Please note that all information and content on the UK Health Radio Network, all its radio broadcasts and podcasts are provided by the authors, producers, presenters and companies themselves and is only intended as additional information to your general knowledge. As a service to our listeners/readers our programs/content are for general information and entertainment only.  The UK Health Radio Network does not recommend, endorse, or object to the views, products or topics expressed or discussed by show hosts or their guests, authors and interviewees.  We suggest you always consult with your own professional – personal, medical, financial or legal advisor. So please do not delay or disregard any professional – personal, medical, financial or legal advice received due to something you have heard or read on the UK Health Radio Network.

In episode 17, Jess welcomes Kelleen and Kimmy, who are both older siblings of autistic adults. Kelleen is an SLP, and Kimmy is a BCBA, both at the University of Washington's Autism Center. In today's discussion, they share how their experiences with their autistic siblings shaped them as people, but also as compassionate practitioners and advocates in their fields. We look at the joys and challenges they experienced as older siblings and some of the issues that continue to arise as they navigate the present and future. And last, but not least, they offer parents some helpful advice for helping their neurotypical children understand and embrace autism. We hope you enjoy the episode!     Resources –Websites for Siblings: Sesame Street (young children) – http://autism.sesamestreet.org/ Rocking Mountain Sibs – https://www.rmsibs.com/ A Sibling's Guide to Autism – https://www.autismspeaks.org/sites/default/files/2018-08/Siblings%20Guide%20to%20Autism.pdf Siblings of Autism – https://siblingsofautism.org/ Sibling Leadership Network – https://siblingleadership.org/ Sibling Support Project – https://siblingsupport.org/ The Organization for Autism Research has a number of sibling resources – https://researchautism.org/how-we-help/families/sibling-support/ The Arc of New Jersey has several helpful resources for siblings of all ages –  https://www.thearcfamilyinstitute.org/resources/sibling-resources/young-sibs.html Parent to Parent – https://www.p2pusa.org/ The Sibling Transformation Project – https://www.siblingtransformation.org/ Growing Up Alongside a Sibling with a Disability –https://www.nytimes.com/2020/05/11/parenting/children-sibling-disability.html  Books for Parents about Siblings: Siblings of Children with Autism: A Guide for Families by Sandra Harris PhD & Beth Glasberg PhD Autism Spectrum Disorder Sibling Support: 15 Practical Tips for Parents & Caregivers by Trish Thorpe Here are links to picture book lists featuring Autistic children.  Amazon: https://www.amazon.com/shop/maistorybooklibrary/list/14VLE2C1F0T17 Bookshop: https://bookshop.org/lists/autism-acceptance-picture-book-list   Sibling books: Benji, the Bad Day, and Me by Sally J. Pla My Brother Otto by Meg Raby (preschool to early elementary) My Brother Charlie by Holly Robinson Peete & Ryan Elizabeth Peete (elementary age) Leah's Voice by Lori DeMonia (elementary age) Tacos Anyone? By Marvie Ellis (elementary age) - Bilingual book Brotherly Feelings: Me, My Emotions, and My Brother with Asperger's Syndrome by Sam Frender & Rob Schiffmiller (elementary age) What About Me? A book by and for an Autism Sibling by Brennan & Mandy Farmer (elementary age) Understanding Samantha: A Sibling's Perspective of Autism by Dustin Daniels (elementary age) Everybody is Different by Fiona Bleach (elementary/middle school age) Autism: The Invisible Cord by Barbara Cain (middle school) Rules by Cynthia Lord (middle school) The Reason I Jump by Naoki Higashida (middle school) Same but Different: Teen Life on the Autism Express by Holly Robinson Peete, Ryan Elizabeth Peete, & RJ Peete (middle school/high school) The Sibling Survival Guide: Indispensable Information for Brothers & Sisters of Adults with Disabilities by Don Meyer & Emily Holl (high school/adults)  Memoirs by Siblings: Boy Alone: A Brother's Memoir by Karl Greensfeld How to be a Sister: A love story with a twist of autism by Eileen Garvin The Ride Together: A Brother & Sister's Memoir of Autism in the Family by Paul & Judy Karasik At Home in the Land of Oz: My Sister, Autism, and Me by Anne Barnhill Crystal Puzzle: Growing Up with a Sister with Asperger's by Ashley Nance How autism shapes sibling relationships By Emily Laber-Warren

I love talking with interesting people doing interesting things—especially when what they're building impacts those of us in the caregiving world. That's why I sat down with Dr. Severance McLaughlin, the CEO of DeLorean AI. His team is using artificial intelligence to predict serious health events—like heart attacks, mental health crises, or hospitalizations—before they happen. As someone who's spent four decades in the thick of caregiving, I've had to be more than a husband. I've had to be the historian, the advocate, and often the one holding the entire narrative together. But what if that burden could be shared? What if technology could actually lighten the load—and even save lives in the process? This conversation dives into chronic pain, suicide risk in veterans, dialysis, depression, and the future of precision healthcare. If you've ever felt overwhelmed by the medical system—or like you're the only one keeping track—this one's worth your time. Lean in and listen. Peter Rosenberger is the host of Hope for the Caregiver, the nation's largest broadcast for family caregivers. After four decades of caregiving, he's learned a few things the hard way—and shares them with heart, humor, and hymns. His newest book, A Caregiver's Companion: Scriptures, Hymns and 40 Years of Insights for Life's Toughest Role, releases this August. Learn more at PeterRosenberger.com Follow on X: @hope4caregiver  

NH+C Wound Healing Center Director Kayla Zandstra and nurse practitioner Christina Richardson talk about the rise in chronic wounds, the expertise and range of treatment options with Northfield Hospital + Clinics, and how to watch for wounds that could cause problems.

In the second segment of Something I Have Always Wondered About, KYMN News Intern Maya Betti talks with Anika Rychner and Lisa Percy of the Community Action Center. Among the several topics that they discuss, they talk about what the CAC does, the funding of the organization, and its expansion from just Northfield to operating […]

Mayor Erica Zweifel along with Northfield Fastpitch Softball Association’s President Nick Capatina and Fundraising Coordinator Jessie Skobrak discuss the $15,000 grant NFSA received from the Minnesota Twins Community Fund to help improve Rock Fields in Northfield.

Steve Grove, the current CEO and Publisher of the Minnesota Star Tribune and the former head of the Minnesota Department of Employment and Economic Development, a Northfield High School graduate, discusses his new book, “How I Found Myself in the Midwest.” Grove will be hosting a reading from the book on tonight, 6:15pm – 8:30pm at […]

In this deeply honest episode of Everyone's Talkin' Money, Shari sits down with Dr. Rachel Piltch-Loeb — public health expert and author of The Millennial Caregiver — to explore the hidden reality of caregiving during the busiest years of your life. You'll walk away learning: You're not alone — why millennials are increasingly becoming caregivers and why it feels so shocking How to have critical conversations with aging parents early, before a crisis hits Practical strategies for balancing caregiving, parenting, and work without burning out The financial truths of caregiving — what you need to budget for now and how to set boundaries Skills caregiving builds that you should add to your resume How to use social media thoughtfully on your caregiving journey Whether you're already in a caregiving role or know it's on the horizon, this episode will help you feel seen, supported, and prepared. Buy Rachael's Book: The Millennial Caregiver: Caring for Loved Ones in the Busiest Years of Your Life Learn more about Rachael at: https://www.rpiltchloeb.com/ Stay up to date with everything Everyone's Talkin' Money on Instagram at  @everyonestalkinmoney Learn more about your ad choices. Visit megaphone.fm/adchoices

Risa Arin doesn't just talk about health literacy. She built the damn platform. As founder and CEO of XpertPatient.com (yes, expert with no E), Risa's taking a wrecking ball to how cancer education is delivered. A Cornell alum, cancer caregiver, and ex-agency insider who once sold Doritos to teens, she now applies that same marketing muscle to helping patients actually understand the garbage fire that is our healthcare system. We talk about why she left the “complacent social safety” of agency life, how her mom unknowingly used her own site during treatment, what it's like to pitch cancer education after someone pitches warm cookies, and why healthcare should come with a map, a translator, and a refund policy. Risa brings data, chutzpah, and Murphy Brown energy to the conversation—and you'll leave smarter, angrier, and maybe even a little more hopeful.RELATED LINKS• XpertPatient.com• Risa Arin on LinkedIn• XpertPatient & Antidote Partnership• XpertPatient Featured on KTLA• 2024 Health Award BioFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship inquiries, email podcast@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 makes working with parents and caregivers feel smooth—or challenging—in play therapy? In this insightful episode, Lisa Dion explores three distinct types of relationships that shape our interactions with parents and caregivers in the therapeutic process. Understanding these dynamics can transform your approach, helping you create deeper, more conscious relationships that honor both you as a therapist and the parents you support.

What is survival mode really costing you?  In this eye-opening episode, Charlotte breaks down the hidden toll that caregiving stress takes on your mind, body, and identity.  You'll discover how chronic stress reshapes your brain, disconnects you from joy, and rewires your nervous system to live on high alert, even after the crisis has passed.  Through deeply personal stories, practical nervous system tools, and powerful micro-shifts, this episode invites you to start reclaiming your presence, one conscious breath at a time. Find the free Scanxiety Toolkit at https://www.cancercaregiverpodcast.com/tools

A woman from the Gem State was selected to represent Idaho in the 2025 Class of Dole Caregiver Fellows, a group dedicated to raising awareness for military caregivers.

Show SummaryOn today's episode, feature a conversation with Robin Kelleher, the CEO and co-founder of Hope For The Warriors, a national nonprofit dedicated to uplifting service members, veterans, and military families as they navigate the complexities of military life.   Provide FeedbackAs a dedicated member of the audience, we would like to hear from you about the show. Please take a few minutes to share your thoughts about the show in this short feedback survey. By doing so, you will be entered to receive a signed copy of one of our host's three books on military and veteran mental health. About Today's GuestRobin Kelleher is the CEO and co-founder of Hope For The Warriors®, a national nonprofit dedicated to uplifting service members, veterans, and military families as they navigate the complexities of military life. For 20 years, Robin has led HOPE with a unique blend of strategic insight and compassionate leadership. Through cultivating meaningful partnerships, driving the vision and impact of HOPE's mission across diverse communities, and building teams that deliver tangible outcomes, Robin has created countless opportunities to meet the evolving needs of our military families.Under her guidance, Hope For The Warriors has become a trusted voice in veteran and military family advocacy and a catalyst for restoring self, family, and hope within the military communityLinks Mentioned During the EpisodeHope For The Warriors WebsitePsychArmor Resource of the WeekThis week's resource of the week is the PsychArmor course Invisible Wounds at Home: Understanding Invisible Wounds. In this course, you will learn about four unseen wounds of military service, and be introduced to our series that includes specific courses on myths and facts about PTSD, Depression, TBI and Substance Use Disorder. You can find the resource here:  https://learn.psycharmor.org/courses/invisible-wounds-at-home-understanding-invisible-wounds Episode Partner: Are you an organization that engages with or supports the military affiliated community? Would you like to partner with an engaged and dynamic audience of like-minded professionals? Reach out to Inquire about Partnership Opportunities Contact Us and Join Us on Social Media Email PsychArmorPsychArmor on TwitterPsychArmor on FacebookPsychArmor on YouTubePsychArmor on LinkedInPsychArmor on InstagramTheme MusicOur theme music Don't Kill the Messenger was written and performed by Navy Veteran Jerry Maniscalco, in cooperation with Operation Encore, a non profit committed to supporting singer/songwriter and musicians across the military and Veteran communities.Producer and Host Duane France is a retired Army Noncommissioned Officer, combat veteran, and clinical mental health counselor for service members, veterans, and their families.  You can find more about the work that he is doing at www.veteranmentalhealth.com  

Val Mertesdorf, Director of Finance, and Justin Raabolle, Director of Facilities, discuss the summer projects going on this year in the school district.

Host Kosmo Esplan talks with Northfield native Ben Wang, who is currently starring in the new film Karate Kid: Legends alongside Jackie Chan and Ralph Macchio, about what it was like moving from China as a child to Northfield, and how he came to be a professional movie actor.

Dundas City Administrator Jenelle Teppen discusses the June 24th City Council Meeting, as well as the Annual Capital Improvement Plan and open city employment positions.

This episode is different. It is personal.Because for the first time, I will be sharing something I have not yet spoken about publicly.My father passed away this March. Just two days before my birthday.And in the weeks that followed, I gave myself permission to fully grieve, to feel, to remember, to process.It was a conscious act of mourning, supported by ceremony, solitude, and also by ketamine therapy, medically supervised at our clinic in Santa Monica.It helped me meet the waves of grief and let them move through me, not around me.And in that space, I kept returning to one question: Why, in our culture, is death treated as something to avoid, deny, or sanitize?Why is something so universal, so sacred, still held in so much fear?Today's guest has devoted her entire life to shifting that.Barbara Karnes is a hospice pioneer and one of the most respected voices in end-of-life education.Her booklet Gone From My Sight, known as The Little Blue Book, has sold over 40 million copies and changed how countless families understand and approach death.In this conversation, Barbara offers profound wisdom: she offers a map, a presence, a way of holding death that allows us to also hold life more fully.This is much more than a conversation about dying. It is a conversation about what it means to live without fear, and to love more openly, even at the edge of goodbye.Episode highlights:02:45 Ariana's Personal Story of Grief and Healing05:29 Understanding the Dying Process10:40 The Role of Caregivers and Cultural Myths About Dying21:51 The Emotional and Spiritual Costs of Caregiving31:36 The Role of the Witness in the Dying Process33:04 Creating a Sacred Experience Before Death34:08 Saying Goodbye and Processing Grief42:16 The Importance of Personal Choice in End-of-Life Care44:44 Cultural Perspectives on Death and Aging52:32 Rehearsing for Death Through Life's Changes54:25 Barbara's Personal Relationship with Death56:22 Understanding Grief as Part of the Dying Process01:02:39 Barbara's Legacy and ResourcesResources mentioned:https://bkbooks.com/pages/about-barbarahttps://bkbooks.com/collections/allSOCIAL MEDIALinkedIn https://www.linkedin.com/in/barbarakarnesrnInstagram https://www.instagram.com/barbarakarnesrnFacebook https://www.facebook.com/barbarakarnesrnYouTube https://www.youtube.com/channel/UCXVqIQdyP2OBTop8-jboRww

Send us a textIn this episode, I had the pleasure of speaking with Dr Erin Von Klien, who is now a third year Neonatology fellow at Monroe Carell Children's Hospital/Vanderbilt University, Nashville. Erin described her research project on exploring association between caregiver employment decisions and having a preterm infant. Erin describes her project which was also recently published in JAMA pediatrics (Preterm Birth and Caregiver Employment Decisions | Reproductive Health | JAMA Pediatrics | JAMA Network) where she investigated the impact of prematurity in parental employment decisions. She describes how she got interested in this impactful topic and how she found her mentor. She is a 2024 recipient of the AAP Marshall Klaus Award in Health Services Research and a participant in the Vanderbilt Patient/ Practice Outcomes Research in Effectiveness and Systems Science (PROgRESS) T32 Program. In this episode she describes her experience in grant writing and winning the AAP Marshall Klaus award. She also provides valuable advice to incoming fellows who are interested in the physician scientist pathway in health services research. As always, feel free to send us questions, comments, or suggestions to our email: nicupodcast@gmail.com. You can also contact the show through Instagram or Twitter, @nicupodcast. Or contact Ben and Daphna directly via their Twitter profiles: @drnicu and @doctordaphnamd. The papers discussed in today's episode are listed and timestamped on the webpage linked below. Enjoy!

Conscious Caregiving with L & L is "Tackling the Tough Conversations."   The topic of this episode is "National Resources & Seniors" featuring hosts Lori La Bey and Lance A. Slatton.   Lori La Bey speaks with Lance A. Slatton about his coverage of the 10th Annual National Elizabeth Dole Foundation Convening in Washington D.C.   About Lori La Bey:   Lori La Bey is the founder of Alzheimer's Speaks and is co-founder of Dementia Map global resource directory and the co-host of Conscious Caregiving with L & L. Lori's mother who lived with dementia for 30 years.   Her goal has always been to shift dementia care from crisis to comfort around the world. She offers a variety of free resources to educate, empower, connect, and decrease stigmas; helping families and professionals live graciously alongside dementia.   Lori is an international speaker known for her multiple platforms and training programs.   Connect with Lori La Bey: Official Website:  https://alzheimersspeaks.com/   Official Dementia Map Website: https://www.dementiamap.com/   About Lance A. Slatton - known as "The Senior Care Influencer"":   Known as “The Senior Care Influencer” Lance is a Writer, Author, Influencer, and Healthcare professional with over 20 years in the healthcare industry. Lance A. Slatton is a senior case manager at Enriched Life Home Care Services in Livonia, MI. He is also host of the award winning podcast & YouTube channel All Home Care Matters and Co-Host of Conscious Caregiving with L & L with Lori La Bey along with The Care Advocates and The Caregiver's Journal. Lance's book, "The All Home Care Matters Official Family Caregivers' Guide" was the recent recipient of the 2024 International Impact Book Awards.     Connect with Lance A. Slatton - "The Senior Care Influencer": Official Website:  https://www.lanceaslatton.com   Official Website for All Home Care Matters: https://www.allhomecarematters.com   Lance A. Slatton and Lori La Bey Co-Host and Produce Conscious Caregiving with L & L.   Visit their website at: https://consciouscaregivingll.com/ To learn more about Lance A. Slatton and Lori La Bey you can visit their websites.

Happy Pride Month GeriPal listeners! Transgender issues are in the news. Just today (June 17th) as we record this podcast: Ezra Klein released a wonderful interview with Sarah McBride, the first openly transgender member of congress A judge ruled that cuts to NIH grants focused on minority groups, including transgender people, were illegal and ordered the government to restore funding.  It's Pride month, and our guests remind us of the leadership of two trans women in the Stonewall riots, which started the modern fight for LGBTQI+ rights and liberation. Today's guests are Noelle Marie Javier, a geriatrician and palliative care doc who tells her story of transitioning as a faculty member at Mt. Sinai in New York, and Jace Flatt, who started their journey as a gerontology researcher at UCSF and is now faculty at UNLV. Jace was in the news recently for having multiple federal grants cancelled because they included transgender participants. We cover many topics, including: Terminology: gender identity, sexual orientation, gender expression, transgender, nonbinary, intersex, what's in LGBTQI+ Gender affirming care Major health and medical issues associated with aging as a transgender person Allostatic load Accelerated aging What can clinicians do - pointers, pearls, and attitudes Dementia risk  Caregiver issues Hormone replacement therapy at the end of life Sexual orientation and gender identity (SOGI) data, what is it, how to collect it respectfully and safely Mentioned: Harvey Chochinov's Dignity Therapy question, and our prior podcast on LGBT Care for older adults and serious illness with Carey Candrian and Angela Primbas So pleased to sing True Colors by Cyndi Lauper, with Kai on guitar for those of you listening to the podcast. -Alex Smith Many links! -Rainbows of Aging: Jace Flatt's research site. -LGBTQcaregivers -Callen-Lorde gender affirming trans health services -GLMA: organization for health professional advancing LGBTQ+ equality -Center of Excellence for Transgender Health at UCSF -World Professional Association for Transgender Health -Sage advocacy services for LGBTQ+ Elders: focus on impact of Medicaid cuts -Trans bodies, Trans selves: resource guide 

1091.  Is the em dash a sign of AI writing? I looked at where the idea comes from, and we have the final answer! Then, we look at the difference between "caregiver" and "caretaker."The "'caregiver" and "caretaker'" segment was written by Jim Norrena, MFA, who has been writing and editing for more than thirty-five years. He's the founder of TypoSuction.com, an independent editing/writing service. He's taught grammar and copyediting intensives and professional proofreading workshops at Media Alliance and served as events coordinator for Bay Area Editors' Forum (BAEF). Visit Linkedin.com/in/jimnorrena/ for his complete work history and highlighted projects.

All Home Care Matters and our host, Lance A. Slatton were honored to welcome back Elizabeth Field the Chief Operating Officer for the Elizabeth Dole Foundation for the post-Convening recap. About Elizabeth Field: recognized expert on military quality-of-life and defense policy. Prior to joining the Foundation, she held senior roles at the Government Accountability Office and the U.S. Department of State, and has testified before Congress on issues ranging from defense reform to veteran support. Her work has been featured by NPR, CNN, and The New York Times. A proud daughter of an Army veteran, she lives in Washington, D.C. with her two sons and rescue dog. About the 10th Annual National Elizabeth Dole Foundation Convening: On May 20, 2025, the Elizabeth Dole Foundation hosted its 10th Annual Convening, A Blueprint for Action: Mapping the Future of Caregiving in a Changing World. This event featured leaders from government, industry, non-profits, and academia gathered for dynamic discussions, engaging keynote speakers, and interactive working sessions focused on shaping the future of support for military and veteran caregivers. Connect with the Elizabeth Dole Foundation: Official Website: https://www.elizabethdolefoundation.org/

Hear John's answer on our Mens Room Question: What's the craziest phone call you've made or taken?