My Husband would like me to place my mother, I am not ready for that. My mother is not easy to handle, but we have been doing well. I left my job to care for our child, and in 2017 my mother moved in with us when my father passed away and she was no longer able to stay in her apartment.
My husband wants her out, he wants his space, and has even pulled the he pays the bills card on me. How can I explain to my husband that I want to enjoy all the time my mother has left. I have tried to tell him this but he just does not get it. I do understand dementia is a handful, and thanks to the fact my husband is able to support us on his own income is helpful cause it allows me stay home. I wish for our child to get to know his grandmother in a place she is comfortable with not in a nursing home, he did not have the chance to know his grandfather I do not want to rob him of that.
My mother and our son to get along wonderfully, and my mother loves having him around. I do understand that this was not meant to be a forever thing, but I am not ready to send my mother away. I use to work in a Medicaid SNF I know the horrors that go on. My husband downplays the quality of care they are capable of provide. I could not live with myself if I did that to her knowing full well how they operate.
My family told me to tell him if he wants her out then he has to pay for her placement to a better quality place, but in truth MC is not really the best wherever you go and the cost associated with private care is insane. By no means am I burnt out. I used to do this for a living so I am better equipped to handle it. My husband is the one that is burned out. He wants his home back. My husband is not much of a people person and have never really meshed with my family.
Am I being unreasonable for wanting to spend as much time as humanly possible with my mom and child? Having both of them around has been pure joy for me. Sure she is complicated show me a person with dementia that is not. I understand his feelings, but I do not think it is fair to have him tell me when it is time to place my mother. I get it he just wants it to be the three of us, but that is not how things are right now. I have told him we still have many years together we can make up for lost time, please find some enjoyment. Our son has a chance to spend time with his last living grandparent do not rob that from him.
He was not pleased by this, I get it might be heavy handed but that is what he is doing. I have seen it many times I know many families say their loved ones are doing great in MC, and sure some are. Though they are not around all day. My mother, hell no one deserves to die in such a place if the a family member is able to and willing to put in the work at home. I get it I can do this because of him, but even still that should not give him a reason to tell me how to care for my mother.
Please advise what should I say or do, we have tried to talk it out and he is hard stuck on this.
Clearly you are a kind and wonderful person. Your mother is lucky to have such a caring daughter who wants to do right by her.
It's been five years though. How long is your husband supposed to sacrifice for your mother? How many years does his home have to double as a memory care facility for his MIL?
Your man and your child are the priorities here. There are beautiful MC and AL facilities.
Now, I've worked in elder homecare almost 25 years. Many of my clients had to go into facility placement. You having worked in a SNF yourself know how to guarantee someone gets good care. It's because the family comes around all the time. It's because they stay on admnistrators and nursing staff night and day to make sure. When my father was in an SNF after a stroke, I had to on several ocassions reduce some of the care staff to tears. I did not care. They were being paid enough to decently care for my father and they were going to. They knew my All-Seeing eye was everywhere at all times. I knew CNA's in his facility and if you take care of them, they help you out. It's not easy to have to be like that, but you'll do it for your mother the same as I did for my father.
It's time to place your mother. Your husband is growing to resent you and her. That's never good. I am my mother's caregiver. The constant neediness, gaslighting, manipulating, instigating, and her lifetime of mental illness gone untreated is pretty much what broke up my good marriage to my second husband. He was a good guy. Patient and very generous too. He couldn't deal with it anymore and we divorced. I live a lonely, impoverished life in my now elderly mother's house as her caregiver. I don't tolerate a second of abuse or ill behavior from her and she keeps it mostly in check because she's needy. She knows she'll be ignored and will get nothing from me if she starts up, but still it's not a good life. It's not a good life at all.
Please, don't let my life of lonely, isolated sadness become yours and it will if you don't place your mother soon. Your husband will go and rightly so because he knows he's not your priority. Your kid will get a lot of time with grandma, but he'll be growing up in a broken home because he won't have his dad living with him. Dad will be a guy he sees on weekends and summer vacations.
Your husband and son are more important than keeping your mother at your house. You can still be a good caregiver to her if she's placed. You become her advocate then.
But... HASN'T he been understanding for the last 5 years, though? For five years he understood, and supported you - that's a LOT of support. When is it his turn? When DOES he get a say in his own living situation, marriage, and family life? How many more years does he have to put his own needs on hold? How long do you? And your son? At the very least, you should work out a timeline with a firm date for when this is going to end. Or it's going to end itself, the hard way.
I agree with others that perhaps you are the one who is not able to see the other side and that now it's time to consider your husband and son and decide what and who to prioritize. I know it's incredibly hard. I have been there, and no matter what you do, you feel pulled in several directions at once.
But your mother has a great chance of thriving in a care facility. Maybe we're just lucky, but my mother, who is still youngish, healthy, and spry, with moderate Alzheimer's is in a wonderful facility with amazing caregivers who treat her so well and love her dearly. She does have behavioral disturbances, but they know how to manage her, they involve me and communicate with me regularly, and they are able to get medications adjusted so much more easily and quickly than I ever could because there is a doctor available regularly and nurses on staff. My mom quite a handful, too, but she is doing far better in her facility than she ever did in her own home or living with us, which she did for awhile. We have kids at home and there was absolutely no way we could keep her here long term while prioritizing our kids and marriage. Placing Mom was the best thing we could have done - for all of us, including her. I never would have guessed that, based on her behavior before, but she's doing better than I could have ever expected, and her caregivers are truly wonderful, loving, knowledgeable, and competent people. Great places do exist.
I do fall in the camp of aging in your home is best but it is a luxury many cannot afford. The OP is trying to do something only a select few are capable of doing and while commendable the OP should come to terms and operate within her means. For her to find placement she has to accept the flaws with LTC and the risks that come with it. This fact is easier for those not involved in the back end and have not seen the darker shades of a certain job. Everyone probably has their horror stories for the field they are in and probably cringe a little when people try to put a positive spin on their profession. This is life when you work in a field you just naturally become hyper critical.
One factor I think many of us are forgetting that often does not get discussed. The toll placement puts on the family member that placed them. We tell people not to feel guilty but that is hard if your LO does nor adjust well to their new situation. Visits become less about quality time and more about redirecting them when they ask to go home, potentially chasing down staff to get questions and concerns addressed.
It is unreasonable to expect someone to go every single day to see a LO in MC especially now with covid and with a child. I do not envy the OP many here including myself are making it seem like this is an easy choice future or past. What we have to remember is the present choices define who we are in the future. If this choice of the OP leads her to become guilt ridden the husband and her child very well may lose their mother either way.
My family was never the same after we had to place our grandma. Holidays become lifeless, the warmth was taken away, resentment permeated the air because one blame the other. This is not a binary choice has many degrees that we as a general reader are not aware of. As many said I hope the OP seeks outside professional help. Cause OP has to make a choice that will leave scars, question is which set of scars is she able to live with.
You said they told you to tell him what? That he is selfish? That he has no right to want something else? A lot of families like" the way things are" because they don't have to do anything. Many years ago I had a coworker who was overly focused on her ailing mother. She was not there for her family. Completely ignored them during her mother's final years. To this day her kids hate her and her husband is long gone. You are not the solution to everything as Beatty likes to say.
Of course that's not the right answer. If you want out of your marriage, that's one thing; you shouldn't die a martyr on the caregiver cross. But if you want to remain happily married, then it's time to find another place for mom. And if the siblings don't like it, that's too bad.
Now go do the right thing.
You are saying your husband has put up with your Mum living in the family home for coming on 5 years.
You are saying he is the soul provider for your family.
You are saying he has reached the end of his rope.
He is telling you he needs his home back.
He is telling you he is feeling like his needs are not being met.
You say I love my Mum and feel it is ok to put her first over your husband.
You say Mum can be a handful.
So basically you are saying your husband and his feelings do not matter, he has no say in his home, his marriage, his family?
I expect you will be a single parent sooner than later.
You say that you do not like care facilities.
You say that you want your child to spend time with Granny.
What is stopping you from placing Mum, and going to visit her with your child every day? You will be able to oversee her care, your child will still spend time with Granny and you can save your marriage.
We got really worried when mom started wandering from home and had no choice. Even living with family this could occur. I hope this gal thinks of what's best for her mother and not herself.
how long will your mom live ? When she becomes totally incontinent with both bowels and urine, what happens ?
When things become too much to handle and ultimately you HAVE to place your mom… where will your marriage be ? Will your marriage be gone? Did you marry your husband or your mom ?
when my husband’s family started the “ have to take care of them in their home” since we were retired we were the obvious choice… I told my husband absolutely not, I didn’t marry him to become his parents caregiver, clean up diarrhea off the floor( yes , who did my husband call when that happened ?) altering my marriage , my retirement … finally FIL placed after ER visit.. and much family destruction, MIL placed .. took a toll on my marriage ..
I understand your husbands point of view…
when I say look down the long road , will you be alone?
I would be searching for an appropriate place , visit as much as you want…
Everyone loved them very much, and everyone came to the conclusion that this would be how they would help versus blowing up their marriages.
You are wholly being supported by him. In addition he's been supporting her for half a decade now. You are not in the position to issue ultimatums--he is. And frankly, it doesn't sound like something he came up with last Tuesday and will blow over. It sounds like he's been thinking along these lines for awhile.
If he pursues divorce, you could lose this house even if you own half. You would almost certainly have to work. In NYC? It'd probably be joint custody meaning three days one week, four days the next, not raising the kid.
The fact your hubs put up with this for five years indicates he's not just some misogynistic uncaring man--rather the opposite--but we all have limits. He is expressing those, and frankly you ignore them at your peril and your child's too.
OP doesn’t realize the wrath of Hades that if hubs hires a real Pitt-Bullie type of divorce attorney as to just what they can do. If they own a home, his atty files for a segregation of assets to happen & with time limit. So 90 -120 days to come to equitable settlement on joint property or placed up for sale. So if she wants to stay in the home, she has to buy it from hubs at FMV. She has no job so not getting lending. If they have a ton of savings that might get split (but his atty may ask for $ placed into educational trust) & she clear outs her 401k but unless she starts working again FT she’s losing house. And no home means APS gets called in to deal with the vulnerable adult position her 66 yr old mom is now in. If she goes back to work, who then takes care of a mom “who cannot be left alone”? If OP uses her moms SS mo income to float household expenses, or moms credit to buy or rent, hubs atty can ask APS to look into her taking advantage of a vulnerable adult…. will not be pretty.
His attorney can get her to pay 50% of all the sons educational costs…. so 50% of tuition, uniforms, camp, fees, dental work, etc. If hubs gets custody, then on her parental weekends she has to provide comparable living, so if hubs has his son in his bedroom, she has to do the same. This is why often noncustodial spouse will have their kids weekends / summer be at a hotel or a resort as the comparable living situation does not have to happen if they r staying away.
If she asks son to do any oversight for grandma, his atty can use that against her. I’m not talking kid and grannie watch TV or share a meal. It’s more that she asks kid to do oversight, like telling kid to make sure grandma take her meds or leaves kid alone with wandering risk grandma. His atty can ask APS & CPS to open a investigation. For a pittbull atty it’s like doing a whack-a-mole… constantly filing something to haul her butt back into court or document or getting others, like APS & CPS, to get her having to be accountable to them. So she folds.
OPs mom is a mere 66; living with them FT now 5 years.
OP posted “she’s extremely healthy, no diabetes / hypertension, cannot b left alone…, is wandering risk…., difficulty w redirection”
OP & hubs maybe mid 30’s early 40’s w kid elementary age or so.
Hubs is as per OP “at his breaking point”;
He has a well paying job in NYC.
They don’t live in a vacuum, there will b women who have him on their radar. None are going to play nice about him paying for or bothering w a MIL or ex wife beyond what a court requires. And there’s going to be one who is absolutely all in having the son become a part of their new family.
if OP wants to stay married, she needs to get them into marriage counseling, be willing to have her mom use her $ to have caregivers come in regularly asap & look into moms LTC placement in senior living situation. Maybe then hubs will stay; otherwise imo he & his wallet r gonna bail & she’ll be destitute.
I think we should stop using custody as a point to persuade the OP cause it could go either way.
You visit at different times. You encourage family to visit. If you motive things that are unacceptable, you report them to administration. You involve the ombudsman.
The OP also might be hesitant cause I know as family we can encourage others to visit but sooner or later she probably will end up being the one to visit and that will become a chore the traveling and dealing with staff will become a annoying to say the least. I loved my grandma but visiting her every weekend got old very quick as I got older by the time I was in elementary school I remember asking if I could just stay home.
No matter how hard we try for the most part visits start to dry up even for the most diligent. Exceptions to every rule but I can see the fears now if they have lived that.
No facility is perfect, not nursing homes, not schools. A very wise friend told me once, vis a vis public vs private school "you can be unhappy for thousands of dollars a year, or you can be unhappy for free".
My mom was in a Medicaid-accepting NH (not in NYC) because we didn't know if she'd run out of money--she lived for 4 1/2"years there. It was not the "best"--they were terrible at communication and I spent many, many hours on the phone, untangling problems.
There is no "easy" way to have a parent with dementia; we sometimes joke here that we are all in the club no one wants to join. Sometimes there are no "good" choices, only the least bad ones. But do gives me thought here to where your loyalties and priorities need to be.
With the breadwinner and the future generation?
I am almost always on the side of placing dementia patients early enough so that they can adjust to new circumstances. You will have to place her eventually--no one person can do this 24/7 in the end stages. Give it some thought and take some tours.
I stood firm and took care of my parents while my husband complained.
My three young children pitched in here and there. (My husband refused to help, but paid the bills). He was very antagonistic at times.
For my young children, this experience was extremely beneficial. They became more responsible, caring, capable and empathetic. They developed a priceless grandparent bond.
It was very difficult at times, but I recall these times with great tenderness and have no regrets.
:)
Every one I know with a parent with dementia on Medicaid in NYC lives on their own with a 24/7 aid. Did you explore that possibility?
Having a parent with a broken brain on psychotropic meds is not "sedating" them. It is treating the panic, agitation and depression that often accompanies dementia. I was happy to be able to give my mother the gift of "calm" in her last years when no one, not me, not around the clock private paid help was able to ease what appeared to be existential dread.
You really want the EMT to do chest compressions to bring your mom back from a cardiac event? So she can linger until she is a drooling shell of a person who can't swallow? THAT is the reality of where this awful disease leads.
I know that none of us here will change your mind. I just think you have an awful sense of where your priorities should lie.
I really think you need to seek a good marital therapist to work this out.
My husband does not get how dated the system is with dementia care, it was a battle just to get her 4 hours, and even with that her aids sometimes do not even show.
I know the difference, and when I worked that night shift I would take the time to validate their concerns and comfort them as best as possible. People would be amazed how simple things like holding their hand and looking at them in the eyes telling them it will be okay goes to sooth them and relax them. Sometimes I would even take them around for a walk if they are getting restless, and engage with them. You can do other things before going whelp time to get the medication because person in 6A keeps bothering us while we bullshit at the front desk watching tik tok.
If they have a life threatening condition then sure DNR is reasonable, but I always tell people make sure you talk to a doctor about it not the social worker. Discuss their concerns with the doctor, the social worker may not have what is in the best interest of the family in mind. As I mentioned I have seen social workers get families to sign a DNR for someone on short term rehab. I am sorry that should not even come up in the conversation in my opinion. They are here for rehab not to die, this is why I also tell families unless you have ZERO means do not use these SNF for short term rehab. At most they will get 30 min, and unless the person speaks up or has a family member present they will often "forget" about the person and they will miss their time. The system is flawed to the core.
I fall in the camp of positive approach advocated by Teepa Snow. Yes medications play a role and have a use do not get me wrong. I am not denying that. What I am saying is often people are quick to use that as the first course of action when I do not feel that should be the way unless someone is truly expressing harmful behavior.
I have seen someone make the claim that a 82, 4'1 female posed a danger to a 5"11 worker because she kept getting up asking for milk at night.
When I did not back up their claims that she posed a danger I lost all respect from the staff, people would go out of their way to make my job harder because I did not back up their claims which would allow them to have an easier night shift. The quality of worker some of these places hire is jarring to say the least.
1. I work in the business and I completely understand how disheartened she feels about it.
2. Among our clients, the ones who are most often afraid of us and afraid of receiving care are those who have worked in care. Not afraid for long! - I'm happy to say, because our team is different from the run of the mill; but it's noticeable how apprehensive they are and how low their expectations are compared to the overall client base.
I've been in my job for over two years now. I have nothing but praise for my co-workers who I know to be good, caring, dedicated people. I have learned that I am not the only one who cares, and I need to be more accepting of not solving every problem. I have also learned that my lifelong habit of being vocal about standards because "I'd rather be right than popular" simply does not work here. If you try it, people will just stop listening to you. They won't have it. They won't be told *by you.* They will think you are an arrogant cow who needs taking down a peg or two and you will achieve nothing to the benefit of your client.
And I work for a *good* service, and our clients are not vulnerable in the way that residents in facilities are, wholly dependent on the staff 24/7.
You can do your best to set an example, you can get as close to the standards you believe in as possible in that moment; but you cannot create the time it takes to deliver excellent care and you cannot just barge in and tell your co-workers to change their attitude, method, insight, understanding and personalities. Much as you might like to!
And actually, it all comes from the top. Good leaders make good teams, because they make standards an aspiration for their people instead of a threat.
Stuck, keep looking for a facility that is well led. Meanwhile, what about additional support at home, or respite care, or anything that might take the pressure off?
You're emotionally abusing your husband who has no peace in his own home.
He's gonna walk and sue for full custody. And he'll win.
You'll have no financial support and will have to get a job thus being unable to tend to your mother and will end up having to place her.
It's a nightmare scenario you're is creating.
As for him paying?!...So, YOUR family thinks that HE should take money away from your child's future to cover their future inheritance??? Your mother pays, medicaid, and her children pay if they want her to have more perks.
I do not agree with what my family said, and I am not proud of even bringing that up in the first place. Where exactly do you see inheritance. She is on Medicaid and her only source of income is SS? What are they are going inherit? Credit card debt? If she had assets I would have a far easier time placing her because I know of many great private pay entire MC facilities where I do feel my mother would thrive. No aspect of isolation every resident has some form of memory related condition and their safe to resident ratio is fairly small. Problem is quality care costs money, I wish my mother had money I would easily use it to pay for her care in a heart beat.
Some say I should voice my concerns, I do but then you are considered a snitch and at that point you have to work in a toxic environment because you dared to put the patient first above a paycheck. Sure, I have also worked in some wonderful facilities but generally those are few and far in-between at least in NYC. The truth is everyone who has worked or has experience in LTC knows the gritty truth about what really goes on behind the doors. To hide between the few places that are run well is what is truly disingenuous in this conversation.
That said I understand the my husband is at the breaking point, but what he does not understand is placing my mother will be a tall order. She is still physically fit, active, and does not respond well to unfamiliar places and people. Isolation also triggers her anxiety, with covid she will be fairly isolated. I also know placing her then taking her out for the weekends will be a bad call, because under the slim chance she adjusts all that will do is reset her and make the staff's job that much harder because they will have to readjust her. She also has a big mouth, and still has some grasp as how to use her phone, I will be getting calls left and right not like it is will be all that much easier. Placement does not remove the stressers it just slightly adjusts them. She only has SS and Medicaid, I am in a shitty situation cause I know my mother she will not adjust well to placement at least not yet. I will be stressed because my mother will be calling me constantly, and with what I know I will not be able to just to chalk it up to her overexerting I will feel the need to check on it myself. Do you really think having to drag our son around each time my mom has a panic attack is more ideal then having her home with us? What life is that? His father works during the week not like he will be able to watch him while I take care of my mother. Me going back to work also limits our sons interaction with his parents. As I told my husband I am sorry I will not be able to turn off the part of me that will be concerned for my mother, that is something to a degree you have to do when you place someone. You have to have a sense of faith in the staff that they will do right, I do not have that for any place in NYC that has availability. I have reached out to contacts and the ones that are accepting have horrible staff retention and mortally rates.
I am not sorry for what I said about placement. It is my experience, you may have your own but it matters very little cause I bet no one would be saying that if they lived in NYC. If my husband is willing to leave me because I care for my mother so be it, that is something he will have to start. I am willing to work something out but placing my mother is not it. If it was my MIL I would also be against it even if we did not get along. Proud to be a good kid.
I will say for certain in the NYC area our Medicaid eligible facilities
I do hope if he does grow to hate me, when he is older he comes to understand why I had to do what I did. It is not an easy choice, nothing about this disease is, every family has to make difficult choices that we do not know if they are the right choice end of the day all we can do is making the choice that we feel we can live with in that moment and try not to beat ourselves up. When you have seen others pass alone in a NH it does something to you, and by no means if I can avoid I do not want to put my mother through that. No one should ever have to die alone if it can be helped. That is where I am coming from.
What comes of this because of my choice so be it, I am sorry for evening coming her. This was my fault I knew generally many would not understand, but for those that do thank you I appreciate it.
The system can be improved but to try and sell they were horrible because of a few bad apples is disingenuous.
Have you stopped to think about the impact on your son, should your husband decide he's had enough and leaves? How do you think your son is going to feel, when he puts together that dad left mom because mom wouldn't choose dad over grandma? Who do you think he's going to be the most angry with? His "wonderful" relation with grandma might very well fly out the window.
And, suppose you get your wish and keep grandma until the bitter end? I don't know how old your child is. Are you prepared to tell him why you all can't go on vacation like the rest of his friends, because of your mother? Why you can't make his games, concerts, plays, etc. like the rest of the moms because your mom can't be left alone and you can't find a sitter? What about when he wants to invite friends over, but he can't, because grandma is now saying inappropriate things, or behaving in an inappropriate manner? Or maybe he's just too embarrassed with grandma to invite friends over. How are you going to handle HIS stress, when your mother's dementia really worsens, and you're dealing with wandering, incontinence, possible violence? You say you've worked with dementia patients, so this might be "normal" to you, but to a child? It's going to be dreadfully traumatic. Could it be your husband is already seeing shades of this?
My kids were 19 and 23 when my mom got so sick; and her illness was "mild" in comparison to ALZ. Mom lived with us - in her own apartment - since my eldest was 2. And my mother's illness and decline was terribly hard on them, from the fear of seeing their grandma so sick to the resentment - yes, resentment - that our lives as a family were in hiatus while my mom was ill and dying. Her death was very traumatic for them as well. And my kids were adults by that time.
I think you need to *hear* - not just listen to- to your husbands very justified concerns about this living arrangement. And take into consideration that there are 3 other lives here whose well-being have to be taken into consideration as much as your mother.
I think you're out of line.
Place her while your son still has good relationship with her.
Hubby’s $$ should not pay for it..this is your mother’s $$ should pay. Your family is worried about inheritance. If she qualifies for Medicaid, the facility can help apply.
I side with hubby . Hugs 🤗
Think about all the people whose parents retired, moved to FL or AZ and only saw their grandkids once or twice a year? It's not the end of the world. You mom can also have a life separate from you.
If you are really struggling with this I also strongly agree that some couples therapy would help. Moving your mom out does NOT mean you don't love her (even though she may not be fond of the idea). It does mean you do love and respect your husband. You won't regret it.
As to the rest of the family saying that HIS money should be used for this, they are out of this world full of nerve. That is nonsense.
I cannot know how strong your marriage is at this point. I think I would recommend you see a marriage counselor, a psychologist or a licensed social worker to work out some sort of agreement. You may be able to compromise on how much longer Mom will stay with you.
I challenge you to put the shoe on the other foot; think about if this was your mother in law, your husband's mother who was suffering from dementia, living in your home and intruding on your privacy for 5 years already, taking up all of your husband's time and attention. And it was you begging him to place her so the two of you, together with your child, could have a normal family life once again. And he was the one who was throwing around wild stories about the horrors of managed care and how he didn't want his son 'robbed' of the opportunity to spend every waking moment with his last living grandparent. But you were feeling otherwise, and robbed of YOUR family time due to your mother in law and her ever-worsening dementia. How would YOU feel? Unheard and like you had no voice in your OWN HOME, I would imagine. Like your marriage came second to his mother, and you'd be correct.
No, he is not the one being 'heavy handed'.......YOU are.
When is enough enough? He's paying all the bills and you are saying that "he has even pulled the he pays the bills card on me." Unless he has a money tree in the backyard, he IS paying all the bills and with inflation being at an all time high, his point is valid. Sorry.
As far as 'your family told me to tell him if he wants her out then he has to pay for her placement to a better quality place', isn't that rich? What about THEY take their mother into THEIR home instead of YOUR husband footing the bill for her placement in a Memory Care ALF which you've already said isn't a great situation anyway?
My mother has lived in a wonderful Memory Care ALF for nearly 3 years now, and in regular AL for 5 years prior, and let me tell you something, she's getting MUCH better care THERE by a team of people working 24/7 than ONE person could EVER provide her in a house setting. Don't kid yourself. And don't put the burden of that cost on your husband either, it's not his burden to bear.
You're looking for justification that your 'my way or the highway' shtick is the proper way to go here, but you won't get it from me or most of us here on the forum; you're barking up the wrong tree I'm afraid. I'm sorry for your husband in this situation that he's married a woman who has no interest in his feelings whatsoever.
In a normal marriage, you'd accommodate your husband's wishes and arrange it so that you and your son would go visit your mother on a regular basis. Not only would she have a whole new social environment in the SNF, but she'd also get to see both of you on a regular basis, making it a win-win situation for ALL involved, not just you.
Would you consider looking for a memory care unit where you might take a part-time job, either now or in the near future? - not as your mother's caregiver, but as a member of the team working with others to improve standards. As someone who has worked in the vocation, don't you think it's up to us to try to make it better rather than to fight to the last ditch to keep anyone we care about away from residential care?
For anyone on the fence or scared Please do not let others negative experiences deter you from doing what is best for yourself and LO. Do the leg work find the best possible placement and do not second guess yourself. If anything happens it is not your fault they failed not you. Please do not buy into the fear and bad rep medicaid facilities get. Many factors come into play state, temperament of patient, staff, location, size etc... you are important and you deserve a life.
I have to say, I am appalled at the number of LTC workers that come here and say how horrible they are. It's your job to make it not horrible and to provide care, yet you talk about the nightmare care. Think about the part you played in creating that environment for those poor people. I'd be worried about karma too.
If you don't prioritize your marriage, you will have your mom as long as you want. To bad for your husband that he married a selfish, self-centered female, he sounds like he deserves so much better then you.
Two things for you to think about:
1) You worked in a Medicaid NH which you thought was not good. How much effort have you put into finding a better one? They are not all the same.
2) Have you considered how you, your son and your mother will live if DH gives up and leaves? DH will pay some child support for your son, but he won’t be obliged to pay for M, and (depending on local laws) he won’t be obliged to pay for you. (Where I am, he wouldn’t pay for YOU, only child support on a scale depending on his income, and certainly nothing for M). Property settlement on divorce will probably force the sale of the ‘family’ home – fair enough, DH needs his share to start the new life without you and M. So where will you go, where will M go, and how much ‘quality time’ will son then be spending with M?
How old is M? What is her life expectancy? How much longer do you expect to keep her at home? What is YOUR sticking point for giving up? What is DH’s sticking point for getting out? How much do you know about divorce? We have had posters who seemed to think that DH would leave (possibly taking the car and the sound system), keep paying the bills, and nothing else would change.
You are stuck in your mind about keeping things the way they are now. They will NOT stay that way indefinitely. If you can't see it, you certainly need a counselor and some legal advice.
And that's assuming husband doesn't sue for custody and win; if he can make a case that living in a home with a person with dementia is not ideal for a child; and he might be able to prove that he can provide a more stable, stress-free environment for his child.
Your comments about residential care for the dependent elderly are by no means universal, but you are allowing yourself to justify making unilateral decisions that will impact on your whole family with no attempt to find a placement that would satisfy you.
You’ve already expressed your displeasure with your husband, but you are actually doing the same thing to him.
Many, MANY of us have experienced situations similar to yours. I slept on the floor next to my mother’s bed for months while we made a horrendously difficult attempt to care for my mother in my home.
Together, my husband (who loved my mother dearly) and I decided that my mother needed more care than we could provide for her, and we found a fine SNF near enough to my home that I could (and did) make daily visits, which I did (twice each Saturday and Sunday) for the 5 1/2 years before she died.
The Bible says “A man shall leave his mother, a woman leave her home….”I
If you want a life with your husband, honor his right to a wife and a mother for his child.
After my grandfather died fairly suddenly at 79 my grandmother lived with one of those sons doing all I mentioned above despite her grief. She was 10 years younger.
After many years her health declined and a Greek AL facility was found for her. This was a wonderful place as everyone spoke the language. Sadly after a few years her health declined further and she could no longer walk. She was then placed in a NH facility. I visited her there and left crying each time but she simply needed too much care. She lived to be 98.
My point is that there are circumstances that make sense for an aged parent to live with family but there can come a time when the burden is too great. All your family's needs should be considered. It would be wonderful if each of us could simply pass in our sleep when the day to day life becomes so difficult that we wonder what is the point of all the suffering. Of vourse that is not the case and we must weigh the options that is best for all family members living together.
I learned so much from my grandmother. My mother was not overly maternal. She was a dancer and then she became depressed spending periods of time in bed which confused me. I have wonderful memories of living with my grandmother. I feel her qualities live on in me when I am around my grandchildren. Your husband and child are your future. With the background you mention perhaps you could find a facility you would find decent. It is wonderful you have housed your mother this long but perhaps it is time for a change.