All Home Care Matters

All Home Care Matters is an informative podcast and YouTube show that helps viewers and listeners learn about resources, tips, & discussion on all things home care.

All Home Care Matters is a education podcast hosted by Unknown Host, with 100 episodes on record and a Required Pod Score of 80. PitchCentric scores this show on Booking Probability, Listen Score, and live audience signals refreshed every 24 hours.

Unknown Host hosts All Home Care Matters, a education show with 100 episodes published.

Our AI reads these to draft pitches. Use them as grounding for a pitch that cites a real guest and a specific topic.

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  Episode #436

  Explore the Mackenzie Meet Alzheimer's Community

  Aug 19, 202618 min

  All Home Care Matters and our host, Lance A. Slatton were honored to welcome Alder Allensworth as guest to the show to share the Mackenzie Meets Alzheimer's Community. About Alder Allensworth, Co-Founder of Mackenzie Meets Alzheimer's: Alder Allensworth, MM, RN, is a registered nurse and retired hospice counselor who supported families caring for loved ones with dementia at the end of life. Her professional background spans working with both children and older adults, including those living with Alzheimer's disease. The inspiration for this project grew from Alder's personal experience witnessing her mother, who had Alzheimer's, connect meaningfully with her grandchildren—Alder's nieces and nephews. This powerful family experience, combined with her clinical work, deepened her commitment to helping families navigate dementia with compassion, creativity, and connection. Alder is also an accomplished writer, having published several articles in professional journals and books. As a speaker and presenter in the field of disabilities, she has shared her insights on local, national, and international stages. Her advocacy and dedication to promoting quality of life for people with disabilities have been featured on CNN, as well as in international media and local news outlets. About Mackenzie Meets Alzheimer's: The Mackenzie Meets Alzheimer's Program (MMAP) is a family-centered multimedia educational program created to help children, parents, caregivers, educators, and healthcare professionals better understand and navigate Alzheimer's disease together. Designed especially for families in the "sandwich generation," MMAP provides practical guidance, age-appropriate education, and meaningful activities that help children stay connected with a loved one living with Alzheimer's—from diagnosis through the severe stage of the disease. At the heart of MMAP is the Mackenzie Meets Alzheimer's Awareness Program (MMAAP), a 5-video educational series that explains the different stages of Alzheimer's while also providing guidance for adults who are simultaneously raising children and caring for an aging loved one. The program includes: • A 5-video educational series covering the stages of Alzheimer's • Guidance for parents and caregivers helping children understand the disease • Simple, meaningful activities children can do with their loved one • A quick-reference guide and video transcripts • Accessible audio and visual resources for different learning needs • An online community component offering additional connection and support One of the most important goals of MMAAP is helping children understand Alzheimer's in ways that are appropriate for their age—while showing them that even as the disease progresses, there are still opportunities to connect, interact, and create meaningful moments with the person they love. The program is complemented by the Mackenzie Meets Alzheimer's Disease Picture Book, a gentle, child-friendly introduction to Alzheimer's that follows a young girl as she learns to understand and remain connected with her grandmother throughout the progression of the disease. The book also includes a QR code providing access to a free Story Song download. The lyrics of the song are the text of the book, creating an engaging and memorable learning experience for young children, early readers, and families. MMAP can also serve as a valuable educational resource for Adult Day Centers and Memory Care Communities. The ready-to-use program gives organizations a structured way to educate and support families, proactively answer common questions, and provide families with resources they can return to throughout their caregiving journey—allowing staff to devote more time to care, engagement, and meaningful connection. Ultimately, the Mackenzie Meets Alzheimer's Program goes beyond explaining the disease. It helps families understand what is happening, gives children a meaningful role in the caregiving journey, and provides families with tools to preserve relationships, create positive memories, and remain connected throughout Alzheimer's and other dementias.

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  Episode #435

  Discover MemoryBoard with CEO & Co-Founder Tyler Zanini

  Aug 18, 202623 min

  All Home Care Matters and our host, Lance A. Slatton were honored to welcome the CEO & Co-Founder of Memoryboard Tyler Zanini as guest to the show. About Memoryboard: Memoryboard is a digital display and mobile app designed to help families stay connected with loved ones experiencing memory loss, dementia, Alzheimer's, or other cognitive changes. Family members and caregivers use the Memoryboard app to remotely send reminders, messages, photos, daily updates, appointments, and words of encouragement directly to a dedicated screen in their loved one's home. The person receiving the messages does not need to download an app, remember a password, navigate menus, or learn new technology. Messages simply appear on the screen in clear, easy-to-read text. Memoryboard was created after its founders experienced the challenges of memory loss within their own family. They wanted to create something that could help families provide structure and reassurance without making technology another source of confusion. Today, Memoryboard supports more than 20,000 families. Families use it to help loved ones stay oriented throughout the day, remember appointments and routines, maintain independence, and feel connected to family members who may live nearby or hundreds of miles away. Memoryboard is designed to support the human side of caregiving rather than replace it. The goal is to give caregivers a simple way to communicate, provide reassurance, and stay involved while giving their loved ones greater confidence and independence in their daily routines. About Tyler Zanini, CEO & Co-Founder of Memoryboard: Tyler Zanini is the co-founder of Memoryboard, a caregiving technology company focused on helping families support loved ones experiencing memory loss, dementia, and other age-related cognitive changes. With a background in healthcare innovation and entrepreneurship, Tyler created Memoryboard alongside his father-in-law, David, after their own family experienced the challenges of caring for loved ones with memory loss. Seeing how difficult it could be to stay connected, communicate changing plans, and provide reassurance from a distance inspired them to build a simpler solution for families and caregivers

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  Episode #434

  Discover Nana's Books Foundation

  Aug 13, 202641 min

  All Home Care Matters and our host, Lance A. Slatton were honored to welcome Dr. Dennis Dulniak, Mark Dulniak, and Craig Dulniak of Nana's Books Foundation for a meaningful conversation about Alzheimer's disease, family caregiving, children's literacy, empathy, and the lasting legacy of Nancy Dulniak. About Nana's Books Foundation: Nana's Books Foundation is a nonprofit 501(c)(3) organization dedicated to promoting literacy, empathy, and awareness through the power of books. The Foundation was created in honor of Nancy Dulniak, a lifelong librarian who passed away from Early-Onset Alzheimer's disease at age 69. Nancy believed books could open minds, inspire compassion, and help children better understand the world around them. Founded in 2020, Nana's Books Foundation provides age- and grade-appropriate books and educational resources focused on Alzheimer's disease, dementia, disabilities, caregiving, empathy, resilience, and acceptance. Through partnerships with schools, public libraries, and community organizations, the Foundation helps families begin important conversations that can otherwise be difficult to navigate. Special emphasis is placed on supporting Title I schools and underserved communities. Since its founding, Nana's Books Foundation has expanded across 16 states and the District of Columbia, distributing more than 26,000 books to nearly 12,000 students and classrooms, as well as 29 school libraries and 20 public libraries. At its heart, the Foundation carries forward Nancy's lifelong commitment to children, education, libraries, and compassion. About Dr. Dennis Dulniak: Dr. Dennis Dulniak is Founder and President of Nana's Books Foundation. After a 40-year career in higher education, including serving as University Registrar at the University of Central Florida and as a Vice President at Parchment, Dennis became a caregiver when Nancy was diagnosed with Early-Onset Alzheimer's disease in 2014. For more than seven years, Dennis served as Nancy's care partner, gaining firsthand insight into dementia caregiving, changing relationships, communication, and advocacy. Following Nancy's passing, he dedicated his retirement to honoring her through Nana's Books Foundation. Dennis is also a Co-Founder of Central Florida Dementia-Friendly Dining, a facilitator and resource for a large men's caregiver support group, and a member of the Central Florida Dementia Care and Cure Initiative. Today, he shares his family's journey to help caregivers, children, and communities better understand dementia. About Mark Dulniak: Mark Dulniak, the eldest son of Nancy and Dennis Dulniak, is Co-Founder and Treasurer of Nana's Books Foundation. The Foundation's roots began in 2018 when Mark started donating books to Knoxville-area classrooms in honor of his mother. Students wrote thank-you notes to Nancy, bringing her tremendous joy during her journey with Early-Onset Alzheimer's disease. That tradition eventually grew into Nana's Books Foundation, ensuring Nancy's lifelong love of books and learning would continue to impact future generations. Mark now helps expand the organization's reach to Title I schools, school libraries, public libraries, students, and families. He also advocates for families to begin age-appropriate conversations with children about dementia, using books as a compassionate way to help them understand what is happening to someone they love. About Craig Dulniak: Craig Dulniak, the youngest son of Nancy and Dennis Dulniak, serves as Secretary Emeritus of Nana's Books Foundation and lives with his wife and son in Philadelphia. During one of Nancy's final visits to Philadelphia, Craig took her to his local public library to sign her grandson up for his first library card at just one year old—a fitting reflection of Nancy's lifelong connection to books and libraries. Craig hopes Nana's Books Foundation will help children better understand dementia, Alzheimer's disease, disabilities, and caregiving by increasing access to books addressing topics often underrepresented in children's literature. Through the Foundation, the Dulniak family continues Nancy's legacy through every book shared and every conversation inspired about kindness, empathy, understanding, and inclusion.

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  Episode #433

  Jacqueline Larsen 2025 Dole Caregiver Fellow North Carolina

  Aug 11, 202627 min

  All Home Care Matters and our host, Lance A. Slatton were honored to welcome Jacqueline Larsen as guest to the show. About Jacqueline Larsen, 2025 Dole Caregiver Fellow, North Carolina: Jacqueline Larsen cares for her husband, Jeffery (Jeff) Larsen, a retired Air Force pararescueman (PJ) who served for 18 years and deployed 20 times. From a young age, Jeff knew he wanted to become a PJ and serve his country. After graduating high school in 2010, he enlisted in the Air Force, completed the rigorous training, and earned his place in the elite unit. Over the years, he sustained multiple injuries, including traumatic brain injuries (TBIs), post-traumatic stress disorder (PTSD), carpal tunnel in both hands, shoulder pain, and herniated discs, which ultimately led to his medical retirement. Jacqueline met Jeff in early 2020 through a dating app—just as she was about to give up on dating to focus on fixing up her newly purchased farm. Jeff had only recently joined the app as a New Year's resolution, and the two instantly connected. Their relationship quickly deepened, and by July 2020, they had eloped, with plans to celebrate with friends and family later that summer. However, on the eve of their planned celebration, tragedy struck when he fell when trying to move bales of hay on his own, leaving him quadriplegic. At the time, Jacqueline was eight weeks pregnant with their second child and navigating the overwhelming reality of Jeff's hospitalization during the height of the COVID-19 pandemic. Jeff spent months in hospitals and rehabilitation centers, including the Shepherd Center in Atlanta and the VA in Augusta, before finally returning home just before Christmas. Since then, Jacqueline has dedicated herself to his care, balancing physical and occupational therapy sessions, pain management treatments, and adaptive rehabilitation activities that help Jeff regain independence. He is working toward riding a hand bike, using adaptive equipment for long-range shooting, and assisting with farm chores from his wheelchair. Their family, which includes their two sons, 11-year-old Lucas and 4-year-old Jackson, have adapted to a new normal—one filled with resilience, adjustments, and an emphasis on kindness and understanding. They have learned that while their family is not able to do all the things other families can do, they now create quality time where they can celebrate with new traditions. The boys have learned to be kind, courteous, and helpful to all people. Living in rural North Carolina, just outside Fort Bragg, Jacqueline faced challenges securing reliable respite care due to the limitations of the VA Caregiver Support Program and Tricare's lack of in-network providers in their county. Her experience has fueled her advocacy for systemic change to better support veteran caregivers, particularly those who have had to leave successful careers due to their caregiving responsibilities. She is passionate about raising awareness of the financial strain that unpaid caregiving places on families, including the burden of student loans for caregivers who can no longer pursue their careers. Currently, Jacqueline is working to turn their hobby farm into a sustainable business that will provide employment opportunities for both her and Jeff. About the Dole Caregiver Fellowship: The Elizabeth Dole Foundation Dole Caregiver Fellows Program is a selective leadership and advocacy fellowship for individuals who provide care and support to wounded, ill, or injured service members and veterans of all generations. Participants—spouses, parents, adult children, friends, or other loved ones—are chosen from across the United States to represent caregivers across their communities and nationally. During a two-year term, Fellows receive training, build networks, and work with policymakers, organizations, and the public to raise awareness of the value of caregivers and the challenges they face. They advocate for improved support and resources and advise the Foundation on programs and policy priorities affecting military and veteran families. In addition, by sharing their stories and experiences, they help other caregivers recognize themselves as caregivers, connect to resources, and feel welcomed in a community where every caregiving journey is valued.

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  Episode #31

  Conscious Caregiving with L & L "Covering Care Costs"

  Aug 10, 202622 min

  Conscious Caregiving with L & L is "Tackling the Tough Conversations." The topic of this episode is "Covering Care Costs" 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. About Lance A. Slatton - known as "The Senior Care Influencer"": Known as "The Senior Care Influencer" Lance is a Writer, Author, Influencer, and Healthcare professional with over 20 years in the healthcare industry. Lance A. Slatton is a senior case manager at Enriched Life Home Care Services in Livonia, MI. He is also host of the award winning podcast & YouTube channel All Home Care Matters and Co-Host of Conscious Caregiving with L & L with Lori La Bey along with The Care Advocates and The Caregiver's Journal. Lance is also the new President of AlzAuthors. Lance's book, "The All Home Care Matters Official Family Caregivers' Guide" was the recent recipient of the 2024 International Impact Book Awards. To learn more about Lance A. Slatton and Lori La Bey you can visit their websites.

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