I’m in a bit of a quandary tonight. Mom (a young 90) and dad (93 with advanced Alzheimer’s) have been with us for 14 months. We have always held out that they need to be in assisted living/memory care because we work full time and Mom is exhausted caring for Dad. We finally have a placement available in a lovely facility that can provide independent living for Mom and intensive assisted living for Dad in the same unit. Mom does not want to go, and Dad is comfortable where he is, here at home with us. They are very well off financially, and I can retire now with full benefits. They could back fill my salary for the next 5 years (until I had planned to retire) if I retired to care for them full time. This past year has been so difficult trying to balance work and elder care. I’ve got 35 years in and could walk away tomorrow, even though I’m only 57. Thoughts as I consider retiring to care for them in their final chapters?
You could also think about ‘post deal breaker’. If the situation deteriorates quickly and they go into a nursing home at $5000 a month each, how does this work with the finances? And will you miss your work if you take quite an early retirement, and then end up living on your own? I am sure that you could find other worthwhile things to do, but if you are really committed to what you do now, you could regret an early retirement that turned out not to be necessary.
This may be the last thing on your mind, but demographics today mean that a 57 year old man (I guess you are male) with his finances in order is a highly attractive marriage proposition. How could a relationship in three or four years' time alter things?
These are all fairly negative ‘what if’s’. Living together might be a good idea that works well for you, your mother and your father. However thinking about the down side is the best insurance for not regretting things that are hard to change later. Doing it should make you more confident about your decision, whichever way it goes. Best wishes.
Then my mother’s only brother was also diagnosed with AD (their mother suffered from it for many years and finally died from it). Then my mother’s maternal aunt (the youngest of her mother’s siblings) ended up in the same facility as my folks, also with AD. My education quickly began to include prevention measures given this seemingly strong genetic link.
I quickly realized I needed to go back to work. Supporting the parts of my parents’ care that were not covered by insurance/Medicare was becoming a source of stress, as financially it limited my ability to visit, and their care was quickly becoming my world. I was disengaged, not mentally stimulated, stressed out over finances, depressed and not coping well in terms of diet and exercise (sounds like early motherhood, except, in most cases, you have a sense of hope that things will improve as your baby grows). This, along with genetics made a perfect recipe for me ending up exactly like my folks.
I am now back to working full time and I have no plans to retire this time until/unless I become physically, mentally, or emotionally unable to work. Being at work has also helped me build better boundaries with my folks and rely on the facility in a more healthy way. I know this is what the parents who raised me would want for me, and I am a better daughter, wife, aunt, and person for it. As I said, this was my decision and may not be the best for you. I only tell you this in hopes of providing more food for thought. Wishing you clarity and peace as you navigate the road ahead.
that the caretaker will die of burnout and resentment after the work had all been done by the son, taking his father to church with dressing,bathing,not sleeping
in other room close by to listen to father so he does not get up at nite and fall..I have only to live with myself as I never thought my brother would predecease
Dad..............i was not watching carefully...brother had some mysterious illness to do with an infection, going to his brain,being sick for a year prior...as well as Dad having multiple bouts of dementia,uti's and irritablility...also blind...this weighed down on brother... So advice to all of you this is a very unselfish,giving,humanitarian gift to give your parents but in this case caregiver
died waiting for his Father to diminish but it went the other way, brother and I were waiting to go to Europe and live together when the folks died but they both
Dad and son died six months apart............so planning sometimes is impossible..yes...and there were no savings here other than a house........could this have had a different outcome.........?
The NH,where i admitted Dad four weeks after funeral of brother caretaker son, was paid with social and a pension from the VA........also Medicaid coming in two mos later after I bought a Funeral Trust with the 10,000 in his account which really belonged to the caretaker son who refused to touch it..............i,daughter, got Aid And Attendance from the VA for Dad,at 96yrs old, to help my brother, ..up until then it was
living modestly on 2 low soc.sec.1100 per mo and son taking care bill paying etc. and giving to their church.............why more people do not know about the help from the VA is a mystery to me however to those on this site my parents were low income.......and Dad had a subarachnoid hemmorage five years prior to gettting A&A........we just did not know about it...........do elder lawyers tell you?.....I never thought my brother would die at 69 years old before Dad at 98 years.Also the VA and Medicare would have sent in help for Dad but again they were like two buddies and bringing in strangers was not in the cards i suppose...brother did not want me there although I noticed his resentment sometimes....especially when the mother started becoming sick...and died...
Last night she violent & curse me called me prostitute, piece of sh—, threatens to kill me, twists my wrists, punches me in breasts, pulls my hair..otherwise, just a nightmare..To save $$$, & because my mother kept complaining about SNF, I discharged her & took her home...where she’s been the last year & 1/2 . She was in SNF for 10 months but insurance ran out due to not progressing. My mother has turned into a person who puts herself first before anyone else including her daughter (me). She’s a bully and an abuser. I’m beginning to forget the good mother that she was sacrificing her career to stay home to take care of me & brother...but then when my father faced unemployment, she took a job....that person is gone and a very selfish person remains.
I took her to hospital last week & all tests come back “normal “!!! They could not get enough urine for culture, but tested the few drops Nurse got ...& they sent her home w stupid me who didn’t insist they keep her there till they can get culture...she also had stopped eat, drinking & refusing meds. Decline since tooth extracted 2 weeks ago...I could go on & on but you get picture
so are they financially well off with at least 800k+? 1M+? More?
If not, then they will likely outlive their $. I’ve been on this site now for years and over & over folks think their parents will have enough $ only to find that the costs of care are horrendously expensive.
If they live long enough, their needs will get beyond your ability & they will run out of assets so the requirements for Medicaid eligibility need to be a consideration. Plus caregiver burnout is a very real thing.
The costs of private pay NH could easily run 8k -15k a mo each. NH avg stay is 2.5 years so 240k-450k each.
In-home care seems to average $20 hr. So 2Ok a year part time for each; 40k paid to you via a legally drawn up caregiver agreement with taxes & FICA done. If by “backfill” you mean your folks match your current salary, that could pose a problem if they outlive their $ and they end up applying for Medicaid.
Really you as their dpoa need to pull together exactly what their financials are and take them with you to meet with an elder law atty. I’d suggest you get with one that is NAELA or CELA level of experience as their situation is more an estate planning if they truly have significant assets.
ALSO really where is your husbands input in all this?
Does he share your view of his own late 50’s & 60’s as having your parents living with you both and your life as a couple revolving around being 24/7 oversight and caregiver to your parents?
As selfish as it sounds, I should’ve kept my job/friends it’s important to your own mental health. Nothing will change the trajectory of these diseases.
I kept her home far longer than I should through numerous falls with little to no outside help - it took a huge toll on me - I tried to bring in caregivers for 12 hours a day while I worked but she did not cope well with strangers in the house - ran outside and fell - caregivers too are not reliable and will leave in the middle of a shift
nearly 3 years ago, I placed mom in a "nice private pay memory care facility" straight from the hospital following a fall - it has been an incredibly difficult journey as well and we are nearing the depletion of financial resources as it has been necessary to have private caregivers with her in the facility
set expectations realistically for both yourself and your parents - assume the cost of the facility is double of what you think going in and you'll need 10 years of care and if their resources can cover it then that should make the decision easier
if you keep them at home, is the situation set up for advanced care needs - think wheelchair access and use of the bathroom and shower
my mom went from being able to stand and walk a few feet to being immobile in a couple of days
is your dad exhibiting any behavior issues - wandering, sleep disorders or aggressive actions - these are often the reason families place loved ones in a facility
There is no right answer and cost and quality of care depends a lot on where you are located but if you can make a decision before you are in a crisis or medical emergency then your road should be easier than most
The biggest thing i realized was that a lot of seniors fear being dumped and forgotten. If y’all decide a community would be the best decision, it’s important to commit to being present, and following through on that commitment.
Should you change your mind later on and decide to place both your dad and your mom in a living facility, make sure you will always have someone to watch over them - that's very important. Regardless of how nice and confortable a place might seem or look you never know how your parents will be treated or taken care of by all the staff.
At present, it sounds like you go out to work, home is not a prison. Do you really want to be around parents 24/7? Retirement can be a big change in this sense.
Have you considered, It they have the means, that they pay for caregivers' services to come into your home? Would that work for you or would you feel your privacy is violated?
Your mom may be happy with the situation as it is, but that is not the point here. Are You happy?
First, if Mom is exhausted then her health is at risk. One day sooner than you think you may get up one morning or come home from work to find your mother has collapsed. Over 30% of primary care givers die before the person they care for.
Second the stress of balancing work and care giving can get to a very extreme level where you do not function well at either task.
The third point you need to consider is that at some point your father will need 7/24/365 care that one person and an aging spouse cannot provide alone. You will either need in home care givers or a facility at some point in his decline.
Moving your parents to AL and MC is the easiest path to provide good quality care, particularly if the facility is a good one and it seems your parents have the resources to provide for a good one. Are your parents alone while you're working? If you retired, would you need to stay home with Dad or could Mom attend a Senior Center while you take care of Dad? Your mother is socially isolated now while she cares for your father. Whether she wants to go or not, she may do much better in AL where she can be with your father as much as she wants, but still get a good night's sleep in her own room and see other people in her age bracket when she wants.
I wouldn't retire early now because that's something that's a permanent change and difficult to impossible to back out. You can always take that road later. How would you feel if you retire now and then your father passes in a few months? Would you want to be back at work or would the lighter load of taking care of your Mom keep you busy enough?
If you want to honor your mother's wishes and keep your parents at home, I strongly suggest hiring in home care attendants to take over your father's direct care for at least 12-16 hours a day. Be prepared to take that to 24/7 or move your father to MC at a moment's notice if/when circumstances change. A case manager who will handle engaging the attendants, taking your parents to routine doctor appointments, etc would also be a good choice to minimize the impact on your work schedule. Since your mother wants to remain at home, I suggest negotiating she attends/socializes at a senior center 2-3 mornings each week to preserve her own health.
I supported my mother taking care of my father with vascular dementia at home for nearly 20 years. When dementia took over to the point my father became a danger to himself and my mother and he needed better management of his other health issues, I placed him in a good MC against his wishes. Mom moved in with me; she has no short term memory and MCI but no true dementia. Her personality is intact and she can make good decisions if she can remember everything she needs to know to make them. She recently fell twice in just three months; the second fall impairing her mobility (in the short term until she heals) and requiring more direct care. So even though she doesn't like it, we now have in home care covering the hours I need to be in the office or attending some event like a kid's ball game. Because of the falls, I expect to keep this arrangement in place even when Mom is back on her feet again. I understand wanting to honor your parent's wishes but you also need to ensure their safety and over all well being. To make this work well both sides need to be willing to compromise when needed.
That allowed me to bring my 87 yo mom out of assisted living to live with me & my hubby. She has the funds to pay me for taking
Care of her, which is way less than the assisted living was costing her. It has been 6 months, so far so good. Yes I do all her meals, laundry, shopping, financial, legal, Dr appointments, dressing her, showers, and including diapers.
When I need to go out for a few hours, I pay someone to be with her.
If we left her in the AL, her funds would have been depleted in a few short years.
I am determined to see this through.
Fortunately she is very grateful & appreciative of what we are doing for her.
I have had doctors who do rounds in those homes say to me, "shoot me twice before you put me in one of these places". The amount of neglect and abuse that goes on in nursing homes is unbelievable.
You all make it seem like a nursing home is a happy ending. It isn't. If you cannot provide that level of care and it's a 1:1 ratio, what do you think will happen there?
People are living longer, and so the elderly are now trying to care for their elderly parents.
My wife and I are on our fourth parent. It is very hard to find a place for them and move them comfortably when they are coming from houses. The care before and after takes its toll in stress which sometimes, as in my case, causes physical disease. Not something I planned on in my 60s. Siblings? there are none.
I refuse to be a full time caregiver for my mother. I have no obligation to do so, especially when I am constantly verbally and emotionally abused. My inlaws were wonderful and a joy to be around. But even then caregiving takes a great toll when you are trying to maintain a job and adult children with serious problems of their own.
Something I have heard a lot - "but she gave you life and raised you." Yes she did. But if I had somehow known what a burden the last few years would become I would have definitely turned down being born. No hesitation.
My mother did not care for her elderly parents in her declining years. Very few of her generation did. It would be a whole lot easier if I was 40, but I do not have the strength, health, or energy now. Stress kills. Look at the statistics of caregiver survival rates. It is pretty grim.
Please do not shake your shame finger at the good folks here until you understand more about their journeys.
However with the blessing of the correct meds, she has calmed down considerably. Also she realizes that this is her last stop, & if she doesn't behave, she may be out.
I agree that unless your senior can afford a very Nice AL, many NHs are undesirable. The care is minimal. I know people who have worked in them, and their workload is unrealistic.
Anyway we all do what we can.