Episode 44

An Interview with A Special Guest – Lance A. Slatton CSCM – Host of the Award Winning Podcast, All Home Care Matters

Lisa has invited a very special guest onto her Truth, Lies, & Alzheimer’s Show Today. His name is Lance A. Slatton, CSCM. Lance is a Certified Senior Case Manager at Enriched Life Home Care Services and the Host of the Award Winning Podcast, All Home Care Matters. Lisa and Lance discuss what shifts they are seeing in this post-COVID world in terms of the way our loved ones, especially those living with dementia, are being cared for.

  •     For example, are more people being cared for at home post-COVID vs. the more institutionalized settings?
  •     How has COVID changed the way people are being cared for today,  if at all?
  •     Lisa and Lance dive deep into the future of care and what the culture of care might look like moving forward post- COVID, especially for those living with dementia.  

About the Guest:

Lance A. Slatton is a Certified Senior Care Manager at Enriched Life Home Care Services in Southeastern Michigan, providing people with an enriched life through their home care services. Lance is also the host of the award-winning Podcast, ‘All Home Care Matters’, and the winner of the 2023, ’50 under 50’ award, issued by the NYC Journal. Lance’s website is https://allhomecarematters.com

About the Host:

Author Lisa Skinner is a behavioral specialist with expertise in Alzheimer’s disease and related dementia. In her 30+year career working with family members and caregivers, Lisa has taught them how to successfully navigate the many challenges that accompany this heartbreaking disease. Lisa is both a Certified Dementia Practitioner and is also a certified dementia care trainer through the Alzheimer’s Association. She also holds a degree in Human Behavior.

Her latest book, “Truth, Lies & Alzheimer’s – Its Secret Faces” continues Lisa’s quest of working with dementia-related illnesses and teaching families and caregivers how to better understand the daunting challenges of brain disease. Her #1 Best-seller book “Not All Who Wander Need Be Lost,” was written at their urging. As someone who has had eight family members diagnosed with dementia, Lisa Skinner has found her calling in helping others through the struggle so they can have a better-quality relationship with their loved ones through education and through her workshops on counter-intuitive solutions and tools to help people effectively manage the symptoms of brain disease. Lisa Skinner has appeared on many national and regional media broadcasts. Lisa helps explain behaviors caused by dementia, encourages those who feel burdened, and gives practical advice for how to respond.

So many people today are heavily impacted by Alzheimer's disease and related dementia. The Alzheimer's Association and the World Health Organization have projected that the number of people who will develop Alzheimer's disease by the year 2050 worldwide will triple if a treatment or cure is not found. Society is not prepared to care for the projected increase of people who will develop this devastating disease. In her 30 years of working with family members and caregivers who suffer from dementia, Lisa has recognized how little people really understand the complexities of what living with this disease is really like. For Lisa, it starts with knowledge, education, and training.

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Transcript
Lisa Skinner:

Hi, everybody. Welcome back to a another new episode of the truth lies and Alzheimer's show. I'm Lisa Skinner, your host. I have a really special guest here with me today. And I'd love to introduce him to you. So let's let's get on with the show as they say, this is Lance, a Slaton. And he actually was a speaker at my summit week before last and so I invited him back on because we are going to talk about a really not only interesting, but important topic today. So let me just tell you a little bit about Lance and then we'll get started with our discussion. So Lance is a certified senior care manager at enriched life homecare services, and he's also the host of the number one rated podcast in the US for the last several years called all homecare matters. He has been a senior case manager for is it eight years, Lancer, 10 years, 10 years, okay 10 years, and has been the host of course of all homecare matters since its inception in the year 2020. Lance finds joy in helping families and those needing care and support. And this led him and his team at enrich life home care services, to create the podcast. All Home Care matters in 2020, to act as a continuation of his work that they have been doing for families and communities throughout South Western Michigan. His commitment to the families and communities in Michigan has led enrich life homecare services to be recognized and awarded the number one home care provider in Michigan for the past four years in a row. Wow, that is quite a remarkable achievement. Congratulations,

Lisa Skinner:

Lance A. Slatton: thank you.

Lisa Skinner:

As host of all Healthcare Matters, he's always looking for ways to help listeners and viewers to find and have the information, have accessible resources and support that everybody as we know, needs as they face long term care issues, and letting them know that they are definitely not alone. He also serves as a member of the Board of Directors for a senior center in Monroe County, Michigan. And he has won the honor and award in 2023 of 50, under 50, which was issued by the New York City Journal, while you have really made a lot of just unbelievable achievements in your work. And so congratulations to you, and all the wonderful work you're doing for this, you know, tough situation for most families. So I want to start our conversation with this question to you, Lance. Because I personally, as you know, I've been counseling families for 30 years now. And plus, I've had eight of my own family members live with one of the brain diseases that cause dementia. And I have personally witnessed since COVID, a shift in the way we're caring for not only our elders, but for people living with Alzheimer's disease and related dementia. So my question to you is in this post COVID world that we are all living in today, what shifts are you seeing that since you do own and operate in home care service company, in the way people are being cared for? And why do you think that we have seen significant shifts since the COVID? pandemic?

Lisa Skinner:

Lance A. Slatton: Yeah, well, first, thank you for the invitation to be here with you, Lisa. And the kind introduction. What we've noticed ourselves on the professional side is when COVID started, you know, a lot of people didn't know what to expect, they didn't know what to do, how to handle it, how to even prepare a plan for what was coming or what they're dealing with. And a lot of families, you know, we you know, I said to somebody just yesterday, you know, we look at our health care providers with reverence. You know, we don't we don't question a doctor, we don't question our pastors or our priests, right. It's, you know, it's a respect for their positions, their trainings their education and experiences. But I feel a lot of families started taking notice when they had to visit their mom or their grandmother or their dad or whoever it may be through a window in the middle of winter in Michigan, to be able to see them and to have any sort of interaction with them. So we started seeing a dramatic shifts to people discovering who didn't even know that a homecare industry existed, to having their loved ones be taken out of these facilities and placed into a home. You know, that's one of the biggest shifts we've seen is families are starting to stay away from where the institutionalized care if you will, and trying to get more into the personalized care. But the other shifts we've seen, though, is almost the polar opposite. We're seeing more people leave the health care industry leaving the home care industry and not returning, you know, and I don't know that anybody really has the answer for why that shift away from those types of services and employment have happened and continue to this day,

Lisa Skinner:

what are they doing? instead?

Lisa Skinner:

Lance A. Slatton: Your guess, would be as good as mine, you know, are they going into an another industry? Were they not returning to the workforce at all? I don't know that anybody has a clear answer, you know, get it, you know, I don't want to make this about, you know, numbers and unemployment. But, you know, we see where unemployment numbers are going down. But the Help Wanted, signs are going up. And a lot of that is I feel people who, you know, went on to, you know, like the COVID relief and unemployment, they're in COVID. You know, they just stayed there, they never returned into the workforce. And so a lot of those people have been on there for so long, they no longer qualify, so they're not getting an unemployment claim. But they're not being counted as being unemployed, because they just drop off altogether. So they're kind of in that abyss of, well, they're not on unemployment, but they're not gainfully employed. And you know, it's COVID really wreaked havoc on, you know, our society as a whole for, you know, services and, you know, work and, you know, factories, you know, health care. I mean, I know, even here just a couple months ago in our communities, a lot of our local emergency rooms and our more community style hospitals, they actually would divert everybody to the major like University Hospitals, because they could not stop there. Er,

Lisa Skinner:

yeah, yeah, I'm aware of that. Yeah, one of the statistics that came out after COVID, and I believe it was the world Alzheimer's annual health study report. And this was probably after the vaccines came out that we saw a dramatic rise in deaths of people that were in assisted living communities in memory care communities, I would say, especially memory care communities in long term care facilities. And interestingly, it was the number one cause of these deaths that occurred in the these populations was due to what you brought up a few minutes ago, isolation and loneliness. And I don't think any of us saw that coming. But they really didn't have a choice, but to close not allow visitors and you know, think about it, it's especially hard in a memory care arrangement environment. How do you communicate to people with cognitive decline, that they have to stay six feet apart, and they have to wear masks? You ever, if you ever tried to get a person living in their mid to later stage of dementia to wear a mask? 24/7? It's, you know, it's almost very challenging.

Lisa Skinner:

Lance A. Slatton: Yeah, it, you know, it's frightening, right? They don't know what's going on, they don't understand this, and you were invading their very close personal space. You know, and, you know, it was just, you know, people were trying to make do with what they had, right, we're trying to do the best with the circumstances given to us. But ultimately, you know, these families just realized, you know, I need to get my mom, I need to get my loved one in, we need to get them home. Because, you know, you don't know if your roommate might have had COVID Now he's getting passed on to your mother. And, you know, they just, you know, it was very trying times, very trying times, and I know, at least here in Michigan, you know, we had a big movement supporting these frontline workers in the frontline was the caregivers and the home health aides who are trying to keep the people who are home, keep them safe, and quarantine them so that they're not going out to the public and contracting it and then going here going there. work. And you know, we noticed it months before, at least in our state situation before we were shut down. Because we would do a lot of community events, educational talks, dementia seminars, fun activities, concerts, offer, you know, the senior centers and different, you know, facilities just to, you know, bring a smile to their face just to lighten the load and brighten their day. And we started noticing these events where you'd get 50 to 100 people now, it's like, there's eight people, then there's four people in. So before we officially got shut down, we made the decision, okay, we're gonna haul to all of our events, you know, and that's where we decided, you know, let's, let's start a podcast. And we can do that for a couple of weeks, right, thinking that's what it was going to be. And that couple of weeks turned into several years, in our I remember here at our offices, because our governor, you know, deemed and labeled us as essential. We would always watch the press conferences every two weeks Friday at you know, one o'clock, there's going to be an update. And you know, the first week we're like, okay, let's, what's the latest news, and then that second shot down, then the third, you know, every two weeks, then it got to the point where it's like, we're not even going to watch because it's just another announcement that we're going to, it's going to be a continuation of the shutdown. And that's when I think a lot of people, you know, the general public started realizing, you know, this is something a lot more serious than just a two to four week situation. And so yeah, so we'd like, let's just use the power of audio and video and help the communities that way. So

Lisa Skinner:

I, I totally agree with you, because I do my show. Because people really don't know where to turn or who to, to find information on the day to day challenges that they're faced with when it comes to Alzheimer's and related dementia. And that surprises me because my first experience dates back 50 years when my grandmother was showing obvious signs of what they call back then senile dementia. And understandably, I mean, I don't even talk about it, let alone call it by, you know, its its current name, Alzheimer's disease, it was senile dementia, which kind of infers that you have a crazy person on your hands. So nobody knows the way things were, then I've been doing this professionally for 30 years. And I know that it's been a real struggle for people to because they don't get a direction or resources or expectations from the primary care physicians or the neurologists. They're not trained in these areas in the psycho social approach to living with Alzheimer's disease and related dementia on a day by day by day basis. But you know, here, fast forward 50 years, 30 years, I have not seen a huge change in people's ability to access, reliable resources and information to help them through the daily challenges. And as you know, Lance, this is a disease that impacts every single person who is involved with somebody living with a brain disease that causes dementia. Absolutely. Go ahead.

Lisa Skinner:

Lance A. Slatton: I was just gonna say if I could piggyback on that for a moment, you know, a good friend of mine, and I know a friend of yours, Pete Hill, from the D word. You know, that name, I think really just epitomizes what families are going through, you know, my grandfather had cancer, you know, 30 plus years ago, and back then it was the C word. Right? Because the medical community. I don't want to say they're afraid, but it's almost like they're afraid of saying the word of something that they don't have an answer for, right, because the doctors and nurses the Hippocratic Oath, you know, we want to help heal, you know, heal and cure and treat cancer back then there was very limited options on what you could do other than, you know, surgically removing it and cutting it out. Right. Or, you know, the radiation and chemo, you know, has made some leaps and bounds since then. But now it's almost like dementia has replaced cancer as that b word which was the C word. So now they don't want to say dementia because it's like what they dealt with with cancer there. You don't have real solutions for curing, treating, and, you know, any sort of positive prognosis. So they want to, you know, I know families that have gone to their doctor, with all of these concerns, the signs the symptoms, but they yet would never read receive a diagnosis of dementia of any form type from that physician because physician didn't know how to tell them. This is what you have, but I have nothing to offer you after I tell you you have this diagnosis, you know, so they feel almost like a, you know, a failure in some level, I think. And so, you know, it's just like almost unspoken, they want some other doctor to give you that diagnosis.

Lisa Skinner:

Yeah, yeah, this is probably the toughest one of the toughest things that any family members will ever encounter in their lifetime. Because it's a long process, the average person lives with it for eight to 15 years, my grandmother was 20 year old woman, a speaker at our summit, I was blown over when she said her mom lived with it for 30 years, I don't think I'd ever heard that length of time. So that's a long time to kind of watch your loved one or, or even caring for somebody that you know, will be living with this for a long period. So let's talk about the dementia aspect. Because there's a very significant difference between caring for people in their home environments who do not live with Alzheimer's disease or dementia. And those who do it, you know, it's just 100 times more challenging and difficult. So how do you as a company, how have you adapted to the shift that we've both agreed we're seeing that I, you know, I think the whole COVID thing freaked a lot of families out, right, because they weren't allowed access. But the thing is, I wanted to bring this up a little earlier, one of the challenges, I think, that nobody really factored in until they actually saw it happening is it's not uncommon for caregivers to work at more than one facility. So what we saw happening was they you know, the facilities, whether they were assisted living or memory care, were inaccessible to family members and visitors. But the caregivers were coming and going, can you speak to Yeah, cuz?

Lisa Skinner:

Lance A. Slatton: Yeah, I will say, you know, you hit the nail on the head, we had so many families, because so our staff weren't working for the facilities, but they were working for families. So oftentimes, Lisa, you know, and I'll get deeper into this in a minute. But we have staff who are taking care of Mrs. Jones at her house, family decided, you know, what, let's downsize. Because we, you know, property taxes, homeowners insurance, utilities, you know, lawn care, snow removal in Michigan, and let's put her in a facility. But yet, we still want, you know, Mary, who her caregiver is to stay with her. I mean, we have families, we continue with them, and hospital admissions and nursing home admissions, and when they move into some type of senior living community, because it has that familiarity. And it's a great, you know, way for the family to have an extra pair of eyes and ears, right. And so, often families would say to us, we don't understand, you know, Mary can go in and take care of mom, Mary's working at a couple of other homes, she's going shopping, you know, she's doing, you know, she's not quarantined from the outside world, like all of the residents are. So why can't we go in and see our mom, but Mary can? What is the difference?

Lisa Skinner:

And that's a really good point. So what was the response to that?

Lisa Skinner:

Lance A. Slatton: Well, the facility would just say, you know, health care professionals, you know, that's what they would kind of put it off on. So like, for us, you know, we would have, all of our staff would pre screen do a questionnaire survey before going on to a shift. But again, that wasn't foolproof, you know, you don't you could be carrying the, you know, the germs you could be carrying COVID Right now, and not even know it until two or three days later, you start showing symptoms, isn't it? It's too late. But then the other part of that is how can you trace it back if you've been to 17 different places in the past two days, you can't pinpoint where or who you might have contracted it from. But then you got to go back and do the, you know, contact awareness. We were working with like our Department of Health and Human Services. Thankfully, honestly, we did not have one single person ever test positive for COVID during those that two and a half, three year period. And we only had one lady stepped down from employment. And that was because she was in her 60s and her family was asking her to do that for their own peace of mind. They were concerned mom was going to get some One thing, and you know, you know, because it was terrifying families were terrified and rightfully so of their loved ones are themselves getting COVID. And then you know, are they going to die? Or they're going to be in the ICU, or they're going to need a ventilator all these different things. And so she voluntarily stepped down. And then once that was resolved, then she did come back. But yeah, I mean, it's just, it was terrifying. But your point, though, you know, those caregivers working at multiple different facilities or going to different homes, I never did really understand other than they felt like, again, they use the professional versus a lay person, they're gonna be responsible, because they're, you know, professional versus a lay person may not take the appropriate steps or measures and, you know, things like that. So I don't know that there was really a good answer to it. But that's the explanation we had gotten.

Lisa Skinner:

So in the very beginning, you know, I agree with you, it was a terrifying prospect to think about contracting COVID. Because it was like the Spanish flu epidemic. I mean, if you contracted it, it meant it could have been a death sentence for you. And it turned out that it hit the elderly population worse than any other population. Do you remember how many years the facilities were shut down and losing track of time? I

Lisa Skinner:

Lance A. Slatton: want to, I could be wrong. I'm guessing here. I believe it's about three years. Yeah, that's what I did. I believe it's about three years, it might have been three years in some months or two years in some months. But it was right, because when we launched the show, in May of 2020. It was we spent several months researching and you know, I took some training with a broadcaster and things. And that was at the later stages of 19. Right around there. Yeah, so it was I think it was March 2020 is when things officially became shut down.

Lisa Skinner:

And then until the vaccines came out, yeah. But that was, I think,

Lisa Skinner:

Lance A. Slatton: late, late 2.1. Yeah. How

Lisa Skinner:

does that impact your business during the shutdown period?

Lisa Skinner:

Lance A. Slatton: You know, it did, but it didn't. So, you know, I tell people, you know, our staff already had PPE, we were already practicing, you know, safety precautions, you know, if the staff, you know, had a sniffle. And this is unrelated to COVID, you know, they would wear a mask when they're with their client. If they had a fever, they didn't go to work. If they were doing hands on care of any nature, they're always wearing gloves. Now, the difference is now they're also going to wear a mask. So, it what being in the industry, there weren't a lot of changes for us. Other than, you know, the staff all had to do their, you know, pre assessment survey before going to work, you know, do you have a temperature? Have you been exposed, anybody knowingly that tested positive for code, you know, things like that. But it really amplified the need for home care. It amplified it dramatically. Because, you know, families weren't who maybe they're a retired couple, and they would take care of mom on Monday, Wednesday, Friday. And you know, the other siblings would do it Tuesday, Thursday, Saturday, Sunday, or whatever the case may be. They're not even going to mom's now. Because, again, a lot of unknowns, they're being extra cautious. They don't want to go to mom's house to help her on Monday, Wednesday, Friday. So now they're looking, who can we get to help mom because we can't leave her alone either. And Mom is, you know, older, highly susceptible to getting sick. And it just it really shined a light on the home care industry. People that have never even known of home care didn't even know that you could have helped come right to your home. They're doing some serious research and learning about all kinds of things. So in a way, it was a positive and I don't mean that and from a business standpoint, but it's a positive that people became more aware of resources for their loved ones than thinking, you know, my option is assisted living, nursing home or hospital. You know, a lot of families they thought that's just what their choices were. Right.

Lisa Skinner:

So since the especially the memory care environments shut down, and we're not even an option for people for three years. And since then, we've agreed that we've seen a shift and a pivot to more people staying home with in home care. What How did you as a company and adapt to caregivers now caring for people with Alzheimer's disease and related dementia in their homes and keeping them safe and stimulated when it's just more of a one on one relation Shouldn't ship versus a bigger care staff taking care of a group of people and they have programs in place and things like that? Because we know it's even more important to be able to provide these things. We live with dementia. So how did you adapt your approach to the new kind of the new way of caring for people in their homes?

Lisa Skinner:

Lance A. Slatton: The biggest adaption because we we already, you know, we offer families, specialized, customized memory care programs already before COVID was ever a thing. The biggest thing, though, that we had to adapt to was we're not taking, you know, Mrs. Jones to her chair exercises, or to her ladies church group, you know, luncheons, they weren't able to go out places. So we were filling that time and with more engagement, more, you know, stimulation and things, but especially for the people, you know, living with dementia, or cognitive impairments of some nature. We were always doing these activities, these engagement, stimulations different things, but what we were sharing with families who never heard of home care, and they're finding, hey, you know, my mom is at, you know, ABC nursing home, I can't stand it anymore. You know, it's eight degrees out snowing, and I'm standing out in a window outside her room. And it's upsetting my mom more than helping her because she can't hear me, I can't hear her. She looks just, you know, out of sorts, what choices do we have? So they would meet with us at our office, we do kind of like when you go to the doctor the first time, there's a lot of questions, a lot of history to get medications, you know, conditions and different things. And then we would work with them to customize a Memory Care program specifically for their mom, you know, and we tell people Lisa all the time, you know, if your loved one has dementia, there's no reason they can't continue living at home, as far as their care goes. Now, what I will clarify that though, when our case managers go in, and if the person is excessively violent, if they're going to be trying to assault or attack staff, that person probably needs a locked Memory Care Unit or Geriatric Psychiatry, because we can't put our staff in harm's way or that person's heart, well being in harm's way either. And but I would say 99 out of 100, people were able to care for them better in their own home. And we explained to you, you will know this too, the longer you keep that loved one in their home, and those familiar surroundings, the far better they're going to perform and be because, you know, they may not remember what you and I had for breakfast this morning with them. But they'll remember, this is my living room, this is my bathroom, I and they'll have that innate, built in sense of being safe, because his home rings true to them. Because that's in their long term memory. So they know where they're at is okay. You take that person out of that environment, and you put them into a white walls Summit, you know, everything. Strange people coming in and out long hallways, they're not going to have the ability necessarily to adapt and adjust to this new place. So they're never going to have that sense of safety and comfort. And I just more families, I feel like have to have that education part of dementia. Yes, we can all say, dementia makes you forget things and this and that. But there's a lot more to dementia than just that. And one of them is understanding that long term versus short term memory. You know, I just met with a lady a couple of weeks ago with her daughter, and the daughter is doing most of the talking. And her mother very pleasant, just sweet lady, you know, a lot of smiles and yes, and you know, very superficial. And the daughter says, Well, we think my may have the beginning signs of dementia. And so why do you think that? Because she'll ask me the same questions a lot. And you know, but I'm not so sure she's not sure if mom really does. I said, Well, what did you ladies do before you came to us? She says, Well, mom and I went and had breakfast at her favorite place. This was like 10 minutes ago, right? And I said, Okay, let me try something. So I said, you know, Mrs. Jones, yes. You know, when she's smiling, I said, What did you have for breakfast today? She looked at her daughter. She looked at me and she says, I haven't had breakfast yet. I said there's your prime example of dementia. 10 minutes ago, you guys just had breakfast. Mrs. Jones, where do you live at 124 Squirrel lane. There's your long term memory. She's been there for 60 years. That part is not affected yet. So it was it was so I mean, I didn't want to embarrass the mom but I wanted the daughter to have a better understanding. I don't think it's my mom may have dementia. Your mom does have dementia, you know in but again it goes back to What we originally talked about doctors sometimes shying away from giving that diagnosis. Because once they give that diagnosis, the next question the family is going to have is, well, what can you give us to cure it? What can you do to help it? There's not a lot the doctor can offer you once you get that diagnosis. So now the doctor, you know, feels like he's not doing the job. And a lot of the average layperson is not going to understand there's not a lot of options available that the doctor is going to be able to give you. They're making some great headway and a lot of great trials and different things. But you know, your average GP or you know, internist is not probably going to be as up to speed on it, because they're not a geriatric psychiatrists. They're not a gerontologist, they're a general practitioner, you know, they are your family doctors, which are wonderful, and they're great, and they're needed. But I always tell families get a referral to a geriatric psychiatrists get a referral to a gerontologist that specializes in dementia, there's gonna be a lot more options and resources from them than necessarily your family doctor who doesn't specialize in this.

Lisa Skinner:

Correct. Yeah. So now that the COVID, and I'm going to say, quote, unquote, pandemic part is kind of behind us. I mean, it's still out there, it's still alive and well, and we all still need to take a certain amount of precautions. Are you starting to see a shift back to the more institutionalized facilities? Or are they pretty much kind of staying status quo with people trying to keep their loved ones at home? As long as they can?

Lisa Skinner:

Lance A. Slatton: I would say in our area right now, I think we don't see us going back to the status quo yet. And maybe we never will, Lisa, I don't know that I think time will tell. But right now, there are more people asking for help for their loved ones in their home than not. Which is a good thing, because I feel like you know, if homecare is done the right way, you have a legitimate reputable company. It can be one of the greatest benefits not only for your loved one, but also for the family. Right. But the one of the unfortunate things about Michigan anyhow, in we try to do a lot of education on this. We're actually a non licensed state for home care. What does that mean? Mean? You know, my neighbor who you know, works as an IRS agent, she could decide tomorrow to start a home care company in the state of Michigan. That's all she'd have to do is decide to start it. There's no BHS there's no government, there's no Health and Human Services involvement. No regulatory departments, you can just start a homecare company and say you're a homecare company and hire whoever you want. And you're well within your legal means in Michigan to do so. And that's terrifying to us, you know, we do with our company as much as you possibly can, because some resources aren't available, because we don't fall under DHS or Health and Human Services, right. But we do complete screenings, background checks, the whole nine yards, we require a minimum of, you know, X amount of professional experience. And the other big thing is, we don't hire temp service. Employees, all of our employees are direct hires, so they're not subcontractors. We don't use temp companies. And they're not, you know, paid cash under the table, if you will, you know, but there's certain things we can't do, like licensed states, you would have, there's a registry where, you know, when people are hiring, it would just be like a nurse going to the hospital, they're going to check their license, make sure there's no, you know, complaints or violations against it. We don't have that per se in Michigan, being in homecare.

Lisa Skinner:

What are some of the biggest concerns that you hear from people that you interview and do assessments on from the family members, when they are really kind of feeling torn between cuts, you know, the family members, they're just so scared of not doing the right thing for their loved one and making a wrong choice? And that's natural and understandable. And I think everybody kind of lives with that fear. It's very real situation. But how do you address that when? Well, you know, for three years, it wasn't an option, but now they're back to having options. Do you get that that concern a lot from people that you know, I don't know if having my mom stay at home with homecare services is the right choice for us. But I don't know if putting her in a memory care facility is going to be the best choice for her either. So how do you address that? Because I'm sure you get that a lot. One

Lisa Skinner:

Lance A. Slatton: of the biggest questions we get is is, if my mom or my dad or whoever it may be, if you're not able to properly care for them, and you don't feel like they should still remain in the home, would you let us know. And we tell them absolutely, unequivocally, we're not here to provide a service, that's not going to be helpful to you, you know, our reputation means more to us and the care and the safety of your loved one means more to us than, you know, just telling you what you want to hear. And we so when we do that evaluation, we this, we can determine usually within the first half hour, 45 minutes, this is a good candidate for care in the home. And if they're not, will tell the family, you know, these are your options, you can do memory care, right, or you can go into a facility, you can't just go from home to nursing home, though, because Medicare's not going to pay for it, you got to have an admission into the hospital for 72 hours before you can do that. But if we don't feel it's safe for your loved one to remain in the home, or we don't feel that we're going to be qualified to give them the care that they need in the home, we will let you know immediately, you know, we care probably as much if not more than you do. Because we want your loved one to be properly cared for. And we'll tell them the differences, you know, memory care, you're going to be in a locked unit, some have outside grounds, you can wander some don't, you know, some have very restricted visiting hours, you know, and one of the hard decisions families need to make if they decide to do memory care facilities, at least in our area, is your loved one really at that point, because some of these memory care facilities, these people are very far gone on the stage, you know, they're late late stages. And if your loved one is still semi coherent, and able to, you know, relate and things like that, that might do a lot more harm to them than good. You know, you want to make sure there are at least around people of equal abilities that are as close as possible with the care in the home. As long as there's not a safety risk of your loved one or to our staff, you know, we can create, and we do create, you know, memory care programs for them do, you know engagement of all the senses, and, you know, it's not just putting them in front of the television and, you know, sitting there, you know, it's very hands on, and everything is custom tailored to each individual family. You know, I tell people, you've seen one person with dementia, you've only seen one person because everybody's going to react and relate to it differently and have different levels of capabilities, even in the same stages.

Lisa Skinner:

I think one of the problems that needs to be factored in to this whole EU scenario is most family members don't aren't aware of what their loved one needs to provide them with the highest, most meaningful, purposeful, and quality, high quality of life, because they've never dealt with this before. So how do they know that what their loved one needs is the person centered approach to care and not just being plopped in front of a television because we all know that that can accelerate their decline. So I'm sure if they meet with you, you're going to explain that to them. But what if they, you know, they don't even know that that's really what they should be looking for in a good care approach? Because they don't know what they don't know. Right? Well, you

Lisa Skinner:

Lance A. Slatton: hope that they trust what you're telling them, right? You know, we go in, and part of I think, helping them to realize we're not there just to quote unquote, sell them something. We we don't need to nor do we have any interest, we want what's going to best benefit that loved one in the family. One of the reasons Lisa, we don't even use contracts with our families. And you know, I mean, tell me a business that's gonna do that without contracts. We tell them you use us as long as you want, maybe, maybe we start this we get the care plan put in place, the memory care put in place. And then after, you know, the second or third visit, you guys decide, You know what, maybe this isn't what's going to best suit our family, then we just stop coming. You know, it's really that simple. But I tell people, you know, talk to your doctors about it, you know, again, hoping you have a doctor that has a good understanding of, you know, the effects and, you know, process of dementia. And you know, sometimes they do sometimes they don't and but every doctor regardless of their experience, they tell the families the best, most effective treatment for your loved one is keeping them in their comfortable, familiar surroundings for as long as you are able. Now one of the things that homecare does have going against it, unfortunately, but it is a reality for any home care company. You can't build Medicare. You can't build private health insurance. You know, it's either done. Yeah. I was gonna say you can either do it through long term care insurance, veterans benefits. Veterans has Aiden attendance. Michigan has auto injury coverage like all the other states, but ours had gotten reduced on the reimbursement. It's a whole nother topic for another show. And then it's private pay. But I tell them, your assisted livings and your memory care facilities? They're not gonna take anything different than what homecare well, so it's not, you know, then you're down to nursing home? And, you know, that's about it. Right. Unless it's for families,

Lisa Skinner:

there's not, you know, really

Lisa Skinner:

brings me to my, the next question I was gonna use and so kinda of, it's relevant to what you just said, are you also seeing a new trend? Because, you know, we've, we've talked about, and I agree with every single thing that we've been talking about today, it's just so important for families to understand all of this. We agree that somebody's staying in their familiar environment for as long as possible, is a good thing, for a lot of different reasons, until it's no longer safe, or, you know, really, they're gonna get probably better care when they really need help with every activity of daily living. And, you know, it's probably now the option that makes sense. But we want to prolong that as long as possible. But are you seeing that happening more regularly, then families bringing their loved one into their homes with their families? And then you see, so what are you seeing out there in terms of keeping them in there? Oh, with with maybe their spouse living there too, but having caregivers, primary care partners, but they live, they're still living together as husband and wife, or by themselves versus a lot of families are, you know, this, probably better than I do. But a lot of families are kind of being put in a position where they have to move their mom or their dad in to excuse me to their homes. And maybe they have younger children. So what are you seeing there,

Lisa Skinner:

Lance A. Slatton: I have not seen a lot of the children having to move their parent into their home. I've seen I've actually seen more of the child, of course, adult child moving into their parents. But But overall, I would say the child and the parent have typically stayed in their own address their own home. And that's just you know, the benefit of the parent usually have already paid off their house or, you know, maybe 10 years ago, they sold the home and bought a nice little condo. But for the most part, they have stayed in their own home. What we have seen no, and again, not common, but it happens. I say semi regularly, where we'll meet with families. Like I said, we would you know, families that we started off helping their loved ones either in a facility or in their home. And if they transition to another type of living environment, they nine out of 10 times we continue on with them until they no longer need our services, which is usually on their passing. But what we have seen a lot of is families discovering homecare, after they sold mom or dad's home, put them in assisted living. And then after their probationary period, the assisted living says, well, we've determined mom is not a candidate for our, you know, community. Here are your choices, you either bring an outside company in to take all responsibility to provide the care for her. Or we can advance her up to our next level of care, which just means more money. And that's usually a locked unit in the family stop because they've already sold mom's house or dad's house, they can't move them out and just say, Well, no, we're just going to take that out and put them back in his home. Because a lot of them sold that property to then fund the living in the senior community. Right. So we've actually counseled a couple of families who ran into that. And they ended up going and getting mom or dad just a one bedroom apartment because essentially, that's what they're going to have at the assisted living. It's a one or two bedroom apartment. And why pay all that money to the facility who is now saying we're not going to retain any responsibility or liability, because we're now officially informing you that mom or dad's no longer a viable candidate for our living and arrangements here. You have to get an outside company that's going to assume all responsibility, but they can keep their room All

Lisa Skinner:

right, I think for a lot of people who are listening will be listening to this, if they're not aware, so assisted living and memory care are what's called a social model, not a medical model, which is actually synonymous with nursing home. And the difference is, you don't get one on one care in assisted living in even in memory care, because they are, they do fall under the category of a social model. And so if a person needs more care with with, you know, either if it's socialization, interaction, or because of activities of daily living, they do ask you to bring in outside help, and you're still paying the cost of the assisted living, and or the Memory Care Plus the cost of the additional care and a lot of families want to, you know, feel that their loved one is getting adequate attention. So you want to speak to that, I know that we have to,

Lisa Skinner:

Lance A. Slatton: yeah, I can close with this. I, I just implore families and you know, your listeners, when shopping for assisted living and weighing your options for care. Ask yourself two questions. One does my mom or dad do? Would they be happier living in a facility or in their own home? I think number one is always going to be happier in their own home. But is it safe for them to do so if we have outside care come to them? The other nice thing about that is you can make the schedule, maybe they only need help every couple of days for you know, for five hours, maybe they need 24 hours, seven days a week care. But if your answer is they need care, assisted living is probably not going to be the right choice for you. But if you decide maybe it is and you go that route, and you're doing a tour, I always recommend do a tour unannounced, don't let them know you're coming. Just go in, walk around, they're going to think you're a family member just visiting somebody in one of the rooms, they're not even going to ask you a question. But you also want to ask the tough questions when you are ready to talk to them, find out exactly what's covered what's not covered, and how do they judge and you know, assess the resonance. How do you know your mom's going to be a good fit, even though she is today that she's going to be a good fit in six months or 12 months, you might be making another move either to another level at that facility? Or having to take her out and put her into a different facility? Just ask the tough questions. You know, we had a family real briefly that, you know, we were helping five days a week, we kept telling the family mom needs more help. Mom needs more help. They had long term care insurance. So they were very fortunate they weren't having to private pay or anything. And the son lived out of state you'd call mom, everything always sounded fine on the phone, very superficial conversation. The daughter was, you know, a very busy business person working you know, seemed like seven days a week. And she also had young children. So she wasn't and she lived about an hour away. So she couldn't come and see things firsthand, quite often. mom ended up taking a serious fall. We weren't at the home. Because again, we were only there a few days a week. Mom took a serious fall. The family called us the next day and said, you know mom's in the ICU, they found her at the bottom of the stairs. I mean, we were devastated because those nicest lady. While she was in ICU, they set up an interview with an assisted living in our community. They came while moms in the ICU and evaluated her as being qualified to move into their community. And the family we explained, we said we don't think your mother is going to be a good candidate, not at all. And they went ahead and moved her in within 48 hours. The daughter's calling us in tears just devastated. The facility said Mom's not really a good candidate. Well, I mean, we knew that and the facility probably knew that to Lisa. But they moved around because you know, once you get them in, a lot of families aren't going to bother loading and packing and moving out. And so they paid for the next level of care. So it was like almost double what they moved mom in that she got to that level. And after a month, the facility is saying Mom's not a good candidate for this level of care either. Now your choices are move mom out, or you have to hire an outside help to come in to be with her 24 hours a day, seven days a week. And I mean, it was it. I've just my heart went out to that family because they just were so taken advantage of you know, and the daughter finally was realizing, you know, how could you say my mom was a good candidate when she's laying in an ICU bed, to be in your assisted living. You had no way to judge her abilities or capabilities and it was just it was really hard, it was a tough decision. So we always tell families make, make time to really ask the tough questions and get direct answers.

Lisa Skinner:

Yeah, that's really, really good advice. So before we let you go, Lance, I've got two questions for you. Do you? You only, you know, correct me if I'm wrong. We serve this state of Michigan, southeastern

Lisa Skinner:

Lance A. Slatton: Michigan. Yes. It's like the bottom half of the state. Okay.

Lisa Skinner:

But your podcast is broadcast. Is it globally or global? You know, I'm sure a lot of people that have been listening to our very powerful discussion today would love to tune into your podcast, you are a you know, wealth of information. And so how, tell tell us about how you can access your pot of

Lisa Skinner:

Lance A. Slatton: well, they can go to our official website, which is all homecare, matters.com, all one word, but they can also find us on all the major podcast streaming platforms or the videos are all on YouTube and social media. Just type in all home care matters.

Lisa Skinner:

Good. Okay. Thank you so much for taking the time to be here. I really enjoy. Thank you are our conversations. This is our second network. We had the one at the summit and now today and I hoped that you would

Lisa Skinner:

Lance A. Slatton: come back on and we can go anytime

Lisa Skinner:

to have and I appreciate you being here. My pleasure. Okay, well, you take care and we're gonna have

Lisa Skinner:

Lance A. Slatton: you on our show. So

Lisa Skinner:

I'd love that. Okay. So that all that's our episode for today's show of the truth lies in Alzheimer's. I'm Lisa Skinner, your host I hope you've enjoyed my very powerful conversation with Lance Slaton today. And if you are interested in what else he great advice he has to offer you then now you've got two podcasts to turn into two. Bye bye bye bye

About the Podcast

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Truth, Lies & Alzheimer's

About your host

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Lisa Skinner, CDP, CDT

Author Lisa Skinner is a behavioral specialist with expertise in Alzheimer’s disease and related dementia. In her 30+year career working with family members and caregivers, Lisa has taught them how to successfully navigate the many challenges that accompany this heartbreaking disease. Lisa is both a Certified Dementia Practitioner and is also a certified dementia care trainer through the Alzheimer’s Association. She also holds a degree in Human Behavior.
Her latest book, “Truth, Lies & Alzheimer’s – Its Secret Faces” continues Skinner’s quest of working with dementia-related illnesses and teaching families and caregivers how to better understand the daunting challenges of brain disease. Her #1 Best-seller book “Not All Who Wander Need Be Lost,” was written at their urging. As someone who has had eight family members diagnosed with dementia, Lisa Skinner has found her calling in helping others through the struggle they can have a better-quality relationship with their loved ones through education and offering workshops on counter-intuitive solutions and tools to help people effectively manage the symptoms of brain disease. Lisa Skinner has appeared on many national and regional media broadcasts. Lisa helps explain behaviors caused by dementia, encourages those who feel burdened, and gives practical advice for how to respond.