Podcast appearances and mentions of sue ryan

Are you feeling overwhelmed trying to care for aging parents while raising children? Do you find yourself stretched thin between different generations, each with their own unique needs? My name is Sue Ryan. As a caregiver for loved ones with Alzheimer's and other types of dementia, I understand the unique challenges faced by those in the sandwich generations. I recently spoke with Christy Byrne Yates, a licensed educational psychologist and author of “Building a Legacy of Love: Thriving in the Sandwich Generation.” Christy has personally navigated the challenges of caring for aging parents while raising her own children, and she brings both professional expertise and lived experience to help families thrive during this demanding season of life. Connect with us and share your tips: Website: https://thecaregiversjourney.org/Donate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/thecaregiversjourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.org, nancy@thecaregiversjourney.org Full Show Notes Additional Resources Mentioned Chirstyyates.com - https://www.christyyates.com/Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Tip 1: C — Choose Your Role as a Caregiver The first step in successfully navigating the sandwich generation is making a conscious choice to embrace your caregiving role. Many people say “I didn't choose this.” or “I had no choice.” We always have a choice. Even not making a choice is still a choice. Tip 2: A — Address the ‘Elephants' in the Room Successful sandwich generation caregiving requires having difficult conversations early and often. These are the ‘elephants' dancing in every family room that everyone sees — but no one wants to discuss. Tip 3: R — Recharge Through Ruthless Self-Care Recharging takes on critical importance when you're caring for multiple generations. Self-care isn't selfish — it's essential for everyone you're caring for. Tip 4: E — Enlist Your Support Team You're not meant to journey alone, and this is especially true for sandwich generation caregivers who face multiple competing demands. Building a comprehensive support team is essential for sustainable caregiving. Tip 5: S — Surrender Control and Embrace Grace Perhaps the most challenging aspect of sandwich generation caregiving is accepting that you cannot control everything, even though you desperately want to. If everyone could just do things your way, life would be so much easier — but that's not reality. Read More in This Blog here

Do you know what you need to do immediately after your loved one passes? Many caregivers don't. Are you worried about missing important tasks or feeling overwhelmed by the sheer volume of administrative, financial, and legal responsibilities? We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've navigated the challenging process of handling death-related responsibilities firsthand. Between us, we've experienced the loss of multiple loved ones and learned valuable lessons about what needs to be done and when. Connect with us and share your tips: Website: https://thecaregiversjourney.org/ Donate: https://give.cornerstone.cc/thecaregiversjourney Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/thecaregiversjourneys/ Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/ Email: sue@thecaregiversjourney.org, nancy@thecaregiversjourney.org Full Show Notes If you are following along with our 20 step Navigating Dementia Caregiving Roadmap guide this is part of Step 20. This is the first guide listed on our guides page. There are many things that can be done ahead of time. We covered these in podcast episode 30 - End of life preplanning and blog as well as in the matching worksheet you can find on our website in the guides section called ‘End of Life Service Worksheet'. Click here to get to the Guides page, scroll down to find the sheet. Tip 1: Prioritize these things immediately after death1. Tip 2: Move to this list within the first few days and weeks Tip 3: Over the next few weeks and months - manage their estate Tip 4: Focus on the things to prioritize once the estate has been closed

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 their caregiving journey. Show notes with product and resource links: http://bit.ly/HHCPod218 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

Have you noticed yourself feeling sad when your loved one can't remember their phone number? Do you find yourself withdrawing from friends or losing patience more easily? These feelings might be grief—and you may not even realize it's happening. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned that grief doesn't only come after our loved one passes away. It's present throughout our entire caregiving journey, from the moment of diagnosis through each individual change along the way. The good news is that understanding grief—recognizing it, honoring it, and learning to move through it without getting stuck—can transform how we experience our caregiving journey. Today we're sharing six essential tips to help you navigate grief with grace and compassion. Connect with us and share your tips: Website: https://thecaregiversjourney.org/Donate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/thecaregiversjourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.org, nancy@thecaregiversjourney.org Full Show Notes https://thecaregiversjourney.org/47-navigating-grief-throughout-caregiving-six-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned Guide: Navigating Dementia Caregiving Roadmap: https://thecaregiversjourney.org/guides/Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Read More in This Blog here

Are you struggling to pull your family together to create a working support system for someone living with dementia? Do you find family members disagreeing on what needs to be done or how to help? You're not alone, and there's a path forward. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned that transforming family dynamics into effective teamwork is one of the most challenging—yet most rewarding—aspects of the caregiving journey. In this episode, we spoke with Dr. Barry Jacobs, a clinical psychologist and family therapist who brings both professional expertise and personal caregiving experience to this conversation. Barry cared for his mother with vascular dementia and his stepfather with Alzheimer's disease for seven years, and he co-authored the AARP Caregiver Answer Book with his wife, psychologist Julia Mayer. This content aligns with Step 8 of our Navigating Dementia Caregiving Roadmap: Start Planning for the Next Stage of Care, particularly when building your personal support network of family and friends. Connect with us and share your tips: Website: https://thecaregiversjourney.org/Donate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/thecaregiversjourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.org, nancy@thecaregiversjourney.org Full Show Notes https://thecaregiversjourney.org/50-family-dynamics-in-caregiving-four-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned Barry's website www.caregiveranswerbook.comBuy the Caregiver Answer Book on Amazon https://amzn.to/4i9V9ZLNavigating Dementia Caregiving Roadmap guide https://thecaregiversjourney.org/guides/#guidesSupport the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Transforming your family into an effective caregiving team isn't easy. It's worth the effort — not just for your loved one with dementia — but for every member of your family. These four tips provide a framework: Create consensus (everyone on the same page).Define an ongoing format for decision making (regular meetings with clear rhythm).Build a family caregiving plan (who does what and when).Plan to deal with conflict (don't let disagreements become disrespectful).

Have you completed the first six essential steps of the comprehensive 20-step caregiving journey roadmap guide Navigating Dementia Caregiving: Your Resource Roadmap for Every Stage? Are ready to take on more? Do you find yourself wanting to learn faster and more easily than trying to figure everything out on your own? If you answered ‘Yes', you're in the right place for the next phase of the dementia “In the Beginning” journey. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned that building knowledge, and preparing for progression, are crucial for sustainable caregiving. We recently talked with Jenny Gay, licensed clinical social worker with Emory Integrated Memory Care, about our comprehensive 20-step caregiving journey roadmap guide: Navigating Dementia Caregiving Roadmap. In this podcast, we're sharing steps 7–10. Connect with us and share your tips: Website: https://thecaregiversjourney.org/Donate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/thecaregiversjourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.org, nancy@thecaregiversjourney.org Full Show Notes https://thecaregiversjourney.org/44-navigating-dementia-caregiving-roadmap-in-the-beginning-steps-7-10-alzheimers-and-other-dementias/ Additional Resources Mentioned Navigating Dementia Caregiving Roadmap Guide In the Beginning - continued Next Steps - You are ready for more  7. Continue your education: Take the Savvy Caregiver course in person or online.Read this magazine:  Mayo Clinic Living with dementia: A guide to caregiving and support. Find and take a virtual dementia tour near you. In the United States, in your search engine, type ‘virtual dementia tour' + 'your state'. For example: ‘virtual dementia tour Florida' or, outside the US, replace your state with your country. 8. Start planning for the next stage of care. Build your personal support network:21 minute TCJ podcast: 40. Create Your Personal Support NetworkTCJ blog: 40. Create Your Personal Support Network.Find and try a memory cafe (Caregivers and care receivers go together).Investigate dementia day centers (also known as adult day centers that include dementia care programs) for your care receiver. Community resource finder: Select Community Services and choose Adult Day Centers for your search.Ask your loved one's medical team for a home safety assessment.The goal is to have someone evaluate your home for safety and dementia care needs. This is usually available through palliative care, GUIDE program, or an order from a physician.You can get a free assessment from social services with this order, or you can pay for an independent assessment from a private organization. 9. Investigate your local government community support:  In the US, contact your local Area Agency on Aging. Search for yours at Eldercare.acl.gov or call 1-800-677-1116.Call and set up a screening for eligibility:They will point you to any free government services where you are eligible. Be sure to find out if you are eligible to get paid to be a caregiver.  10. Evaluate driving risks.  Some US states have specific requirements for individuals with dementia to report their diagnosis and potentially undergo driving evaluations. Listen to this podcast or read this blog:21 minute TCJ podcast: 5. Taking Away the KeysTCJ blog: 5. Taking Away the Keys.  Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways The Three Stages of the Dementia Caregiving Journey 1. In the Beginning - Your loved one receives a diagnosis.  2. The Messy Middle - You begin asserting control; this is when it gets messy! 3. Later On - You are managing all aspects of their care. 

Are you feeling overwhelmed by the complexity of dementia care? Do you find yourself wishing you had more support navigating medical decisions and planning for the future? You're not alone - and there's specialized help available that many caregivers don't fully understand. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we both wish we had understood what palliative care is and how to leverage it earlier in our journeys. Unfortunately, when palliative care was first explained to us, it was explained incorrectly, and neither of us took advantage of all the great things palliative care has to offer. We recently spoke with Dawn Kolderman, a registered nurse and Senior Clinical Director of Palliative Care Services at Avow, who has more than 30 years of nursing experience with the last 20 focused on palliative and hospice care. Dawn shared invaluable insights about palliative care that we wish we had known sooner. Connect with us and share your tips: Website: https://thecaregiversjourney.org/Donate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/thecaregiversjourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.org, nancy@thecaregiversjourney.org Full Show Notes Additional Resources Mentioned Avow Palliative Care LinkSupport the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Tip 1: Understand What Palliative Care Actually Is The first step is clearing up common misconceptions about palliative care.  Palliative care is a holistic approach to a life-limiting disease. This includes dementia — which is indeed a life-limiting disease.  The key difference between palliative care and hospice care: Palliative care patients are at the beginning of their journey and are still seeking aggressive, curative treatment while seeing all their providers and specialistsHospice care patients are generally at the end of their journey, no longer seeking aggressive treatment, and focusing on comfort care. Palliative care is an additional supportive layer of care that works collaboratively with all your existing medical providers. Most importantly, palliative care focuses heavily on the caregiver. Tip 2: Call Palliative Care In — Here's How Many caregivers don't realize how accessible palliative care is or when to call it in. The answer is simple: the earlier, the better. Tip 3: Understand the Goals of Palliative Care Palliative care has specific, comprehensive goals that address both immediate and long-term needs. Primary goals include: Relieving physical symptoms first Supporting the caregiver and family Education and collaboration Advanced care planning (ACP). This crucial component involves sitting down with the patient, caregiver, and family to discuss important decisions while your loved one can still participate in these conversations. Tip 4: What Else You Need to Know About Palliative Care There are several important aspects of palliative care that many people don't realize. Your loved one won't look sick. The goal is to help them live their life fully. Early intervention builds stronger relationships. The nurse navigator's role is specifically to connect you with community resources you might not know about.  Read More in This Blog here

Have you ever thought, "I wish I knew how to have a constructive conversation with my manager about how to align my work responsibilities and my caregiving responsibilities?" Today we're sharing strategies to help working family caregivers thrive at both work and at home. We're sharing four tips. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we understand how caregivers often feel torn between their responsibilities at home and their professional responsibilities, which they're trying desperately to fulfill, often without support. Connect with us and share your tips: Website: https://thecaregiversjourney.org/Donate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.org, nancy@thecaregiversjourney.org Full Show Notes https://thecaregiversjourney.org/41-aligning-work-and-caregiving-responsibilities-four-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Tip 1: Self-Identify and Strategically Disclose Assess your company culture firstExamples of supportive company policiesDisclose early in the journeyPlan your conversationFrame it collaborativelyDocument everything Tip 2: Build Flexibility Explore flexibility options in your organizationPropose pilot arrangementsConsider team involvementCreate backup plansLeverage technologyConsider career flexibility Tip 3: Leverage Your Resources Connect with colleagues who are also caregiversExplore Employee Assistance Programs (EAPs)Look for community resourcesTake things off your plate Tip 4: Plan for the Unplanned Understand your benefits and protectionsCreate a caregiving budgetExplore financial resourcesBuild an emergency fundPrepare for career transitions Read More in This Blog https://sueryansolutions.medium.com/40-building-your-personal-caregiving-support-network-9f9639e9ae87

Have you ever felt overwhelmed because you don't know what information you need, can't find reliable sources, or feel frustrated by too much conflicting advice? We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned having a step-by-step roadmap is crucial for navigating the beginning of your caregiving journey. We recently talked with Jenny Gay, licensed clinical social worker with Emory Integrated Memory Care, about the comprehensive 20-step caregiving journey roadmap guide Navigating Dementia Caregiving: Your Resource Roadmap for Every Stage. This podcast is bringing the first six essential steps to take immediately after diagnosis. Connect with us and share your tips: Donate: https://give.cornerstone.cc/thecaregiversjourney Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/thecaregiversjourneys/ Full Show Notes Here In the Beginning - First Steps - Right after the diagnosis 1. Choose a palliative care organization. This will likely also serve as your hospice organization later in your journey. In your search engine, type ‘Palliative Care' + ‘the name of your country' or, in the US ‘the name of your state'. Schedule an initial consultation with more than one so you can compare. Educate yourself on what palliative care is: 27 minute The Caregiver's Journey (TCJ) podcast: 42. When To Call In Palliative Care 2. Create an Advance Care Plan. Get your legal documents in order and do some initial end of life preplanning with your loved ones input: Contact your attorney or an elder law attorney NAELA.org. Listen to this podcast or read this blog on elder law attorneys: 32 minute TCJ podcast: 31. Elder Law Attorneys Alzheimer's Association legal documents overview: Leverage this End of Life Planning Worksheet. 3. Understand the financial situation. Work with a financial advisor - especially those who focus on seniors. Elder law attorneys can also advise in this area. Alzheimer's Association resources overview of financial planning 4. Find support groups. First and foremost for you. If possible, find a support group you can attend in person: The Alzheimer's Association support group finder has support groups for a variety of types of dementia. If your loved one is interested a support group: Dementia minds has online groups for people living with dementia. Many local senior centers have support groups for your loved one to increase socialization: In the US, go to your ‘countyname'.gov website and search for a senior center. The Alzheimer's Association 24/7 helpline in the US: 1.800.272.3900. 5. Educate yourself on early caregiving journey topics. Listen to these two podcasts or read these two blogs. Memory Loss: 29 minute TCJ podcast: 2. Memory Loss Communication: 20 minute TCJ podcast: 3. Communication – in the Beginning 6. Investigate the US Medicare GUIDE program. Listen to this podcast or read this blog: 23 minute TCJ podcast: 39. Is the Medicare GUIDE program for you Understand if your loved one may be eligible: https://www.cms.gov/priorities/innovation/guide/faqs#ben-cgs. If you think you might be eligible, find a US Medicare GUIDE program provider near you. There may be several who cover your zip code so explore options. Go here to find a GUIDE program: Enter your state. Under models select ‘Guiding an Improved Dementia Experience (GUIDE) Model'. Click ‘Display selected'. You can use the plus and minus signs in the upper right corner to zoom in closer to your area. When you find the location you want, click on the blue dot and detailed contact information will show. The Three Stages of the Dementia Caregiving Journey 1. In the Beginning - Your loved one receives a diagnosis. 2. The Messy Middle - You begin asserting control; this is when it gets messy! 3. Later On - You are managing all aspects of their care. Full blog here

“In the marathon that is caregiving, the difference between exhaustion and endurance isn't willpower, it's the strength of the support network we build around us.” Sue Ryan Are you feeling overwhelmed by the responsibilities of caregiving? Do you find yourself thinking, “I don't have time to get everything done.” or “I should be able to do this myself.”? You're not alone, and there's a better way forward. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned building a strong personal support network is crucial for sustainable caregiving. Studies show that dementia family caregivers face overwhelming emotional challenges. Connect with us and share your tips: Website: https://www.thecaregiversjourney.comDonate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Full Show Notes: https://thecaregiversjourney.org/40-create-your-personal-support-network-five-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned 27. The Realities of Caregiver Self-Care https://thecaregiversjourney.com/the-realities-of-caregiver-self-care-four-essential-tips-alzheimers-and-other-dementias/32. Navigating the Caregiver Hiring Process https://thecaregiversjourney.com/32-navigating-the-caregiver-hiring-process-five-essential-tips-alzheimers-and-other-dementias/Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Tip 1: Assess Your Needs and Make a List Ask yourself: Do I have time to get everything done that needs to be done?Am I physically strong enough to handle all caregiving tasks?Do I find myself losing patience or empathy?Is my loved one struggling with activities of daily living that I can't manage alone? If you answered yes to any of these questions, it's time to ask for help.  Tip 2: Create a List of Who Can Help and What They Can Do Think about all the people who have offered to help or who might be willing to help. Map your list of potential helpers to your list of needs. If multiple people can help with a particular task, list them all—it's better not to rely on just one person. Tip 3: How to Effectively Ask for Help Recognize that some people want to help your care receiver, while others want to help you. Be specific and direct about what you need and why you need it.Remember that the people on your list have likely already offered to help or have shown willingness to support you.Adapt your approach based on the person you're asking.  Tip 4: When People Offer to Help, Say "Yes" Avoid these common traps: "It would be easier just to do it myself.""No one can care for my loved one like I can.""I should be able to do this myself.""I feel guilty—they have their own busy lives." Tip 5: Maintain Your Support Network and Adjust as Things Change Encouraging open communication with your support team membersBeing proactive about finding new support team members when neededChecking in regularly with your helpers to keep them informed and engagedWatching for signs of burnout in your helpers—they may experience caregiver fatigue tooAddressing inflection points in your loved one's care needs Read More in This Blog https://sueryansolutions.medium.com/36-building-your-personal-caregiving-support-network-9f9639e9ae87

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 “grip 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 their caregiving journey. Show notes with product and resource links: http://bit.ly/HHCPod218 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

This morning's service is led by Sue Ryan, one of our elders. Sue speaks on the subject 'The Holy Spirit'. The scriptures read in this service were taken from Genesis 1:1-2, John 14:16-17, John 16: 16-24 [NIV-UK translation].

Our worship service is led by one of our elders, Sue Smith with the address given by another or our elders, Sue Ryan. The address is entitled 'Secrets of the Holy Spirit', and the scripture read beforehand is from John 16 : 5 - 15.

Sue Ryan came to rowing through her journey as a breast cancer survivor, and she's embraced the sport as both a challenge and a source of community. We talk about how the sport helped her move past childhood trauma, how it has shaped her cancer recovery, and the ways she's found strength on and off the water as a member of Whitmarsh Boat Club, WeCanRow Philadelphia, and the Survivor Rowing Network.   QUICK LOOK 00:00 - Episode intro and welcome 01:59 - Rowing Week 03:58 - The Huddle 04:20 - Hot Seat Q&A 07:28 - Despite being “horribly uncoordinated,” Sue got hooked when she learned to row with WeCanRow Philadelphia 09:45 - Trauma in Sue's youth led to disassociation from her body but rowing and therapy have helped her reconnect 13:15 - Social network as key to cancer recovery, and finding a welcoming club culture at Whitemarsh Boat Club 17:49 - Recovery: strength training, lymphedema, lifting, asking for help 21:00 - Being a voice of strength for her teammates 22:00 - Working with a sports psychologist, and Sue's mantra 29:14 - How rowing has changed Sue and paying it forward to help new rowers 33:04 - Sue's rowing “sales pitch” 33:40 - What Sue wishes someone had told her before she learned to row 34:00 - Sue describes the perfect stroke 36:50 - Steady State Network news and notes . To see photos of Sue, and get links to the people, clubs, and events mentioned in this episode, check out the show notes on our website. . This episode was made possible in part by Breakwater Realty, RowSource, and our Supporters. . Steady State Podcast is hosted and edited by Rachel Freedman and Tara Morgan. Tara provides additional audio engineering, books show guests, and is our sponsor and donor coordinator. Rachel writes our scripts and e-newsletter, and manages the website and social media. Our theme music is by Jonas Hipper. . SHOP SSN GEAR: www.steadystatenetwork.com/shop SIGN UP FOR THE SSN NEWSLETTER: www.steadystatenetwork.com/newsletter MAKE A DIFFERENCE: www.steadystatenetwork.com/support  Check out more Steady State Network here:  FB - /SteadyStateNetwork IG - @SteadyStateNetwork BLUESKY - steadystatenetwork.bsky.social FB - /AllieswithOars IG - @AllieswithOars Connect on FB and IG with the hosts: Rachel Freedman - @RowSource Tara Morgan - @CmonBarber    

This mornings service is led by one of our elders, Dave Dodd with the address, titled 'Back From The Dead', given by Sue Ryan. Scriptures read before the address are from John 11.

Is the Medicare GUIDE Program for you? Today Nancy and I are sharing insights from Amy Imes of Emory's Integrated Memory Care about the new Medicare Program GUIDE. We're going to help you understand what it is and how to know if you can leverage it. We're sharing three tips. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we are so excited to share this information with you. This is an awesome opportunity to learn about the US Medicare GUIDE Program. With big announcements happening on July 1, 2025, we're excited to give you an overview so you can understand how you might participate in the GUIDE program. Let us introduce you to Amy. Amy Imes is a gerontological nurse practitioner who is a trusted expert in geriatrics, demonstrating a deep understanding of the unique healthcare needs of the aging population. Throughout her career, Amy has played a pivotal role in building care models—that's important to the GUIDE program—and developing teams that yield superior outcomes. In addition to her clinical work, she is a member of the team at Emory's Integrated Memory Care, which is a nurse practitioner-led primary care practice for patients living with dementia. She's also the program lead for the Medicare GUIDE Program at Emory Healthcare. GUIDE stands for Guiding an Improved Dementia Experience. It is a US Medicare pilot program that aims to provide better support and resources for persons living with dementia and their caregivers. Which is awesome. You should know that it's a pilot program. Please let's all support it because we need to prove that this pilot program which focuses on helping dementia caregivers actually works so that this can become a standard part of Medicare and can also be expanded globally. It would be ideal for the US to prove it's worth so that we can help other countries take advantage of these kinds of support because they're watching and they're aware of it. This is a groundbreaking program that is being offered around the country. So definitely we want to show up and show out as people tend to say sometimes. As of today, July 1st, there are approximately 390 programs across the country that have been vetted by Medicare to provide this program, and so it is really going to have an impact for persons living with dementia. Full Show Notes https://thecaregiversjourney.org/39-is-the-medicare-guide-program-for-you-three-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned To find a guide program near you: Go to this CMS website page and put in your state and under models select ‘Guiding an Improved Dementia Experience (GUIDE) Model' Then click ‘Display selected' You can use the plus and minus signs in the upper right corner to zoom in closer to your area and find the program closest to you. There may be several who cover your zip code so explore options Emory Integrated Memory Care: https://www.emoryhealthcare.org/centers-programs/integrated-memory-care-clinic Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways What the Medicare GUIDE Program Offers One-on-one support and coaching by dementia prevention providers Care navigation through an often difficult and chaotic healthcare system Education and training resources for caregivers Respite care Tip 1: Understand Your Eligibility Tip 2: How to Find a GUIDE Program Near Me Tip 3: How to Integrate GUIDE with Your Existing Medical Team About Emory's Integrated Memory Care GUIDE Program For those in the Atlanta area, Emory's Integrated Memory Care is led by nurse practitioners who are all dementia specialists and geriatric specialists. They bring everything under one umbrella with geriatric psych, licensed social workers, and RNs on their team. This eliminates doctor hopping and multiple visits. Read More in This Blog here

Do you wish you could get a good night's sleep? We do too! We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we appreciate the insights Dr. Glenna Brewster, PhD, RN, FNP-BC, Assistant Professor at Nell Hodgson Woodruff School of Nursing at Emory University, shared for all of us about her sleep study titled SLEEPMATE, and how we can all create good sleep habits. Dr. Glenna Brewster's background is impressive, and her passion for good sleep is inspiring! In addition to her responsibilities as a professor, she is a nurse scientist, family nurse practitioner, and she leads the Emory University Mind at Rest research team, which develops and tests practical, evidence-based programs to reduce sleep problems and improve health outcomes for people living with memory loss or dementia and their caregivers. Good sleep isn't just for your care receiver, this is for you too! According to Dr. Brewster: Sleep problems, especially if you're a caregiver or person living with cognitive impairment, are significant. You might have a hard time falling asleep, wake up multiple times during the night, or notice that as the disease progresses there is daytime sleepiness. Sleep disturbances are prevalent both in care partners or caregivers and people living with cognitive impairment. Dr. Brewster has developed the SLEEPMATE study for caregivers and people living with cognitive impairment and types of dementia. It's a six-week virtual intervention where you participate together. The study examines whether the intervention is feasible, acceptable, and if it improves sleep outcomes. At the end of this blog post is the link you can use if you're interested in participating in this virtual study. This topic is incredibly valuable for us as caregivers. We've learned the need for quality sleep — and what not having it is like. We've also learned that we're often so focused on quality sleep for our care receiver, we don't prioritize our own sleep as caregivers! One important take-away from Dr. Brewster for caregivers it's so easy not to consider — or to lose sight of: Your quality of sleep is every bit as important — and sometimes even more — important than your care receiver's. Full Show Notes here Additional Resources Mentioned Dr. Glenna Brewster, assistant professor, shares her innovative study designed to improve the sleep outcomes of persons living with preclinical and early-stage dementia and their caregivers. Brewster is also founder of the Mind at Rest research lab.For more information about joining this study, visit mindatrest.org/contact/.Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Tip 1: Practice Good Sleep Hygiene Tip 2: Limit Daytime Naps Tip 3: Make Your Bedroom Like a Cave Tip 4: Schedule Worry Time Earlier in the Day Tip 5: Keep Your Bedroom for the Three S's About the SLEEP-MATE Study Dr. Brewster's study is recruiting pairs. The person who is receiving the care doesn't have to be diagnosed with dementia, just have a complaint or an experience of cognitive changes. Caregivers or care partners—different people want to be called different things based on where in the dementia journey they are—both people participating, both having some type of sleep disturbance or sleep problems. That could be difficulty falling asleep, difficulty staying asleep (meaning that you fall asleep and then you wake up, and when you wake up, you have a hard time falling back asleep), or significant daytime sleepiness or some other type of impairment during the day. It's for people who are living within the contiguous US. Each of you gets an honorarium for participating as a thank you for your time and investment in participating in the study. If you have any questions or want to find out more about the study, please reach out at 404-712-9164 or you can check out their lab's website at www.mindatrest.org.

What would happen if you were suddenly thrust into the role of caregiver for someone you love? Would you have any idea what to do or how to do it? It's estimated that as many as 50 million people in the United States are caregivers, a job that virtually none of them trained for. We all know someone who became a caregiver and had to learn on the fly. Unfortunately, there are precious few resources that can help. Sue Ryan and Nancy Treaster experienced it first-hand. These inspiring women worked together in the software industry before finding themselves facing a similar life challenge: becoming caregivers for their husbands, both of whom were battling dementia. There was plenty of information about their husbands' diagnoses. Doctors were happy to provide them with hordes of information about what to expect as the disease progressed, but nobody was there with practical information about how to be a caregiver for someone with dementia. Their lived caregiving experience gave Sue and Nancy all the training they needed to make sure nobody else would have to figure it out on their own. That's when they founded the sensationally popular podcast, The Caregiver's Journey. Each episode features truly practical advice about how to manage as a caregiver. Topics range from self-care to advice for clipping your loved one's fingernails. They truly cover it all. The Caregiver's Journey has since grown to a powerhouse brand that fills a hugely meaningful gap for anyone who finds themselves having to be a caregiver. The organization was recently granted nonprofit status. In this episode, Sue and Nancy discuss their former careers, their friendship, and their own personal journeys. It's at times compelling, heart wrenching and funny, but it's entirely inspirational and helpful. To learn more about The Caregiver's Journey, visit them at thecaregiversjourney.org. And look up “The Caregiver's Journey” on any podcast app. ******* If you enjoy Second Act Stories, please leave us a review here. We may read your review on a future episode! Subscribe to the Second Act stories Substack. Check out the Second Act Stories YouTube channel. Follow Second Act Stories on social media: Facebook LinkedIn Instagram Second Act Stories theme music: "Between 1 and 3 am" by Echoes.

What would happen if you were suddenly thrust into the role of caregiver for someone you love? Would you have any idea what to do or how to do it? It's estimated that as many as 50 million people in the United States are caregivers, a job that virtually none of them trained for. We all know someone who became a caregiver and had to learn on the fly. Unfortunately, there are precious few resources that can help. Sue Ryan and Nancy Treaster experienced it first-hand. These inspiring women worked together in the software industry before finding themselves facing a similar life challenge: becoming caregivers for their husbands, both of whom were battling dementia. There was plenty of information about their husbands' diagnoses. Doctors were happy to provide them with hordes of information about what to expect as the disease progressed, but nobody was there with practical information about how to be a caregiver for someone with dementia. Their lived caregiving experience gave Sue and Nancy all the training they needed to make sure nobody else would have to figure it out on their own. That's when they founded the sensationally popular podcast, The Caregiver's Journey. Each episode features truly practical advice about how to manage as a caregiver. Topics range from self-care to advice for clipping your loved one's fingernails. They truly cover it all. The Caregiver's Journey has since grown to a powerhouse brand that fills a hugely meaningful gap for anyone who finds themselves having to be a caregiver. The organization was recently granted nonprofit status. In this episode, Sue and Nancy discuss their former careers, their friendship, and their own personal journeys. It's at times compelling, heart wrenching and funny, but it's entirely inspirational and helpful. To learn more about The Caregiver's Journey, visit them at thecaregiversjourney.org. And look up “The Caregiver's Journey” on any podcast app. ******* If you enjoy Second Act Stories, please leave us a review here. We may read your review on a future episode! Subscribe to the Second Act stories Substack. Check out the Second Act Stories YouTube channel. Follow Second Act Stories on social media: Facebook LinkedIn Instagram Second Act Stories theme music: "Between 1 and 3 am" by Echoes.

“An educated and confident family caregiver who knows what to do in their role is really the absolute best medicine for the care receiver.” Dr. Carolyn Clevenger Do you know extensive research specifically focused on dementia caregivers is being conducted? Are you aware of innovative studies designed to equip family caregivers with navigation skills? Now you will, and you'll be learning about valuable opportunities to strengthen your caregiving journey. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we are continuously learning new ways to support our health and well-being, and that of our care receivers. We recently discovered the groundbreaking dementia caregiver research, the CANDO Study, Dr. Carolyn Clevenger, DNP, RN, GNP-BC, AGPCNP-BC, FAANP, FGSA, FAAN, Professor at the Emory University Nell Hodgson Woodruff School of Nursing is conducting. When most people think about dementia research, they focus on studies involving people living with dementia or pharmaceutical treatments. This crucial area of research focuses on supporting the family caregivers themselves. Dr. Clevenger is a professor and gerontological nurse practitioner who is nationally recognized as an education leader in advanced practice nursing and geriatrics. Carolyn founded, and directs, the comprehensive dementia care model called Integrated Memory Care (IMC), which provides memory and primary care in a single integrated approach for people living with dementia and their care partners. Full Show Notes https://thecaregiversjourney.org/36-learn-to-navigate-support-systems-four-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned Dr. Carolyn Clevenger, a nationally recognized educational leader in advanced practice nursing, geriatrics and gerontology, shares her groundbreaking work on dementia family caregiver education programs that teach new caregivers how to transition into the role and navigate various support systems.For more information about joining this study, visit scholarblogs.emory.edu/CAN-DO/.Savvy Caregiver course: Available face-to-face or online (in-person version includes support group benefits)“Best Programs for Caregivers” website: A collaboration between the Benjamin Rose Institute on Aging and Family Care Alliance featuring only research-proven programs.Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Additional Resources Mentioned Takeaways Tip 1: Understand Different Levels of Care Early Home-Based CareCommunity-Based ProgramsResidential Care Options Key considerations: Each level has different eligibility requirements and payment structuresAvailability varies by state—some follow federal guidelines, others have state regulationsPeople often wait until they desperately need memory care but try to access assisted living instead, creating unnecessary stress Tip 2: Stay Ahead of Financial Challenges Protect your assets while maintaining oversightUnderstand the early warning signsWatch for judgment impairment issues Tip 3: Leverage Legal Support from Elder Law Experts What sets elder law attorneys apartSpecialized dementia expertiseLong-term benefits Tip 4: Take Evidence-Based Classes What makes evidence-based courses effectiveMeasurable outcomes The CAN-DO Study: Training Caregivers as Navigators Dr. Clevenger's current research project, CAN-DO (Caregiver As Navigator Developing Skills Online), trains family caregivers to navigate four critical systems: healthcare, financial, legal, and family systems. Course structure: Six-week online course following three families through different types of dementiaEach day presents real-life scenarios with appropriate responses and preventive measuresVideos from subject matter experts including elder law attorneys, investigators, estate planners, and healthcare providers

"When it comes to caregiving, the assumption about being able to take what we've learned and just naturally grow is not always going to be true." How do you think you would feel if you were caregiving for a second or third person living with dementia? Would you feel more prepared because of your previous experience? If you answered "yes," you might be surprised by what research is revealing about experienced caregivers. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, both of us have been caregivers more than once, and we recently learned about enlightening research from Dr. Emily Mroz, a researcher at Emory University's School of Nursing who coined the phrase "experienced caregiver." Her research is shedding light on a common phenomenon that affects millions of families: providing dementia care for multiple loved ones throughout adulthood. Dr. Mroz is a tenure-track assistant professor and social behavioral scientist who studies how people think, feel, and act within their social and personal situations. With training in developmental psychology, gerontology, geriatrics, and public health, she uses her multidisciplinary perspective to develop resources and interventions that support people living with serious illness, family caregivers, and those who are bereaved. Through her research and interviews with caregivers, Dr. Mroz has identified crucial insights about experienced caregivers that challenge common assumptions and offer practical guidance for those stepping into the caregiving role again. Full Show Notes https://thecaregiversjourney.org/37-studying-experienced-caregivers-four-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned Dr. Emily Mroz, assistant professor and social-behavioral scientist, discusses her research on improving how patients and caregivers navigate serious illnesses such as dementia, end-of-life care and bereavement. Link to study flyer here To join this study, visit survey.qualtrics.emory.edu/jfe/form/SV_cYfshxWcThSSV5s.Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Tip 1: Avoid Assumptions About Who Is Prepared to Be a Dementia Caregiver Tip 2: Assess How Prepared You Really Feel Tip 3: Don't Hesitate to Get Involved in Skills Training and Support Groups Tip 4: Share Your Stories with Grace, Not Judgment The Importance of Research for Experienced Caregivers Dr. Mroz's study is part of a growing recognition that experienced caregivers represent a significant population with unique needs and strengths. Her virtual research study involves participants completing surveys about their caregiving experiences and sharing their stories to help researchers understand the differences between new and experienced caregivers. Study details: Focuses on people currently in active caregiving roles, including those early in their journey with a second or third care recipientParticipants receive a $50 gift card honorariumSessions are conducted virtually and take about one to two hoursCan participate alongside other dementia caregiver research studiesResearch is crucial for developing resources specifically tailored to experienced caregivers Read More in This Blog here

Is your loved one in a memory care community, or are you considering moving them into one? Understanding how to build a collaborative relationship with the care team is crucial for ensuring the best outcomes for your loved one. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned that creating a true partnership with care community staff can dramatically improve quality of care and reduce stress for everyone involved. We recently spoke with James Lee, CEO and co-founder of Bella Groves, an award-winning memory care community. With over 17 years of experience in senior living and memory care, James has developed valuable insights on how to transform what is often an adversarial relationship between family caregivers and professional caregivers into a collaborative partnership. Full Show Notes https://thecaregiversjourney.org/35-build-a-partnership-with-your-care-community-six-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Takeaways Tip 1: Assess the Overall Fit When looking for a memory care community, many families focus on practical aspects like location, price, and amenities. While these factors are important, James suggests that philosophical alignment and rapport with the management team are even more crucial for long-term success. When evaluating potential communities, James recommends shifting your mindset from "us versus them" to "us collectively versus dementia." This perspective can transform the relationship from the beginning. Tip 2: Embrace the Community Aspect Moving your loved one from home to a community setting represents a fundamental shift in their care environment—from one-on-one care to being part of a group. Tip 3: Acknowledge Your Role Has Changed When your loved one moves into a care community, your role shifts from being the primary caregiver to being a care partner working alongside professional caregivers. Tip 4: Recognize That the Diagnosis Will Progress A critical aspect of the care partnership is understanding that your loved one's condition will continue to change over time. In fact, by the time someone moves into a memory care community, they're often in the steeper part of their dementia journey where changes happen more rapidly. Tip 5: Acknowledge Your Grief The dementia journey involves ongoing loss, a phenomenon Sue calls "drip grief." As your loved one's condition progresses, you experience new losses almost daily—abilities that disappear, memories that fade, personality changes that emerge. Tip 6: Engage with the Community Caregiving Team The families whose loved ones have the best quality of life tend to be those who actively engage with the care team. This engagement goes beyond basic communication to building genuine relationships with the people caring for your loved one. Building a True Partnership Creating a collaborative relationship with your loved one's care community team isn't just about being nice—it's about achieving the best possible outcomes for your loved one with dementia. By reframing the relationship from "us versus them" to "us collectively versus dementia," you can transform what is often an adversarial dynamic into a true partnership. As James explains, "You are your loved one's expert, we are dementia experts. And the two together give us the best chance to get this right." Read More in This Blog here

Are you prepared for others to take care of your loved one? Do you have a care plan in place? Having a comprehensive care plan is one of the most important tools a caregiver can create — not just for emergencies, but for everyday peace of mind. We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned the importance of creating a care plan for our loved one. We spoke with Amanda Lukoff, co-founder and CEO of Eleplan, about what a care plan is and how to create one that works for your unique situation. Amanda's journey to creating Eleplan was deeply personal. Her brother Liam, who has autism, is her "North Star" and the inspiration behind her career path, including going to law school for special education law. Through observing her parents' caregiving journey with Liam, Amanda recognized the need to capture all the knowledge that lived in her parents' heads so that others could provide care that truly honored who Liam is as a person. Connect with us and share your tips: Website: https://www.thecaregiversjourney.comDonate: https://give.cornerstone.cc/thecaregiversjourneyInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Additional Resources Mentioned Episode 32: Navigating The Caregiver Hiring Process https://thecaregiversjourney.com/32-navigating-the-caregiver-hiring-process-five-essential-tips-alzheimers-and-other-dementias/Eleplan Website: https://www.eleplan.com/Support the nonprofit The Caregiver's Journey: https://give.cornerstone.cc/thecaregiversjourney Full Show Notes https://thecaregiversjourney.com/33-how-to-create-a-care-plan-five-essential-tips-alzheimers-and-other-dementias Takeaways Tip 1: Start with the Basics The first step in creating a care plan is to document the essential information that would allow someone to provide short-term care (even for just 30 minutes) while you step out. This includes: Emergency contactsMedications and dosagesHigh-level meal preferencesAllergiesRelevant medical conditions Tip 2: Outline Preferences and Daily Routines Beyond the basics, a good care plan should capture what makes your loved one unique—their preferences, personality traits, and daily routines. Your care plan should include: Likes and dislikesDaily schedule and routinesBedtime and morning ritualsBehavioral patternsEmotional triggers (both positive and negative) Tip 3: Document What to Do in an Emergency Crisis situations demand clear instructions. Your care plan should outline: What constitutes an emergency for your loved oneWhen to call 911 vs. other resourcesWho to contact and in what orderSpecial instructions for EMTs or ER staffLocation of important medical documents Tip 4: Collect Key Contacts and Documents Gathering important documents in one accessible location is critical for seamless care. This includes: Insurance cardsHealthcare directivesPower of Attorney documentsGuardianship formsMedical history and medication lists Tip 5: Keep Everything Accessible and Current A care plan is only effective if it's up-to-date and easily accessible. Amanda frames this with an important question: "Do I have a system that is as dynamic as the needs of my loved one and the ever-changing piles of documents and information?" Whether you're using a physical binder, shared digital documents, or a specialized platform like Eleplan, the key is having a system that makes updates easy and ensures the information is available whenever and wherever it's needed. Read More in This Blog

Caregiving in the workplace is a conversation too few leaders are having—and it's costing businesses more than they realize. Hidden behind turnover rates, disengaged employees, rising healthcare costs, and inconsistent performance is a workforce silently struggling to manage dual roles. Employees at every level, from entry-level staff to the C-suite, are balancing the demands of their careers while caring for aging parents, children with special needs, or loved ones facing health challenges. Yet most organizations aren't equipped to support them, and many employees never speak up. Sue Ryan, Chief Inspirationalist and a strategist for workplace caregiving solutions, brings this challenge into sharp focus. Drawing from over 30 years of personal caregiving experience and professional leadership, Sue shines a light on what she calls the workforce blind spot—an exponentially growing crisis that's costing U.S. businesses an estimated $33 billion annually in lost productivity and turnover. The issue isn't just personal—it's systemic. And it's avoidable. As the U.S. population ages rapidly, with those over 65 set to outnumber those under 18 by 2030, the pressure on working caregivers is increasing fast. The fastest-growing demographic in the country is now adults over 85. This demographic shift is creating ripple effects in every industry, affecting employee well-being, engagement, and long-term retention. Leaders who ignore this trend risk falling behind—not just in compassion, but in performance. Supporting caregiving in the workplace doesn't mean overhauling business models or adding burdensome policies. In fact, many solutions already exist within organizations; they just haven't been adapted to meet this need. Sue breaks down how simple shifts in culture—starting with top-level leadership—can make a meaningful difference. It begins with normalizing the conversation. When employees feel safe acknowledging their caregiving responsibilities, it opens the door to flexibility, planning, and improved collaboration. Business leaders often assume caregiving is an HR issue. That's a costly mistake. When the executive team leads with clarity and openness, human resources can activate systems, provide training for managers, and integrate caregiving into team planning and scheduling. But without visible, top-down acknowledgment, the conversation stalls before it ever starts. Employees who can't speak up often leave, taking their skills and institutional knowledge with them. Sue also draws attention to what she calls the “sandwich generation”—employees, often in their 40s or 50s, who are supporting both aging parents and dependent children while maintaining full-time roles. These team members bring valuable experience and insight to their companies, but their capacity is being stretched thin. Ignoring their reality leads to burnout, disengagement, and missed opportunity. Normalizing caregiving in the workplace can be as straightforward as updating onboarding conversations, creating safe spaces for disclosure, and encouraging leadership to model openness. Organizations like Deloitte, Starbucks, and Amazon are already seeing measurable results from acknowledging and addressing this reality—improvements in productivity, employee satisfaction, and retention. The shift doesn't require large financial investments—it requires intention. Companies already have many of the operational, legal, and financial structures in place to support this evolution. The missing piece is leadership. When executives set the tone, the culture follows. It becomes easier for teams to adapt, cross-train, and collaborate in ways that support both business goals and employee well-being. This is more than a human resources initiative—it's a business growth strategy. Addressing caregiving in the workplace is about keeping your best people, increasing engagement, and reducing the hidden costs of turnover. With the right awareness and tools, organizations can create environments where employees bring their full selves to work—without hiding a critical part of their lives. Watch the full episode on YouTube. Don't miss future episodes of Fordify LIVE! every Wednesday at 11 AM Central, streaming on your favorite social platforms. Catch new episodes of The Business Growth Show Podcast every Thursday for a weekly dose of business growth wisdom. About Sue Ryan Sue Ryan is a speaker, strategist, and Chief Inspirationalist dedicated to transforming how organizations support family caregivers in the workplace. With over 30 years of experience navigating her own caregiving journeys while maintaining a professional career, she equips business leaders with the tools and insights to turn caregiving from a hidden liability into a competitive advantage. Sue helps organizations reduce turnover, improve engagement, and build cultures of empathy and performance. Learn more at SueRyan.Solutions. About Ford Saeks Ford Saeks is a Business Growth Accelerator who has helped generate over a billion dollars in sales for companies ranging from startups to Fortune 500s. As President and CEO of Prime Concepts Group, Inc., he focuses on customer acquisition, brand visibility, and innovation. With over 20 years of experience, Ford has founded more than ten companies, authored five books, and holds three U.S. patents. His expertise also extends into AI-driven content strategy, showcased at the Unleash AI for Business Summit. Learn more at ProfitRichResults.com and watch his TV show at Fordify.tv.

When you're grieving, the last thing you need to be doing is planning a service. Pre-planning allows you to make only two decisions when death occurs: what day and what time the service will be held. Everything else can be arranged in advance, giving you the space to honor your loved one while processing your grief. We are Sue Ryan and Nancy Treaster, and we recently spoke with Greg Cannon, who has more than 45 years of experience in the funeral profession, including as a funeral director. Greg shared his expertise on planning ahead for a loved one's service, offering eight essential tips that can make all the difference during a difficult time. Rate, Subscribe, Share the Podcast and Share Your Tips on Social Media! Please click here to review, follow, subscribe to and share our podcast. Connect with us and share your tips: Website: https://www.thecaregiversjourney.com Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/TheCaregiversJourneys/ Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/ Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Full Show Notes https://thecaregiversjourney.com/finding-peace-in-preparation-end-of-life-service-preplanning-eight-essential-tips-alzheimers-and-other-dementias/ Additional Resources Mentioned End of Life Service Worksheet here Takeaways Tip 1: Choose a Funeral Home Select a funeral home that will meet your needs. This choice may be based on location, previous experience with them, or their reputation. Tip 2: Decide on Burial or Cremation This fundamental decision shapes many subsequent choices. If choosing burial, consider: Cemetery location If the person is married, reserving an adjoining space for the spouse Whether traditional burial or green burial options are preferred. For cremation, consider: Whether the cremation will happen before or after the service. What will be done with the cremated remains afterward. In both cases, you'll need to decide what clothing the person will wear. Greg advises bringing a complete set of clothing, including undergarments and outerwear. Shoes are optional and often difficult to put on, but can be included if they're meaningful. Tip 3: Decide on the Type of Service Funeral services have evolved beyond the traditional. Traditional Service (for either burial or cremation) Memorial Service Green Burial Direct Cremation or Direct Burial Tip 4: Choose a Location The location for the service could be: A funeral home A place of worship A location meaningful to the deceased Tip 5: Prepare the Obituary Rather than writing the complete obituary under time pressure, prepare by: Compiling all necessary information ahead of time Creating a comprehensive list of family members to include Selecting a photo or photos to accompany the obituary. Tip 6: Create a Notification Tree Decide ahead of time: Who needs to be notified of the death Who will notify whom Create a “notification tree” so you're not responsible for contacting everyone. Tip 7: Plan the Service Consider these elements and include your care receiver as much as possible: Officiant: Choose the clergy or person who will lead the service Eulogies: Decide who will deliver them and provide guidance Music: Select meaningful songs or hymns Readings: Choose scripture, poetry, or other readings Personal touches: Include memorabilia, photos, or items that represent the person's life. Consider alternatives to traditional floral arrangements: Family quilts Meaningful objects (like golf clubs for an avid golfer) Photos. Tip 8: Plan the Gatherings Consider various types of gatherings: Private family dinner before the service Reception after the service for all attendees Informal gathering at home with close family and friends.

Sue Ryan and Nancy Treaster with The Caregiver's Journey join host Carol Morgan on this week's Atlanta Real Estate Forum Radio episode. In this podcast episode, Ryan and Treaster discuss transitioning into a caregiver role for a family member with dementia. How does The Caregiver's Journey support dementia patient caregivers? “I wanted other people to learn faster and more easily than I did because I was so frustrated and overwhelmed and sometimes frightened,” said Ryan. “I prefer to feel confident, balanced and supported, and I wanted to give that to others.” Before starting The Caregiver's Journey, Ryan and Treaster realized there was a need for easy answers to daily caregiver challenges related to dementia. Ryan points out that there are 100+ types of dementia, each with unique characteristics. Dementia affects everything from cognitive function and mood to depth perception and movement. The nonprofit podcast and online course offer niche advice for caregivers, simplifying the process and promoting the well-being of dementia patients. What are some best practices for caregivers? “The hardest thing for anyone to realize when they walk in the door if they're a first-time caregiver is that when your loved one gets a diagnosis of dementia, you just got a diagnosis of caregiver, and you're not just a caregiver for the person with dementia,” said Treaster. “You are responsible for your care.” Ryan highlights a few tips to keep yourself and your loved one happy and healthy. Give yourself permission not to be okay: She recommends caregivers acknowledge that while your loved one's life is changing, so is yours. You must accept the change and the feelings that come with it. Find support in others: There are dozens of support groups and resources available to caregivers; you just have to look for them! Talking to others about the challenges, successes and everything in between is essential. Seek an accountability partner: While supporting your loved one, ensure someone is looking out for you. Ryan emphasizes that caregivers can easily neglect their own needs to prioritize the diagnoses of loved ones, but accountability is crucial not to burn out. “It's so easy for us to lose ourselves in our caregiving, and if we don't have someone who holds us accountable for caring for ourselves, we can lose that,” said Ryan. “So, we want to prioritize learning about the diagnosis, but not feeling we need to do it alone.” Stay curious: One of the best ways to care for loved ones is to continue looking for new methods and helpful tips. Don't compare yourself to others but be willing to learn more. What are some dementia warning signs to look out for? Treaster says that dementia patients are often skilled at hiding cognitive decline. You might brush off the signs the first couple of times, but it may be time to visit the doctor if the same issues keep recurring. Other short-term medical diagnoses can also present as cognitive decline, including vitamin deficiencies and minor infections. “It's easy to brush off the excuses because nobody really wants to answer to be dementia, right?” said Treaster. “But don't let it go because the sooner you could find out it might be something else, or the sooner you can start treating their dementia, the better as well.” How are continuing care communities transitioning to accommodate residents with dementia? There are over 7 million individuals over the age of 65 in the United States with various dementia diagnoses. That statistic is expected to double by 2060. Continuing care communities are implementing day programs that allow dementia residents and outside participants to mingle during the day and special wings that allow residents with similar diagnoses to live near each other. Treaster recommends testing out various programs. Maybe the first program isn't a great fit; try another one! Day programs offer caregivers a break to care for themselves while loved ones enjoy exciti...

As caregivers for our loved ones with Alzheimer's and other types of dementia, we often face the challenging question: "Is it time to change my care receiver's living situation?" We are Nancy Treaster and Sue Ryan, and through our experiences, we've developed five essential tips to help you navigate this complex decision-making process. Connect with us and share your tips: Website: https://www.thecaregiversjourney.comInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Full Show Notes https://thecaregiversjourney.com/time-for-a-change-home-and-community-living-options-five-essential-tips-alzheimers-and-other-dementias/ Takeaways 1. Understand Your Financial Resources This foundational step requires a thorough assessment of both current and future financial resources. Professional Resources to Consult: - Financial advisors (especially those specializing in senior care) - Elder care attorneys - Government program specialists Income Sources to Consider: - Care receiver's savings - Pensions - Long-term care insurance - Public health insurance (Medicaid in the US) - Social Security disability benefits - Family contributions Expenses to Evaluate: - Home modifications - Safety adjustments - In-home caregiving costs - Day program fees - Potential lost income if reducing work hours - Care community costs 2. Research Care Options There are three main categories of care options to evaluate: Non-Residential Options: - Respite programs - Memory cafes - Day programs In-Home Options: - Professional caregiving services - Government programs (VA benefits, Medicare services) - Family caregiver arrangements Care Communities: - Memory care specific facilities - Communities with memory care units - Different care models and staffing levels - Waiting list considerations 3. Assess Home Safety This evaluation should include multiple perspectives: Medical Assessment: - Get an updated medical evaluation - Discuss current and future safety risks - Request occupational therapy assessment Key Safety Considerations: - Wandering risk - Cabinet and door safety - Mobility challenges - Fall prevention - Depth perception issues - Stairs and accessibility - Emergency services access 4. Evaluate Medical Needs Current and Future Medical Considerations: - Impact of multiple diagnoses - Care complexity - Required medical procedures - Medication management - Physical care requirements 5. Prioritize Wellbeing for Both Care Receiver and Caregiver This final tip focuses on quality of life considerations for everyone involved. Socialization Needs: - Care receiver's social preferences - Community engagement opportunities - Caregiver isolation prevention - Balance of stimulation and comfort Safety and Emotional Considerations: - Physical safety for both parties - Emotional wellbeing - Caregiver burnout prevention - Managing aggressive behaviors - Personal boundaries Making the Final Decision: - Consider all evaluation points - Involve family members - Maintain awareness of available options - Stay connected with potential care communities - Be prepared to act when needed

Nancy Treaster and Sue Ryan, co-founders of The Caregiver's Journey https://thecaregiversjourney.com/, share their deeply personal experiences as longtime dementia family caregivers and their mission to provide practical support to others navigating similar challenges. With over 25 years of caregiving experience each, they both struggled to find the guidance they needed and decided to create a platform to help others learn faster, feel more confident, and find balance in their caregiving journey. Through The Caregiver's Journey Podcast, they provide practical tips, candid conversations, and real-life stories that address the everyday struggles of dementia caregivers, from bathing and dressing to navigating emotional and logistical challenges. Their mission is to make dementia caregiving easier by offering resources in multiple formats-podcasts, blogs, workshops, and books-so caregivers can access information in the way that suits them best. Now a nonprofit organization, The Caregiver's Journey aims to expand globally, ensuring that no caregiver has to feel alone or start from scratch. With a strong emphasis on building a support system, setting boundaries, and taking care of oneself, Nancy and Sue are dedicated to equipping caregivers with the knowledge, confidence, and community they need to provide the best possible care for their loved ones. Learn more at TheCaregiversJourney.com or connect with them on YouTube, Spotify, Apple Podcasts, Facebook, and Instagram.

Imagine being on a journey where love, divine guidance, and ice cream are your compass. That's exactly what Sue Ryan experienced throughout her caregiving path. With over 40 years of personal caregiving and a strong background in enterprise software, Sue joins us to share her incredible story. From caring for her grandmother, father, and husband, Sue managed to balance these responsibilities while maintaining a thriving professional life. Her experiences offer a powerful blend of practical advice and spiritual insight, promising to empower anyone navigating similar roles.Sue brings to light the surprising gifts that caregiving can offer, not just to those receiving care but to the caregivers themselves. She reveals how small acts, like offering a favorite treat, can profoundly impact a care receiver's emotional state. Through Sue's storytelling, we explore the beauty in the seemingly mundane and find honor in caring for those who can't care for themselves. These moments, guided by love and a touch of divine intervention, shape our purpose and transform how we serve others, turning challenges into true wisdom.Our conversation celebrates the unique and perfectly imperfect nature of caregiving. Perceived failures? They're just stepping stones for learning and growth. We embrace the curiosity often lost in adulthood, finding joy in exploration and life's unanswered questions. As Sue shares her personal story of God's presence during life's final stages, faith emerges as a comforting ally. Through all these experiences, hope remains a steadfast companion, inviting listeners to connect deeply with our caring community, always ready to support and inspire.

1-8-25 Morning Rush - Apocalyptic California Wildfire UPDATES - Justin Baldoni's Lawyer Plans To Sue RYAN REYNOLDS & Shares New Voice Note On Megyn Kelly Show & Bachelorette Jenn DISSES ALL HER MEN We're following the devastating wildfire hitting the Pacific Palisades in Southern California. I'll have updates as cars are parked on major road ways, folks evacuating on foot, institutions up in flames. Plus we've got more info coming out from the Blake Lively v Justin Baldoni lawsuits as Bryan Freedman, Justin's lawyer, goes on a controversial program to share a new voice note from Justin himself. Plus Bachelorette's Trista Sutter explains how tough Special Forces kicked her butt Plus James Kennedy of Vanderpump Fame breaks his social media silence following his domestic violence arrest, Ill share what he had to saygo to patreon.com/daveneal for more bonus content!

“We've both had ‘that' trip — the last trip that you take when you decide we're not traveling ever again with our care receiver. Or, as we like to say, it's the trip after the last trip you should have taken!” We are Sue Ryan and Nancy Treaster. As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned travel decisions require careful consideration. Through our experiences, and what we've learned from support groups and others on their journeys, we've developed four important tips to help you decide whether you and your care receiver should stay home or go on what could be ‘that' trip. See Full Show Notes here Rate, Subscribe and Share Your Tips on Social Media! Please click here to review, follow or subscribe to our podcast. If you don't see your preferred platform click on Podchaser and click at the bottom “Write my review” You can log in with Twitter, Facebook or Google On the right you'll see a box with “Follow”, “Rate and Review” and “Share” Connect with us and share your tips: Website: https://www.thecaregiversjourney.com Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/TheCaregiversJourneys/ Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/ Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Additional Resources Mentioned These resources contain affiliate links so we may receive a small commission for purchases made at no additional cost to you. Fidget blanket here Takeaways Tip 1: Pre-test Travel Readiness Key points: Test longer car rides (at least an hour round trip) Try interstate driving if that will be part of your journey Experience crowds and noise if those will be present Test unfamiliar environments Pay attention to any existing signs of travel difficulty. Tip 2: Evaluate All Trip Components Key points: Assess sleeping arrangements and bathroom accessibility Consider the need for quiet space Evaluate support options at the destination Think about familiarity with locations Listen to your inner voice about the decision — is this the wisest choice? Tip 3: Plan Comprehensively Key points: Minimize advance information to avoid overwhelming your care receiver. Pack comfort items: Fidget blankets Familiar snacks Favorite music and headphones Photo books Familiar entertainment (DVDs, etc.) 3. Plan around normal routines: Meal times Sleep schedule Best times of day for different amounts of activity 4. Prepare for emergencies: Take IDs and insurance cards Bring extra medications Pack legal documents Consider anti-anxiety medication options Share detailed itinerary with family members Have your emergency contact information easy to find on your care receiver and in case something happens to you. Tip 4: Prepare Others Key points: Explain current abilities and challenges Provide conversation guidance Demonstrate proper approach techniques Give permission for others to opt out if they're not comfortable Show grace toward those processing their own emotions Read More in This Blog here

As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned that full incontinence is an inevitable part of our journey. It's a topic not often discussed, yet it's a reality for us to navigate with compassion, dignity, and preparation — for both us and our care receiver. We are Nancy Treaster and Sue Ryan. Through our experiences, we've developed 2 valuable tips to help you navigate bowel and bedbound incontinence in your caregiving journey. Watch Bowel and Bedbound Incontinence: Two Essential Topics / Alzheimer's and Other Dementias https://youtu.be/PD4zOctyfPw Takeaways Read More in This Blog here Additional Resources Mentioned Episode 10 - Incontinence Begins hereEpisode 11 - Cleaning Your Care Receiver hereChanging a bedbound care receiver YouTube video here Changing a Depend with a bowel movement hereDisposable incontinence underwearFor women hereFor men hereWheels for bedBed with railsWedge pillowAdaptive clothingShorts snap up herePants snap up hereVery nice adaptive clothing here Non-rinse bathing wipes hereAdult washcloths/wipes hereDisposable incontinence pads hereRound tipped scissors hereScented small trash can liner hereAdult incontinence can here Rate, Subscribe and Share Your Tips on Social Media! Thanks for listening! If you enjoyed this episode, please leave a review and subscribe on your favorite podcast platform. Please click here to review, follow or subscribe to our podcast.   If you don't see your preferred platform click on Podchaser and click at the bottom “Write my review” You can log in with Twitter, Facebook or GoogleOn the right you'll see a box with “Follow”, “Rate and Review” and “Share”  Connect with us and share your tips: Website: https://www.thecaregiversjourney.comInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com

Support for Caregivers, with Sue Ryan and Nancy Treaster, The Caregiver’s Journey (North Fulton Business Radio, Episode 805) In this episode of North Fulton Business Radio, host John Ray welcomes Nancy Treaster and Sue Ryan from The Caregiver’s Journey. They discuss the significant challenges faced by caregivers of loved ones with dementia, emphasizing the emotional and […] The post Support for Caregivers, with Sue Ryan and Nancy Treaster, The Caregiver’s Journey appeared first on Business RadioX ®.

Support for Caregivers, with Sue Ryan and Nancy Treaster, The Caregiver’s Journey (North Fulton Business Radio, Episode 805) In this episode of North Fulton Business Radio, host John Ray welcomes Nancy Treaster and Sue Ryan from The Caregiver’s Journey. They discuss the significant challenges faced by caregivers of loved ones with dementia, emphasizing the emotional and […]

As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned managing incontinence is one of the most challenging aspects of our journey. It's a topic where having detailed information is vital to our adjusting to this part of our journey mentally, physically, and emotionally. We are Nancy Treaster and Sue Ryan. Through our experiences, and insights we've learned from others in support groups, we've developed three indispensable tips to help you navigate the important component of incontinence care with your care receiver — cleaning them Takeaways here Additional Resources Mentioned Episode 10 - Incontinence Begins here Episode 12 - Bedbound and Bowel Incontinence here Episode 13 - Incontinence Overnight here Adaptive clothing Shorts snap up here Pants snap up here Very nice adaptive clothing here Disposable incontinence underwear For women here For men here Adult washcloths/wipes here Non-rinse bathing wipes here Disposable incontinence pads here Round tipped scissors here Rate, Subscribe and Share Your Tips on Social Media! Thanks for listening! If you enjoyed this episode, please leave a review and subscribe on your favorite podcast platform. Please click here to review, follow or subscribe to our podcast. If you don't see your preferred platform click on Podchaser and click at the bottom “Write my review” You can log in with Twitter, Facebook or Google On the right you'll see a box with “Follow”, “Rate and Review” and “Share” Connect with us and share your tips: Website: https://www.thecaregiversjourney.com Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/TheCaregiversJourneys/ Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/ Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com

Who knew that understanding the stages of incontinence could make such a difference in our caregiving journey? As caregivers for our loved ones with Alzheimer's and other types of dementia, we've learned incontinence is an inevitable - and can be - a challenging part of our journey. It's a reality and a topic that's not often discussed. It's helpful for us to be prepared to navigate incontinence with compassion, dignity, and grace for our care receivers and for us. We are Nancy Treaster and Sue Ryan. Through our experiences, we've developed four tips to help you navigate the pre-incontinence and early incontinence phases on your caregiving journey. Takeaways Before we introduce your tips, it's helpful to understand what we mean by ‘pre-incontinence' and ‘early incontinence'. Pre-Incontinence This is the phase before actual incontinence begins, when our care receiver is showing signs incontinence may be on the horizon. Signs include: Using the trash can instead of the toilet for toilet paper Not flushing the toilet Resisting drinking to avoid bathroom trips Looking around anxiously (potentially for a bathroom) Early Incontinence When actual incontinence begins, it usually starts with urinary incontinence. Your loved one may still be trying to find the bathroom but often doesn't make it in time. Signs include: Not getting to the bathroom fast enough Holding their stomach, bottom, or between their legs Tip 1. Make it Easy to Find the Bathroom Yes, to us this sounds simple. To our loved one, they are disconnecting with the signs their bodies are telling them they need to go, and the steps to use the bathroom. One of the most effective ways to support your loved one during pre-incontinence and early incontinence is by making the bathroom as accessible and easy to find as possible. Tip 2. Schedule Bathroom Breaks Establishing a consistent bathroom routine can significantly reduce accidents and make the transition into full incontinence more manageable. Tip 3. Simplify Cleanup As incontinence progresses, accidents will happen. Being prepared can make cleanup easier and less stressful for both you and your loved one. Tip 4. Think Positively and Have Lots of Grace Perhaps the most important tip of all is to maintain a positive attitude and extend grace to both you and your loved one. Read More in This Blog here Additional Resources Mentioned Episode 11 - Cleaning Your Care Receiver here Child proof door knob cover or double deadbolt locks for external doors Child proof door knob covers here Extra tall pet gate from (40” to 70”) - 57” here Disposable incontinence underwear For women here For men here Pads Mattress pads 34”x36” here 72”X36” here Disposable incontinence pads here Brown large pet pee pads here Easy mops Swiffer mop here Bona here Hard surface cleaners Pine Sol here Pooph here Odoban here Fabuloso here Carpet cleaning Resolve Urine Destroyer here Resolve Ultra Pet here Bissell Pet Carpet Cleaner here Resolve Urine Destroyer Carpet Cleaning Machine Formula here Rate, Subscribe and Share Your Tips on Social Media! Thanks for listening! If you enjoyed this episode, please leave a review and subscribe on your favorite podcast platform. Please click here to review, follow or subscribe to our podcast. If you don't see your preferred platform click on Podchaser and click at the bottom “Write my review” You can log in with Twitter, Facebook or Google On the right you'll see a box with “Follow”, “Rate and Review” and “Share” Connect with us and share your tips: Website: https://www.thecaregiversjourney.com Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/TheCaregiversJourneys/ Linkedin: https://www.linkedin.com/in/suearmstrongryan/, https://www.linkedin.com/in/nancytreaster/ Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com

Description When a close family member is diagnosed with dementia, it can be uniquely challenging for young adults to navigate this new reality. We are Nancy and Merritt Treaster. When Merritt was in his early twenties, his dad, who was 60 at the time, was diagnosed with Frontotemporal dementia. A few short years later, his grandfather, at the age of 85, was diagnosed with Alzheimer's disease. Merritt's experiences led us to create this episode to help other young adults. He has distilled his thoughts on how to be better prepared into four essential tips for young adults facing a family member's dementia diagnosis. Takeaways For takeaways click here Rate, subscribe and share your tips on social media! Please click here to review, follow or subscribe to our podcast. If you don't see your preferred platform, click on Podchaser and click at the bottom “Write my review” Connect with us and share your tips: Website: https://www.thecaregiversjourney.com Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/TheCaregiversJourneys/ Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Keywords Young adult, teenager, boundaries, incontinence, Alzheimer's, dementia, caregiver, caregiving, dementia care, memory care, dementia caregiver blog, Alzheimer's blog, caregiver blog, senior caregiver blog, dementia caregiver tips, how to care for someone with dementia living alone, information on dementia for caregivers, how to be a caregiver for someone with dementia, family caregiver, frontotemporal dementia, dementia caregiver tips, family caregiver, Sue Ryan, Nancy Treaster, Susan J Ryan, Merritt Treaster

You're going to wish you'd known about padding hard corners earlier in your caregiving journey! We are Nancy Treaster and Sue Ryan. Through our experiences as caregivers for our family members and loved ones with Alzheimer's and other types of dementia, we've learned ensuring home safety is both vitally important and ever-changing. In this post, we're sharing three main tips for managing safety — both inside and outside the home. These help you keep your loved one safe while giving you peace of mind. Takeaways For takeaways click here Additional Resources Mentioned File of Life: Create a document called File of Life. Child proof door knob cover or double deadbolt locks for external doors Child proof door knob covers here Double dead bolt or code based lock here Child proof cabinet locks here Child proof stove knob covers here Child proof refrigerator latch here Child proof switch plate for garbage disposal here Window sash here Extra tall pet gate from 40” to 70” here Child padding foam here Cameras or baby monitor for the bedroom and bathroom Baby monitors - some come with motion alarms as well here I use Nest Cameras and pay for the Nest Aware feature which gives me access to video history. A friend of mine uses a Ring and swears by it. Whatever kind you get, if your care receiver is still staying home alone, consider one with an intercom Indoor here Grip Socks here Floor lift chairs Indeelift here Lift chairs here Rate, subscribe and share your tips on social media! Please click here to review, follow or subscribe to our podcast. If you don't see your preferred platform, click on Podchaser and click at the bottom “Write my review” Connect with us and share your tips: Website: https://www.thecaregiversjourney.com Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/TheCaregiversJourneys/ Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Keywords Home safety, child proof, dementia proof, reduce falls, Alzheimers, dementia, caregiver, caregiving, Alzheimers care, dementia care, memory care, best dementia podcast, alzheirmers podcast, caregiver podcast, dementia caregiver podcast, dementia podcast, alzheimers podcast, caregiver podcast, senior caregiver podcast, dementia caregiver tips, frontotemporal dementia, dementia caregiver tips, how to deal with dementia as a caregiver, information on dementia for caregivers, how to be a caregiver for someone with dementia, family caregiver, Sue Ryan, Nancy Treaster, Susan J Ryan

Welcome to Good Girls Get Rich! I'm your host, Karen Yankovich, and today's episode hits close to home for so many of us—balancing the demands of caregiving while still building a successful, profitable business. We've all heard of the “sandwich generation,” right? Those of us who are caring for our aging parents while still supporting our children and running our businesses. It's tough, it's real, and it's not talked about nearly enough in the entrepreneurial world. That's why I'm so excited for you to meet my guest, Sue Ryan. Sue is an expert in caregiving AND business strategy, and she's walked the walk. She knows how it feels to juggle these roles and come out on the other side with success—not just surviving, but thriving. If you're like me and so many of the incredible women in my She's LinkedUp program, this conversation is going to speak to your soul. #GoodGirlsGetRich  We want to hear your thoughts on this episode! Leave us a message on Speakpipe or email us at info@karenyankovich.com. Episode Highlights: Sue and I dive into the real-life challenges we face as women caring for loved ones while still showing up as leaders in our businesses. We talk about why it's crucial to normalize these conversations in our workplaces and how you can set yourself up for success in both areas of life without burning out. In this episode, we cover: How caregiving can impact your business and what you can do to stay profitable while still being there for the people who matter most. The importance of creating boundaries and why having honest conversations with your family and business team is key to reducing stress. Practical tips for building a support system—from leveraging technology to outsourcing tasks—so you don't feel like you have to do it all on your own. Why it's essential to remove the stigma of caregiving in business and how you can lead by example for your employees and contractors. Strategies for keeping your business running smoothly while still being present for your family. Sue and I both understand that you don't have to choose between being a great caregiver and running a successful business. In fact, the strategies we share in this episode will help you thrive in both roles—without sacrificing one for the other. There is a way to support your loved ones AND continue to build wealth and influence. We've got your back! Magical Quotes from the Episode: Sue Ryan: "The goal is to help family caregivers become confident, balanced, and supported in all phases of their journey, without sacrificing their professional lives." "By 2030, more people will be over 65 than under, and the available pool of caregivers is shrinking. It's critical for businesses to start recognizing and supporting the caregiving role." "You don't have to navigate caregiving and business alone. Leverage your support systems and get creative—whether it's technology or a community of people who understand the journey." Karen Yankovich: "Caregiving is a reality for so many entrepreneurs, and it's not something we talk about enough—but it absolutely impacts how we run our businesses." "I've realized over the years that running a business while supporting aging parents isn't something you just ‘figure out'—it requires real strategy, boundaries, and planning." "As a business leader, I'm not just thinking about myself. I have employees and contractors who are also juggling these same challenges. We need to create support systems that work for everyone." Resources Mentioned In This Episode: Sue Ryan's Caregiver's Journey Program (7-day free access!) Help Us Spread The Word! It would be awesome if you shared the Good Girls Get Rich Podcast with your fellow entrepreneurs on Twitter. Click here to tweet some love! If this episode has taught you just one thing, I would love if you could head on over to Apple Podcasts and SUBSCRIBE TO THE SHOW! And if you're moved to, kindly leave us a rating and review. Maybe you'll get a shout out on the show!   Ways to Subscribe to Good Girls Get Rich: Click here to subscribe via Apple Podcasts Click here to subscribe via PlayerFM Good Girls Get Rich is also on Spotify Take a listen on Podcast Addict

If your loved one can't do three of the things we discuss in this episode, they should not be home alone. As caregivers for our husbands, parents, and other loved ones with Alzheimer's and other types of dementia, we both know that one of the early goals for our loved one is to help them maintain their independence as long as it's reasonable. You'll be balancing your concern for their safety with their independence, remembering their ability to stay home alone is temporary. We are Sue Ryan and Nancy Treaster, and through our experiences, we're sharing six key tips for supporting your loved one's ability to be home alone. Show Notes During this phase your focus will be to observe and adjust regularly. Tip 1: Conduct an Audit of Activities of Daily Living Regularly observe and document your loved one's ability to perform daily tasks. This helps identify patterns of decline and areas where support may be needed. Tip 2: Monitor Food and Hydration Ensure your loved one is eating properly and staying hydrated. Set up systems to make food easily accessible and track fluid intake. Tip 3: Ensure Communication Capabilities Verify that your loved one can communicate with the outside world and call for help if needed. Consider implementing technology solutions to enhance communication. Tip 4: Manage Medication Establish a reliable system for medication management. If your loved one can't take their medication independently, it may be time to reconsider their living situation. Tip 5: Track for Safety Implement safety tracking measures, including monitoring driving abilities and using personal tracking devices to ensure your loved one's whereabouts. Tip 6. Create a Support Team Build a network of family, friends, and neighbors who can assist in caregiving and emergencies. Keep everyone informed with up-to-date information about your loved one's needs. Remember, leaving your loved one with dementia at home alone is a temporary situation. While it requires continuous monitoring and can be anxiety-inducing, implementing these strategies can help you navigate this phase more effectively. We're all on this journey together, and with proper planning and support, you'll get through this situation just fine. Thermostat control Through app https://www.amazon.com/s?k=app+controlled+thermostat+for+house&crid=27O5EFJOCSLLR&sprefix=thermostat+for+house+with+app%2Caps%2C85&ref=nb_sb_ss_pltr-data-refreshed_6_29 Thermostat cover https://www.amazon.com/s?k=thermostat+cover+with+lock&crid=3OHIO7E2YQ8SP&sprefix=thermostat+cover%2Caps%2C146&ref=nb_sb_ss_pltr-data-refreshed_2_16 Electronic medication dispensing and monitoring devices https://www.amazon.com/s?k=Electronic+medication+dispensing+and+monitoring+devices+with+app&crid=2AOUSNW2CGOF5&sprefix=electronic+medication+dispensing+and+monitoring+devices+with+app%2Caps%2C73&ref=nb_sb_noss Inside and outdoor cameras Indoor https://www.amazon.com/s?k=indoor+cameras+with+intercom&i=tools&crid=1RTJWUD6C53DD&sprefix=indoor+cameras+with+intercom%2Ctools%2C72&ref=nb_sb_noss Outdoor https://www.amazon.com/s?k=outdoor+cameras+with+intercom&i=tools&crid=2ERD6HT2QIK5W&sprefix=outdoor+cameras+with+intercom%2Ctools%2C78&ref=nb_sb_noss Tracking devices for their person Watches https://www.amazon.com/s?k=person+tracking+device&crid=OPZ28JRM2KDU&sprefix=person+t%2Caps%2C96&ref=nb_sb_ss_ts-doa-p_2_8 Shoes https://www.amazon.com/s?k=gps+smart+sole&crid=2DM2XBGVTA5VJ&sprefix=GPS+smart+sole+%2Caps%2C95&ref=nb_sb_ss_ts-doa-p_1_15 Website: https://www.thecaregiversjourney.com Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/TheCaregiversJourneys/ Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com

We are Sue Ryan, Nancy Treaster, and Merritt Treaster. In this episode, we're introducing ourselves to you and sharing why we are so passionate about bringing you practical tips and candid conversations for Alzheimer's and other dementia family caregivers.  Show Notes Takeaways Nancy and I have known each other for many years and have often discussed our caregiving journeys together. We're both passionate about helping you navigate your caregiving journeys with fewer surprises and more confidence.  Our podcast offers practical tips and we have candid conversations to help you tackle day -to -day common dementia challenges. Our purpose is to give you the knowledge and the resources you need to navigate your journey with strength, patience, and peace of mind. We're all on this journey together. Rate, subscribe and share your tips on social media! Thanks for listening! If you enjoyed this episode, please leave a review and subscribe on your favorite podcast platform. Please click here to review, follow or subscribe to our podcast.   If you don't see your preferred platform click on Podchaser and click at the bottom “Write my review” You can log in with Twitter, Facebook or GoogleOn the right you'll see a box with “Follow”, “Rate and Review” and “Share”  Connect with us and share your tips: Website: https://www.thecaregiversjourney.comInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Keywords Alzheimer's, dementia, caregiver, caregiving, Alzheimer's care, dementia care, memory care, best dementia podcast, best Alzheimer's podcast, best caregiver podcast, best caregiving podcast, best caregiver podcast, dementia caregiver podcast, dementia podcast, Alzheimers podcast, caregiver podcast, senior caregiver podcast, dementia caregiver tips, frontotemporal dementia, dementia caregiver tips, how to deal with dementia as a caregiver, information on dementia for caregivers, how to be a caregiver for someone with dementia, family caregiver, Sue Ryan, Nancy Treaster, Merritt Treaster, Susan J Ryan

Does it feel like a punch in the gut every time you realize something new your loved one has forgotten? As caregivers for our husbands, parents, and other loved ones with Alzheimer's disease and other types of dementia, we've learned that memory loss in the early stages is a challenging journey. In the beginning (the early season of the diagnosis), our primary goal is to help our care receivers maintain as much dignity and independence as possible while providing support behind the scenes. We are Sue Ryan and Nancy Treaster, and through our experiences, we have four main tips that we'd like to share with you. Show Notes Takeaways In this episode, we're talking about memory loss “in the beginning”. When we say “In the beginning” we mean when you're mostly helping your care receiver manage things (often behind the scenes), while also helping them maintain their independence.  We offer four tips to help you. Tip 1: Figure Out What Information They're Struggling to Remember One of the most effective ways to support your loved one is by identifying what information they're having trouble remembering. This involves careful observation and adapting your approach to help them maintain their dignity and independence. Tip 2: Understand and Help with What They Can No Longer Do As the condition progresses, it's important to adapt tasks your loved one can no longer manage independently. Tip 3: Get Other People Involved, As Appropriate Sharing the diagnosis with others can be a sensitive topic, but it's often crucial for both the caregiver and the care receiver. Tip 4: Watch Out for UTIs - They Can Muddle the Whole Situation Urinary Tract Infections (UTIs) can significantly impact cognitive function and behavior in people with dementia and there can often be no symptoms except a sudden cognitive decline. At the beginning it's hard to get your head around what is happening. You will get through this phase, and your confidence will grow as you learn to handle each new situation.  Related episodes 3. Communication - in the Beginning: Four Essential Tips / Alzheimer's and Other Dementias / Practical Tips and Candid Conversations Rate, subscribe and share your tips on social media! Thanks for listening! If you enjoyed this episode, please leave a review and subscribe on your favorite podcast platform. Please click here to review, follow or subscribe to our podcast.   If you don't see your preferred platform click on Podchaser and click at the bottom “Write my review” You can log in with Twitter, Facebook or GoogleOn the right you'll see a box with “Follow”, “Rate and Review” and “Share”  Connect with us and share your tips: Website: https://www.thecaregiversjourney.comInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Keywords Alzheimers, dementia, caregiver, caregiving, Alzheimers care, dementia care, memory care, best dementia podcast, best alzheirmers podcast, best caregiver podcast, best caregiving podcast, best caregiver podcast, dementia caregiver podcast, dementia podcast, alzheimers podcast, caregiver podcast, senior caregiver podcast, dementia caregiver tips, frontotemporal dementia, dementia caregiver tips, how to deal with dementia as a caregiver, information on dementia for caregivers, how to be a caregiver for someone with dementia, Sue Ryan, Nancy Treaster, Susan J Ryan

You are going to wish you knew about the third tip in this episode much earlier! As caregivers for our husbands, parents, and other loved ones with Alzheimer's disease and other types of dementia, we've learned that communication is a constantly evolving process. In the beginning (the early season of the diagnosis), our primary goal is to help our care receivers maintain as much dignity and independence as possible. We are Sue Ryan and Nancy Treaster, and through our experiences, we've developed four tips to help you communicate.  Show Notes Takeaways In this episode, we're talking about communication “in the beginning”. When we say “In the beginning” we mean when you're mostly helping your care receiver manage things (often behind the scenes), while also helping them maintain their independence.  We offer four tips to help you. Tip 1: Help Them Plan Their Day One of the most effective ways to support your loved one is by assisting them in planning their day. This involves understanding what they can realistically accomplish and creating a manageable list of tasks for them to do. The list also helps you support them, making it easier to prompt them gently throughout the day to complete these tasks. This approach helps them feel valued and accomplished at day's end. Tip 2: Simplify and Minimize As cognitive abilities decline, it's important to simplify instructions and minimize distractions. What worked one week might be too complex the next, so constant observation and adjustments are necessary.  Tip 3: Use Positive Reinforcement and Body Language Positive reinforcement can have a profound impact on your loved one's mood and cooperation. Even if it feels unnatural at first, offering praise for completing simple tasks can boost their confidence and create a more positive atmosphere. Tip 4: Share the Truth They Need to Hear While honesty is important, we've learned that it's often more beneficial to share "the truth they need to hear" rather than the whole truth. Rather than think of this as lying, think of it as providing information in a way that minimizes their – and often our - anxiety and frustration. Everything you're experiencing in terms of communication during this early season of their dementia may feel challenging and strange. You'll be constantly adapting and adjusting your approach. But, this is just a phase. You will manage through this situation, and it will get better. Related episodes 2. Memory Loss: Four Essential Tips / Alzheimer's and Other Dementias / Practical Tips and Candid Conversations Rate, subscribe and share your tips on social media! Thanks for listening! If you enjoyed this episode, please leave a review and subscribe on your favorite podcast platform. Please click here to review, follow or subscribe to our podcast.   If you don't see your preferred platform, click on Podchaser and click at the bottom “Write my review” You can log in with Twitter, Facebook or GoogleOn the right you'll see a box with “Follow”, “Rate and Review” and “Share”  Connect with us and share your tips: Website: https://www.thecaregiversjourney.comInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Keywords Alzheimer's, dementia, caregiver, caregiving, Alzheimer's care, dementia care, memory care, best dementia podcast, best Alzheimers podcast, best caregiver podcast, best caregiving podcast, best caregiver podcast, dementia caregiver podcast, dementia podcast, Alzheimers podcast, caregiver podcast, senior caregiver podcast, dementia caregiver tips, frontotemporal dementia, dementia caregiver tips, how to deal with dementia as a caregiver, information on dementia for caregivers, how to be a caregiver for someone with dementia, family caregiver, Sue Ryan, Nancy Treaster, Susan J Ryan

I wish I had known about this child proofing tip before I spent so much money on locksmiths. In this episode we talk about wandering. As caregivers for our husbands, parents, and other loved ones with Alzheimer's and other types of dementia, we've learned that wandering is a complex and often frightening behavior that requires careful management. Wandering can occur both inside and outside the home, during day or night, and each scenario presents unique challenges. We are Sue Ryan and Nancy Treaster, and through our experiences, we have four tips to address wandering while maintaining our loved ones' dignity as well as ensuring their safety. Show Notes Takeaways Outside Wandering Tip 1: Use your grapevine   Tip 2: Consider wearable tracking devices Tip 3: Register them with EMT's and police Tip 4: Consider child proof door knob covers on doors that lead to the outside Tip 5: Consider window sash locks and a pole for any sliding doors Inside Wandering Tip 1: Safety proof the areas you allow them to go during the day Tip 2: Discuss sleeping medication with their doctor Tip 3: Allow them access at night to only the bedroom and a bathroom Tip 4: Consider cameras or baby monitors to make sure you can watch them especially at night  Tip 5: Safety proof access to stairs  Additional Resources Mentioned Tracking devices for their personWatcheshttps://www.amazon.com/s?k=person+tracking+device&crid=OPZ28JRM2KDU&sprefix=person+t%2Caps%2C96&ref=nb_sb_ss_ts-doa-p_2_8Shoeshttps://www.amazon.com/s?k=gps+smart+sole&crid=2DM2XBGVTA5VJ&sprefix=GPS+smart+sole+%2Caps%2C95&ref=nb_sb_ss_ts-doa-p_1_15Child proof door knob cover or double deadbolt locks for external doorsChild proof door knob covershttps://www.amazon.com/s?k=child+proof+door+knob+covers&crid=1VBY69F9OQN3T&sprefix=child+proo%2Caps%2C105&ref=nb_sb_ss_ts-doa-p_3_10Double dead bolt or code based lockhttps://www.amazon.com/s?k=2+key+both+sides+deadbolt+lock+set&i=tools&crid=32L214IRSRSLU&sprefix=2+key+both+sides+deadbolt+lock+set%2Ctools%2C69&ref=nb_sb_nossWindow sash https://www.amazon.com/Defender-Security-9928-Security-Unlocks/dp/B00BOZBGF8?pd_rd_w=1gyHe&content-id=amzn1.sym.378a0f29-5acb-4c80-bc6e-087cd6806daf&pf_rd_p=378a0f29-5acb-4c80-bc6e-087cd6806daf&pf_rd_r=F9XR7F8R8B4H0PHGYRGY&pd_rd_wg=hFzlD&pd_rd_r=9e98be86-af00-40b7-b783-6f58d7839b31&pd_rd_i=B00BOZBGF8&ref_=pd_bap_d_grid_rp_0_1_ec_sr_ppb_i&th=1Extra tall pet gate from 40” to 70” https://www.amazon.com/s?k=extra+tall+pet+gate&i=tools&crid=1ZJ0VGQK13QAV&sprefix=extra+tall+pet+gate%2Ctools%2C86&ref=nb_sb_noss_2 Cameras or baby monitor for the bedroom and bathroomBaby monitors - some come with motion alarms as wellhttps://www.amazon.com/s?k=baby+monitor+with+motion+detection&i=tools&crid=27MFODCOG9GBV&sprefix=baby+monitor+with+motion+de%2Ctools%2C84&ref=nb_sb_ss_fb_1_27I use Nest Cameras and pay for the Nest Aware feature which gives me access to video history. A friend of mine uses a Ring and swears by it. Whatever kind you get, if your care receiver is still staying home alone, consider one with an intercomIndoorhttps://www.amazon.com/s?k=indoor+cameras+with+intercom&i=tools&crid=1RTJWUD6C53DD&sprefix=indoor+cameras+with+intercom%2Ctools%2C72&ref=nb_sb_nossOutdoorhttps://www.amazon.com/s?k=outdoor+cameras+with+intercom&i=tools&crid=2ERD6HT2QIK5W&sprefix=outdoor+cameras+with+intercom%2Ctools%2C78&ref=nb_sb_nossMotion alarmhttps://www.amazon.com/s?k=person+indoor+motion+alarm&crid=393V3S00L1T5W&sprefix=person+indoor+motion+alarm%2Caps%2C75&ref=nb_sb_noss Please click here to review, follow or subscribe to our podcast.   Connect with us and share your tips: Website: https://www.thecaregiversjourney.comInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/

If you can successfully leverage tip one in this episode you will have an easy path to removing driving privileges. As caregivers for our husbands, parents, and other loved ones with Alzheimer's and other types of dementia, we both learned that driving privileges are a sensitive and important issue to address. In the beginning stages of dementia, our primary goal is to balance safety with our care receivers' desire for independence. We are Sue Ryan and Nancy Treaster, and through our experiences, we've offer four key tips for removing driving privileges. Show Notes Takeaways We offer four tips to help you. Tip 1: Understand Legal and Insurance Considerations One of the most effective ways to approach the driving issue is to familiarize yourself with the legal and insurance implications in your area. This involves researching local laws and understanding the potential consequences of allowing someone with dementia to continue driving. Tip 2: Implement Tracking Measures For those in the early stages of dementia who are still able to drive safely, tracking can provide peace of mind for caregivers while allowing the care receiver to maintain some independence. Tip 3: Gradual Transition: Riding Along and Taking Over As dementia progresses, it's helpful to start riding along frequently and gradually take over driving responsibilities. Tip 4: Removing Driving Privileges Completely Sometimes, for safety reasons, we need to take more decisive action to prevent our loved ones from driving. Additional Resources Mentioned State laws on dementiaWe found this state by state summary online but can't vouch for the source.  https://www.dementiacarecentral.com/caregiverinfo/driving-problems/#state-lawsCheck you state law specifically by searching like this “state name law driving with dementia”Tracker for their carIphone users - Airtaghttps://www.amazon.com/s?k=airtag&crid=1BY7R7PYXTG6J&sprefix=airt%2Caps%2C166&ref=nb_sb_ss_ts-doa-p_1_4Android user - Tilehttps://www.amazon.com/s?k=android+tile&crid=2KQYC4CI78EZO&sprefix=android+tile%2Caps%2C99&ref=nb_sb_noss_1Tracking device for their carhttps://www.amazon.com/s?k=person+tracking+device&crid=OPZ28JRM2KDU&sprefix=person+t%2Caps%2C96&ref=nb_sb_ss_ts-doa-p_2_8Tracking device for their personWatcheshttps://www.amazon.com/s?k=person+tracking+device&crid=OPZ28JRM2KDU&sprefix=person+t%2Caps%2C96&ref=nb_sb_ss_ts-doa-p_2_8Shoeshttps://www.amazon.com/s?k=gps+smart+sole&crid=2DM2XBGVTA5VJ&sprefix=GPS+smart+sole+%2Caps%2C95&ref=nb_sb_ss_ts-doa-p_1_15 Rate, subscribe and share your tips on social media! Thanks for listening! If you enjoyed this episode, please leave a review and subscribe on your favorite podcast platform. Please click here to review, follow or subscribe to our podcast.   If you don't see your preferred platform click on Podchaser and click at the bottom “Write my review” You can log in with Twitter, Facebook or GoogleOn the right you'll see a box with “Follow”, “Rate and Review” and “Share”  Connect with us and share your tips: Website: https://www.thecaregiversjourney.comInstagram: https://www.instagram.com/thecaregiversjourney/Facebook: https://www.facebook.com/TheCaregiversJourneys/Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Keywords Alzheimers, dementia, caregiver, caregiving, Alzheimers care, dementia care, memory care, best dementia podcast, best alzheirmers podcast, best caregiver podcast, best caregiving podcast, best caregiver podcast, dementia caregiver podcast, dementia podcast, alzheimers podcast, caregiver podcast, senior caregiver podcast, dementia caregiver tips, frontotemporal dementia, dementia caregiver tips, how to deal with dementia as a caregiver, information on dementia for caregivers, how to be a caregiver for someone with dementia, family caregiver, Sue Ryan, Nancy Treaster, Susan J Ryan

Does it feel like a punch in the gut every time you realize something new your loved one has forgotten? As caregivers for our husbands, parents, and other loved ones with Alzheimer's disease and other types of dementia, we've learned that memory loss in the early stages is a challenging journey. In the beginning (the early season of the diagnosis), our primary goal is to help our care receivers maintain as much dignity and independence as possible while providing support behind the scenes. We are Sue Ryan and Nancy Treaster, and through our experiences, we have four main tips that we'd like to share with you. Show Notes Takeaways In this episode, we're talking about memory loss “in the beginning”. When we say “In the beginning” we mean when you're mostly helping your care receiver manage things (often behind the scenes), while also helping them maintain their independence. We offer four tips to help you. Tip 1: Figure Out What Information They're Struggling to Remember One of the most effective ways to support your loved one is by identifying what information they're having trouble remembering. This involves careful observation and adapting your approach to help them maintain their dignity and independence. Tip 2: Understand and Help with What They Can No Longer Do As the condition progresses, it's important to adapt tasks your loved one can no longer manage independently. Tip 3: Get Other People Involved, As Appropriate Sharing the diagnosis with others can be a sensitive topic, but it's often crucial for both the caregiver and the care receiver. Tip 4: Watch Out for UTIs - They Can Muddle the Whole Situation Urinary Tract Infections (UTIs) can significantly impact cognitive function and behavior in people with dementia and there can often be no symptoms except a sudden cognitive decline. At the beginning it's hard to get your head around what is happening. You will get through this phase, and your confidence will grow as you learn to handle each new situation. Related episodes 3. Communication - in the Beginning: Four Essential Tips / Alzheimer's and Other Dementias / Practical Tips and Candid Conversations Rate, subscribe and share your tips on social media! Thanks for listening! If you enjoyed this episode, please leave a review and subscribe on your favorite podcast platform. Please click here to review, follow or subscribe to our podcast. If you don't see your preferred platform click on Podchaser and click at the bottom “Write my review” You can log in with Twitter, Facebook or Google On the right you'll see a box with “Follow”, “Rate and Review” and “Share” Connect with us and share your tips: Website: https://www.thecaregiversjourney.com Instagram: https://www.instagram.com/thecaregiversjourney/ Facebook: https://www.facebook.com/TheCaregiversJourneys/ Email: sue@thecaregiversjourney.com, nancy@thecaregiversjourney.com Keywords Alzheimers, dementia, caregiver, caregiving, Alzheimers care, dementia care, memory care, best dementia podcast, best alzheirmers podcast, best caregiver podcast, best caregiving podcast, best caregiver podcast, dementia caregiver podcast, dementia podcast, alzheimers podcast, caregiver podcast, senior caregiver podcast, dementia caregiver tips, frontotemporal dementia, dementia caregiver tips, how to deal with dementia as a caregiver, information on dementia for caregivers, how to be a caregiver for someone with dementia, Sue Ryan, Nancy Treaster, Susan J Ryan

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All of the questions in this episode were sent in by listeners via Instagram, Patreon messages, or Spotify responses. Support Creative Codex on my Patreon and get access to exclusive episodes, including the RED BOOK READING series and all the Episode Exclusives:  ⁠⁠https://www.patreon.com/mjdorian⁠⁠ Questions (in order of appearance, with timestamps): Do you think sadness / heartache / trauma is the secret ingredient to making great art? - Nikita ( 3:33 ) Of all the artists featured so far in Creative Codex, who would you most like to spend a day with – perhaps even working alongside or collaborating on a project? And what question would you most like to ask them? - Tamara ( 6:24 ) Will you ever do an autobiography? - X ( 9:03 ) What is the relation between Alchemy and Christianity, I know Jung wrote some pieces on it? - Tim Susss ( 10:16 ) How the hell do you do it? Is this your full time job? How do you read and dive into so many heads and worlds and then share it in this rich and atmospheric podcast? - Vika ( 11:48 ) What's something you learned about a creator that caught you off guard and made you laugh? - Nolo ( 13:54 ) In episode 39: Carl Jung and Alchemy Part 1, 15 minutes and 17 seconds in, I would love to know the name of that beautiful piece of music. - Daniel ( 16:41 ) Do you think AI could ever independently tap into individual, animal or human collective consciousness? How will we know what art (say something done by hand like a painting or sculpture) is authentically from that artist anymore? Will imagination become an unused skill through laziness? - Sue Ryan ( 22:05 ) I have started a YouTube channel but I get discouraged very quickly. How do I stop getting discouraged? - Priyanka ( 34:27 ) What are your thoughts on the subject of channelling? - Diana Grigorieva ( 37:22 ) Sylvia Browne clip: https://www.youtube.com/watch?v=9yzz8vaZgE8 I'd love to know about your writing process, I enjoy your work. Where do you start? - Thomas Widner & Vida013 ( 42:50 ) Do you think the Collective experience of archetypes (to articulate beliefs and ideas) has contributed to the rise of fantasy / collaborative storytelling games and entertainment in the recent years? - Nathan Grabosch ( 45:20 ) I have been reading Jacques Sadoul's “Alchemy and Gold”, and it states that alchemists wrote their discoveries in metaphors, since true knowledge has to remain occult. Why do you think this is? - Romina ( 47:10 ) How do you reconcile the tension between the desire to create something absolutely original with the idea that creativity seems to be the revealing of a truth? Is there anything new under the sun and should we strive for that if there is? - J Kent ( 48:39 ) Do you consider that genius is someone fixated in the stage of the albedo? This stage is the closest point between the ego and the collective unconscious. It's a fascinating yet perilous stage (psychosis). - Trudy ( 52:45 ) How does Jung remember all these dreams and poignant symbolism so clearly? How could we follow his genius processes of the internal if our dream memories are not nearly as clear, if even present? - Mulnah ( 54:26 ) I'm curious what your feelings are about drugs and creativity? Are drugs a crutch, a useful tool, or something else? - Ben Thurnhoffer ( 56:00 ) I'm curious about how symbolism works in alchemy as well as in Jung's work, the origin of symbols and such. - Chris DeHaven ( 59:25 ) Do you think that knowledge that Jung left behind was for the creatives and perhaps neurotypicals of today to be re-discovered to heal from modern madness and unlock potential? - Talos_draws ( 01:00:46 ) What is the relationship between art and value? What is the value of art? To elicit an experience? To convey a message? To transform the subjective into the objective? - Al Spaulding ( 01:02:34 ) How has this podcast changed your life? - Clinton King ( 01:05:30 ) Creative Codex Soundtrack Vol.1: https://mjdorian.bandcamp.com --- Produced by MJDorian

All Home Care Matters is honored to welcome the founder of Sue Ryan Solutions, Sue Ryan. Sue's mission is to empower and embolden individuals to maximize the opportunities and potential change will bring. As a speaker, change strategist, author, executive coach, caregiving coach and mentor, she lives this through two passions of her purpose. She guides and inspires leaders and emerging leaders committed to business growth and next-level leadership to be great leaders of themselves and others. She guides non- professional caregivers to become confident, balanced, and supported in all phases of their caregiving journey. Sue specializes in helping individuals and teams thrive during times of change. Working with them to clarify, align, develop, and implement solutions in highly competitive markets, while creating their culture poised to face the challenges of change with resilience and right action in the direction of their goals, they successfully deliver long-term brand growth and value. Whether change is due to external factors such as market shifts, technology innovation, economic changes - or setting their sights on growth and expansion - understanding the dynamics and psychology of change enhances their ability for success. Sue delivers these through her signature offerings Intentionally Navigating Transitions - Leadership Through the Dimensions of Change, The Prodigy ZoneTM, Leadership C.A.R.E.S.TM, and The Caregiver's Journey. Sue's corporate career of more than 30 years was in enterprise application software sales to companies across industries including Healthcare, Financial Services, Information Technology, Manufacturing, Hospitality, and Utilities. She was responsible for ensuring individuals were poised for change and their organizations were positioned for predictable success. While her performance was consistently recognized in the top tier, her most satisfying achievement was her nearly 100% client retention rate. Sue has been in roles of family caregiving support for more than forty years. She's moved from feeling frustrated, overwhelmed, and yes - sometimes frightened - to confident, balanced, and supported, navigating the transitions in her life, her care receivers, and those who support them on their journey. As a speaker, coach, author, educator, and mentor, she shares the lessons, tips, and strategies she's learned to help others positively navigate their caregiving journeys. Sue has been a volunteer mentor of emerging leaders for Menttium since 2011. Sue volunteers in the children's ministry of Gulf Community Church, is a member of the Blue Zone's Engagement Committee, and a passionate technology educator for seniors. Sue is a member of the International Coaching Federation. Through her coaching, Sue earned the John Mattone Platinum-Elite Executive Coach ranking. Sue supports the Leadership Collier Foundation and is a 2023 graduate of Leadership Collier. She volunteers as a speaker and Community Educator for The Alzheimer's Association, and is a speaker and volunteer for AlzAuthors. She has authored or co-authored three International best-selling books. Two are in the field of business. Her non-professional caregiving book is Our Journey of Love, 5 Steps to Navigate Your Caregiving Journey. She created the online course The Caregiver's Journey to support caregivers through their entire caregiving journey. Sue recently gave her first TEDx talk. Next stop, the TED platform.