My mom has been living by herself many states away and we're moving her home. Over the last few years we've noticed she's been progressively getting forgetful but things have really progressed. Her neighbors have been in contact with my brother and me and based on what we're learning I'm doubtful she'll be able to continue to live on her own. Her home is sold and her belongings will be loaded up soon, but we don't have a place for her to move to as of yet. I'm thinking we'll need to store her belongings until we figure out a long-term solution for her and that is where my questions begin. I figure we need to find her doctors and get her assessed first. Second we then need to find the appropriate type of home for her, whatever that might be. Third it would seem we also need to understand what kind of resources there might be for her, i.e. government, etc. She does not have a lot of money and lives pretty much off social security. This is all new to me and I'd like to find a single point of contact who is trustworthy that can guide me through this process. Does anyone have recommendations? I'm not sure if I should go through an elder care attorney or a government agency. I'm concerned the former will have his or her interests first while the latter I worry about competence. Thank you for any input anyone can provide.
Maybe mdmess couldn't tell over the phone the degree of impairment her mom has.
mdmess, this journey has started out backwards. Usually, all this information has been collected, then research has been conducted and THEN the house sells and the move to assisted living or memory care is a smooth transition. Your road will be bumpier because you did not do your homework before you needed to act. I'm not shaking a stern finger....I did the same thing. I thought my mom had "more time" before the dementia progressed, therefore giving ME more time to check out where she would end up. She took a fast turn down dementia lane. It was "do something within the next 2 weeks " time.
You will need Power of Attorney for health care and finances. If she will sign you on her bank accounts, even better. Do it soon before her mind is so far gone the bank would refuse. You need to establish doctors in the area that she'll be living. You will be taking her to the appointments and you need to understand her ailments. Have her examined by a geriatric neurologist for dementia. Whether you pick a board and care home (cheapest alternative), a nursing home, an assisted living facility or memory care (most expensive), you should get a list (mine was available as a senior directory at the library), look over the possibilities, then go without her to check them out. If they pass your approval, then take her. Ask her old doctor what type of facility (s)he would recommend. Get her signed up in your county for whatever services she would be eligible for. Look for a senior listing under county social services (Google it).
Just because you started out backwards doesn't mean you can't finish facing forward.
Good luck. You're taking on a project much bigger than you can imagine.
I think she meant that the daughter will need to find (or search, locate, etc.) doctors where she WILL be living.
In my experience (I cared for my mother from mild dementia onset to moderate to severe dementia and eventually her death several years ago), it is best to have a talk with your mom and ask her what she thinks. My mother, though her memory was impaired, was quite aware that she needed help. She was able to tour several facilities with me and pick a senior housing place where she thought she'd be most comfortable, and was able to live there for a good number of years till her dementia worsened and we eventually moved her to an assisted living facility. We made mistakes along the way, but I was always glad we respected Mom enough to ask her opinion and try to honor her choices as much as we could. It was nice for her, having the more independent life of the senior housing before she needed more care such as given in the assisted living homes. There, she met many people more disabled than her, but in the senior housing facility she was able to have more friends who could get out and do more things and it kept her feeling more "normal" and part of her community.
Not everyone is aware of their own needs and capabilities though, so you do need to observe her to find this out. If you want to move her in with you, that's one way. But in my area, we have wonderful senior citizen facilities where individuals can live independently, in their own apartments, while having support of an onsite person (not a nurse but someone who can assist when needed) and other government agency support services (meals-on-wheels, home health care etc.). When she is close to you geographically, you will be able to stop in on her frequently while also giving her the independence she may desire (that was a big thing with my mom, that she wouldn't "burden" her children by living with them). Sadly, there probably will be no one point of contact to guide you,but you'll learn along the way and the Aging agency is a good place to start. What I learned is that I was that point of contact for my mother, her advocate and caregiver and friend/daughter/confidante and consoler. Enjoy this time with your mother, and be kind to yourself if you don't do everything right. I learned to appreciate the new way her mind worked and just get into it with her, even if it involved repetition and meanderings that didn't always make a lot of sense to me. I loved to laugh with her so I tried to find lots of ways to keep her joyful. The one regret that I have is that I didn't spend more time with my mother, even when she was severely incapacitated with her dementia, because I miss her smile, and those hugs, which never disappeared throughout!
IMO, it's important to provide the doctor with a list of things you have observed about the patient. If the doctor takes everything the patient says at face value, then they fail to see the real problem. My cousin reported to her doctor that she was able to prepare meals, bathe, take medications, run her household, etc. when in fact, she could NOT do any of those things. If I had not been there to let the doctor know of the lapsed insurance, 911 calls, spoiled food in fridge, weight loss, repeating, no short term memory, etc. he would not have known, based on their short office visit. So, it's important to know what her deficits are. I'm not sure how you can do that without watching her closely for at least a couple of weeks. It is important that while she is competent that she appoint someone to be her Durable Power of Attorney, Healthcare POA, etc. I'd see an attorney pronto about that.
For my mom, we suspected she had dementia. She knew she had memory problems. I talked to her one day and brought up the memory issues and suggested she get tested for it. She was thoughtful and did she had never thought about dementia, she thought it was just the normal aging memory decline. I wasn't able to get her to a neurologist, but her PCP did a test and diagnosed her with mild cognitive impairment. She is pretty good (normal aging memory decline) unless she's stressed or tired. How bad her memory is tells me how stressed/tired she is. We suspect my stepdad has a form of alzheimer's/dementia, but we're at the early stages of dealing with that. However, again there are many resources available today to help elders live independently for so much longer than before. Yes, things can cost but it's still less expensive than a facilty. We use lifeline alerts, we have cameras in my father in laws house since he is alone most of the time (there is a monitoring service available but we don't want to pay for it. Instead we have many family members with access to them so we peek in on him frequently. Yes, he knows about them and jokes about mooning us), we pay a family member to stay there 5 nights a week and assist as needed (who does a lot more than she gets paid for as its dad afterall). We use notes all over the place with reminders. He was also in the habit of calling my husband for everything before dementia, so this habit continues thankfully. He'll call about the strange car in the driveway (a family members car), he'll call about the TV not working (sometimes he pushed a wrong button), etc. Thankfully he normally doesn't call frequently about the same thing as I've heard some dementia people do. Both our parents live about an hour away from us and each other (think of a triangle) so we can't easily run over frequently. And we haven't convinced them to move closer, so you're lucky.
Another resource to contact is the Alzheimer's Association. They also have some counseling and other resources, tips, support groups, etc.
Almost half of the folks with dementia have some form other than ALZ. One thing they all have in common is that they progress. That is, they get worse in time. Keep that in mind as figure out Mom's housing needs. What is fine now may be inadequate over time, so a place where you can add on more services is desirable.
Good luck to you! Keep us posted.
It's been difficult with her there and us here and her reluctance to get help, but getting her to move home should help us get more involved in her care. I appreciate the recommendation related to the geriatric care manager and will look into that. Her will is done and the POA is something we're working on currently.
We appreciate your input. Thank you!
If it was me, I'd want to research most of the questions myself, so that when I consulted an attorney or government resource, I'd have enough information to know if I was being bamboozled. You could also consider a geriatric care manager, who is a private pay person who can act as a quarterback for all of the things you need to do. They often have a nursing background.
Your mom needs to get her will in order, along with her Powers of Attorney (for health and property) if she doesn't have those done and is still capable of making those kinds of decisions. That would require an attorney's help. You could also contact your area agency on aging to find out about local resources in your area.
I'm sure others will have more good suggestions.