Podcasts about caregivers

After years of carrying the weight of lead, Shannon and Cooper find a path out from under the darkness and into the sunlight.LEAD: how this story ends is up to us is an audio docudrama series that tells the true story of one child, his mysterious lead poisoning, and his mother's unwavering fight to keep him safe. A true story written by Shannon Burkett. Directed by Alan Taylor. Starring Merritt Wever, Alessandro Nivola, Cynthia Nixon, and Cooper Burkett.Lead was produced by Shannon Burkett. Co-produced by Jenny Maguire. Featuring Amy Acker, Tom Butler, Dennis T. Carnegie, James Carpinello, Geneva Carr, Dann Fink, Alice Kris, Adriane Lenox, Katie O'Sullivan, Greg Pirenti, Armando Riesco, Shirley Rumierk, Thom Sesma, and Lana Young. Music by Peter Salett. “Joy In Resistance” written by Abena Koomson-Davis and performed by Resistance Revival Chorus. Casting by Alaine Alldaffer and Lisa Donadio. Sound Design by Andy Kris. Recording Engineer Krissopher Chevannes.For corresponding visuals and more information on how to protect children from lead exposure please go to https://endleadpoisoning.org.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

In a conversation that challenges stereotypes and brings to light the unexpected realities of caregiving, this episode reveals the experiences of three men who stepped up to care for their mothers with dementia. It's a heartfelt exploration of grief, growth, and the bonds that are both tested and strengthened through caregiving. Shattering Stereotypes: Men as Caregivers We often associate caregiving with daughters, wives, and sisters, yet over 40% of caregivers are men. Many of them, like guests David Bredbenner, Alfredo Botello, and Vincent Zappacosta, find themselves in this role simply because "there really was no other option." Their stories reveal that caregiving isn't just a woman's job—it's a human one. Vincent shares, “My mother and I were always close and I just didn't trust anyone else to take care of her, because nobody knew her as well as I did.” David talks about “reacting, firefighting, and suddenly you're just drawn in, and before you know it, it becomes part of your routine.” Alfredo, navigating life as an only child, speaks honestly about how necessity and love for his mother collided the moment his stepfather passed away. Lifestyle Overhauls and Personal Sacrifice For each son, caring for their mothers led to seismic shifts in their daily lives. Plans are always tentative, boundaries are tested, and a new form of “parenting” emerges. As Alfredo vividly describes: “Nobody told me growing up that I'd have another kid in my 50s—only she'd be in her 80s and have opinions!” From rearranging work schedules to leaving reassuring Post-its for an anxious parent, the logistics become second nature, though the emotional toll lingers. The men openly discuss balancing frustration, guilt, and even resentment with deep love. They offer comfort in recognizing that no one is “superhuman”: “It's almost like we do expect ourselves to be perfect...and that never happened,” Christy reflects. While the stories in “Sons Caring for Mothers” circle around men, the lessons ring true for anyone on a caregiving journey. There are no perfect solutions, only the imperfect, beautiful bonds of love, memory, and forgiveness. After the Podcast Learn more about David, Vincent, and Alfredo and purchase their books here. Learn about the Moderators Marianne Sciucco Christy Byrne Yates About the Podcast AlzAuthors is the global community of authors writing about Alzheimer's and dementia from personal experience to light the way for others. Our podcast introduces you to our authors who share their stories and insights to provide knowledge, comfort, and support. Please subscribe so you don't miss a word. If our authors' stories move you, please leave a review. And don't forget to share our podcast with family and friends on their own dementia journeys. We are a 501(c)(3) charitable organization totally reliant on donations to do what we do. Your generosity will help cover our many operating costs, which include website hosting and maintenance fees, service charges to keep things running smoothly, and marketing expenses to promote our authors, expand our content, improve our reach, and more. Our ongoing work supports our mission to lift the silence and stigma of Alzheimer's and other dementias. To sustain our efforts please donate here Ideas and opinions expressed in this podcast belong to the speakers and not AlzAuthors. Always consult your healthcare provider and legal and financial consultants for advice on any of the topics covered here. Thanks for listening. We are a Whole Care Network Featured Podcast Proud to be on The Health Podcast Network Find us on The World Podcast Network and babyboomer.org Want to be on the podcast? Here's what you need to know. We've got merch! Shop our Store

Feeling overwhelmed by the weight of your responsibilities as an entrepreneur and caregiver? You're not alone.   In this remix moment, I want to share my current challenges and the lessons I've learned about leading from where you are. We'll explore how to navigate the tension between business demands and personal needs, as well as the power of authenticity in building trust with your clients and community.   You'll discover my top three anchors for sustainable leadership during tough times, which can help you find harmony in your life and business.   I know many of you may be facing your own challenges, whether it's caregiving, grief, or other personal burdens. My hope is that by sharing my journey, you'll find encouragement and tools to navigate your own difficult seasons.   Remember, you don't have to prove anything to anyone. You can show up, even imperfectly, and still make a meaningful impact. Life and business are intertwined, and it's okay to lean into that reality.   Thank you for your continued support, and I look forward to sharing more of this journey with you in future episodes.  

In this informative episode of Chatting with Betsy, host Betsy Wurzel shares valuable caregiver insights in her conversation with Dr. Barry J. Jacobs and Dr. Julia L. Mayer about their newest collaboration, The AARP Caregiver Answer Book — a must-have resource for caregivers at any stage of their journey. Structured in a helpful Q&A format, the book answers real-life caregiving questions and provides emotional, practical, and spiritual guidance.Betsy and her guests explore critical topics, including the importance of education, self-care, and end-of-life planning. The conversation also dives into how caregiving transforms us, why it's important to find purpose afterward, and the benefits of mental health counseling and support groups. They stress how vital it is to keep communication open with spouses, partners, and children throughout the caregiving process.These caregiver insights highlight the need for resources that validate the caregiver's journey and provide practical support. Betsy shares her heartfelt opinion that this book belongs in every physician's office and wishes it had been available during her own caregiving experience. She considers it an essential resource that every family should have access to.

This episode is the closing session of the Caregiving Connection series from the Benjamin Goldberg Foundation, where Wendy Goldberg and Dr. Sheetal Ajmani reflect on the wisdom shared throughout the series and answer audience questions about the caregiving journey.Together, we revisit insights from our special guests:Cindy Griffith on empathy and the difference between being empathic and empathetic—plus tools to protect your own energy.Dr. Kapil Kapoor on patient–caregiver communication, advocacy, and preserving autonomy in the medical setting.Monica Rao on the healing power of her channeled meditation, offering practices to move from the mind into the heart.In this Q&A, Wendy and Dr. Ajmani expand on these themes with real-life reflections, exploring how caregivers can recognize early signs of burnout, reframe self-care as essential rather than selfish, and use simple rituals to stay grounded and resilient.Even if you missed the earlier sessions, this conversation brings the whole series together—reminding us that while we can't always change outcomes, we can change the story of the caregiving journey.

What happens when a caregiver decides she's done facing it all alone? Ellen Gullett took her experience caring for her mom and turned it into something powerful: a support group that now brings comfort, laughter, and honesty to caregivers at Second Presbyterian Church. In this episode, she shares how the group began, the surprising things she's learned, and the stories that stay with her. You'll also hear the kind of support caregivers really need, what not to say, and how one small act of kindness can carry someone.Show notes:www.Joyshouse.orghttps://visitcaregiverway.com/https://www.secondchurch.org/supportgroupsSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Author and caregiver Jess Ronne joins me to share her story and her new book, Caregiving with Grit and Grace. As the mother of a son with profound disabilities and the young wife who walked through her husband's brain cancer, Jess has lived the struggles many caregivers face but few talk about. Together, we discuss the loneliness of caregiving, special needs parenting, the reality of grief and anger, and the hope that comes through faith in Christ. This conversation is for anyone navigating the challenges of family caregiving, special needs, or long-term illness — offering encouragement, honesty, and spiritual strength for the journey.

Former Golden Gopher, turned assistant coach, Eric Carter of the Raider Football team joins us to talk about his journey here and what he hopes to bring to the team for a successful 2025 season under the tutelage of Head Coach Brent Yule. We Meet Raider Captains of the Girl’s Swim and Dive team, Evy […]

Robby Dilmore welcomes Peter Rosenberger and Jasmine Hyatt to discuss A Caregiver's Companion and the life-changing work of Crossroads Kids Clubs bringing the gospel into public schools.

Are financial challenges from caregiving impacting your financial stability and well-being? You are not alone. This episode addresses the significant costs involved—from medical expenses to lost income—and offers practical guidance on financial planning and maintaining faith. Learn how to explore resources such as Medicaid and VA benefits while trusting in the promise of Philippians 4:19: My God will supply all your needs. Transform financial stress into an opportunity for reassurance and provision.#CaregiverStress #FinancialPeace #GodsProvision #ChristianCaregivers #FaithAndFinance #CaregiverSupport #TrustGod #PodcastForCaregivers #StrongerTogetherPodcast"To partner or to learn more about our ministry visit https://s2c2gministry.com/.To receive a free to help you as it relates to space, click here.

Click here to receive today's free gift on the Radio Page: Grieving with Hope – In Grieving with Hope, Randy gives perspective and practical advice to help readers on the grieving journey, so that in time, your grief will be accompanied by joy and hope. Use the coupon code: RADIOGIFT for free shipping!*Limit one copy per person* --------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.

[REBROADCAST FROM April 16, 2025] Death comes for everyone. Registered Nurse and End of Life specialist Suzanne O'Brien believes we can make that time better. Her book, The Good Death, offers guidance for how caregivers can help their loved ones. It also offers practical advice on how to have a 'good death' so that everyone can be involved.

Our August episode has host and gerontologist, Sherri Snelling, talking with Savenia Falquist of HomeShare Oregon about a roommate finding service for older adults. Looking to support older adults who are living at home and help them with avoiding loneliness while also boosting their financial resilience, this is what we call “Golden Girls 2.0.” Savenia explains how it works. In CAREGIVER WELLNESS NEWS, Sherri celebrates one of the biggest entertainment stars of our lifetime sharing her caregiving story: Taylor Swift joins the 63 million caregivers in the U.S. Sherri talks about why this type of spotlight on caregiving is important. Sherri shares insights from her book, “ME TIME MONDAY” for National Wellness Month and also talks about “broken heart syndrome” as part of National Grief Awareness Day (8/30). In honor of wellness month and National Relaxation Day (8/15) Sherri shares 7 Relaxation Hacks from her “Self-Care in 7 Minutes Solutions” video series on YouTube. And, for National Social Wellness Month in August Sherri provides statistics from a recent national poll on friendships and aging – how do you rank? In our WELL HOME DESIGN NEWS, Sherri talks about recent studies that show how environment wellness is key in longevity showing how Parkinson's risk is connected to golf courses and how dogs can help. Also, August 26 is National Dog Day and Sherri shares more info on how our furry best friends help is live longer and now how we can do the same for them. And finally, Sherri celebrates the 2-year-anniversary of her book, ME TIME MONDAY, which is coming out in audio format; and Penny the wonder dog makes her annual appearance! (2:50) – Caregiver Wellness News (15:30) Interview with Savenia Falquist – Executive Director of HomeShare Oregon (41:36) – Well Home Design News Take Care and Stay Well! Find out more at: caregivingclub.com/podcast/

Mike Tyson is famous for saying, “Everybody has a plan until they get punched in the nose.” When suffering punches us in the nose, our plans - and clichés - don't hold. In this episode of Truth Talk Live, I explore why “drive-by ministry” fails and why true comfort begins with seeing people in their pain—just as Christ sees us. You'll hear: My reflections from the ICU after Gracie's 98th surgery. The danger of empty phrases like “God has a plan” or “just trust Jesus.” A listener in tears, struggling to accept God's forgiveness. A reminder from Scripture: not why, but who. Gracie also sings Breathe on Me, Breath of God a cappella—an anchor of hope in moments when words fail. If you've ever wondered what to say (or not say) when someone is in trauma, this episode points to solid ground in Christ.   ORDER THE NEW BOOK …TODAY!    

Kate Ford and local Girl Scouts Ella, Amelia, and Maddie discuss the upcoming recruiting event for Girl Scouts on Monday, September 8th, and some of their favorite things about being a Scout.

Today in the ArtZany Radio studio Paula Granquist features The Fesler-Lampert and Acoustic Roots Performing Arts Series with Tami Resler and Dr. Benjamin Downs from the Shattuck-St. Mary's School and composer, arranger, and pianist Kavyesh Kaviraj who will be featured in all three of the Jazz Series concerts within the series. https://www.s-sm.org/news-events/fesler-lampert-performing-arts-series https://www.kavyeshkaviraj.com/about The Fesler-Lampert and Acoustic Roots Performing Arts Series features an exciting array […]

Carrie Carroll and Jariya Goerwtiz from Northfield Shares discuss Goerwitz’s new role, the upcoming grant deadline, and more.

Both Rich and Danny are card carrying members of the E Street Nation, so this is something regular listeners should have seen coming pretty clearly. This week marks the 50th anniversary of the release of Born to Run. The boys mark the occasion by breaking the album down. It’s not quite having your face simultaneously […]

All Home Care Matters and our host, Lance A. Slatton were honored to welcome Michele Bolton as guest to the show.   About Michele Bolton:   Michele Bolton, Founder and CEO of MY911 Inc., is a Canadian entrepreneur redefining healthcare technology. Inspired by personal health challenges and a profound commitment to patient empowerment, she established MY911® to revolutionize emergency medical communications, seamlessly connecting patients, first responders, and healthcare professionals. With an illustrious career spanning 30 years in agriculture and wealth management simultaneously, Michele brings a unique blend of expertise to her visionary leadership.   Her innovative approach, rooted in empathy and a dedication to enhancing the patient experience, has positioned MY911® as a pioneering, patient-centric solution that has transformed the healthcare landscape. Michele's trailblazing efforts have garnered international recognition, earned her an invitation to Global Healthcare Week in Abu Dhabi and prominent features in esteemed publications such as Forbes, Business Insider, MSN, and Insights Success, among others. Through her unwavering commitment to empowering patients as active participants in their healthcare journey, Michele continues to drive transformative change on a global scale.   About MY911 Inc.:   MY911 Inc. is a service that provides users with a customized wallet card displaying a QR code linked to an online profile, designed to streamline emergency medical communications through written and smart technology for patients and healthcare professionals. The user is in control of their online profile, and fills out the information they wish to share. MY911 Inc. is a company founded in London, Ontario, Canada.   CEO Michele Bolton started the service after her own challenges with the healthcare system. It's comforting to see others experience the same benefits of streamlined medical communications she personally receives from using her innovative, customized MY911® wallet card. A MY911® subscription makes a great gift, providing loved ones with awareness, peace of mind, and convenience! 

Research shows that simple practices such as self-hugs, soothing touch, and hand-to-heart can calm the nervous system, supporting caregivers and the children in their care.Summary: From parents to teachers, caregiving can be overwhelming and exhausting. This episode of The Science of Happiness dives into simple touch-based strategies that promote calm, reduce stress, and foster stronger connections. Researchers share how even brief moments of self-soothing or supportive touch can improve mental and physical health for caregivers and children. How To Do This Practice:  Sit or stand comfortably and take a moment to notice your body. Soften your jaw and shoulders. If it feels safe, close your eyes or lower your gaze. Place one hand on your belly, both hands over your heart, or give yourself a self-hug— whatever feels most comfortable and natural. Let the weight of your hands feel steady and supportive. Take a slow inhale through your nose and a longer exhale through your mouth. Silently repeat a kind phrase to yourself, like “How can I be a friend to myself today?” and “It's okay to make mistakes.” Feel the warmth and weight of your hands. On each exhale, invite a little ease into your face, shoulders, belly, and back. Notice any tiny shift toward calm. Wrap your arms around your torso and apply comfortable pressure, finishing with a gentle self-hug before returning to your day.  Scroll down for a transcription of this episode.Today's Guests:THERESA ALEXANDER is a pre-K teacher based in Arlington, Virginia, with nearly 20 years of teaching experience. She's also a new mother.MICHAEL BANISSY is a psychology professor at University of Bristol and the author of “Touch Matters: Handshakes, Hugs, and the New Science on How Touch Can Enhance Your Well-Being.”Learn more about Michael here: https://www.banissy.com/Related The Science of Happiness episodes:  Caring for Caregivers Series: https://tinyurl.com/4k2hv47jRelated Happiness Breaks:The Healing Power of Your Own Touch: https://tinyurl.com/y4ze59h8Our Caring for Caregivers series is supported by the Van Leer Foundation, an independent Dutch organization working globally to foster inclusive societies where all children and communities can flourish. To discover more insights from Van Leer Foundation and others on this topic, visit Early Childhood Matters, the leading platform for advancing topics on early childhood development and connecting diverse voices and ideas across disciplines that support the wellbeing of babies, toddlers and caregivers around the globe.Tell us about your experience with this practice. Email us at happinesspod@berkeley.edu or follow on Instagram @HappinessPod.Help us share The Science of Happiness! Leave us a 5-star review on Apple Podcasts and share this link with someone who might like the show: https://tinyurl.com/2p9h5aapTranscription: https://tinyurl.com/4ppzs8kw

Take cover, everybody, Producer Nick has the reigns! Over the years, Talk About It has received so many questions from viewers ranging from how to deal with an epilepsy diagnosis, to what to do if you are a caregiver, to practical quesitons about establishing routines and how to prevent seizures. Every episode, we are all privileged to hear these incredible conversations from a range of guests and experts, but we have an expert sitting right there, every time: Greg! He has gone through what caregivers go through, he has dealt with medication and emerging treatments, he has become an expert on what to do when his son Jake has a seizure, and so has his family. In this special two-part AMA series of Talk About It, Greg will be in the guest seat answering questions in a real and candid way to provide a peek behind the curtain of his experiences and offer advice from one person in the community to another.  This is part one, and you don't want to miss it!  Talk About It with Greg Grunberg is excited to be sponsored by Neurelis and by Jazz Pharmaceuticals.

In this week's episode, Brain & Life Podcast hosts Dr. Daniel Correa and Dr. Katy Peters discuss some of their favorite articles in the most recent issue of Brain & Life Magazine. The dive into the effects of ultra-processed foods, helpful innovations like smartphone apps and specialized gyms, and the support sibling caregivers provide to their loved ones. If you would like to read these articles and more, check out the latest issue!   Brain & Life Articles Mentioned How Ultra-processed Foods Can Have a Negative Effect on Brain Health Smartphone Apps Can Help Manage Parkinson's, Migraines, Epilepsy, and More How Specialized Gyms Empower People with Neurologic Conditions Sibling Caregivers are Supporting Brothers and Sisters Through Chronic Conditions   Other Brain & Life Podcast Episodes on These Topics The Many Faces of Cerebral Palsy with Micah Fowler, Phoebe Rae Taylor, and Kelsey Cardona We Are Brave Together with Jessica Patay Cheryl Hile is Running Around the World with Multiple Sclerosis Exploring Longevity with Author Dan Buettner   We want to hear from you! Have a question or want to hear a topic featured on the Brain & Life Podcast? ·       Record a voicemail at 612-928-6206 ·       Email us at BLpodcast@brainandlife.org   Social Media:   Hosts: Dr. Daniel Correa @neurodrcorrea; Dr. Katy Peters @KatyPetersMDPhD

This week, Diane sues te Parable of the Sower to share different reactions to LTC planning occur in the United States.   Are you the hard soil?  The rocky soil? The thorny soik?  The fertile soil? After listening, you can scheudle a phone or zoom meeting with me to start planing to prepare for your family's tomorrow

In this podcast episode, Mary Allen-Des Jardins discusses the Uplifting CareGivers Association (UCA), a nonprofit organization dedicated to supporting healthcare and community caregivers.

Today on Spill the Beans, Mox, Lindsay, and Ashlee talk about a few of their favorite things.

CC Linstroth of Age Friendly Northfield discusses upcoming events with Age Friendly, and touches on her receiving this year’s Joseph Lee Heywood Award for Distinguished Service.

Northfield Area Fire & Rescue Services Chief Tom Nelson discusses the NAFRS budgeting process, Defeat of Jesse James Days safety and events, and more.

      All Home Care Matters and our host, Lance A. Slatton (@lanceaslatton) were honored to welcome Andrew Karesa CEO and Founder of @bluebellvillage as guest to the show.     About Andrew Karesa:   Andrew Karesa is a member of the Muskeg Lake Cree Nation and a proud husband and father of two young sons.   After witnessing how his family coped to support his grandmother with her Alzheimer's diagnosis, Andrew realized he needed to take action. This inspired the creation of blueBell Village, aimed at Restoring the Personhood and Independence of those living with dementia™. With blueBell, Andrew has seen lives transformed for both individuals living with dementia and their caregivers, and he is passionate about fostering a world where care is tailored to each individual's needs.   Additionally, he is pursuing his doctorate at the University of Calgary, where his research explores Indigenous entrepreneurship in the health sector, with a particular focus on the role of data in new venture creation. Andrew also holds an MBA from the University of Alberta. Before founding blueBell Village, he worked as a practicing engineer in the energy sector.     About blueBell Village:   blueBell Village is a health innovation company rooted in Indigenous values, dedicated to transforming the dementia care experience for families and caregivers. Founded in Canada, blueBell Village focuses on bridging clinical best practices with cultural and community-based knowledge to improve quality of life for people living with dementia—particularly in underserved and Indigenous communities.   Its flagship tool, blueBell Connect, is a digital support platform that helps care teams deliver personalized, culturally appropriate, and clinically grounded care. Unlike traditional caregiver tools, Connect doesn't just share information—it guides action. It enables caregivers to coordinate with one another, share updates in real time, and receive recommendations that are tailored to the specific needs, routines, and cultural contexts of the individual they support. With a focus on inclusion, personalization, and dignity, blueBell Village is building tools that meet people where they are—and helping communities take care of their own.        

Episode 112 - Mother-daughter duo Mollie and Maureen share their heartfelt journey with ALS, caregiving, genetic testing and hope for the future. 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.

Charlotte Bayala, host of the award-winning Cancer Caregiver Podcast, joins Dr. Leah Sherman to discuss the unique challenges caregivers face. Charlotte shares her journey of becoming a caregiver for her husband with cancer and how she developed practical, emotional, and self-care strategies for caregivers. The conversation covers how to ask for help, integrating meditation and breathwork into daily routines, and the unexpected benefits of self-compassion for caregivers. Listeners can also learn about Charlotte's Scanxiety Toolkit, a resource designed to help manage the anxiety leading up to medical appointments.Tell us your thoughts on this episode!Support the showBecome a member of The Cancer Pod Community! Gain access to live Q&As, exclusive content, and so much more! Join us today! Check out our website! Looking for more information? We have blogs, merch, and all of our episodes listed by season and category. Shop our favorite reads! We've joined with Bookshop.org to offer some of our fave books! Have a comment or suggestion? Email us at thecancerpod@gmail.com Follow us wherever you browse. We're always @TheCancerPod: Instagram Bluesky Facebook LinkedIn YouTube THANK YOU!!

There's a caregiving crisis in America, and taking care of our parents is just one part of the struggle.It's caring for adults with a disability. It's grandparents raising kids again, or parents as primary caregivers for a medically complex child. Then there are friends caring for friends like they're family. Today is dedicated to highlighting resources to help caregivers of all kinds – both paid and unpaid. And, we're taking your calls. Call 615-760-2000 to ask the experts – or join us live streaming on YouTube at noon and pop your question into chat!Plus, we hear about actor Bradley Cooper's new PBS documentary about caregiving in America, which probably hits home because most of us will spend part of our life playing the role he played for his father. As first lady Rosalynn Carter said, "There are only four kinds of people in the world – those who have been caregivers, those who are currently caregivers, those who will be caregivers, and those who will need caregivers.”This episode was produced by LaTonya Turner and Mary Mancini.Guests Chris Durrance, director and senior producer of PBS documentary, Caregiving LaTonya Turner, editor and afternoon host, WPLN News Sandy Ewing, caregiver, medically complex child Aimee Luchterhand, caregiver, child with special needs Tina Lemon, caregiver, grandparent raising grandchildren Dr. Feylyn Lewis, Asst. Dean Student Affairs, VU School of Nursing; National Alliance for Caregiving researcher Dr. Megan Schwalm, President & CEO, Tennessee Caregiver Coalition

This summer, we're revisiting some of Hina and Marla's greatest hits from the first 10 seasons of The LowDOWN. On the Season 10 finale of The LowDOWN: A Down Syndrome Podcast, Dr. Susan Fawcett and a panel of caregivers give us the lowdown on mental wellness for parents and caregivers.Support the showThe LowDOWN: A Down Syndrome Podcast is produced by the Down Syndrome Resource Foundation. Learn more and support the podcast at DSRF.org.Follow @DSRFCanada on Facebook, Instagram, and Twitter.Leave us a rating and review on Apple Podcasts.

Northfield Public Schools Superintendent Dr. Matt Hillmann talks the first day of school, family engagement days, and more.

Host Joe Moravchik talks with St. Olaf College Distinguished Professor of History Steve Hahn about piracy in colonial North America and the Caribbean, the pardoning of over 200 pirates at this time, and much more from his book A Pirate's Life No More: The Pardoned Pirates of the Bahamas.

Northfield Mayor Erica Zweifel and Northside Boards owner Tyler Westman discuss Phase 2 of the Northfield skate park.

The deficits from the lead poisoning continue to intensify, Shannon channels her anger and grief into holding the people who hurt her son responsible.LEAD how this story ends is up to us is a true story written and produced by Shannon Burkett. Co-produced by Jenny Maguire. Directed by Alan Taylor. Starring Merritt Wever, Alessandro Nivola, Cynthia Nixon, and Cooper Burkett.EP4 features Eboni Booth, Sasha Eden, Kevin Kane, April Matthis, Alysia Reiner, and Mandy Siegfried. Casting by Alaine Alldaffer and Lisa Donadio. Music by Peter Salett. Sound Design by Andy Kris. Recording Engineer Krissopher Chevannes.For corresponding visuals and more information on how to protect children from lead exposure please go to https://endleadpoisoning.org.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Shaucha (To Organize) is about more than just physical cleanliness—it's the practice of creating external order to support inner clarity and peace. By organizing our spaces, schedules, and influences, we create a calm foundation for family life. Tapa (To Discipline) builds on this by channeling that order into resilience, helping us and our children grow stronger and more present, even in discomfort.Interested in registering for our live, virtual course with Vivekji and other guides? Visit http://bit.ly/cmn-2025.In this season of Live Vedanta, we are sharing insights on Courageous Caregiving through Vibhishana Gita. These discourses are from our Parenting Culture community, a space for seekers striving to be better in their caregiving responsibilities through the practice of self-development. You can always catch up on the previous episode.For those on the journey of self-development, Chinmaya Mission Niagara provides a community forum to listen, reflect, and contemplate. Follow us on Instagram and Facebook for more updates about upcoming live workshops, courses, and more! Chinmaya Mission is an international non-profit organization working to transform individuals through the knowledge of Vedanta.

 Show SummaryOn today's episode, we feature a conversation with Dr. Qwynn Galloway – Salazar, Senior Vice President of Engagement and Transformation at PsychArmor and founder and CEO of In Their Honor, an organization that supports veterans and those who care for them through the end of 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 GuestDr. Qwynn Galloway-Salazar is a veteran of the United States Army (01-06) and spouse to a retired combat Veteran. Her work has spanned the last 20 years, supporting our Nation's Military and Veteran communities. As the founder of In Their Honor, LLC, Qwynn serves as an End-of-Life Doula and Trainer. This Spring, she is slated to roll out state-specific training for End-of-Life Professionals supporting Veterans and their Caregivers; and training specifically geared towards the Veteran Caregiver community. In addition, serving as the Co-Principal Investigator of the Brooklyn College Veterans History Project, Qwynn conducts oral history interviews of Veterans, listening to how Veterans make meaning of their experiences and sharing with larger audiences. She believes, as a society, the way we make sense of the Veteran experience shapes the care and support future generations of Veterans receive.While blending her heart work with her head work, her doctoral dissertation entitled “Post-9/11 Women Veterans' Experiences Transitioning Into the Civilian Workforce” landed her the opportunity to serve as a qualitative researcher for the FY21 National Defense Authorization Act (NDAA), § 9104, Study on Unemployment Rate of Women Veterans Who Served on Active Duty in the Armed Forces after September 11, 2001. Along with co-authoring a chapter on “Vicarious Trauma and Compassion Fatigue” in Veteran care providers.Qwynn earned her Ph.D. from Walden University, specializing in Industrial and Organizational Psychology. She holds a Master of Arts degree in Professional Counseling and a Bachelor of Science degree in Criminal Justice. She serves on the Board of Directors for the American Association of Suicidology and the Advisory Board of the Veterans Studies Association.Links Mentioned During the EpisodeDr. Qwynn Galloway – Salazar on LinkedInIn Their Honor web site PsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week is the PsychArmor Course Library. Whether you're a health care provider, educator, employer, caregiver, or simply someone who wants to make a difference — PsychArmor courses are designed for you.  You can find the resource here:  https://learn.psycharmor.org/collections Episode Partner: Are you an organization that engages with or supports the military affiliated community? Would you like to partner with an engaged and dynamic audience of like-minded professionals? Reach out to Inquire about Partnership Opportunities Contact Us and Join Us on Social Media Email PsychArmorPsychArmor on 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  

Caregivers often struggle with the emotional and physical drain of caring for an elderly mother, especially when dealing with anxious personalities, physical and mental health concerns. In this episode, caregiving expert Pamela D Wilson offers essential caregiver tips and effective strategies for managing challenging caregiving situations. Learn how to set boundaries and communicate directly and honestly to create a better caregiving experience. By implementing these caregiver support strategies and techniques, you can create balance in your life while providing the necessary support for your aging loved ones.To find show transcripts and links mentioned in Episode 226 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, visit Pamela's website at www.PamelaDWilson.comLearn about Pamela D Wilson, her professional background, and her experience: https://pameladwilson.com/pamela-d-wilson-story/Are you interested in a 1:1 elder care consultation by telephone or video call with Pamela? Schedule time and learn more here: https://pameladwilson.com/elder-care-consultant-aging-parent-consultation-managing-senior-care-needs-meet-with-pamela-d-wilson/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/ Twitter: https://x.com/CaregivingSpeakPamela D Wilson | Caregiving Expert provides caregiver tips, support for caregivers, and resources for aging and elder care. Caregiving and aging for parents doesn't have to be challenging with expert caregiver advice, solutions, and strategies based on Pamela's 25 years of experience in care management and developing care solutions for families and individuals.©2025 Pamela D Wilson. All Rights Reserved

Rick and Doug are joined by Dr. Jen Wertalik of Georgia Southern University and Dr. Pam Wolfe, retired from Penn State University, to discuss their groundbreaking new book on sexuality education for individuals with disabilities. The conversation explores why sexuality education is essential, the heightened risks of abuse faced by this population, and how comprehensive instruction extends far beyond physiology to include relationships, self-advocacy, and decision-making. The guests highlight both the challenges and opportunities of preparing teachers, parents, and caregivers to navigate an often-taboo topic with empirical, practical strategies. Listeners will come away with a deeper understanding of how sexuality education empowers individuals with disabilities to live safer, more fulfilling lives.   To earn CEUs for listening, click here, log in or sign up, pay the CEU fee, + take the attendance verification to generate your certificate! Don't forget to subscribe and follow and leave us a rating and review.   Show Notes: Coming Soon!

Hosts Rob Ryden and Will Healy play a lot of songs they think are related to the Minnesota State Fair, or just fairs in general. Some of them are, while others… Anyway, your hosts also talk in depth about the Great Minnesota Get Together, and even offer a contest to win fair related prizes. It’s […]

Dundas City Administrator Jenelle Teppen and Caitlyn Otis from Dundas Oktoberfest discuss the upcoming event on Saturday, September 20th and how to get involved.

Tim Freeland and Ali Feldman from the Defeat of Jesse James Days committee discuss the annual Horseshoe Hunt starting tomorrow, Wednesday, August 27th.

On the 137th episode of What is a Good Life?, I'm delighted to welcome Diane Button. Diane is a founding partner of the Bay Area End-of-Life Doula Alliance in Northern California, and the best-selling author of Dear Death: Finding Meaning in Life, Peace in Death, and Joy in an Ordinary Day and The Doula Tool Kit: The Complete Practical Guide for End-of-Life Doulas & Caregivers (co-authored with Angela Shook and Gabby Jimenez). She holds a master's degree in Counselling Psychology, works as a practicing end-of-life doula, and serves as a lead instructor in the University of Vermont Larner College of Medicine's End-of-Life Doula Certificate Program. Her latest book is the inspiring What Matters Most.In our conversation, Diane shares the profound insights she has gained through her work, emphasising the power of presence, the value of embracing all emotions, and the joy found in life's simplest moments.Together, we explore how the beauty of ordinary days and the wisdom of those facing death can illuminate what it truly means to live well and meet life's final chapter with grace.For Diane's latest book, What Matters Most:To buy your copy: https://www.penguinrandomhouse.com/books/768705/what-matters-most-by-diane-button/About the book: https://www.dianebutton.com/what-matters-mostWebsite: https://www.dianebutton.comContact me at mark@whatisagood.life if you'd like to explore your own lines of self-inquiry through 1-on-1 coaching, my 5-week group courses, or to discuss experiences I create to stimulate greater trust, communication, and connection, amongst your leadership teams.- For the What is a Good Life? podcast's YouTube page: https://www.youtube.com/@whatisagoodlife/videos- My newsletter: https://www.whatisagood.life/- My LinkedIn: https://www.linkedin.com/in/mark-mccartney-14b0161b4/00:00 Reflections on the book02:10 The depth of the role of an End of Life Doula04:45 Experiencing everything08:44 The cultivation of presence14:00 Pausing and slowing down17:00 An awareness of joy21:20 An expression of gratitude25:30 The process of writing the book31:55 Not waiting to celebrate life36:30 Distilling what matter most40:30 The simple moments43:30 Legacy work with the dying48:00 Regrets over the little things52:30 Self-love, acceptance, and authenticity1:00:00 Comfort with grief and conflicting emotions1:08:00 The importance of our small acts

Ever wondered how far you'd go to care for someone you love? How much dignity you'd sacrifice? I found my answer on the side of I-20 during Atlanta rush hour.When my mother started talking to people who weren't there, walking into walls, and fidgeting constantly, I suspected a UTI—those sneaky infections that can make dementia symptoms appear dramatically worse. After three grueling weeks of attempting to collect a urine sample from my incontinent mother, we finally succeeded. With my precious cargo secured, I had exactly one hour to reach a lab 45 minutes away.What followed was nothing short of a caregiver's nightmare. Halfway to the lab, my body betrayed me, forcing an emergency roadside stop that left me sweating, shaking, and utterly humiliated—but still clutching that precious urine sample. You'll have to listen to the episode for all that went down - listener discretion advised!This raw, unfiltered story illustrates the invisible battles caregivers fight daily. We sacrifice comfort, dignity, and sometimes even our own health in service of those who depend on us. But in those moments of chaos and desperation, we discover reservoirs of strength we never knew existed.If you're caring for someone with dementia, remember this: UTIs are the worst. They can cause dramatic behavioral changes that mimic worsening dementia. Before assuming your loved one's condition is deteriorating, check for infection. And never, ever stop advocating—even when it means pulling over on a busy highway or challenging medical professionals who stand in your way.Subscribe to Parenting Up for more unvarnished truths about the caregiving journey. Because sometimes the messiest stories offer the most valuable lessons.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/channel/UCDGFb1t2RC_m1yMnFJ2T4jwPatreon: https://patreon.com/jsmilesstudiosTEXT 'PODCAST" to +1 404 737 1449 - to give J topic ideas, feedback, say hi!Be sure to leave us a review!

In this week's episode of Hope for the Caregiver, I continue my two series: Difficult Issues Caregivers Face but Don't Want to Talk About and Hymns Every Caregiver Should Know. I start with a memory of a pastor who once told me, “Peter, you do yourself a disservice—you make this look easier than it is.” He was right. For years I made caregiving look manageable, even while quietly drowning inside. That appearance of strength often kept others from stepping in or even knowing what to say. Meals and casseroles are thoughtful, but they're not enough. Caregivers need more than temporary relief—we need sustainable support. Vocational direction, financial guidance, and mentors willing to walk with us can make the difference between barely surviving and building a life that endures. Scripture reminds us of El Roi, the God who sees. Just as He saw Hagar, Zacchaeus, and the multitudes, He also sees caregivers who mask their exhaustion. And if God sees, the church must learn to see too—not just the obvious needs, but the hidden cracks in a caregiver's life. I share about Gracie's 98 surgeries, including a recent five-month stretch in the hospital, and how impossible it has been to plan a “normal” career or even a five-week calendar. Caregiving has reshaped everything in my life, and for too long I didn't have people asking the deeper questions about what was sustainable. Then I take you to the Caregiver Keyboard, where I introduce this week's hymn. I not only play it, but also show how its harmonies—tension, dissonance, and resolution—mirror the emotional weight caregivers carry. The story behind the hymn ties directly into this theme: before we can encourage or rescue anyone, we first have to see them. I close by sharing from my new book, A Caregiver's Companion: Scriptures, Hymns, and 40 Years of Insights for Life's Toughest Role. I wrote it to give caregivers—and the church—a vocabulary of hope. Because healthy caregivers make better caregivers.   Get this book today!    

Host Dr. Matt Hillmann, the Superintendent of Northfield Public Schools, talks with Northfield Middle School Family and Consumer Science teacher, as well as the President of the Northfield Education Association, Amanda Miller.

Manager of Riverwalk Market Fair Derek Meyers discusses tomorrow’s monthly 4th Tuesday market at the Northfield Community Education Center from 3-6:30pm, and other goings-on at the weekly Saturday market.

Project Friendship Executive Director Holly Schoenbauer and Program Coordinator April Kopack discuss the mentorship program between Northfield students and St. Olaf and Carleton students.

The Caregiver's Journal hosted by Lance A. Slatton with Cindy (PT) & Christina (ST) Hardin-Weiss.   The Caregiver's Journal is the show where we are sharing the caregiving experiences, stories, and wisdom of family caregivers.   Chapter 15 - "Caregiving Love":   About Mary Whitehead:   Mark & I have been partners in life since our first date, a Heart concert, in 1978 followed by our marriage in 1979. Together we raised two children, and along the way we helped care and provide for parents & grandparents throughout their illnesses and aging in place or in senior living centers. I call myself a care partner vs. caregiver because Mark does not need my assistance for everyday tasks. We both use our strengths that complement each other on this path with Parkinson's and several other chronic illnesses he lives with.   My late mother was my inspiration. In my mid-teens I watched her, over the course of two years, lovingly care for my dying father (lung cancer). I could not have had a better, in-home example of someone who did everything, including care for him, with love. I am married to the most wonderful man who insisted that my mom live with us for what totaled the last 12 years of her life so that she could have a comfortable life with no expenses and be cared for by us after having a massive heart attack two years before she passed away.   When Mark was 47, as we became empty nesters and were poised to live out some dreams that were not feasible during our first 2+ decades together, a diagnosis of young onset Parkinson's Disease brought our hopes, plans, and his career to a screeching halt. But it couldn't completely stop this incredible human being, artist, musician/composer, man of many hobbies and a higher math maniac. I like to tease him about trying to share multi-page equations with me for discussion. Side note: he even took an online math course through MIT and I insisted that he buy one of their hoodies to wear proudly. There is so much to Mark that we could never cover in one conversation but rather than dwell on the PD, he prefers to pursue and concentrate on what he CAN do.   We cultivate humor and wit in our relationship. That's where “Tenacious M” - my care partner/gansta moniker comes from. I combine it with my Cornermam enthusiasm to encourage Mark's boxing workouts (excellent for PD) and – like a beagle in a brush pile - I pursue every challenge face head on, whether it's an insurance or pharmacy snafu, etc. Together, we face every aspect of living with PD. And we are both are dedicated PD research participants at Washington Univ., St. Louis, MO, also the location of Mark's neuro, Dr. Joel Perlmutter (definitely the top doc). I, along with two of our friends are in the non-PD control group. We all have pledged to donate our brains at the end of our lives for PD research.   In 2013, inspired by a Parkinsons Foundation resource kit, we created a PD Awareness & Research fundraising blitz, raising nearly $3k for Dr. P's research. Friends, family & my coworkers held Pancakes for PD, Dine-out nights, a proclamation by our city mayor, and, among many other activities, we raffled a beautiful quilt that Mark & I designed, and I did the hand-embroidery.   Like the motto in our Parkinson's & Dystonia private FaceBook group, we will never give up.   And I'd like to credit the group's founder/lead admin, Erika, for creating a safe and supporting space for people with PD and the caregivers & care partners.