Podcasts about caregiver support

All Home Care Matters and our host, Lance A. Slatton were honored to welcome Katrina Love Prescott as guest to the show.   About Katrina Love Prescott:   Katrina Love Prescott is an award-winning Caregiver Advocate, Coach, and Media Producer. As co-founder of Care Nation, a non-profit dedicated to supporting caregivers, she has partnered with leading organizations for over a decade to enhance the quality of life for those with chronic illnesses and their caregivers. Her acclaimed web series, Therapeutic Fibbing, exploring a family's journey with dementia, has garnered over 2 million views.   Her latest project, Things Not to Say to a Caregiver, has surpassed 1 million views and continues to resonate widely. Passionate and innovative, Katrina is committed to transforming the caregiver experience.   About "Things Not To Say To A Caregiver":   A sharp, funny web series where a no-nonsense Care-y Godmother rewrites the awkward, hurtful things people say to caregivers—turning missteps into moments of empathy, growth, and comic relief. Synopsis: Things Not to Say to a Caregiver is a comedic web series that tackles the awkward, misguided things people say to caregivers—and how we can do better. Each episode, led by a sharp-tongued “Care-y Godmother,” flips a cringeworthy moment into a teachable one. Blending sketch comedy with real-life insight, TNTS validates caregivers' experiences while educating the public with humour and heart.    Connect with Katrina Love Prescott: Official Website: https://www.katrinaloveprescott.com Instagram: @katprescott  Tik Tok: kat.prescott LinkedIn: https://www.linkedin.com/in/katrina-love-prescott-5799157/ Facebook: https://www.facebook.com/katrina.prescott/   Watch "Things Not To Say To A Caregiver": YouTube Playlist: https://www.youtube.com/playlist?list=PLNKwjxd98HaUZ-hY7tzB8DDXLvJI1BHzh

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 14 - "Caregiver Support":   About Heidi Lee Cross:   Heidi Lee Cross is a North London-based copywriter, poet, and caregiver. She shares a home with her partner, 12-year-old son, and their cherished dog Bailey. After graduating with a BA Hons Degree in Drama & Theatre Arts in 1996, Heidi embarked on a television career that spanned two decades.   Starting as an intern with Planet 24's The Big Breakfast, she progressed through roles as a runner, researcher, bulletin presenter, and eventually studio and location producer across various television networks. Her passion for writing led her to transition into a successful copywriting career. In 2023, Heidi published a poignant collection of poems about parenthood titled Mum of a Boy.   Her caregiving journey began in 2017 after her father's unexpected passing, which left her to support her mother as she faced early cognitive decline and an Alzheimer's diagnosis. This deeply personal experience inspired her second book, Milk Tulips, a blend of stories, poetry, practical advice, and insights. The book serves as a companion for caregivers navigating the complexities of dementia, especially those raising young children at the same time. Heidi hopes her work provides comfort and encouragement to those facing similar challenges. (both books available on Amazon in hardback, paperback and for Kindle).   About Marielle Molette:   Marielle Molette is a projects officer with an NHS and Social Care background, complemented by her expertise in French and Translation Studies. She lives in North London with her husband and two sons. Her most recent role as a commissioning officer for Barnet Council allowed her to use her skills to lead on various initiatives, including the national Changing Places Toilets campaign. This initiative ensures the provision of fully accessible toilets for individuals with significant disabilities, equipped with specialised facilities such as hoists and adult-sized changing tables, offering dignity and independence to those who need it most.   Passionate about creating positive change and improving the lives of others, Marielle has been a dedicated advocate and caregiver for her mother, who has lived with Alzheimer's for the past 10 years. Her journey inspired her participation in a video campaign by the Royal Free Trust, where she shared her experiences caring for her mum. This initiative aimed to improve outcomes for dementia patients in hospitals, raising awareness about the unique challenges they face, advocating for better care solutions.

You will never regret being kind to your spouse.  In a strong marriage, the sexual expression of love is the sinew that ties two hearts together and forms the kind of bond we depend on to get us through life's greatest challenges. As we age, the intensity of physical passion burns more ember than flame, but the bonds of love can be just as strong, even stronger, than ever.  Alzheimer's forces a wedge in the relationship. Caregiver stress is more devastating than you imagined. Frustration and Anger barge into your home and wreak havoc in your daily world. Anticipatory grief destroys your dream of the future.  Whether the dementia caregiving journey takes a few years or a decade or more, love doesn't fade from a strong marriage. The challenge is learning how to express that love in a new way.  After marrying more than 150 couples, publishing 3 historical romance novels with Harper Collins, and being married for 41 years to a man I loved deeply, I've learned some things about weddings, romance, intimacy, and dementia. I share a few of those thoughts in this episode.   Mentioned in the episode:  John van Gurp's YouTube channel: John and Heather's Dementia Journey Be sure to listen to episode 28 about how using improv can help caregivers enter the world of their loved one. Let me know if you'd like to be part of an online improv class where all the participants are dementia family caregivers. I'm working a future episode about how it feels to have to care for a family member with dementia when you would never refer to that person as your "loved one." If that's you, please contact me. Email: zita@myspousehasdementia.com   

Do you ever feel like no matter what you try, your loved one with dementia still refuses your help, gets upset, or acts in ways that make no sense? You're not alone — and you're probably not doing anything wrong. In this video, I share 5 often-overlooked reasons behind challenging dementia behaviors — including the #1 mistake most caregivers make without realizing it. Once you understand what's really going on, you can stop taking things so personally and start using strategies that actually work.  If you'd like to see this episode on video, you can hop on over to my YouTube channel here. Get Weekly Dementia Tips in Your Inbox! Sign up for our FREE Dementia Dose newsletter at https://careblazers.com/dementiadose It's our mission to make dementia caregiving easier for families caring for a loved one with Alzheimer's disease, frontotemporal dementia, lewy body dementia, vascular dementia, or any other type of dementia. We believe that in order to create a more dementia-friendly world, we must first create a caregiver-friendly world. That's why we create free educational training videos like this one so that anyone with an internet connection can get access to dementia care information. **This channel and any information by Dementia Careblazers is not a substitute for healthcare. This is not healthcare advice. Please talk to your healthcare providers for specific feedback on your situation.

Struggling with challenging dementia behaviors — and nothing you've tried is working? In this episode, I'll show you 3 proven ways to respond that can make a real difference, even in the most frustrating situations. These simple but powerful shifts have helped thousands of Careblazers feel more confident and less overwhelmed.  If you'd like to see this episode on video, you can hop on over to my YouTube channel here. Get Weekly Dementia Tips in Your Inbox! Sign up for our FREE Dementia Dose newsletter at https://careblazers.com/dementiadose It's our mission to make dementia caregiving easier for families caring for a loved one with Alzheimer's disease, frontotemporal dementia, lewy body dementia, vascular dementia, or any other type of dementia. We believe that in order to create a more dementia-friendly world, we must first create a caregiver-friendly world. That's why we create free educational training videos like this one so that anyone with an internet connection can get access to dementia care information. **This channel and any information by Dementia Careblazers is not a substitute for healthcare. This is not healthcare advice. Please talk to your healthcare providers for specific feedback on your situation.

Most dementia caregivers are making at least one of these 5 mistakes—and they don't even know it. If caregiving feels overwhelming, frustrating, or like nothing you're trying is working, this episode is for you. In this episode, I'll walk you through the most common mistakes caregivers make that actually make things harder for themselves and their loved one with dementia. You'll learn how to shift your mindset, reduce stress, and start getting better results with less emotional burnout. If you've ever said “I've tried everything and nothing works,” this might be the breakthrough you've been needing. If you'd like to see this episode on video, you can hop on over to my YouTube channel here. Get Weekly Dementia Tips in Your Inbox! Sign up for our FREE Dementia Dose newsletter at https://careblazers.com/dementiadose It's our mission to make dementia caregiving easier for families caring for a loved one with Alzheimer's disease, frontotemporal dementia, lewy body dementia, vascular dementia, or any other type of dementia. We believe that in order to create a more dementia-friendly world, we must first create a caregiver-friendly world. That's why we create free educational training videos like this one so that anyone with an internet connection can get access to dementia care information. **This channel and any information by Dementia Careblazers is not a substitute for healthcare. This is not healthcare advice. Please talk to your healthcare providers for specific feedback on your situation.

Psychiatrist Carolyn Rodriguez studies hoarding disorder and says that all of us have attachments to our possessions. But for many, these attachments can disrupt daily life and even pose health risks. For those with loved ones who struggle with hoarding disorder, she says treatments exist, including cognitive behavioral therapy (CBT). Lately, she's been studying how virtual reality can augment CBT through virtual discarding practice and ways brain stimulation may improve symptoms. But, Rodriguez says, never underestimate the value of empathy for those in need of help, as she tells host Russ Altman on this episode of Stanford Engineering's The Future of Everything podcast.Have a question for Russ? Send it our way in writing or via voice memo, and it might be featured on an upcoming episode. Please introduce yourself, let us know where you're listening from, and share your question. You can send questions to thefutureofeverything@stanford.edu.Episode Reference Links:Stanford Profile: Carolyn RodriguezConnect With Us:Episode Transcripts >>> The Future of Everything WebsiteConnect with Russ >>> Threads / Bluesky / MastodonConnect with School of Engineering >>> Twitter/X / Instagram / LinkedIn / FacebookChapters:(00:00:00) IntroductionRuss Altman introduces Carolyn Rodriguez, a professor of psychiatry and behavioral science at Stanford University.(00:02:47) Motivation to Study Hoarding DisorderWhy Carolyn chose to focus her research on hoarding disorder.(00:03:44) Collecting Versus HoardingDistinguishing between normal behavior and clinically significant hoarding.(00:05:47) Prevalence of Hoarding DisorderThe universality and pervasiveness of hoarding disorder.(00:07:11) The Brain Science Behind HoardingEarly neuroscience findings on attachment and discarding behavior.(00:08:47) Dopamine and Excessive AcquisitionThe connection between hoarding and potential dopamine reward pathways.(00:09:55) Risk Factors and Cognitive ChallengesPersonality traits, genetics, and processing difficulties involved in hoarding.(00:11:14) Gender Differences and Insight IssuesGender prevalence in treatment-seeking and the concept of anosognosia.(00:12:35) The “Why” Behind HoardingHow motivations and emotional attachments influence behavior.(00:13:50) Onset and Progression of DisorderTypical onset age, aging effects, and early warning signs.(00:15:05) Historical References to HoardingAccounts from ancient literature of hoarding-like behavior(00:17:16) Attachment to ObjectsThe emotional, aesthetic, and identity-based reasons people retain objects.(00:20:45) Current Treatment OptionsThe treatment landscape, including lack of medications and focus on CBT.(00:22:30) Chronic Nature of Hoarding DisorderFraming hoarding as a long-term condition with hopeful outcomes.(00:23:08) Virtual Reality for TreatmentA study on using VR to safely practice letting go of personal items.(00:25:58) Neuromodulation ResearchUsing non-invasive brain stimulation to reduce acquisition urges.(00:27:00) Advice for Individuals and FamiliesThe importance of empathy and self-care for individuals and caregivers.(00:28:47) Conclusion Connect With Us:Episode Transcripts >>> The Future of Everything WebsiteConnect with Russ >>> Threads / Bluesky / MastodonConnect with School of Engineering >>>Twitter/X / Instagram / LinkedIn / Facebook

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

This episode of Marrow Masters brings us an incredible conversation with Kitrena Young, a two-time cancer survivor whose story spans decades and highlights the unique challenges faced by adolescents and young adults (AYAs). We begin by learning about Kitrena's initial diagnosis of B-cell ALL with a Philadelphia chromosome at the age of eight, followed by a shocking relapse 23 years later. Her candor about how she recognized the early signs the second time around—bruising and fatigue—underscores the importance of self-awareness and advocacy.We discuss how navigating the adult healthcare system differed drastically from her pediatric experience. Kitrena takes us through her rapid efforts to get an urgent appointment and the emotional toll of being thrust back into the cancer world. With support from her brother and eventually finding care at the Memorial Sloan Kettering Cancer Center (MSKCC)  through a compassionate voice on the phone, she exemplifies what it means to be proactive in your care journey.Fertility preservation is another focal point. Kitrena recounts her decision to freeze 15 eggs before starting treatment and how her perspective on parenthood has evolved. She walks us through the emotional and physical realities of exploring surrogacy and genetic testing post-transplant—particularly the complex issue of donor DNA requiring a skin biopsy for viable results.Kitrena doesn't shy away from discussing post-treatment life: weight gain linked to early menopause, a challenging international trip filled with setbacks and triumphs, and the frustrations of altered tastes and capabilities. Despite it all, she maintains a remarkable sense of humor and determination to continue traveling and living fully.Family and caregiver dynamics are woven throughout her story. She speaks lovingly about her partner's unwavering support and the strength of her younger brother, who stepped up when needed most. Her message to caregivers includes practical advice—especially around vigilance with medical billing, noting errors she encountered from appointments she never attended.Finally, Kitrena emphasizes the growing importance of therapy for both patients and caregivers. She encourages the AYA community to use available resources to work through trauma, grief, and uncertainty—pointing to virtual options that didn't exist in her earlier experience.Kitrena's journey is one of persistence, clarity, and empowerment. She brings vital, firsthand wisdom to the AYA cancer space, reminding us that while every survivor's path is different, no one should walk it alone.Thanks to our Season 17 Sponsors:Leukemia and Lymphoma Society (LLS): https://lls.org/and Incyte: https://incyte.com/FInancial Resource from the LINK: https://www.nbmtlink.org/financebookresources/ National Bone Marrow Transplant Link - (800) LINK-BMT, or (800) 546-5268.nbmtLINK Website: https://www.nbmtlink.org/nbmtLINK Facebook Page: https://www.facebook.com/nbmtLINKFollow the nbmtLINK on Instagram! https://www.instagram.com/nbmtlink/The nbmtLINK YouTube Page can be found by clicking here.To participate in the GVHD Mosaic, click here: https://amp.livemosaics.com/gvhd

In this episode, we sit down with Dr. Chris Dandoy, Associate Professor of Clinical Pediatrics and bone marrow transplant physician at Cincinnati Children's Hospital. Dr. Dandoy shares his deep experience working with adolescents and young adults (AYAs), focusing on the unique challenges they face during and after cancer treatment. Our conversation centers around empowering AYAs to take ownership of their healthcare journey, improving outcomes, and restoring quality of life.Dr. Dandoy introduces us to Engraft, a collaborative learning network he founded, which unites providers, patients, families, industry partners, and nonprofits to improve survival and quality of life post-stem cell transplant. Rather than each center working in isolation, Engraft allows for real-time communication and problem-solving across 15 centers, helping everyone learn from each other's best practices.A core message in our conversation is the importance of ownership—encouraging AYAs to ask questions, understand their medications, and advocate for themselves. We explore the concept of “ownership” through examples, like advocating for the removal of central lines after they're no longer medically necessary, and understanding the role and risks of medications such as immunosuppressants and anti-infectives.Dr. Dandoy walks us through strategies to support medication adherence, such as using reminder apps, setting daily routines, and involving friends or caregivers for support. He also emphasizes the temporary nature of this intense medication schedule, helping patients see it as a phase, not a life sentence.We highlight how important it is for AYAs to stay engaged—learning about their labs, asking what new medications are for, and writing down questions for their healthcare team. Chris stresses that they don't have to memorize everything; the goal is communication and awareness, not perfection.For caregivers, Chris offers validation and encouragement, reminding them this is a marathon with tough stretches, but also moments of progress. He urges caregivers to walk beside their loved ones—not behind or in front—fostering independence and shared decision-making.Dr. Dandoy closes with an inspiring story of a young survivor who endured ICU-level complications but is now back to running races and embracing life fully. It's a powerful reminder that while the transplant journey is grueling, it's also transformative.More:Engraft Learning Network: https://www.engraftlearningnetwork.org/Thanks to our Season 17 Sponsors:Leukemia and Lymphoma Society (LLS): https://lls.org/and Incyte: https://incyte.com/ National Bone Marrow Transplant Link - (800) LINK-BMT, or (800) 546-5268.nbmtLINK Website: https://www.nbmtlink.org/nbmtLINK Facebook Page: https://www.facebook.com/nbmtLINKFollow the nbmtLINK on Instagram! https://www.instagram.com/nbmtlink/The nbmtLINK YouTube Page can be found by clicking here.To participate in the GVHD Mosaic, click here: https://amp.livemosaics.com/gvhd

In this episode, we speak with Emily Long Sarro, a board-certified family nurse practitioner specializing in adolescent and young adult (AYA) care at Memorial Sloan Kettering Cancer Center. We focus on the unique challenges AYAs face before, during, and after a stem cell transplant. Emily shares how this age group, defined as 15 years old to 39 years old by the National Cancer Institute, is often overlooked in the healthcare system, stuck between pediatric and adult care settings. They're navigating identity, relationships, careers, and independence—while also managing a serious illness, which can disrupt or halt life milestones.We discuss how Emily approaches AYA care with a holistic mindset—merging clinical treatment with emotional and mental health support. She emphasizes the importance of granting young patients autonomy and private space, especially when families may unintentionally overstep. She urges healthcare providers to always include mental health support in the treatment plan, noting that anxiety, depression, and even PTSD are common in this group, both during and long after treatment.Emily also stresses the need for daily coping tools like journaling, movement, and meditation to supplement infrequent counseling sessions. She encourages us to create trust by really listening, especially since many AYAs feel dismissed in early diagnostic stages due to their age.We then dive into critical but often unspoken topics: fertility preservation, sexual health, and survivorship. Emily outlines time-sensitive fertility options and highlights the emotional toll if these aren't addressed early. She covers the hidden costs of care and offers resource suggestions like Livestrong and Cancer and Careers. She also calls attention to "silent disabilities" that persist post-transplant and affect career and daily function, emphasizing self-advocacy in the workplace. Coworkers and others may not "see" these limitations, but accommodations are often necessary.We discuss milestones missed due to treatment and the emotional weight of watching peers move on through social media. Emily suggests practical ways to stay socially connected, such as virtual events and platforms like Cancer Buddy. For caregivers, she reminds us that support often means just being present and handling small tasks that feel overwhelming to the patient.  It's important to hold space for patients' sadness over missing milestones, but when appropriate, the big picture remains: they may be sacrificing a few milestones now to experience many more later.The episode closes with a deeply moving survivor story—a young man from The Bronx who overcame mistrust in the medical system, underwent a transplant, and now runs a thriving music production business. His resilience and transformation encapsulate the hope and strength that defines this patient group.More:Marrow Masters Season 9, Episode 2, with fertility resources in Show Notes: https://marrowmasters.simplecast.com/episodes/preserving-fertility-through-cancer-treatmentCancerCare – https://www.cancercare.orgImerman's Angels – https://imermanangels.orgLivestrong Fertility – https://livestrong.org/how-we-help/livestrong-fertility/Worth the Wait – https://worththewaitcharity.com/Maggie's Dream (Fertility Preservation Assistance)–https://www.teammaggiesdream.org/Cancer and Careers – https://www.cancerandcareers.orgCancer Buddy App (Bone Marrow Foundation) –https://bonemarrow.org/support-and-financial-aid-2/support/about-cancerbuddyThanks to our Season 17 Sponsors:Leukemia and Lymphoma Society (LLS): https://lls.org/and Incyte: https://incyte.com/ National Bone Marrow Transplant Link - (800) LINK-BMT, or (800) 546-5268.nbmtLINK Website: https://www.nbmtlink.org/nbmtLINK Facebook Page: https://www.facebook.com/nbmtLINKFollow the nbmtLINK on Instagram! https://www.instagram.com/nbmtlink/The nbmtLINK YouTube Page can be found by clicking here.To participate in the GVHD Mosaic, click here: https://amp.livemosaics.com/gvhd

In this episode, we sit down with Nick Giallourakis, Executive Director of the Steven G. Cancer Foundation and co-founder of Elephants and Tea, a digital magazine and support platform for adolescent and young adult (AYA) cancer patients and survivors. We begin by learning about Nick's brother, Steve, whose incredible journey as a five-time cancer survivor—including osteosarcoma, Secondary AML, renal cell carcinoma, and pleomorphic sarcoma—serves as the foundation and inspiration for Nick's work.Nick walks us through the origins of Elephants and Tea, which he co-founded with his mother, Angie. The platform emerged from a need for authentic, uncensored storytelling within the AYA cancer space. They pivoted from a traditional media model to a platform where survivors share their stories in their own words. This decision came from listening to survivors who didn't want their experiences diluted. The magazine's name—suggested through a contest—symbolizes the raw truth of cancer as the “elephant in the room,” while “tea” represents the comfort found in open dialogue.Nick highlights key challenges AYAs face: financial toxicity, unstable careers, insurance struggles, dating, and misdiagnoses due to age biases. He's encouraged by the growing trend of self-advocacy in this group, including the rise in second opinions. We reflect on the post-COVID landscape, noting how virtual platforms opened doors for more isolated individuals, while in-person connections remain essential for others.We touch on caregiving—especially for AYAs where roles can be filled by peers, not just parents. Nick emphasizes the importance of caregivers asking for help and delegating tasks. He also speaks candidly about the emotional toll of losing community members and the need to acknowledge and process that grief.We explore how storytelling fuels community-building at Elephants and Tea. The magazine has contributors from 15 countries, highlighting a global hunger for connection and support. Nick shares how partnerships—like their impactful collaboration with Walgreens—are making tangible changes, such as mandatory fertility counseling for patients receiving chemo for the first time. Behind the scenes, they're working with industry and medical organizations to use these stories for systemic change.As for what's next, Elephants and Tea continues to expand its in-person programming, including regional magazine release events. They're consistently surveying their audience to ensure their efforts are aligned with current needs. Nick leaves us with a heartfelt story of a late community member who, through a simple virtual Halloween hangout, helped spark deeper bonds and outreach across the cancer community.More: Elephants and Tea: https://elephantsandtea.comSteven G. AYA Cancer Research Fund: https://stevengcancerfoundation.orgCancer and Fertility Magazine produced by Elephants and Tea WITH Walgreens: https://elephantsandtea.org/cancer-fertility/YA Cancer Gabfest (Cactus Cancer Society): https://cactuscancer.org/ya-cancer-gabfestStupid Cancer: https://stupidcancer.org/Thanks to our Season 17 Sponsors:Leukemia and Lymphoma Society (LLS): https://lls.org/and Incyte: https://incyte.com/ National Bone Marrow Transplant Link - (800) LINK-BMT, or (800) 546-5268.nbmtLINK Website: https://www.nbmtlink.org/nbmtLINK Facebook Page: https://www.facebook.com/nbmtLINKFollow the nbmtLINK on Instagram! https://www.instagram.com/nbmtlink/The nbmtLINK YouTube Page can be found by clicking here.To participate in the GVHD Mosaic, click here: https://amp.livemosaics.com/gvhd

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

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.

A brand-new study just dropped in Nature Medicine… and the numbers are worse than we thought. In this episode, I'm breaking down the latest dementia statistics that every caregiver, family member, and adult over 55 needs to know. This is more than just data—it's a wake-up call. We're talking risk factors, who's most vulnerable, and why dementia care is on the verge of a national crisis. But don't worry—there's hope too. I'll also share where to turn next and how we can take action now. Click the link below to read the full study: https://drive.google.com/file/d/1tkUsmdUeWIvASlpgkd3seeDHwLUBF9-T/view?usp=sharing  If you'd like to see this episode on video, you can hop on over to my YouTube channel here. Get Weekly Dementia Tips in Your Inbox! Sign up for our FREE Dementia Dose newsletter at https://careblazers.com/dementiadose It's our mission to make dementia caregiving easier for families caring for a loved one with Alzheimer's disease, frontotemporal dementia, lewy body dementia, vascular dementia, or any other type of dementia. We believe that in order to create a more dementia-friendly world, we must first create a caregiver-friendly world. That's why we create free educational training videos like this one so that anyone with an internet connection can get access to dementia care information. **This channel and any information by Dementia Careblazers is not a substitute for healthcare. This is not healthcare advice. Please talk to your healthcare providers for specific feedback on your situation.

Key Topics Discussed:The philosophy of care behind RPM How RPM empowers patients and improves outcomes Common barriers for providers and patients—and how to overcome them The emotional and human impact of being “seen” through RPM Why RPM is essential for proactive care and value-based models How RPM strengthens patient-provider partnershipsWho Should Listen:Providers looking to elevate their standard of care Patients managing chronic conditionsCaregivers advocating for loved onesHealthcare leaders navigating the shift to proactive careTune in to hear why Jennifer believes every Your Health patient should be on RPM—and why the time to act is now. www.YourHealth.Org

When someone we know or love starts to develop psychological issues, we don't often associate it with a form of dementia. However, this trait is one of the most common signs of frontotemporal dementia (FTD) — the most common neurodegenerative disease in people under the age of 65. In his new book, Mysteries of the Social Brain: Understanding Human Behavior Through Science, Dr. Bruce Miller highlights his experiences observing people with FTD and what they have taught him about what he calls the "social brain."Dr. Bruce Miller has been observing people with FTD for decades in the Memory and Aging Center at the University of San Francisco, where he is also Professor of Neurology and the Founding Director of the Global Brain Health Institute. He shares key insights on how to keep our "social brain" healthy and how it can even unlock our creative potential.

Could this vitamin really slow down Alzheimer's? The latest research might change everything. In this video, I'm sharing the surprising study results, how this vitamin works in the brain, and why some neurologists are already taking it themselves. Most people have never heard of this — but if you're caring for someone with dementia or worried about memory decline, you'll want to see this. Link to study: https://pmc.ncbi.nlm.nih.gov/articles/PMC7880246/ If you'd like to see this episode on video, you can hop on over to my YouTube channel here. Get Weekly Dementia Tips in Your Inbox! Sign up for our FREE Dementia Dose newsletter at https://careblazers.com/dementiadose It's our mission to make dementia caregiving easier for families caring for a loved one with Alzheimer's disease, frontotemporal dementia, lewy body dementia, vascular dementia, or any other type of dementia. We believe that in order to create a more dementia-friendly world, we must first create a caregiver-friendly world. That's why we create free educational training videos like this one so that anyone with an internet connection can get access to dementia care information. **This channel and any information by Dementia Careblazers is not a substitute for healthcare. This is not healthcare advice. Please talk to your healthcare providers for specific feedback on your situation.

In this episode, we explore the fascinating phenomenon of Terminal Lucidity - what it is, how it occurs, and why it continues to mystify both science and spirituality. Hear powerful, firsthand stories from those who've witnessed this final moment of clarity, offering insight, comfort, and awe at the threshold between life and death. Some of the references to this episode include: https://pubmed.ncbi.nlm.nih.gov/20010032/ https://theconversation.com/terminal-lucidity-why-do-loved-ones-with-dementia-sometimes-come-back-before-death-202342 https://www.buddhanet.net/bereaved/ https://www.leiferreport.com/poetry-life/ https://www.crossroadshospice.com/hospice-resources/spirituality-end-of-life-care https://en.wikipedia.org/wiki/Moksha https://waterfromrock.org https://en.wikipedia.org/wiki/Turiya www.reddit.com www.quora.com *** The views and opinions expressed in this podcast are intended solely for discussion and informational purposes. They do not necessarily represent the views of the hosts, guests, or affiliated organizations, and should not be taken as professional advice or endorsements. Please consider this content as part of an open dialogue. For more about Kirsty, visit www.kirstysalisbury.com

Careblazer, did you know you could lower your dementia risk by nearly 50% just by changing some everyday habits? In this video, I'm walking you through 14 research-backed lifestyle changes you can start making today—based on the 2024 Lancet Commission Report. These are modifiable risk factors, which means they're things you actually have control over. As a board-certified geropsychologist, I see so many people feel helpless when it comes to brain health. But this video is here to show you that you have more power than you think. From hearing loss and blood pressure to social isolation and air pollution, I'll explain what each risk factor means and exactly how you can take action. If you'd like to see this episode on video, you can hop on over to my YouTube channel here. Get Weekly Dementia Tips in Your Inbox! Sign up for our FREE Dementia Dose newsletter at https://careblazers.com/dementiadose It's our mission to make dementia caregiving easier for families caring for a loved one with Alzheimer's disease, frontotemporal dementia, lewy body dementia, vascular dementia, or any other type of dementia. We believe that in order to create a more dementia-friendly world, we must first create a caregiver-friendly world. That's why we create free educational training videos like this one so that anyone with an internet connection can get access to dementia care information. **This channel and any information by Dementia Careblazers is not a substitute for healthcare. This is not healthcare advice. Please talk to your healthcare providers for specific feedback on your situation.

Episode Notes:Scott shares the recent rapid decline of his father's health and the emotional toll it has takenHow missed diagnostic details revealed a larger issue in communication and coordinationThe critical role of a Senior Solutions Advisor in bridging care gapsWhy primary care must evolve to become the quarterback of patient navigationA look back at models from 2012 and why older frameworks may hold the key to future innovationThe call to hire 287+ RN Case Managers for the 23,000+ homebound patients currently servedPersonal reflections on legacy, family, and the power of leading with empathy  www.YourHealth.Org

Why do so many people with dementia refuse to bathe?

The healthcare system is complex and challenging to navigate, especially for seniors and their caregivers, but preparation and knowledge can help you maintain control, advocate effectively, and achieve better outcomes during healthcare transitions.KISMETWhile most assume senior care facilities and nursing homes operate based on modern nutritional science, many still follow outdated dietary guidelines based on the food pyramid, which may negatively impact metabolic health when seniors need more protein and healthy fats for optimal recovery and function.EPISODE SUMMARYIn this episode, master's prepared nurse Cheryl Field shares insights from her 36 years of experience in senior care. She discusses how understanding the healthcare system can help aging adults maintain control during transitions like emergency room visits and hospital stays. Field explains the critical differences between traditional Medicare and managed care options that seniors must navigate when turning 65. She offers practical advice on preparing for healthcare events, including what to bring to the emergency room and how to approach rehabilitation stays positively. Field emphasizes the importance of advance directives, creating a supportive home environment, and embracing a mindset that accepts assistance when needed. The conversation also explores how improved nutrition and metabolic health can benefit both seniors and their caregivers, potentially reducing medication dependence and improving quality of life.NOTABLE QUOTE"A hundred percent of us will experience a sudden change in health. That's just for certain, whether it's one or the last one, but a hundred percent of us will have some kind of sudden change in health."Cheryl Field Contact Infowebsite: https://www.cherylfield.com/LinkedIn: https://www.linkedin.com/in/cherylfield1621/Facebook: https://www.facebook.com/people/Cheryl-Field-Senior-Care-Consultant/61564158076135/Instagram: https://www.instagram.com/cefield50/Send Dr. Ovadia a Text Message. (If you want a response, include your contact information.) Dr. Ovadia can not respond here. To contact his team please email team@ifixhearts.com If you like what you hear, I wanna make it easier for you to take action on your health.Head over to i fix hearts.com/book to grab a copy of my book, Stay Off My Operating Table, and if you're ready to go deeper or talk to someone from my team, just go to i fix hearts.com/talk. Stay Off My Operating Table on X: Dr. Ovadia: @iFixHearts Jack Heald: @JackHeald5 Learn more: Stay Off My Operating Table on Amazon Take Dr. Ovadia's metabolic health quiz: iFixHearts Dr. Ovadia's website: Ovadia Heart Health Jack Heald's website: CultYourBrand.com Theme Song : Rage AgainstWritten & Performed by Logan Gritton & Colin Gailey(c) 2016 Mercury Retro RecordingsAny use of this intellectual property for text and data mining or computational analysis including as training material for artificial intelligence systems is strictly prohibited without express written consent from Dr. Philip Ovadia.

All Home Care Matters and our host, Lance A. Slatton were honored to welcome filmmaker and long-term care advocate Peter Murphy Lewis as guest to the show.   About Peter Murphy Lewis:   Peter Murphy Lewis is a documentary filmmaker, CNA, and long-term care advocate & founder of Strategic Pete who uses storytelling to spotlight the unsung heroes of caregiving. He is the creator of the docuseries People Worth Caring About, which reveals the real human stories behind the caregiving crisis in America.     With a background in marketing and content strategy, Peter brings a unique blend of empathy and clarity to both film and business. He's also the founder of Strategic Pete, a boutique consultancy helping mission-driven organizations grow through storytelling and scalable marketing systems.     His work has been featured in Care.com, Provider Magazine, Becker's Healthcare, McKnight's, and more. Peter lives next to a zoo in Kansas, sleeps in a hammock under the stars, and spends his mornings teaching his 8-year-old son to golf.    

BrainStorm wants to hear from you! Send us a text.in this episode of the "BrainStorm" by UsAgainstAlzheimer's, George Vradenburg, Co-founder and Chairman of UsAgainstAlzheimer's, and Russ Paulsen, the organization's Chief Operating Officer, discuss the impact of the Trump administration's policies on Alzheimer's research with host Meryl Comer. The conversation highlights the systematic dismantling of the National Institutes of Health (NIH) and other critical agencies, which threatens to undermine Alzheimer's research and public health. Vradenburg and Paulsen express concerns about the lack of transparency in the reorganization and the potential negative effects on drug reviews and approvals due to significant cuts at the FDA. They highlight the importance of protecting key programs that support seniors and the potential global impact of these policy changes. Despite the challenges, both Paulsen and Vradenburg are optimism about scientific advances in diagnosing and treating Alzheimer's, including the development of blood tests and new treatments. Hear the call to action for listeners to advocate for continued support for Alzheimer's research and to contact their members of Congress to ensure that funding remains a priority. This is a must listen episode!  This episode is sponsored by Genentech.Support the show

In this episode of the Gladden Longevity Podcast, Dr. Jeffrey Gladden interviews Dr. Heather Sandison, who discusses her innovative approach to cognitive health and dementia care. Dr. Sandison emphasizes the potential for reversing cognitive decline through functional medicine, lifestyle changes, and a focus on diet, particularly the benefits of ketosis. She shares insights on creating a supportive environment for individuals with memory issues and the importance of personalized strategies based on genetic and environmental factors. The conversation highlights the need for a shift in perspective regarding Alzheimer's treatment and the potential for significant improvements in cognitive function. In this conversation, Dr. Jeffrey Gladden and Dr. Heather Sandison discuss the rising prevalence of dementia and cognitive decline, emphasizing the importance of environmental factors and lifestyle choices in mitigating risks. They explore how to architect living spaces to promote brain health, the impact of toxins, and the significance of hormonal optimization. The discussion also highlights the critical role of caregivers, their mental health, and the need for support systems. Finally, they touch on innovative approaches to Alzheimer's treatment and ongoing research efforts.   For Audience · Use code 'Podcast10' to get 10% OFF on any of our supplements at https://gladdenlongevityshop.com/ !  · Find out more about Dr. Heather's expertise at https://www.solcere.com/ & https://www.maramaexperience.com/about/     Takeaways Dr. Sandison emphasizes a new approach to dementia care.        Functional medicine can optimize cognitive health.        Creating a supportive environment is crucial for healing.        Ketosis can significantly improve cognitive function.        Personalized strategies are essential for effective treatment.        Genetic factors play a key role in cognitive decline.        Dietary interventions can enhance brain health.        Social engagement is vital for cognitive support.        There is hope for reversing Alzheimer's symptoms.        Innovative treatments are emerging in the field of cognitive health. Dementia is increasingly prevalent due to demographic shifts.        Environmental factors significantly influence cognitive health.        Screen time and modern stressors contribute to cognitive decline.        Architecting living spaces can reduce exposure to harmful stimuli.        Toxins like mycotoxins are neurotoxic and should be avoided.        Hormonal optimization is crucial for brain health in aging individuals.        Caregivers face increased health risks and need support.        Caregivers should prioritize self-care to maintain their well-being.        Innovative treatments for Alzheimer's are being developed and researched.        Community support can enhance the caregiving experience.   Chapters 00:00 Introduction to Cognitive Health and Dementia Care 03:09 The Shift in Perspective on Alzheimer's Treatment 06:05 Creating a New Model for Memory Care 09:03 Understanding Genetic and Environmental Factors 11:59 Innovative Approaches to Cognitive Function 15:04 The Role of Ketosis in Brain Health 18:09 Personalized Strategies for Cognitive Improvement 20:56 Exploring Dietary Interventions for Brain Health 26:06 The Rise of Dementia and Cognitive Decline 28:40 Architecting Environments for Brain Health 31:54 The Impact of Toxins on Cognitive Function 35:08 Hormonal Optimization for Brain Health 41:27 Supporting Caregivers in Dementia Care 48:23 Innovations in Alzheimer's Treatment and Research   To learn more about Dr. Heather Sandison: Email: drheathersandison@gmail.com Website: https://www.drheathersandison.com/ YouTube: https://www.youtube.com/channel/UC7D8wkR3j1ZNoI2HHCLs3tg Facebook: https://www.facebook.com/HeatherSandisonND Instagram: https://www.instagram.com/dr.heathersandison/ Reach out to us at:    Website: https://gladdenlongevity.com/     Facebook: https://www.facebook.com/Gladdenlongevity/    Instagram: https://www.instagram.com/gladdenlongevity/?hl=en     LinkedIn: https://www.linkedin.com/company/gladdenlongevity    YouTube: https://www.youtube.com/channel/UC5_q8nexY4K5ilgFnKm7naw    

This episode features a discussion among kidney nurses about the challenges patients face while on their renal replacement journey, and the various ways nurses can support them and their caregivers. The conversation includes suggestions for new nurses entering the field, thoughts on improving patient support, and discusses how approaches may vary in different contexts. Ana Elizabeth Prado Lima Figueiredo – Professor, School of Nursing at the Pontifícia Universidade Católica do Rio Grande do SulElaine Bowes – Senior Clinical Nurse Specialist and Advanced Level Nurse Practitioner in Peritoneal Dialysis at Kings College HospitalFatima de Figueiredo - Renal Vascular Access Nurse, Kings Renal Unit, King's College Hospital Foundation TrustJane van der Jeugd - Nurse Practitioner: Transplantation I Nephrology, Flinders Medical Centre, Southern Adelaide Local Health NetworkZehra Aydin - Assistant Professor at Istanbul Atlas University

This one simple exercise changed everything—for me, for my audience, and it could do the same for you. In this episode, I'll share the 3 things I'd want my caregivers to know if I ever needed care... and show you how this one shift can make dementia care so much easier and more compassionate.

All Home Care Matters and our host, Lance A. Slatton were honored to welcome the team behind the award winning app Memory Lane Games.   About Bruce Elliott, Co-Founder & CEO:   Bruce's life in tech started in the dot com boom (and dot com bust!) era, then into leadership roles in online payments, gaming and blockchain. Then in 2019 Bruce stepped into digital health after he and a friend sat in a pub talking about their Mums, then 86 and 90, imagining how they might turn their memories into games, launching Memory Lane Games.   As Co-Founder and CEO, Bruce leads the team at Memory Lane Games in supporting caregivers and people living with dementia in over 100 countries every month, with their Mayo Clinic award-winning personalized dementia app.   About Lisa Karran, COO:   Lisa's diverse set of skills across marketing, operations and corporate governance have been gained during a 20 year career with much of the latter half having been spent advising and working in startups. At Memory Lane Games she is responsible for marketing, operations and finance and ensuring that the business runs smoothly now and is able to scale. An advocate for women working in technology, Lisa is a founding committee member of LoveTech, a charity established in the Isle of Man to inspire young women into STEM careers.   About Matty Tait, Operations Coordinator:   Matty brings a dynamic background in sales, operations, and business development, with experience spanning both established companies and fast-moving startups. At Memory Lane Games, he plays a key role in operations, partnerships, and growth—helping the team deliver meaningful impact today while building for the future. Passionate about people-first technology and making a difference in the community, Matty is also involved in various entrepreneurial projects that support small businesses and positive social change.   About Memory Lane Games:   Memory Lane Games is transforming dementia care by turning memories into moments of joy, connection, and confidence. Our easy-to-use app offers a growing collection of simple, personalised games designed to gently prompt reminiscence and spark meaningful conversations between people living with dementia and their caregivers.   From familiar TV shows and local landmarks to childhood memories and lifelong hobbies, each game is thoughtfully crafted to celebrate what makes every individual unique. Used by families, carers, and care homes around the world, our clinically informed approach focuses on what people can do—bringing dignity, delight, and a touch of nostalgia to every interaction.    DISCLOSURE: Lance A. Slatton - The Senior Care Influencer is the Official Brand Ambassador for Memory Lane Games.

An Oscar-winning actor with Alzheimer's was left alone for 6 DAYS… and no one knew. What happened to his wife—the person caring for him—could happen to any dementia caregiver. This isn't just a Hollywood tragedy. It's a wake-up call. In this video, I'm sharing two life-saving lessons every caregiver needs to hear. If you care for someone with dementia, this could be the most important 10 minutes of your week. If you'd like to see this episode on video, you can hop on over to my YouTube channel here. If you found this information helpful, consider subscribing to my free email newsletter for even more valuable insights on dementia by clicking here.

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 11 - "Joy in Caregiving":   About Alex Garza:   Alex is a devoted caregiver and digital marketer, balancing her professional life with the profound journey of caring for her husband after his hemorrhagic stroke in 2017. With over 25 years of marriage, she draws on her love and faith to navigate the challenges of caregiving, working from home to provide support and stability.   Through her her instagram channel, she hopes to inspire fellow caregivers, offering hope, encouragement, and practical insights for those facing their own difficult times, showing that resilience and compassion can light even the darkest paths.

In this episode, join host Darleen Mahoney as she engages with Mario Irizarry, Clinical Director of Palmetto in Home RN, to explore the multifaceted challenges of aging in place and caregiver burnout. Mario shares his expertise on innovative home care solutions, emphasizing the importance of supporting individuals who wish to age comfortably in their own homes.We delve into the financial implications of retirement and assisted living, with Mario highlighting the average annual cost of assisted living facilities in the US. He also shares personal experiences of caregiver burnout, illustrating the often unnoticed pressures faced by caregivers. Tune in to learn about the advanced technology used in home care, including HIPAA-compliant systems that provide medication reminders and monitor vital signs. Mario also offers valuable resources for caregivers, such as reaching out to the local Office of Aging for support. Don't miss this insightful discussion on enhancing the quality of life for aging individuals and their caregivers.  www.palmettoinhomern.com.SeniorLivingGuide.com Podcast sponsored by TransMedCare Long Distance Medical Transportation & GoGo GrandparentThe background music is written, performed, and produced exclusively by purple-planet.com.https://www.purple-planet.com/

Why do people with dementia act out, push you away, or refuse your help? In this video, I'm revealing 3 surprising causes behind challenging dementia behaviors—and they're probably not what you think. These aren't just mood swings. They're messages. Learn what your loved one might really be trying to tell you—and how to handle it with less stress and more confidence. If you'd like to see this episode on video, you can hop on over to my YouTube channel here.

Conscious Caregiving with L & L is "Tackling the Tough Conversations." The topic of this episode is "Healthcare Changes & Seniors" 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's book, "The All Home Care Matters Official Family Caregivers' Guide" was the recent recipient of the 2024 International Impact Book Awards. Connect with Lance A. Slatton - "The Senior Care Influencer": Official Website: https://www.lanceaslatton.com Official Website for All Home Care Matters: https://www.allhomecarematters.com Lance A. Slatton and Lori La Bey Co-Host and Produce Conscious Caregiving with L & L. Visit their website at: https://consciouscaregivingll.com/ To learn more about Lance A. Slatton and Lori La Bey you can visit their websites.

Dementia medication refusal is one of the most frustrating challenges caregivers face. If your loved one refuses to take their medication, you're not alone! In this episode, I reveal the #1 mistake caregivers make when handling dementia medication refusal and share proven strategies to make medication time easier. You'll learn: ✅ Why dementia patients refuse medication (confusion, fear, sensory issues, independence) ✅ What NOT to do (why forcing, arguing, or sneaking meds can backfire) ✅ How to make medication time easier (changing medication forms, routines, positive reinforcement) If you'd like to see this episode on video, you can hop on over to my YouTube channel here. And if you need ongoing support, check out our Care Collective—a warm, supportive community for dementia caregivers, with live Q&A sessions, expert advice, and 24/7 access to resources.

All Home Care Matters and our host, Lance A. Slatton were honored to welcome David Knack as guest to the show.   About David Knack:   David Knack serves as Head of Sales at Zingage, a leading platform that helps home-based care providers engage and retain their care teams. Passionate about thoughtful automation and operational excellence, David partners with healthcare entrepreneurs to implement technology solutions that enhance both caregiver and patient experiences. He also hosts “Home Care Hindsight,” a podcast where he explores healthcare innovation and best practices with industry leaders.   About Zingage:   Zingage is the leading caregiver engagement platform for home-based care, transforming how providers connect with and support their teams. By fostering meaningful relationships and celebrating great work, Zingage helps providers reduce turnover, improve compliance, and deliver better care. The company serves hundreds of healthcare organizations across the US and Canada. Organizations using Zingage report up to 70% reduction in turnover and 50% fewer missed visits, enabling them to focus on what matters most—delivering exceptional care. Founded in 2023, Zingage is headquartered in New York.

The Care Advocates is brought to you by the All Home Care Matters Media team and focuses on providing family caregivers and their loved ones with support, resources, and discussion on the issues facing them in the matrix of long-term care.   The Care Advocates are honored to welcome, Christina Keys as guest to the show.   About Christina Keys:   Christina Keys went from career woman to caregiver when her mother had a life changing stroke in 2013. She cared for her for 10 years. Turning a mess into a message. Christina is now a National Speaker, Advocate and Caregiver Community Builder as well as the Founder and CEO of Keys For Caregiving. Christina is also one of the hosts on this coming years Self Care at Sea Cruise. About Keys for Caregiving: Keys For Caregiving helps to Connect businesses, and Family Caregivers. With their consulting services, training, webinars, advocacy projects, podcasts and collaborative creation and production of caregiver events they are working to help collectively transform the Care Space community and amplify all our voices for change.   About Lance A. Slatton:   Lance A. Slatton is an author, writer, host, producer, healthcare professional for over 20 years, and renownedly known as "The Senior Care Influencer". Lance A. Slatton is the host of the Award-Winning podcast & YouTube show All Home Care Matters. He is also a senior case manager at Enriched Life Home Care Services in Livonia, MI.   Lance was named as "50 under 50" for 2023 and received the distinction as the Top Influencer for Healthcare and Advocacy for 2024. Lance is also a columnist for multiple healthcare and news websites and and is the author of the award winning book "The All Home Care Matters Official Family Caregivers' Guide".   About Sharon's Son, George:   Dr. George Ackerman (Sharon's son) is from Brooklyn, N.Y. Now residing in Florida, he works in the fields of law, police, and education. George lost his mother, Sharon Riff Ackerman on 1/1/2020 due to Parkinson's Disease.   George wanted to honor his mother and continue to help in the Parkinson's awareness cause and did not know how to bring change. George started TogetherForSharon® as a family for the purpose of keeping his mother, Sharon Riff Ackerman's, memory alive and to share the message of Parkinson's Awareness and hope for a cure. 

This podcast episode features guest Nicole J. Smith, a daughter faced with her mother's Alzheimer's diagnosis. Nicole J. Smith intertwines heartfelt memoir with practical advice, a vital roadmap for caregivers navigating dementia care. Nicole was blindsided by her mother's post-pandemic cognitive decline and took a deep dive into dementia education after her mother's Alzheimer's diagnosis. Nicole is sandwiched between caring for three aging parents and five children. She wrote the book she could not find in managing the legal, financial, medical, and emotional aspects of becoming a caregiver. Her book Diagnosis Dementia: Your Guide for Eldercare Planning and Crisis Management, shares her story and helpful resources in navigating the terms and turmoil of eldercare. End of life planning conversations are critical to have before a crisis occurs. www.njsmithbooks.comMichelle and Nicole discuss the challenges of managing aging parents' care and finances. The conversation highlighted the importance of having legal documents like powers of attorney in place for both parents and adult children, especially as many people face unexpected health issues, such as Alzheimer's disease. The speakers shared personal stories about their experiences with caregiving, emphasizing the emotional, financial and logistical complexities involved that you might be surprised by.They addressed the broader implications of an aging population, noting that 10,000 baby boomers turn 65 daily, which places significant pressure on the healthcare system. The speakers stressed the need for proactive planning in retirement discussions, as caregiving costs can deplete savings. They provided resources for families navigating these issues, including support groups and websites focused on end-of-life conversations. This episode is important as it raises awareness about the realities of caregiving and the necessity of preparation, encouraging listeners to engage in difficult but essential conversations about aging and care.00:05 - Starting the caregiving journey 10:18 - Importance of powers of attorney 20:51 - Facing caregiving realities 29:50 - Navigating family dynamics 39:18 - Essential resources for caregiving 45:33 - Organizing conversations on aging Key TakeawaysProactive Planning: It is crucial to have conversations about health, finances, and caregiving preferences with family members before a crisis occurs.- Education and Organization: Caregiving requires not only emotional support but also a structured approach to managing medical, legal, and financial aspects.- Community Support: Caregivers are not alone; there are numerous resources and support networks available to assist them in their journey.Resources mentioned in the Podcast:Introduction to various resources such as aging life care managers, financial planners, and elder law attorneys.Recommendations for support groups and educational resources, including:Conversations:https://deathoverdinner.org/https://theconversationproject.org/https://www.fivewishes.org/Caregiver Support:https://daughterhood.org/https://leezascareconnection.org/homehttps://wearehfc.org/For much more on ALL things money mindset, money management, how to earn a great living and take control of your finances…Subscribe to my weekly podcast, Money and You:https://podcasts.apple.com/us/podcast/money-you-with-michelle-perkins/id1365907575?ign-itscg=30200&ign-itsct=podcast_boxPlease share the episode or the podcast with your friends and family members who want to understand money better and feel more confident and in control of their financial lives.And don't forget to join the Limit Free Life email community for valuable, usable content and to learn about upcoming events: Let's Connect… https://limitfreelife.com/newsletter/I'm excited to offer you a proven way to develop a next level relationship with money that will empower your mindset and financial mastery by “dating your money.”  Until you understand how YOU relate to money and what you believe about money, nothing will change. Once you begin to get to know yourself with money, learn the fundamentals of money management, and operate in a new way with money, everything will open up. Join my newsletter so I can let you know when my next "money dating program" is starting and I'll help you make the shift. The next one begins soon! For more information on Limit Free Life & Michelle Perkins: https://limitfreelife.comLinkedIn: https://www.linkedin.com/in/limitfreelife/Instagram: https://www.instagram.com/livealimitfreelifeYou Tube: https://www.youtube.com/@michelleperkins-limitfreel2446

On episode 230, we welcome Michelle Sherman to discuss mental illness within families, the missteps people make in attempting to address it, our tendency to personalize others' struggles, what happens when others aren't aware of why they're struggling and can't explain it, the 4Cs model of navigating mental illness in others, the effects and trauma and neglect, asking for support and overcoming the shame of doing so, and why having a mental illness doesn't necessarily mean one is incapable of being a good parent. Michelle D. Sherman, PhD, ABPP, is a board-certified, licensed clinical psychologist who is a nationally recognized leader in the family experience of mental illness and trauma. She is the editor-in-chief of Couple and Family Psychology: Research and Practice and worked for many years in the Veterans Affairs system. She is a fellow of the American Psychological Association and was named their Family Psychologist of the Year in 2022. Her newest book, co-authored with DeAnne Sherman, available now, is called Loving Someone with a Mental Illness or History of Trauma: Skills, Hope, and Strength for Your Journey. | Michelle D. Sherman, PhD | ► Website | https://www.seedsofhopebooks.com ► Facebook | https://www.facebook.com/profile.php?id=61557940777748 ► Instagram | https://www.instagram.com/seeds_of_hope_books ► Linkedin | https://www.linkedin.com/in/michelle-sherman-phd-lp-abpp-312897100 ► Loving Someone with a Mental Illness or History of Trauma Book | https://amzn.to/3CSwQiR Where you can find us: | Seize The Moment Podcast | ► Facebook | https://www.facebook.com/SeizeTheMoment ► Twitter | https://twitter.com/seize_podcast  ► Instagram | https://www.instagram.com/seizethemoment ► TikTok | https://www.tiktok.com/@seizethemomentpodcast  

Did you know that sudden, unexplained generosity could be a silent warning sign for early dementia? What seems like harmless kindness might actually signal cognitive changes that put your loved one—and their finances—at risk. In this video, I uncover how this subtle behavior can reveal deeper issues, and more importantly, what you can do to protect your loved ones.

1 in 3 people with dementia who visit the ER are diagnosed with a UTI.

In this episode, we dive in deep with Mindy Rice from Hospice & Palliative Care of Iredell County to demystify the often misunderstood concepts of hospice and palliative care. Mindy explains that palliative care is a specialty focused on pain and symptom management for those suffering from serious illnesses, while also differentiating it from hospice care, which is geared towards providing comfort during the final stages of life. She shares personal anecdotes, including her own father's experience with esophageal cancer, to illustrate the profound impact of these services.We also learn about the significant roles that team members like doctors, nurse practitioners, social workers, and caregivers play in both hospice and palliative care settings. Mindy highlights the importance of advocating for a loved one's care and the available resources to support families during these challenging times. Tune in to discover invaluable insights and practical advice that can enhance the quality of life for patients and bring peace of mind to their families.SeniorLivingGuide.com Podcast sponsored by TransMed Care Long Distance Medical Transportation & GoGo Grandparent 855-464-6874 (ext 81714) The background music is written, performed and produced exclusively by purple-planet.com.https://www.purple-planet.com/ *SeniorLivingGuide.com Webinars and Podcast represents the opinions and expertise of our guests. The content here is for informational and educational purposes. It does not necessarily represent the views, recommendations, opinions or advice of Fairfax Publishing/SeniorLivingGuide.com or its employees

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 9 - "Inspired Care":   About Kathleen Quinn, EdD, MBA.: Kathleen Quinn, EdD, MBA, currently serves as the associate vice president for strategic projects at Maryville University in St. Louis and is the founder and president of Kay Inspired, LLC and inventor of the patented Mobility Towel. Her 35+ years in higher education provided opportunities to positively impact students' lives and helped fuel her passion for creating impactful solutions for individuals that genuinely made a difference for others. Aside from her impressive career in education, Kathleen's inventive journey began with a personal story—one marked by love, empathy, and determination.   Kathleen developed the Mobility Towel, an innovative product inspired by her mother, Kay, who battled Rheumatoid Arthritis. This creation was driven by Kathleen's desire to help her mother maintain her functional independence and dignity in daily activities, such as drying off after a shower. The Mobility Towel, designed with unique features like weighted ends and handles, allows individuals to dry their backs, legs, and feet unassisted and without straining, thus catering to those with limited mobility due to aging, surgery recovery, or chronic conditions.   Kathleen's achievements in academia and entrepreneurship reflect her passion for empowering individuals through compassionate and inventive approaches. Her vision and dedication make her a key figure in discussions about caregiving, inclusive design, and the intersection of health and innovation.

Hey Careblazers!

All Home Care Matters and our host, Lance A. Slatton  were honored to welcome Irene Walker the Author of "Forgiving the Man Who Forgot: Grateful Gratitude Attitude" as guest to the show.     About Irene Walker:   Irene Walker is a strong and resilient woman who has faced significant personal challenges. Losing her husband to early-onset dementia is an incredibly difficult experience, and yet, her ability to maintain success in her career and continue to raise her children while managing life's complexities speaks to her inner strength.   Irene strongly believes in practicing gratitude daily. Her background in business administration and financial risk has helped her navigate the uncertainties that come with managing both her professional life and the demands of her personal circumstances. Despite her professional achievements, it's clear that her personal journey has been deeply transformative.     About "Forgiving the Man Who Forgot: Grateful Gratitude Attitude":     We left the doctor's office and my head started spinning. I couldn't remember where I had parked the car. Quite miraculously, Robert managed to navigate us to the correct floor of the parking garage. I felt that all hope had been sucked out of me. I had been struggling to cope since our last appointment with the family doctor, but receiving this final blow was brutal. I put my left hand on the side of the car, leaned over, and threw up. It was just bile. I had to push something out of me--denial, anger, angst--I didn't know. I only knew that I needed it out. I wiped my mouth, my snotty nose and my tear-stained face with jittery hands and then leaned heavily against the back of the car. I took a long, shaky breath in and out in an attempt to pull myself together.     So began the journey with her husband who is diagnosed with early onset Dementia at the age of 51. Forgiving The Man Who Forgot carries the reader along one woman's journey of love, gratitude, honesty, disappointment and courage, detailing her life before, during and after her husband's diagnosis of early onset dementia. Reading this memoir, the reader feels as though the author is sitting across from them and sharing the ups and downs of her life, over a glass of wine or cup of coffee.  

I grew up listening to Walter Cronkite. He signed off each nightly newscast with “And that's the way it is.” As a kid, I was often alarmed by the news. But I reasoned that if Walter Cronkite respected me enough to tell me the truth, then I could handle it. Yes, my reasoning was flawed. Mr. Cronkite didn't know me.  In this episode, I share deeply personal stories from my childhood. That's when my first caregiving experience really began. Both of my parents had enough confidence in me to tell me the truth, even at five years old.  Still, decades later, Mr. Cronkite's respect and my parents' confidence helped me find the resilience I needed to care for my husband. He had Alzheimer's. Today's family dementia caregivers need someone who respects them enough to tell them the truth. Caregivers need the truth to make a plan -- for minimize the chances of falling, to recognize what might be a urinary tract infection (UTI), to serve food not likely to cause choking, to adjust the household budget to hire a CNA (Certified Nursing Assistant), to ask the hard questions about the real costs of memory care facilities. Sometimes, we can plan only one step at a time. But one step IS progress.  I hope that in hearing my childhood story, other caregivers will be able to look into their pasts and recognize times when they found strength. Now is the time to draw on that strength. We need to survive.           

All Home Care Matters and our host, Lance A. Slatton welcome Yati Patel as guest to the show. About Yati Patel: Yati Patel is OTTI's Senior Student Ambassador and Team Captain for this school years HOSA, Future Healthcare Professionals, competition. She is currently a second-year student at Center for Sight and a Senior at Noblesville High School. After graduation she will be entering college as a Pre-Med student with the intent of joining the field of Ophthalmology. Yati's end goal is to be a surgeon, although she does not know which specialty Yati would like to focus her practice around, she is leaning heavily into the ever-growing need in the world of eyes. Yati has been working closely with Center for Sights, Austin Lifferth OD FAAO, on a Glaucoma study around the effects on eye pressure response, and correlation with weight lifting versus low-impact exercise. Yati will be presenting her results at the Indiana 2024/2025 HOSA competition in April of 2025, and hopes to continue developing the study for publication.

Do you ever feel frustrated when caring for your loved one with dementia?  It's easy to forget that their brain no longer processes information the way it used to.  In this coaching episode, we explore how adjusting expectations and understanding your loved one's cognitive reality can help you manage frustration and improve the caregiving experience.   The episode ends with a gentle reminder to lean on God's strength throughout the caregiving process.  The Lord's blessing and guidance provide comfort during stressful moments and help caregivers navigate challenges with greater peace and resilience.   Ever Wonder How To Know What Is Causing Your Caregiver Stress? Take Our FREE Caregiver Stress Assessment Today! https://www.thinkdifferentdementia.com/quiz   Join the FREE Dementia Caregiver Support Facebook Group today for more support:  https://www.facebook.com/groups/dementiacaregiversupportforchristians   Are You A Christian Dementia Caregiver Struggling To Cope With Caregiving? Join the FREE "Ask the Dementia Coach" Monthly Meet Up! And be on the podcast, get support and your questions answered.  https://dementiacaregivingmadeeasy.com/ask   Enjoy our podcast? Please take a moment to leave us a review on Apple Podcasts and Spotify —it really supports our show! https://podcasts.apple.com/us/podcast/dementia-caregiver-support-for-christians-conversations/id1716187550