Happy Healthy Caregiver

Tim Otis is a two-time family caregiver whose journey began in childhood when he helped care for his paralyzed mother and later became the primary caregiver for his father, living with Parkinson’s disease. Through these deeply personal experiences, Tim saw how long-term caregiving—though rooted in love—can quietly impact a caregiver’s health, identity, relationships, and career. In this episode, we discuss the emotional toll of supporting a loved one through serious illness, the ripple effects caregiving has on family dynamics and employment, and why caregivers must be seen as whole people—not just helpers. Tim also shares his desire to create systemic change in how we support caregivers, reflects on his mother’s end-of-life experience, and guides us through a short, restorative reset you can practice anytime. Show notes with product and resource links: https://bit.ly/HHCPod226 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self

After spending more than a decade as the primary caregiver for her mother, living with vascular dementia, Rosanne Corcoran dedicates her work to supporting and empowering family caregivers nationwide. She is a leading voice with Daughterhood, host of Daughterhood the Podcast, and was named a 2024 Advocate for Aging by Next Avenue and the American Society on Aging. In this episode, Rosanne shares practical wisdom on accepting help from community and support networks so that you can carve out time to be off the caregiving clock and learn that it’s ok to share uncomfortable feelings outside your family. We also talk about aging well, navigating in-home dementia care, seeking everyday joy, and what true self-care can look like when caregivers finally take time for themselves. Show notes with product and resource links: https://bit.ly/HHCPod225 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjournal

Betsy Hicks-Russ, Director of the nonprofit Autism Odyssey, shares what it takes to navigate caregiving when your child has high support needs. Drawing on her over three decades of experience as a family caregiver, Betsy discusses overcoming significant obstacles, letting go of victimhood, and choosing to try new things—even when the path forward feels uncertain. In this episode, we explore the powerful gut-to-brain connection and why good nutrition matters for caregivers and care recipients alike. Betsy also reflects on how caregiving has changed over time, comparing today’s information overload with earlier days of lower-tech living and stronger local community connections. Plus, we explore the joy of discovering shared interests with our care recipients—such as a love of Grateful Dead music and nature—and how these shared joys can deepen connection and resilience in caregiving relationships. Show notes with product and resource links: https://bit.ly/HHCPod224 Receive the podcast in your email here:

Meet sandwich generation caregiver Brendan Kelso, who shares his journey caring for his mom with Alzheimer’s while also supporting his son with ASD. Brendan discusses embracing vulnerability and how therapeutic writing—even just 15 minutes a day—helps him process the messy parts of life and the mental traffic that shows up at night when sleep feels impossible. You’ll learn how creativity weaves through Brendan’s caregiving life—from thrifting books with his son to run an eBay bookstore, to adapting extended plays into child-friendly experiences, to writing a debut mystery-thriller inspired by his mother’s Alzheimer’s journey, and even transforming her former tiny home into a brick-and-mortar bookstore. We also dive into the importance of saying no, accessing California caregiver support, and finding meaningful ways to adapt when life doesn’t go as planned. Show notes with product and resource links: https://bit.ly/HHCPod223 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy o

Kathy Stein spent decades as the legal guardian and devoted advocate for her younger autistic brother, Ed. After Ed’s passing in 2024, Kathy and her siblings chose to donate his brain to scientific research—a powerful act of love that supports future breakthroughs in autism and neurodegenerative disorder understanding and leaves a powerful legacy in Ed’s memory. In this episode, Kathy shares what lifelong advocacy really looks like, how compartmentalizing your day can protect your energy, and why navigating state-by-state care systems can be so challenging for families. She also walks us through the brain donation process, her idea for a “compassion pill,” and the creative way she stays active through her beloved “big box walking” routine. Show notes with product and resource links: https://bit.ly/HHCPod222 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjournal For podcast sponsorship opportun

As the navigator for her daughter’s rare disease and a Yale-trained physician, Dr. Maggie Kang, uses her personal and professional training to guide other parents through the healthcare system, helping them turn health challenges into leadership. She is a passionate advocate, TEDx speaker, and contributor to HuffPost and Psychology Today.  In this episode, we explore how caregivers can reclaim agency for themselves and their loved ones, move beyond cycles of suffering or self-comfort, and take meaningful action—especially within the rare disease community. We also discuss the grief that accompanies losing our pre-caregiving life and how to intentionally create a vibrant, empowered “new normal.” And, you’ll learn why fresh parsley is one of Maggie’s go-to self-care strategies. Show notes with product and resource links: https://bit.ly/HHCPod221 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjo

Jeanette Yates spent decades caring for her mother — an experience that inspired her to write a book and host a podcast helping adult children caring for aging parents feel good, not guilty.  In this episode of the Happy Healthy Caregiver Podcast, Jeanette and Elizabeth explore two powerful emotions that every caregiver faces: guilt and grief. Together, they unpack how to let go of perfectionism, embrace self-compassion, and find peace in “good enough” caregiving. Show notes with product and resource links: https://bit.ly/HHCPod220 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjournal For podcast sponsorship opportunities contact Elizabeth: https://happyhealthycaregiver.com/contact-us/ The Happy Healthy Caregiver podcast is part of the Whole Care Network. Rate and Review the podcast: https://bit.ly/HHCPODREVIEW

When Eric Levitan saw his parents’ health decline from afar, he set out to better understand how to impact healthy aging for his family and others. He founded Vivo, a company dedicated to helping older adults stay active and independent. In this episode, we dive into the four cornerstones of healthy aging, fall prevention, and how to make healthy habits stick—plus accessible, fun ways to add strength training into daily life. Eric also shares insights on remote caregiving, the growing AgeTech initiative, talking with loved ones about senior living, and why challenging experiences can strengthen both the body and the mind. Show notes with product and resource links: https://bit.ly/HHCPod219 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjournal For podcast sponsorship opportunities contact Elizabeth: https://happyhealthycaregiver.com/contact-us/ The Happy Healthy Caregiver podcast is part of

Nancy Treaster, a retired software industry executive turned Certified Caregiving Consultant, co-founded The Caregiver’s Journey with longtime friend Sue Ryan after both personally faced the challenges of dementia caregiving for multiple family members. Nancy has supported her father through Parkinson’s, her father-in-law through Alzheimer’s, and her husband through Frontotemporal Dementia. Drawing on her professional background and personal experience, Nancy offers a compassionate yet practical approach that empowers family caregivers to face their caregiving journey with confidence, fewer surprises, and more effective solutions. In this episode, we talk about the difference between palliative care and hospice care—and why both are often underutilized. Nancy also shares insights on the stages of grief (including a unique concept called “drip grief”), her love of travel, the power of podcasting, and how caregivers can access an interactive roadmap filled with practical tools and resources to guide them on

Brian Stifel cared for his brother and continues to provide care and support for his mom. He is a corporate executive, husband, and proud father of three. In this episode of the Happy Healthy Caregiver podcast, we discuss real-life caregiver challenges, including dating while caregiving, the myth of work-life balance, online safety concerns, and finding joy in each day. Even on tough days, Brian says he can string together a few of these “hot dog moments!” Show notes with product and resource links: http://bit.ly/HHCPod217 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjournal For podcast sponsorship opportunities contact Elizabeth: https://happyhealthycaregiver.com/contact-us/ The Happy Healthy Caregiver podcast is part of the Whole Care Network. Rate and Review the podcast: https://bit.ly/HHCPODREVIEW

Dan Contreras is a U.S. Army veteran, proud husband, and devoted caregiver to his wife, Teresa. After years of service and leadership with DAV (Disabled American Veterans)—including his role as National Commander—Dan has become a strong advocate for both caregivers and care receivers. Like many military spouses and family members, Dan didn’t initially see himself as a “caregiver.” That changed when, as a DAV leader, he sought to better understand the DAV’s Caregiver Support Program by completing the onboarding process. Now, he’s on a mission to raise awareness and provide resources for the 70% of veterans who are caring for loved ones. In this episode of the Happy Healthy Caregiver podcast, Dan shares: The resources DAV offers to support veterans who are also caregiversHow his perspective on self-care has shifted as Teresa’s cancer journey has progressedThe creative outlets he and Teresa enjoy together, including Legos, crafts, and hobbies that bring them joyHow something as simple as a karaoke app hel

Kameron Browning is a resilient sandwich generation caregiver and single mom from Oklahoma who’s caring for five people besides herself. She’s navigating life between supporting her father, Jim, who lives with Alzheimer’s disease, and raising four children from toddler to teenager. Over the years, Kameron has worn many caregiving hats—remote caregiver, in-home caregiver, and support caregiver—while balancing work and family life. After experiencing caregiver burnout, she’s redefined “self-care” as simply giving her brain a chance to rest, letting go of people-pleasing, tuning out unsolicited advice, and leaning into advocacy, trust, and intuition for herself and those she loves. Show notes with product and resource links: http://bit.ly/HHCPod215 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjournal For podcast sponsorship opportunities contact Elizabeth: https://happyhealthycaregiver.com/contac

Even though P.K. Beville is considered an expert in psychology and gerontology, she still felt lost and overwhelmed as a dementia caregiver for her dad. P.K. is the founder of Second Wind Dreams, a pioneering nonprofit that fulfills dreams for older adults and champions dignity, hope, and joy in aging. She is the creator of the internationally acclaimed Virtual Dementia Tour®, a training tool that has helped millions better understand and care for those living with dementia. In 2023, she launched Empathic Transitions to support families during end-stage dementia and is currently certifying the first Dementia Doulas. In this episode of the Happy Healthy Caregiver podcast, we talk about why caring for a loved one in any setting is still tricky, how the phrase ‘I wish’ sparked an uplifting non-profit in the older adult space, where we can find sources for humor and joy, and why the end-of-life experience for those living with dementia is different.  Show notes with product and resource links: https://bit.

Our guest is Barry J. Jacobs — he’s a clinical psychologist and author based just outside of Philly who has a real heart for supporting family caregivers. And that passion is personal. Barry’s caregiving journey started young — when he was just 14, his dad was diagnosed with brain cancer and sadly passed away the following year. That experience shaped the direction of his life and career. Later, from 2010 to 2017, Barry stepped into the caregiving role again — this time for his stepfather, who had Alzheimer’s, and his mom, who was living with vascular dementia. He truly understands the emotional rollercoaster that comes with caregiving and has spent his career helping others navigate it with more support and less guilt.  In this episode, we discuss two of his books, co-written with his wife, one on love and relationships after 50, and one focused on addressing common family caregiving questions. We delve deeper into the topics of guilt, family dynamics, and self-care. Barry has much personal and profession

Meet Lisa Musselman, a 2025 Elizabeth Dole Foundation Fellow, military caregiver, and passionate advocate for equitable care for veterans and their families. Lisa talks about her caregiving journey supporting her husband Andy, a pre-9/11 Air Force veteran living with ALS, while raising a family and trying to stay afloat herself. Lisa shares the emotional and physical toll of those early years—missing milestones with her children, struggling to find respite, and putting her own health last. On the brink of burnout, everything changed when skilled nursing entered the home. This support allowed her to rebuild strength through physical therapy, prioritize mental wellness with therapy, and make space for joy through family vacations and visits with friends. What makes Lisa’s story especially powerful is how she turned adversity into a platform for advocacy. Motivated by a friend’s early encouragement that she would “become a voice” for others impacted by ALS, Lisa now champions policy and support changes for

Katie Prentiss is a mother of four, a former professional photographer, and a current filmmaker. When her mother was diagnosed with frontotemporal dementia (FTD), Katie stepped into the role of primary caregiver, balancing her family, business, and her mom’s care. This life-changing experience opened her eyes to the preciousness of life, motivating her to make a bold midlife career pivot into acting and producing. In this episode, Katie shares details about her latest full-length feature film, which she describes as a heartfelt love letter to family caregivers. She shares about how caregiving shaped her personal and professional journey, and how she found acceptance, growth, and healing through what she calls the law of contraction and expansion. Tune in to discover how this powerful concept can help caregivers navigate every stage of the caregiving journey with resilience, purpose, and moxie. Show notes with product and resource links: https://bit.ly/HHCPod211 Receive the podcast in your email here:

J Smiles has been a caregiver to her mom living with Alzheimer’s and NPH for over 13 years—an unexpected journey that began after her father’s sudden passing. Once a globe-trotting consultant who could barely keep a plant alive, J found herself overwhelmed and facing serious health issues just 18 months into caregiving. A wake-up call from her doctor led her to explore self-care through stand-up comedy. In this episode, J shares how comedy became her lifeline, helping her cope, advocate for caregivers, and bring joy to others walking a similar path. Show notes with product and resource links: https://bit.ly/HHCPod210 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjournal For podcast sponsorship opportunities contact Elizabeth: https://happyhealthycaregiver.com/contact-us/ The Happy Healthy Caregiver podcast is part of the Whole Care Network. Rate and Review the podcast: https://bit.ly/HHCPO

Patty Webster is no stranger to caregiving—she helped care for her mom at the end of her life and now supports her sister, who’s the primary caregiver for their dad. In this episode of the Happy Healthy Caregiver podcast, Patty shares how her personal experience fuels her passion for The Conversation Project, a movement helping families talk openly about end-of-life wishes. We chat about why these conversations matter, how to start them, and how they can bring families closer. It's real, relatable, and something every caregiver should hear. We also talk about how to not be a ‘swooper’ as a remote support caregiver, why it’s important to infuse fun in caregiving visits, and why grace is essential for all members of the care team. Show notes with product and resource links: https://bit.ly/HHCPod209 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCjournal For podcast sponsorship opportunities contact

Meet Scott Lien, a working family caregiver and member of the sandwich generation, who navigated the loss of four parents and in-laws over twelve years. His caregiving journey, combined with his extensive tech background, inspired him to co-found GrandPad, a user-friendly platform designed to keep seniors connected and engaged. In this episode of the Happy Healthy Caregiver podcast, Scott and I dive into practical ways families and society can combat senior isolation and loneliness. We also explore the unexpected benefits—such as reducing elder fraud and financial scams—and how fostering meaningful connections can help us all live without regrets. Plus, Scott shares wisdom from the “super seniors” he works with and reveals his secrets to ensuring joy in every day. And…stay tuned for how you can take advantage of an exclusive GrandPad offer for the HHC Community!

Imagine stepping into a marriage knowing you're immediately going to become a full-time caregiver. That was Hope Cross's reality when her husband, Steve, was diagnosed with ALS while they were dating. For nine years, she cared for him up until his passing, and it was a journey filled with love, challenges, and deep emotions. Hope has openly shared the raw and unfiltered sides of caregiving, offering a rare glimpse into the realities many face, but sometimes don't discuss. In this episode, Hope shares how she navigated life after loss, rediscovering herself and ultimately launching a therapy practice focusing on family caregiving, trauma, PTSD, grief and anxiety. We also explore the powerful role of art, nature, friendships, writing, and even our own noses in the healing process. Show notes with product and resource links: https://bit.ly/HHCPod207 Receive the podcast in your email here: http://bit.ly/2G4qvBv Order a copy of Elizabeth's book Just for You: a Daily Self Care Journal: http://bit.ly/HHCj