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Liz Campbell gets you up to date with the latest scores and highlights from the week on the Raider Scoreboard. It’s a wet and wild day as the Raiders Gators swim team takes over the studio. Senior Captains Will Udelhofer, Logan Joyce and Will Redetzke along with Juniors Jimmy Graham and Odin Bergs join their […]
International Women's Day bonus episodeIn this special episode, Danielle Black explores something rarely named in conversations about parenting after separation: the invisible architecture of childhood.The planning.The anticipating.The emotional holding.The daily mental load of raising children that rarely appears in legal documents, mediation rooms, or parenting orders.Across decades of research, we know that primary caregivers - most often mothers - carry the majority of this invisible labour. Yet when families separate, the systems designed to determine parenting arrangements often struggle to see it.In this episode, Danielle explores:• The invisible labour that holds children's lives together• Why the "proximity illusion" can make non-primary caregivers appear equally involved• What the research actually says about caregiving and unpaid labour• Why 'equal parenting time' is NOT the same as 'equal parenting'• How post-separation economic abuse often shows up through child-related costs• The emotional reality of being the parent who provides the secure base children return toThis episode is for women at every stage of the journey: those still in difficult relationships, those navigating separation, those in family court proceedings, those with final orders who are still managing chaos, and those carrying the grief of children being turned against them.On International Women's Day, this conversation honours the work that primary caregivers do every day - even when the world fails to see it.Because the invisible architecture of childhood may be unseen by systems, but it is never invisible to the children living inside it.As always, this episode is not legal advice and not therapy.Explore the supports offered by Danielle Black CoachingThe Post-Separation Parenting Blueprint™
Send a textParent. Partner. Leader. Provider. Caregiver. Professional.But who are you outside of what you do for everyone else?In this episode of In Session, we explore the quiet identity crisis that often hides beneath burnout. Many high-capacity adults have spent years (sometimes decades) being the responsible one, the strong one, the dependable one. Over time, roles become identity. And when that happens, exhaustion isn't just physical, it's existential.We unpack:How early conditioning shapes role-based identityThe difference between purpose and performanceSigns you've lost yourself in responsibilityWhy burnout often signals identity depletionHow to begin reclaiming who you are beyond your titlesThis conversation is for anyone who feels tired in a way sleep doesn't fix.If you've ever asked yourself, “Who am I when I'm not needed?” this episode is for you.Because roles are expressions of who you are. They are not who you are.Support the showDisclaimer: This podcast is for informational and educational purposes only and is not a substitute for therapy or professional mental health care.Want more? Subscribe now and take a seat In Session! https://www.buzzsprout.com/1679131/supportFollow us on Instagram: @insessionthepodcast Join our Facebook group: https://www.facebook.com/insessionthepodcast/
Aging in Place: Safety, Technology, & Dignity w/ Drew Siefried of TruBlue Ally - AZ TRT S07 EP04 (286) 3-1-2026 Things We Learned This Week · America is aging rapidly - By 2030, 1 in 5 Americans will be over 65. · Most seniors want to stay in their homes - More than 80% of older adults prefer aging in place rather than moving to assisted living. · Technology is transforming senior safety - Non-intrusive monitoring systems can detect falls and alert families without cameras or wearables. · One fall can change everything - Falls are one of the leading causes of injury and loss of independence among seniors. · Prevention is far cheaper than crisis care - Simple home safety upgrades can prevent accidents and help seniors maintain independence longer. Guest: Drew Seifried LKIN: https://www.linkedin.com/in/drewseifried/ Company: TruBlue Home Service Ally Website: https://www.trublueally.com/east-phoenix-north-scottsdale With over 25 years of combined corporate and entrepreneurial experience, I currently own and operate TruBlue Home Service Ally, where we support seniors and busy families with home modifications and handyman services. In this role, we prioritize safety, reliability, and exceptional service, ensuring all personnel meet high professional standards. As a Certified Franchise Executive, I also guide aspiring entrepreneurs, including corporate professionals, first responders, and military veterans, toward business ownership through franchising. Leveraging expertise in franchise agreements and processes, I simplify the path to ownership, aligning opportunities with individual goals. My mission is to empower others to achieve their aspirations through purpose-driven ventures. TruBlue Home Service Ally® provides a unique and affordable approach to helping busy adults and seniors live a worry-free life by offering trustworthy handyman, home maintenance and senior modification services. Helping you maintain your home both inside and out, TruBlue's services include: handyman projects and to-do list chores, preventative home maintenance programs, seasonal work, and senior modification services, all handled by a professional, bonded and insured Tru-Pro® Technician. Episode Overview America is entering a major demographic shift. By 2030, 1 in 5 Americans will be over the age of 65, creating what many experts call the "Silver Tsunami." Families across the country will face new challenges as aging parents want to maintain independence while staying safe at home. But aging at home safely requires planning. In this episode, we sit down with Drew Seifried of TruBlue Home Service Ally to discuss how home safety modifications, emerging Age Tech, and non-intrusive monitoring technologies are helping seniors stay independent longer — while providing peace of mind for their families. We also explore the unique needs of veterans and individuals with disabilities, and how communities and organizations can better support them. Segment 1: Aging in Place & The Silver Tsunami Drew Seifried owns three territories with TruBlue, a national franchise focused on helping people safely remain in their homes. The company works primarily with: · Seniors and aging adults · People with disabilities · Veterans · Adult children caring for aging parents Their mission is simple: help people live independently and safely at home. The Growing Senior Population America is rapidly aging. Key statistics: · 61 million Americans are age 65+ · By 2030, about 20% of the population will be seniors · Phoenix and other Sun Belt cities are seeing rapid senior population growth as retirees relocate This demographic shift will place new pressure on: · Healthcare systems · Caregiver workforce · Family members caring for aging parents The Hidden Risk: Falls in the Home One of the biggest threats to senior independence is falling. Key statistics: · 1 in 4 adults age 65+ falls each year · Falls cause over 3 million emergency room visits annually · More than 300,000 seniors are hospitalized each year for hip fractures · Over 50% of falls occur inside the home In many cases, one fall can change everything. A serious fall can lead to: · Hospitalization · Loss of mobility · Long-term disability · Moving into assisted living The Most Dangerous Areas in a Home According to home safety experts, the highest risk areas include: · Bathrooms (tubs and showers) · Entryways and stairs · Poor lighting · Cluttered hallways or walkways Even small modifications can dramatically reduce fall risk. Preventing Falls Before They Happen TruBlue helps families install preventative safety upgrades such as: · Bathroom grab bars · Non-slip shower treatments · Improved lighting · Handrails and stair supports · Walkway hazard removal The company also performs full home safety assessments to identify hidden risks. As Drew explains, the goal is prevention — because once a fall happens, recovery can be much more difficult. Aging at Home vs Assisted Living Another major challenge families face is cost. Average assisted living costs in the U.S.: · $5,000–$6,000 per month · Often $60,000–$70,000 per year By comparison, many safety upgrades or in-home services cost a fraction of that. And most seniors prefer to stay home. Surveys show: · 84% of seniors want to age in place · Independence and familiarity with their home environment matter deeply Segment 2: Age Tech & Smart Monitoring One challenge facing families is the shrinking caregiver workforce. With fewer caregivers available, technology is stepping in to help monitor safety. Adult children want peace of mind that their parents are safe — especially when they live in another city. But many seniors dislike traditional monitoring systems. Common concerns include: · Cameras in the home · Wearable emergency devices · Privacy issues · Technology complexity A New Approach: Radar-Based Monitoring A newer technology solution is radar-based monitoring systems like those from Pontosense. These systems use small radar sensors placed throughout the home. They can detect: · Falls · Movement patterns · Breathing and vital signals Unlike cameras, they are completely non-intrusive. Features include: · No cameras · No wearable devices · No audio recording · No stored video data The system can detect unusual events and send alerts. Smart Alerts for Families If a fall occurs, the system can: · Wait about 90 seconds to see if someone gets up (reducing false alerts) · Send notifications to family members · Contact caregivers · Alert emergency services if necessary Family members can also monitor activity patterns through a mobile app. For adult children balancing careers, families, and aging parents, this technology provides peace of mind without invading privacy. Segment 3: Disability Services & Veteran Support TruBlue also works with individuals living with disabilities and veterans who require specialized home modifications. Organizations supporting the disability community include: · Ability360 · Benevilla These groups offer programs ranging from adaptive sports to community support services. Health Challenges as We Age Many older adults face conditions that impact mobility or independence. These can include: · Arthritis · Balance issues · Progressive neurological diseases like ALS or MS · Reduced strength and coordination Simple tasks — getting into a bathtub, climbing stairs, or reaching shelves — can become difficult. Home modifications can restore independence. Importantly, these upgrades can be designed to blend into the home aesthetically, preserving both function and dignity. Supporting Veterans Veterans represent another group that often needs home safety support. Key statistics: · Approximately 17 million veterans live in the United States · Nearly 8 million veterans are age 65 or older Despite available programs, many veterans do not utilize assistance. Organizations working to support veterans include: · Paralyzed Veterans of America · Veterans of Foreign Wars · Elks Lodge Drew himself served in the military and is passionate about helping veterans access services and resources. Additional Home Safety Monitoring Beyond fall prevention, modern smart homes can also monitor: · Smoke and fire detection · Water leaks and flooding · Utility failures · Entry and exit activity These systems help families create a safer living environment for aging loved ones. Final Takeaway Aging doesn't have to mean losing independence. With the right combination of: · Home safety modifications · Smart technology · Community resources · Family planning Millions of seniors can live longer, safer, and more confidently in their own homes. 'Best Of' Topic: https://brt-show.libsyn.com/category/Best+of+BRT Thanks for Listening. Please Subscribe to the AZ TRT Podcast. AZ Tech Roundtable 2.0 with Matt Battaglia The show where Entrepreneurs, Top Executives, Founders, and Investors come to share insights about the future of business. AZ TRT 2.0 looks at the new trends in business, & how classic industries are evolving. Common Topics Discussed: Startups, Founders, Funds & Venture Capital, Business, Entrepreneurship, Biotech, Blockchain / Crypto, Executive Comp, Investing, Stocks, Real Estate + Alternative Investments, and more… AZ TRT Podcast Home Page: http://aztrtshow.com/ 'Best Of' AZ TRT Podcast: Click Here Podcast on Google: Click Here Podcast on Spotify: Click Here More Info: https://www.economicknight.com/azpodcast/ KFNX Info: https://1100kfnx.com/weekend-featured-shows/ Disclaimer: The views and opinions expressed in this program are those of the Hosts, Guests and Speakers, and do not necessarily reflect the views or positions of any entities they represent (or affiliates, members, managers, employees or partners), or any Station, Podcast Platform, Website or Social Media that this show may air on. All information provided is for educational and entertainment purposes. Nothing said on this program should be considered advice or recommendations in: business, legal, real estate, crypto, tax accounting, investment, etc. Always seek the advice of a professional in all business ventures, including but not limited to: investments, tax, loans, legal, accounting, real estate, crypto, contracts, sales, marketing, other business arrangements, etc.
Dr. Barbara Paldus is the Founder and CEO of CODEX Labs, the sponsor of this episode.She grew up around Nobel Prize winners, built biotech manufacturing equipment for vaccines and cancer therapeutics, and then sold her company after an 8 year old threatened suicide.Her son's severe eczema pushed her into an unregulated $100,000,000,000 skincare market where parents are told to trust labels that nobody verifies. She explains how corticosteroid ladders leave patients with years long withdrawal, why U.S. ingredient oversight lags Europe, and how chemotherapy destroys the same skin and gut barriers seen in inflammatory disease.The conversation tracks the real stakes behind “clean” marketing: a child's immune system, hospital infections like MRSA, and patients trying to survive treatment without new damage. She also details the research path from Irish medical manuscripts to microbiome science and why sick populations become the only reliable regulators when policy fails.RELATED LINKSBarbara PaldusCodex LabsSekhmet VenturesDr Peter LioFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.
This week Andrew talks with executive Katie Rhone — the Sr. Vice President of HERO & Employee Experience at KARE. KARE is an on-demand senior care platform connecting qualified caregivers & nurses with senior living communities. Katie has the extraordinary leadership responsibility over experience design & strategy for 65,000+ caregivers and nurses serving patients. In this conversation, Katie shares many of the ideas & frameworks she utilizes to build an organization (and workforce) that feels connected, appreciated, well-recognized, & an incredible sense of belonging. This conversation has the power to help all of us be better leaders & teammates — and give us the tools to make the communities we care about a little bit more connected. ** Follow Andrew **Instagram: @AndrewMoses123X: @andrewhmosesSign up for e-mails to keep up with the podcast at everybodypullsthetarp.com/newsletterDISCLAIMER: This podcast is solely for educational & entertainment purposes. It is not intended to be a substitute for the advice of a physician, psychotherapist, or other qualified professional.
Our guest today is Pam Cusick Senior Vice President of Rare Patient Voice. Rare Patient Voice is a national community that connects patients and caregivers with researchers who genuinely want to learn from their lived experiences. Through this work, RPV ensures that people living with rare and chronic conditions have a direct voice in shaping studies, treatments, and health innovations. Their model is built on trust, respect, and fair compensation, creating a space where stories become data that can drive meaningful change. Pam Cusick is a leader in patient engagement with more than three decades of experience in research design, implementation, and advocacy. As Senior Vice President of Rare Patient Voice (RPV), she works to ensure that patient and caregiver experiences help shape the future of medical research. Beyond RPV, Pam contributes to the advancement of women in healthcare through her work with Women in Research (WIRe), the Healthcare Businesswomen's Association (HBA), and the International Society for Patient Engagement Professionals (ISPEP). She continues to mentor emerging leaders who share her dedication to connecting patient advocacy with meaningful scientific progress.
Caregivers put so much energy into caregiving yet they still struggle with self-criticism and feeling like their best isn't good enough.Every caregiver deserves self-forgiveness.Listen this week to find out the five areas that can lead caregivers to carry shame, and what they can do about it.Your wellbeing matters.Doctor Deliawww.DoctorDelia.comCoping Courageously: A Heart-Centered Guide for Navigating a Loved One's Illness Without Losing Yourself is available here: www.copingcourageously.com Please review this podcast wherever you listen and forward your favorite episode to a friend! And be sure to subscribe!Sign up to stay connected and learn about upcoming programs:https://trainings.integrativepalliative.com/IPI-stay-in-touchI'm thrilled to be listed in Feedspot's top 15 palliative podcasts!https://blog.feedspot.com/palliative_care_podcasts/
Season 3 | Episode 14 Caring for a teen living with a mental health challenge can push a family to the brink. Recovery College at Ontario Shores is offering a new course on how to care for your teen and yourself in this tumultuous time.
This episode explores the Essential Caregivers Act of 2025 and the lessons learned from the COVID 19 visitation bans in long term care. Our discussion examines how isolation harms residents, why essential caregivers are irreplaceable, and how this legislation aims to protect resident rights during future emergencies. It's a conversation about dignity, safety, and ensuring that no one in long term care is ever left without the people who know and love them most. Guests: Irma Rappaport, National Advocate, Caregivers for Compromise, Connecticut Virtual Family Council; and Amy Badini, Connecticut Caregivers for Compromise, Essential Caregivers Coalition, Connecticut Virtual Family Council
In this heartfelt episode of The Summits Podcast, cohosts Vince Todd, Jr. and Daniel Abdallah sit down with twin sisters Liz Childers and Norma Unser to share an inspiring and deeply personal conversation about their family's journey with cancer. Liz and Norma open up about how cancer has profoundly impacted their lives, with their mom, Liz, and Norma all facing breast cancer diagnoses. They discuss the emotional and physical challenges of their battles, the critical role of routine screenings in early detection, and the strength they've found in each other. The conversation also highlights the groundbreaking work of the Cancer Vaccine Coalition and the hope it brings for the future of cancer outcomes and prevention. Liz and Norma's story is a powerful reminder of resilience, the importance of advocacy, and the strides being made in the fight against cancer. Learn more about the Cancer Vaccine Coalition: https://cancervaccinecoalition.org/ Shop Lizzie Lu's Crew hats! https://lizzielucrew.com/
Dr Eugene Manley grew up in Detroit in the 1980s cycling through emergency rooms 20 to 30 times a year with asthma and anaphylaxis while hospital staff talked past his family and buried them in paperwork they could not decode. He responded by earning a BS in mechanical engineering an MS in biomedical engineering and a PhD in molecular biology cell biology and biochemistry. Along the way he tore his ACL training for a jiu jitsu black belt worked 86 straight days in a lab during his doctorate and learned how academic and clinical systems punish people who refuse to shrink.In this episode Manley walks through a recent post surgery ordeal at Mount Sinai Queens where staff falsified records attempted an illegal discharge and nearly sent him home on the wrong blood thinner. He explains how medical racism shows up in charts staffing and decision making and why measurable equity fails without accountability. Listeners hear how his STEMM and Cancer Health Equity Foundation builds pipelines for underrepresented students challenges clinical trial design and teaches patients how to protect themselves when institutions lie. RELATED LINKS• Eugene Manley Jr• STEMM and Cancer Health Equity Foundation• Village Voice• LUNGevity FoundationFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.
Caring for aging parents is a noble and taxing job. Finding support as a caregiver is vital to both your health and your parents' long-term outcomes. Memory cafes may be just the community you need.If you get a ton of value in this episode, I would love to invite you to subscribe because it costs nothing to subscribe.Bill Cohen's loving and talented mother, Sheila, lost her home to Hurricane Katrina. Then, she lost her health, ability to create beautiful art and, ultimately, her life due to Alzheimer's.For almost 10 years, Bill was her primary caregiver and advocate, not just her son. He turned his personal loss into his passion supporting other caregivers across North America. After “retiring” from state employment eight years ago, Bill is a caregiver support group and memory café leader, a podcast guest, a speaker, a trained elder mediator, and a caregiving support consultant. He has completed several caregiving courses through the Alzheimer's Association and the Society for Certified Senior Advisors (CSA)®, and earned business degrees from Boston and Portland State Universities. Bill is a native New Englander and lives in the Portland, Oregon area with his wife and supporter, Lori. Welcome, Bill!Check out Petite2Queen for more great interviews, podcasts, and blogs to help you achieve more, faster!https://www.petite2queen.com/Support the showCheck out Petite2Queen for more great interviews, podcasts, and blogs to help you achieve more, faster!https://www.petite2queen.com/
Feeling resentment as a cancer caregiver? You are not alone and you are not a bad person.In this powerful episode of The Cancer Caregiver Podcast, we unpack one of the most unspoken emotions in caregiving: resentment.If you're caring for a spouse or loved one with cancer and quietly thinking:“Why is it always me?”“Why does no one ask how I'm doing?”“I didn't sign up for this version of my life.”This episode is for you.Caregiver resentment often hides beneath exhaustion, burnout, scanxiety, anger, and guilt. It can show up when:You feel invisible in your own crisisFamily members offer opinions but not helpFriends check on your loved one but never check on youThe endless oncology appointments and medical tasks never stopYou grieve the life, career, travel, or retirement plans you lostHere's the truth: resentment is not a character flaw. It's an overcapacity signal.When you're stretched beyond your emotional and physical limits, resentment is your nervous system's warning light. It's often grief wearing armor grief for the support you didn't receive, the freedom you lost, or the version of your life you thought you'd have.In this episode, you'll learn:Why caregiver resentment is normal (and common in cancer caregiving)How resentment is connected to caregiver burnoutThe hidden grief beneath bitternessHow to turn resentment into information instead of shameA 3-step reflection practice to respond to resentment with curiosity instead of guiltYou can love your person deeply and still resent what caregiving has cost you. Those truths can coexist.This episode is part three of our four-part series, “The Things You Don't Say Out Loud,” where we explore the hidden emotional realities of cancer caregivers including loneliness, anger, resentment, and the thoughts you only admit in the dark.If you're navigating caregiver stress, compassion fatigue, or emotional exhaustion while supporting a loved one through cancer, this conversation will help you feel seen and less alone.
Show SummaryOn this episode, we have a conversation Today we're having a conversation with Vietnam Era veteran and nurse Joanne Malear, who is the coordinator of the 11th Hour Squadron. They are an all-volunteer organization that believes in taking care of dying veterans like family. They can be there at a loved one's bedside during those final nights when family members are at home getting much-needed rest.Provide FeedbackAs a dedicated member of the audience, we would like to hear from you. If you PsychArmor has helped you learn, grow, and support those who've served and those who care for them, we would appreciate hearing your story. Please follow this link to share how PsychArmor has helped you in your service journey Share PsychArmor StoriesAbout Today's GuestJoanne Melear is a former U.S. Navy nurse and the founder of the 11th Hour Squadron, a volunteer initiative dedicated to ensuring that veterans in hospice care are not alone at the end of life. Drawing on her military medical experience and deep commitment to lifelong service, she created the program to bring trained veteran volunteers to sit bedside, provide companionship, and honor fellow service members in their final hours.Links Mentioned During the Episode11th Hour Squadron Website PsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week is the PsychArmor course Caring for Veterans Through the End Of Life: Compassionate Communities. In this course, you will learn how you can provide compassionate care through the end-of-life for those who have served our country. You can find the resource here: https://learn.psycharmor.org/courses/caring-for-veterans-through-the-end-of-life-1 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
As we close out American Heart Month on Full Circle, this episode centers on a story that is both heartbreaking and life-affirming.Marvale Young has always been a caregiver. A devoted mother, she fostered more than 30 children, opening her home and heart to young people who needed stability, love, and safety. She was the strong one — the one who carried others through their storms.But over time, life carried its own weight. After losing her husband and navigating years of emotional stress, Marvale began noticing subtle shifts in her health. Fatigue. Changes in her body. Signals that were easy to overlook when you are used to putting everyone else first.Then came the diagnosis: heart failure.In this intimate conversation, Marvale reflects on what it felt like to hear those words and whether prolonged stress and unresolved grief contributed to her declining health. Caregivers often ignore their own needs. Women, especially, push through discomfort. Marvale's story challenges us to reconsider that pattern.And then — in the midst of unimaginable grief, just days after losing her son — she received a call that would change everything. A donor heart was available.Her journey from heart failure to transplant is a powerful reminder of the lifesaving impact of advanced cardiac care, organ donation, and medical research. It is also a testament to resilience, faith, and the gift of second chances.Heart disease remains the leading cause of death in the United States. Symptoms are often subtle. Stress is not “just stress.” Fatigue is not always “just being tired.”This episode is about listening to your body before it whispers become emergencies.Call to Action:Make your heart health a priority. Schedule a physical. Monitor your blood pressure. Have honest conversations about stress, grief, and self-care. Learn how you can support heart health education and survivor advocacy through the American Heart Association. Share Marvale's story — it could inspire someone to seek care sooner.
In this opening segment of Hope for the Caregiver, I take us to Matthew 9:9, where Jesus calls Matthew from his tax booth with two simple words: Follow me. Matthew didn't leave a side job. He walked away from wealth, security, and the only system he had ever known. And unlike the fishermen who could return to their boats, Matthew had no way back. The moment he stood up, his old life was over. I explore the historical reality behind that moment and why Matthew's decision mattered so deeply, then I turn the lens toward us as caregivers. Because when a diagnosis comes, when an accident reshapes a family, when surgeries multiply and life changes permanently, something quietly closes behind us too. Caregivers don't return to life before the hospital room. There's no leave of absence from love. No tax booth waiting if we decide this is too hard. Caregiving often feels like having the ships burned behind us. We didn't fully choose the road, and we rarely know what lies ahead. But like Matthew, we are called not into clarity, but into obedience. In this episode, I talk about what it means to move forward when there is no going back, and how caregivers can discover purpose, faithfulness, and the presence of Christ in places we never expected to walk.
BrainStorm wants to hear from you! Send us a text.What happens when your carefully mapped career path collides with an Alzheimer's diagnosis — and you're only 26? In this deeply personal episode of BrainStorm by UsAgainstAlzheimer's, host Meryl Comer sits down with Jessica Guthrie, founder of the online platform Career and Caregiving Collide, whose life changed forever when her mother was diagnosed with early-onset Alzheimer's in 2014.Jessica shares what it means to be a young Black professional thrust into the role of long-distance caregiver — navigating a healthcare system that often didn't listen, workplaces that weren't designed with caregivers in mind, and support spaces where she was frequently the youngest and only Black person in the room. Rather than suffering in silence, she turned her experience into a growing online community where caregivers across generations find connection, validation, and practical wisdom.Meryl and Jessica unpack the hidden barriers facing Black families seeking an Alzheimer's diagnosis, the toll caregiving takes on career ambitions and financial security, and why the people who show up at diagnosis often disappear years down the road.This is conversation for anyone who has ever had to choose between their dreams and their family.Support the show
In honor of TNBC Day, CancerCare is proud to partner with the TNBC Foundation for a special episode of Cancer Out Loud dedicated to the triple-negative breast cancer community.We would love to hear from you! Please share your thoughts or episode ideas at canceroutloud@cancercare.org or leave a comment on this episode!Please follow, rate and share Cancer Out Loud to help others find strength and support through our community.SummaryIn this conversation, CancerCare oncology social worker Christina Monaco, and Caryn Sullivan, a breast cancer survivor and thriver, discuss the importance of support and community for individuals diagnosed with triple negative breast cancer. Caryn shares her personal journey through various stages of breast cancer, emphasizing the significance of hope, positivity, and wellness practices. They explore the role of caregivers, the impact of community resources like the Triple Negative Breast Cancer Foundation, and the importance of mindfulness in navigating the challenges of cancer treatment.TakeawaysCaryn's journey with breast cancer began with an early stage diagnosis.She emphasizes the importance of support from family and friends during treatment.Caryn's cancer mutated to triple negative metastatic breast cancer after several years.Finding hope and positivity is crucial in the cancer journey.Community support, such as the TNBC Foundation, plays a vital role in coping with cancer.Wellness practices, including mindfulness and healthy eating, have helped Caryn manage her health.Building relationships with medical professionals is essential for effective treatment.Caregivers should be mindful of the needs of those they support.Caryn encourages newly diagnosed patients to seek out success stories for inspiration.Gratitude practices can help shift focus during difficult times.
Caregiving rarely arrives with a manual. When Megan Taniguchi's grandmother survived a heart attack and then a stroke, Megan walked away from her job, moved in, and learned how to keep her family together—one blood pressure reading, one bath, one prayer at a time. We invited Megan back to share the unfiltered truth: the daily routines that stabilize fragile health, the medical skills she picked up from generous nurses and a rare doctor who took time to teach, and the mistakes that became lessons, like how an overstrict diet can send sodium and potassium spinning.We dig into what dignity really means when care gets intimate, how tempers cool and repairs happen fast, and why a tight, three-person unit—grandma, mom, and son—can become a quiet fortress. Megan opens up about single motherhood, the logistics and cost of youth sports, and the creative fundraising it takes to show up on the sidelines without dropping the ball at home. Along the way, she describes how therapy, small social moments, and candid communication keep her from burning out, and how simple systems—pill organizers, shared calendars, visible checklists—turn chaos into a plan.Faith threads through every scene. After years of drifting, Megan returned to church, chose re-baptism, and started talking to God daily. Not ritual for ritual's sake, but a living relationship that reshaped how she sees responsibility, provision, and endurance. That shift didn't erase the hard parts; it gave them meaning. The episode is a guide for caregivers, single parents, and anyone standing at the edge of a hard decision, offering practical caregiving tips, mental health tools, and a reminder to say thank you now, not later.If this conversation moved you, tap follow, share it with someone carrying a heavy load, and leave a review with your best caregiving tip so others can learn from you too.
“Patients are waiting…”Those simple but profound words from Dr. Steve St. Onge set the tone for this conversation, and for why this work matters so deeply.Science has always fascinated me. I often joke that I'm not smart enough to be a scientist, but I have endless respect for the people who are, especially those who can take incredibly complex ideas and explain them in a way the rest of us can truly understand. This is why I know you're going to love my conversation with Dr. St. Onge. Steve is the Chief Business Officer at Clarametyx. Dr. St. Onge is a PharmD and MBA with more than 15 years of experience spanning clinical care, medical affairs, and leadership in biotechnology. What stands out most about Steve isn't just his impressive résumé, it's his ability to clearly explain the science, the strategy, and, most importantly, the urgency behind the work Clarametyx is doing.I first met Steve in person at the North American Cystic Fibrosis Conference (NACFC) in Seattle, where we had the opportunity to really connect and talk about Clarametyx's approach. Their work focuses on targeting biofilm-driven inflammation and progressive lung damage, an area of significant unmet need for people living with chronic respiratory diseases, including cystic fibrosis. In this conversation, Steve breaks down what biofilms are, why they're so difficult to treat, and how Clarametyx is thinking differently about tackling the inflammation and lung damage they cause.We also talk about the long road of drug development, the responsibility that comes with working in rare disease, and why the phrase “patients are waiting” isn't just a saying, it's a call to action. This episode is an honest, accessible, and hopeful look at science in motion, and at the people behind the research who are driven by the patients counting on progress.If you've ever wanted a clearer understanding of how innovative science moves from idea to impact—and why time matters so much, his is a conversation you won't want to miss. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y
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Dr. Robert Russell, Chief Medical Officer at Majestic Health, joins us to share what led him into geriatric medicine and why he believes caring for older adults is some of the most meaningful work a physician can do. He explains what his role entails, how families can advocate for their loved ones within a medical team, and the top three concerns facing our aging population today. We also talk about Alzheimer's disease and dementia, including why cognitive decline should never be dismissed as a normal part of aging.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.
Send a textMarisa Toldo on LinkedInMarisa Toldo websiteMarisa's email: hallo@marisatoldo.comSupport the Alzheimer's & Dementia Resource Center
Friend of Them Before Us, Katy Talento is a Harvard-trained epidemiologist, naturopathic doctor, and former Trump White House health policy advisor who spent two decades inside the DC healthcare machine — then left to help everyday people and employers outsmart it. She writes about health policy, natural medicine, and how to live like a human — from real food and hormonal health to how to cut your medical bills in half using rules she personally helped write. All of it's at KatyTalento.com.For some of her recent articles, check out:Infertile, her guest post for our TBU substack - https://thembeforeus.substack.com/p/infertileOutsmart the Medical Billing Trap — a free step-by-step playbook for patients to fight back against medical bills, using rules she personally helped write in the White House https://www.katytalento.com/p/outsmart-the-medical-billing-trap?r=158d0wHospitals are Soviet-style Hellscapes Unfit for Humans - A Patient, Caregiver and Policy Manifestohttps://www.katytalento.com/p/hospitals-are-soviet-style-hellscapesSee more from Katy at @katytalento for IG, X, LinkedIn and https://www.facebook.com/katytalento.nd/
The term “mental load” gets thrown around a lot — but what does it actually mean, and why does it so often fall on moms and primary caregivers? Join us for The Invisible Workload: Why 75% of the Mental Load Lands on Primary Caregivers, a candid, expert-led conversation about the invisible labor that keeps families running — and the emotional, logistical, and identity toll it takes. We're joined by three powerhouse women who are reshaping how we talk about care, support, identity, and the weight parents carry:
CAR T‑cell therapy is redefining what personalized cancer treatment can look like, offering real promise for patients and families. In this episode, we speak with Dr. Richard Maziarz and CAR T Nurse Coordinator Bashi Ratterree of Oregon Health & Science University (OHSU). Together, they explain how CAR T‑cell therapy works, who may be eligible, what patients can expect during treatment and recovery, and the promising advancements shaping the future of this innovative therapy. DOWNLOAD TRANSCRIPT CLICK HERE to participate in our episode survey. Mentioned on this episode: CAR T-cell therapy Clinical Trial Support Center CAR T-Cell Therapy: A Path of Hope and Healing Video Series Bloodline Breakthroughs: innovations and inspiration video podcast: CAR T-cell Therapy Hematology Horizons vlog: CAR T-Cell Therapy and the Patient Experience CAR T-Cell Therapy: Side Effects video Additional Blood Cancer United Support Resources: Information Specialists Financial support Online Chat Free Nutrition Consultations Free telephone/web patient programs Free booklets Young Adult Resources Support groups Caregiver support Caregiver Workbook Survivorship Workbook Advocacy and Public Policy Patient Community Mental Health Resources Episode supported by Bristol Myers Squibb; Johnson & Johnson & Legend Biotech; Kite, a Gilead Company; Novartis Pharmaceuticals Corporation. The post Inside CAR T‑Cell Therapy: How Innovation Is Changing Lives first appeared on The Bloodline with Blood Cancer United Podcast.
Join us in community: Women Connected in Wisdom Community Listen to past episodes: https://womenconnectedinwisdompodcast.com/ Glo from head to toe by joining the shealo glo glo club at www.shealoglo.com ! Stillpoint: A Self-Care Playbook for Caregivers Join Christine at an event! Book a free coaching consult with Christine here: https://christinegautreaux.com Like & Subscribe to get notifications of when we are live: Women Connected in Wisdom Instagram Women Connected in Wisdom on Facebook What does it take to move from survival mode to self-acceptance? This week, we welcome Harper A. Bailey, public health leader, powerful storyteller, and author of It Was Her: A Memoir — a deeply personal journey through loss, resilience, leadership, and transformation. As the first Black woman to lead a prominent national women's healthcare nonprofit, Harper has spent her career championing health equity and amplifying underserved voices. In this conversation, she shares the emotional and spiritual evolution behind her memoir unfolding through four powerful stages: Running, Falling, Sinking, and Flying.
Drew Deraney is a coach, author, and advocate dedicated to empowering caregivers and families of individuals with autism. As The Caregiver & Family Health Coach, he helps parents and caregivers find balance, build resilience, and care for themselves as compassionately as they care for their loved ones. Drew is the proud father of three children, including a son with autism, which inspires his mission to provide guidance, education, and community support. Through coaching, speaking, and his podcast From Caving In To Crushing It, Drew encourages others to live authentically, rise with strength, and lead with purpose. www.autismresourceproject.org/podcast
If you've ever cared for someone with Alzheimer's—or loved someone who has—you know the quiet heartbreak of watching a person you cherish slowly fade, even while they are still physically present. It's a journey marked by grief, exhaustion, and a longing for strength that often feels just out of reach. In today's episode, storyteller Jennifer Roberts from our West Cobb community outside of Atlanta, Georgia, shares her experience of walking alongside her father-in-law as her mother-in-law battled Alzheimer's. With honesty and tenderness, Jennifer reflects on the weight of caregiving, the sorrow woven into the disease, and the unexpected ways God met her family in the middle of it all. Her story is a powerful reminder that when God calls us into a difficult season, He also equips us with perseverance, sustains us with His presence, and leads us forward with hope, joy, and strength. If you are a caregiver—or know someone who is—this is a story you won't want to miss, and one you'll want to share. VERSE OF THE WEEK: "Consider it pure joy, my brothers and sisters, whenever you face trials of many kinds, because you know that the testing of your faith produces perseverance. Let perseverance finish its work so that you may be mature and complete, not lacking anything." James 1:2-4 CHALLENGE OF THE WEEK: If you know someone who is caretaking for a loved one, reach out to them this week by sending an encouraging message, making a call to check in on them, or offering to be of some assistance. ________________________________________________ Listen to Jennifer Roberts' sisters' story from season 8- Ep. 300- Laurel Henson: "The Providence of God: A Story of Love After Loss." Listen to a similar story: Ep. 299- Kenzie Hightower: "When We Can't, He Can: A Sister's Story of Support." Download a phone background of the weekly verse HERE! Give to StoryTellers Live in honor of Jennifer and any of our past storytellers! Join us "In the Room" on Patreon to access new stories straight from our live gatherings around the country! Join us for our Stories of Hope luncheon on March 11th in Birmingham! Shop for our When God Shows Up Bible Study series~ Stories of Hope, Stories of Freedom, Stories of Faith Are you interested in one-on-one coaching with our very own Robyn Kown!? Click HERE! Check out all of our live speaking engagement opportunities on our website. Sign up to receive StoryTellers Live's weekly newsletter for updates and details on our live gatherings.
On this episode of Waves of Awareness, we're diving into the power of early intervention, school partnerships, and family collaboration. Early interventionists Alisha Kelley and Michelle Baker join us to share what it really looks like to support children inside the classroom — and how they help bridge the gap between teachers and caregivers to create consistency, confidence, and growth. What happens when school routines become meaningful developmental moments? How do early learning professionals partner with educators without disrupting the flow of the classroom? And what can families gain when everyone is truly on the same team? You'll get a behind-the-scenes look at early intervention in action — plus real stories that highlight why collaboration between schools and families matters more than ever. Waves CEO Staci Davis is joined by Waves adults Johnny Sunshine and Jeni Tanner as her co-hosts, who share personal updates, including Jeni's upcoming show with Backlight Productions and excitement around the Waves Annual Fundraising Breakfast, where Johnny will be giving the prayer. If you care about early childhood development, inclusive education, or building stronger connections between home and school, this conversation is for you. Press play and join us!
Conscious Caregiving with L & L is "Tackling the Tough Conversations." The topic of this episode is "The Future of AlzAuthors" featuring hosts Lori La Bey and Lance A. Slatton. 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 is also the new President of AlzAuthors. 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 Official Website for AlzAuthors: https://www.alzauthors.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.
Jenny Opalinski has spent more than a decade inside hospitals where people lose the ability to speak, breathe, swallow, and sometimes survive. A medical speech language pathologist by training, she worked in ICU, neuro rehab, and long term acute care settings, including a Level 1 trauma center, where she watched clinicians absorb 10 to 15 traumatic events in a single shift and then get told to move the crash cart faster next time.That lived reality pushed her to co found The Wellness Shift, an advocacy and education platform focused on healthcare worker burnout, suicide, and assault. In this conversation, Opalinski walks through the moment that changed everything for her: standing in a hospital hallway listening to a family wail after a failed code, followed by a debrief that addressed logistics and ignored grief entirely.She also explains how that work led to Humanity Rx, her podcast about the human cost of medicine, and Dragon's Breath: Calming Tricks for Big Feelings, a children's book that translates evidence based breathing and regulation strategies into language kids can actually use. The episode covers moral injury, time scarcity, false wellness, respiratory muscle training, and why empathy keeps getting treated as an optional expense instead of clinical infrastructure.RELATED LINKSJenny Opalinski on LinkedInThe Wellness ShiftHumanity RxDragon's Breath: Calming Tricks for Big FeelingsAspire Respiratory ProductsFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.
Caregiver anger is real and no one talks about it.If you're a cancer caregiver feeling angry at the medical system, frustrated with family, resentful of the constant responsibility, or secretly furious at yourself… this episode is for you.Caregiver burnout doesn't always look like exhaustion. Sometimes it looks like a tight jaw. A short temper. A bathroom cry you don't fully understand.In this episode, we unpack:Why anger is a normal response to caregiving stressThe hidden link between caregiver resentment and griefHow suppressing anger fuels burnoutA simple 2-question tool to process anger without exploding or shutting downIf you're navigating cancer caregiving stress, scanxiety, emotional exhaustion, or caregiver guilt... press play.Because self-preservation starts with telling the truth about what you feel.Find more caregiver support at www.cancercaregiverpodcast.com
Show SummaryOn this episode, we have a conversation Today we're having a conversation Mark Solomon, co-founder of the Veterans Community Project. We talk about their innovative approach to ending veteran homelessness through tiny home communities, wraparound support, and a mission to ensure every veteran has both housing and connection.Provide FeedbackAs a dedicated member of the audience, we would like to hear from you. If you PsychArmor has helped you learn, grow, and support those who've served and those who care for them, we would appreciate hearing your story. Please follow this link to share how PsychArmor has helped you in your service journey Share PsychArmor StoriesAbout Today's GuestMark Solomon is a Naval Reserve Officer and co-founder of the Veterans Community Project, an organization dedicated to ending veteran homelessness through innovative housing and supportive services. Drawing on his own military experience and the challenges veterans face transitioning to civilian life, he helped launch the project in 2014, leading efforts to create a tiny-home village and comprehensive outreach center in Kansas City that connects veterans with resources such as health care referrals, employment assistance, and counseling.Links Mentioned During the EpisodeVeterans Community Project Website PsychArmor Resource of the WeekThis week's PsychArmor Resource of the Week is the PsychArmor course Finding Veteran Support Programs. No matter what issue you're facing, you can use the power of the internet to reach out and get the help you deserve. You can find the resource here: https://learn.psycharmor.org/courses/Finding-Veteran-Support-Programs 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
Allowing adult children to manage healthcare decisions for elderly parents carries significant legal risks and challenges for families. In this episode, caregiving expert and expert witness Pamela D. Wilson explores the complexities of eldercare decision-making and the high-stakes responsibility of a durable power of attorney agent for aging parents.Adult children, caregivers, and parents will gain vital insights into fiduciary duties, liability, litigation risks, and how challenging family dynamics impact family caregiving experiences. Learn practical caregiver advice and access professional-level caregiver support to navigate healthcare decision-making with confidence.Address intrafamily conflict while fulfilling fiduciary responsibilities for elder care. Gain a deeper understanding of why power of attorney agents need clear guidance to protect elderly parents and themselves in this important discussion of eldercare, aging, and power of attorney designation.To find show transcripts and links mentioned in Episode 239 and other The Caring Generation podcasts, click here to visit Pamela's website: https://pameladwilson.com/caregiver-radio-programs-the-caring-generation/For professional-grade caregiving, aging, and elder care tips for your caregiving journey, visit Pamela's website at https://www.PamelaDWilson.comLearn about Pamela D Wilson, her professional background, and her experience: https://pameladwilson.com/pamela-d-wilson-story/Schedule a professional 1:1 elder care consultation by telephone or video call with Pamela: https://pameladwilson.com/elder-care-consultant-aging-parent-consultation-managing-senior-care-needs-meet-with-pamela-d-wilson/Sign up for Pamela's newsletter here: https://pameladwilson.com/contact/Join Pamela's Online Caregiver Support Group on Facebook https://www.facebook.com/groups/thecaregivingtrapFollow Pamela on Social Media:Facebook: https://www.facebook.com/pameladwilsoncaregivingexpert/LinkedIn: https://www.linkedin.com/in/pameladwilsoncaregiverexpert/X: https://www.x.com/CaregivingSpeakPamela D. Wilson, a caregiving expert, expert witness, educator, and caregiver consultant, provides caregiver advice, practical tips, support, and resources for aging and elder care decision-making. Developing caregiving, aging, and eldercare strategies is easier with expert caregiver advice and solutions founded on Pamela's 25 years of professional experience. Visit Pamela's website www.PamelaDWilson.com to access online caregiver resources, courses on care management, power of attorney, and guardianship, plus practical advice and tips for aging adults and family caregivers providing elder care support. ©2018, 2026 Pamela D Wilson. All Rights Reserved
Yes, I am back and this time, I will do my best to not disappear on you all! My life has taken a major turn and now, with this podcast I plan to share my thoughts, frustration and more, so that others who are caregivers know, it is okay to feel what you feel.
Beating Cancer Daily with Saranne Rothberg ~ Stage IV Cancer Survivor
In today's episode, Saranne, the founder of the Comedy Cures Foundation, discusses the importance of support and understanding when facing a cancer diagnosis. She shares her experiences and highlights an article by Jan C. Dunn, emphasizing the three H's: help, hear, and hug. Saranne encourages listeners to communicate their needs to their support circle and reminds them that they sometimes need a listening ear or a comforting hug. Tune in as Saranne explores the power of laughter and the role of caregivers in the cancer journey.2025 People's Choice Podcast Awards Best Health Series FinalistRanked the Top 5 Best Cancer Podcasts by CancerCare News in 2024 & 2025,and #1 Rated Cancer Survivor Podcast by FeedSpot in 2024 to 2025. Beating Cancer Daily is listened to in 140 countries across 7 continents and features over 400 original daily episodes hosted by Stage IV survivor Saranne Rothberg. To learn more about Host Saranne Rothberg and The ComedyCures Foundation:https://www.comedycures.org/ To write to Saranne or a guest:https://www.comedycures.org/contact-8 To record a message to Saranne or a guest:https://www.speakpipe.com/BCD_Comments_Suggestions To sign up for the free Health Builder Series live on Zoom with Saranne and Jacqui, go to The ComedyCures Foundation's homepage:https://www.comedycures.org/ Please support the creation of more original episodes of Beating Cancer Daily and other free ComedyCures Foundation programs with a tax-deductible contribution:http://bit.ly/ComedyCuresDonate THANK YOU! Please tell a friend whom we may help, and please support us with a beautiful review. Have a blessed day! Saranne
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Caregiving for Alzheimer's isn't just hard; it's isolating, invisible, and full of grief that never gets a clean ending.In this episode, Dr. Caron Leid, counselor, educator, author, and caregiver advocate, discusses how her mother's early Alzheimer's diagnosis and later aphasia changed everything and how the system largely left her to figure it out alone. She names the ambiguous grief of losing a parent in slow motion, and the emotional whiplash of being a daughter while also becoming the decision-maker.Dr. Leid gets real about the “impossible choice” caregivers live with, especially in the sandwich generation. She talks about the guilt of choosing between a child and an aging parent, the exhaustion of constant vigilance, and how martyr culture rewards caregivers with praise instead of practical support. That dynamic can keep people stuck, suffering quietly, and feeling like asking for help is failing.She also brings a trauma-informed, schema-based lens to caregiving. What we react to is not only today's crisis, but old family patterns, cultural expectations, and the layered impact of racism and microaggressions on access, trust, and how black and brown families are treated in care settings. She explains why informal caregiving and formal healthcare work are not the same job.Tune in and learn how to center caregivers as the backbone of care, without romanticizing their burnout.Connect with Dr. Leid on LinkedIn here and visit her website! Check out Dr. Leid's books: Alzheimer's: What They Forget to Tell You: A Personal Journey, Self Love: What They Forget to Tell You, Grief: What They Forget to Tell You, and BS and Other Childhood Tales We Learned by Dr. Caron Leid
Send Cathy a text:)Caregiving is not meant to be a solo mission.In this episode of The Caregiver Cup Podcast, we're talking about something many caregivers struggle with — building a support system.Whether you're caring for a spouse, parent, or loved one, the pressure to “do it all” can feel overwhelming. But strength isn't handling everything alone. Strength is building a team.In Season 2, Episode 8 — The Support System Blueprint, we explore:✔️ Why caregivers struggle to ask for help ✔️ How to identify the gaps in your current support ✔️ The difference between emotional, practical, and professional support ✔️ How to create “micro-teams” instead of looking for one superhero ✔️ Delegation and outsourcing ideas that protect your energy ✔️ Why automating and simplifying your life counts as support ✔️ How asking for help protects your rhythm, boundaries, and emotional spaceCathy shares her personal story of preparing for Denis' stem cell transplant — building both a “home blueprint” and a “Milwaukee blueprint” — and how allowing others to step in made the journey steadier, not weaker.You'll walk away with reflection questions and one small action step to begin building your own caregiver support system — even if asking feels uncomfortable.Because you were never meant to carry caregiving alone.
H&P Disability Direct - Live Answers on the Road to VA Compensation
Join in our Live VA Disability Q&A Session in which we answer your questions live. We can't get to every single question so we will answer them as they come in. If you have any questions about the VA Disability Benefits process you can ask the question in the comment section when we go live and a little earlier. We are nationwide VA Accredited Disability Lawyers. We can't wait to answer your questions!For a FREE Case Evaluation go here: https://www.hillandponton.com/free-ca...Visit our website at https://www.hillandponton.com/?utm_so...Like us on Facebook at www.facebook.com/HillandPontonFor questions please email us at Info@hillandponton.comSpeakers: Attorney Matthew HillThe content of this YouTube channel is provided for informational purposes only and is not intended to constitute legal advice. You should not rely upon any information contained on this YouTube channel for legal advice. Viewing this YouTube channel is not intended to and shall not create an attorney-client relationship between you and Hill and Ponton, PA. Messages or other forms of communication that you transmit to this YouTube channel will not create an attorney-client relationship and thus information contained in such communications may not be protected as privileged. Hill and Ponton, PA does not make any representation, warranty, or guarantee about the accuracy of the information contained in this YouTube channel or in links to other YouTube channels or websites. This YouTube channel is provided "as is," does not represent that any outcome or result from the viewing of this channel. Your use viewing of this YouTube channel is at your own risk. You enjoy this YouTube channel and its contents only for personal, non-commercial purposes. Neither Hill and Ponton, PA, nor anyone acting on their behalf, will be liable under any circumstances for damages of any kind.
I'm a full-time caregiver for my parents and now I'm starting to wonder if my own finances are okay for the long haul? Have a money question? Email us here Subscribe to Jill on Money LIVE Subscribe to Jill on Money Newsletter YouTube: @jillonmoney Instagram: @jillonmoney Twitter: @jillonmoney "Jill on Money" theme music is by Joel Goodman, www.joelgoodman.com. To learn more about listener data and our privacy practices visit: https://www.audacyinc.com/privacy-policy Learn more about your ad choices. Visit https://podcastchoices.com/adchoices
If you could switch places with someone and peek into their mind, who would you pick? For journalist Courtney Martin, she chose her aging dad with advanced dementia. Courtney joins Chris to talk about her deep desire to understand her father's experiences, what it's like to witness a loved one's health decline, and why it's important to practice asking for help. This is a perfect episode to listen to if you're taking care of a loved one (or know someone who is) and want practical ways to be kinder to caregivers.Host & GuestChris Duffy (Instagram: @chrisiduffy | https://chrisduffycomedy.com/)Courtney Martin (Instagram: @courtwrites | https://courtneyemartin.com/) LinksHumor Me by Chris Duffy: https://t.ted.com/ZGuYfcLhttps://courtney.substack.com/For the full text transcript, visit go.ted.com/BHTranscriptsLearn more about our flagship conference happening this April at attend.ted.com/podcast Hosted on Acast. See acast.com/privacy for more information.
On this episode of Hope for the Caregiver, I talk about something that has taken me forty years to learn: I'm not chasing happiness anymore. I'm chasing healthiness. Happiness depends on what's happening. Good lab report? I'm happy. Insurance approves something without a fight? That's practically a revival service. But caregiving doesn't offer steady circumstances. If my stability depends on things going well, I won't last long. Joy is different. Joy is anchored. Joy rests in the unchanging character of God. I can be sorrowful and still rejoicing. I can sit in a hospital room and still be steady. I share a real-life conversation with a mother struggling with her alcoholic son and explain how asking one simple question — "Is this healthy?" — can bring clarity when "right or wrong" only creates confusion. I also talk about physical health, financial health, and spiritual health. I say it often because I have to hear it myself: I'm no good to Gracie if I'm fat, broke, and miserable. Healthy caregivers make better caregivers. And I close with one of my father's favorite hymns, Lead On, O King Eternal — a reminder that caregiving is not about swords loud clashing, but about deeds of love and mercy. If you're weary, discouraged, or just tired of trying to feel better in a life that may not improve, this episode is for you. You may not feel happy, but you can be healthier. And you can be anchored.
As co-founder of Soaring Families, Mike George transformed his personal experience into impact, helping families move from survival mode to resilience and joy. He leaned on his background in AI, process improvement, and enterprise systems to develop The Soaring Families Way™, a structured yet compassionate approach that equips families with practical tools to regain control, reduce stress, and find fulfillment. https://www.seniorcareauthority.com/resources/boomers-today/
In this heartfelt interview, Martha shares her journey of resilience and faith following her husband's traumatic brain injury. Discover how community, faith, and perseverance have shaped her path of caregiving, healing, and giving back. Martha Boswell is a full time caregiver for her husband David, a traumatic brain injury survivor. She plans events and hosts Caregiver Coffees for the Brain Injury Association of Louisiana, and she is the author of four books. Her latest novel, Nothing to Lose, is a faith-based fictional account of life with a brain injury—a story of redemption and resilience—available on Amazon. She loves spending time with her family and connecting with other caregivers. Please connect on Facebook @supperontheshelf Instagram @tbiwifelife Chapters 00:00 Introduction and Martha's Background 01:10 Perseverance and Faith in the Journey 02:06 Husband's Injury and Initial Shock 04:39 Life Before and After the Injury 09:23 The Fall and Immediate Aftermath 12:28 Medical News and Family's Response 14:05 Miracle Moment: Eyes Open in January 16:25 Early Rehabilitation and Challenges 19:43 Insurance and Financial Stress 21:28 Living with a Changed Husband 23:30 Rebuilding Marriage and Hope 26:29 Motivation and Purpose in Recovery 28:54 Living Safely and Caregiver Strategies 31:23 Support Groups and Community Resources 33:40 Faith as the Foundation 36:26 Lessons Learned and Resilience 38:37 Dark Moments and God's Use of Suffering 41:08 Creative Outlets and Healing 43:43 Self-Regulation and Spiritual Strength 45:52 Community Events and Support Initiatives 48:54 Connecting and Outreach Efforts 50:25 Recovery, Resilience, and Restoration 52:23 Hope in Eternity and Present Moments 54:20 Closing Remarks and Gratitude
From Fear to Peace: Growing Spiritually as a Dementia Caregiver by Linda Knebel Pruden Lindaknebelpruden.com https://www.amazon.com/Fear-Peace-Spiritually-Dementia-Caregiver-ebook/dp/B0F7J3DJ3F An instant #1 New Release in Dementia. This spiritual growth book explores Linda Pruden’s experience as a dementia caregiver for her husband. Inspired by his own determination to find spiritual gifts embedded in the journey, her story provides encouragement for those living with a chronic illness and the people who love them. “A powerful read for caregivers facing the journey of caring for someone with dementia. Her growth and faith over years of caring for Rob is an amazing blend of self-discovery and acceptance. An incredibly validating and relatable read.” —Lisa M. Brown, MSW, LISW, caregiver services program coordinator for Lyngblomsten Community Services When Linda’s husband, Rob, was diagnosed with dementia, he described it as a gift and an opportunity to grow spiritually. As things grew more difficult, Linda remembered these words and began her mission to live out his hopes. Offering a fresh, positive outlook on serving as a dementia caregiver, From Fear to Peace is a reassuring road map for any faith-testing journey. Linda Knebel Pruden is an author and national speaker residing in St. Paul, Minnesota. She received her master’s degree in speech/language pathology from Purdue University, and went on to write five books for teachers, as well as her award-winning memoir, Reflections on a Changing Family. Having grown through the experience of being a caretaker, it is now her passion to help others unbury their own truths and find beauty in painful times. This book covers caring for dementia, but is also an essential read for . . . people hoping for spiritual growth and peace, those looking to effectively provide caregiver support, and families needing a guide for walking in grace. During the hardest of times, Linda’s words help readers to let go of expectations and hold tight to hope . . . it’s only then that we can move from fear to peace. “Linda has created tools that will guide you through those darkest hours of transitions and fears. It is a story of empowerment and gratitude.” —Kristin Burich, healing facilitator About the author Linda Knebel Pruden is an author and national speaker residing in St. Paul, Minnesota. She received her master's degree in speech/language pathology from Purdue University, and went on to write five books for teachers, as well as her award-winning memoir, Reflections on a Changing Family. Having grown through the experience of being a caretaker, it is now her passion to help others unbury their own truths and find beauty in painful times.
Your Hope-Filled Perspective with Dr. Michelle Bengtson podcast
Episode Summary: Caring for others is one of the most beautiful expressions of Christlike love, yet it can also be one of the most exhausting. Whether someone is caring for an aging parent, a chronically ill spouse, a child with special needs, or a friend struggling through a difficult diagnosis, caregivers often experience emotional fatigue, compassion overload, and spiritual depletion. In honor of National Caregiver’s Day, today on Your Hope-Filled Perspective we are shining a bright and honoring spotlight on caregivers who quietly pour out strength and tenderness day after day. If you are a caregiver who feels seen and unseen all at once, this conversation is for you. Quotables from the episode: In this episode we want to acknowledge the deep emotional and spiritual cost that comes with caregiving, whether it’s caring for children, spouses, parents or someone else. Many caregivers love fiercely yet carry silent burdens. They often neglect their own rest while tending to the needs of others. They juggle responsibilities, appointments, medications, medical decisions, financial pressures, and emotional strain until their own souls feel frayed. If that describes you, know that God sees every moment of sacrifice. He understands every tear cried in private. He knows how heavy this calling can feel. Whether you are in a short-term caregiving season or you have been carrying this responsibility for years, we want to help you find strength, rest, and spiritual renewal. Yet God created rest not as a luxury but as a divine necessity. He invites caregivers to receive the strength they need directly from His presence. Caregivers often do not realize how overwhelmed they are until they are already close to burnout. They believe they should be able to keep going. They think rest is selfish. They feel guilty for asking for help. But caregiving is not meant to be a one-person mission. Caregiver burnout does not happen overnight. It happens slowly and quietly, often while someone is trying to be strong for everyone else. God never intended caregiving to be an isolating burden. Galatians teaches us to carry one another’s burdens. That includes the weight of caregiving. Asking for help is not a failure. It is a biblical principle If you have begun feeling resentful or emotionally disconnected, that is a powerful signal that your soul is in need of restoration. You cannot pour out what has not been filled. I want caregivers to hear this truth. You are not responsible for outcomes. You are responsible to love well and to walk faithfully, but God holds the results. Scripture References: Isaiah 40:29 “He gives strength to the weary and increases the power of the weak.” Psalm 73:26 “My flesh and my heart may fail, but God is the strength of my heart and my portion forever.” Psalm 18:28 “You, Lord, keep my lamp burning; my God turns my darkness into light.” Jeremiah 31:25 “I will refresh the weary and satisfy the faint.” Recommended Resources: Free Caregiver Burnout Warning Sign Checklist Reframing Rejection: How Looking Through a Different Lens Changes Everything By Jessica Van Roekel Sacred Scars: Resting in God’s Promise That Your Past Is Not Wasted by Dr. Michelle Bengtson The Hem of His Garment: Reaching Out To God When Pain Overwhelms by Dr. Michelle Bengtson Today is Going to be a Good Day: 90 Promises from God to Start Your Day Off Right by Dr. Michelle Bengtson Breaking Anxiety’s Grip: How to Reclaim the Peace God Promises by Dr. Michelle Bengtson Breaking Anxiety’s Grip Free Study Guide Free PDF Resource: How to Fight Fearful/Anxious Thoughts and Win Hope Prevails: Insights from a Doctor’s Personal Journey Through Depression by Dr. Michelle Bengtson Hope Prevails Bible Study by Dr. Michelle Bengtson Free Webinar: Help for When You’re Feeling Blue Social Media Links for Host and Guest: Connect with Rev. Jessica Van Roekel: Website / Instagram / Facebook Connect with Dr. Bengtson: Order Book Sacred Scars / Order Book The Hem of His Garment / Order Book Today is Going to be a Good Day / Order Book Breaking Anxiety’s Grip / Order Book Hope Prevails / Website / Blog / Facebook / Twitter (@DrMBengtson) / LinkedIn / Instagram / Pinterest / YouTube / Podcast on Apple Co-Host: Jessica Van Roekel is a worship leader, speaker, and writer who believes that through Jesus, personal histories don’t need to define the present or determine the future. She inspires, encourages, and equips others to look at life through the lenses of hope, trust, and God’s transforming grace. Jessica lives in rural Iowa surrounded by wide open spaces which remind her of God’s expansive love. She loves fun earrings, good coffee, and connecting with others. Hosted By: Dr. Michelle Bengtson Audio Technical Support: Ashton Bengtson Discover more Christian podcasts at lifeaudio.com and inquire about advertising opportunities at lifeaudio.com/contact-us.