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I have a father who has early dementia, yet finds ways to aggravate and pretends not to hear me, a husband with Congestive Heart Failure who doesn't want to move other than from bed to chair, and a mother in law who lives alone with her dog and also doesn't move much. I've been trying to build a home based business before Covid-19. I also feel overwhelmed and want to block everyone out. Can anyone relate? Or am I alone?

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You need to realize you can't do it all. You may need to find a place for Dad. If he has money an AL and transitioning to a LTC facility as he worsens. Husband, CHF can be debilitating, but needs to be ur priority.
MIL, same thing. If husband has other siblings, they need to step up to the plate. You need to tell them you have enough on your plate. If no siblings nearby, then find resources to help her.

I understand why you would be starting up a business, but it maybe part of your problem. Trying to do too much and be there for everyone. My Mom was fairly easy to care for but one person at a time was enough. My disabled nephew had to be put on the back burner.

Dad may not be aggravating you on purpose. He may be losing his hearing. May no longer be able to process what is being said.
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That's very difficult. And too much. Someone else should take care of father and MIL. Your focus should be helping husband. If MIL's children aren't available, then find someone else.

Wish you all the best
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You can’t be in two places at once.

Your priorities lie with your husband.

Best wishes finding care for your parents.

Do not feel guilty about caring for your husband.

Take care of yourself as well. You have a lot on your plate. Prioritize and tackle issues one thing at the time.

It’s so easy to feel overwhelmed when we are smack in the middle of mayhem.
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This is way too much for one person to handle. Good suggestions below. All the best to you and a big hug. Is the paperwork in order for your father and MIL (will, living will with medical instructions, POA for medical and financial decisions, and also some banks have their own POA forms)? If you are the POA, you have to make things possible for yourself to handle. Consider assisted living for father and MIL. Set up as much as possible so that you can handle things online and bills are paid automatically.
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Wow, you do have a lot on your hands.
Im thinking maybe if you alone has to be the Caregiver to all 3 then it would be easier to have all 3 to live with you and out of their combined monies, hire a Caregiver to help you out.

You would need to have access to their funds.
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Frances73 Dec 2020
Are you crazy? How can one person be a full time care-giver to 3 people and run a business? A facility has multiple staff with specialized training to correctly assist in moving and caring for people. And no-one has to be on-call 24/7 to 3 demanding, ill people. Have you ever hired an in-home caregiver? I went through that for my Dad and it was a constant revolving door of people, some he liked, some he hated, some I didn't trust. Her first concern is getting her family members the correct care.
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You need support and help from your family and friends. If they cannot provide that support it is time to put him in assisted living or nursing home. You need to establish BOUNDARIES, a daily routine, and everybody must play their roles in care of him, and must be strictly enforced. Routine is very important. Everybody needs to cooperate or ship him out. Or you will be the one who needs the medical care.

If your father is still "with it" he needs to cooperate too, and make it very clear if he does not he will have to go to a nursing home. And he cannot spend his life on a chair or in bed or you will end up with someone bedridden. You want to avoid that as much as possible. My mom had the most advanced Alzheimer's you can imagine but she was only bed ridden for 2-1/2 months only because she forgot how to stand after 15 years of the disease. If you think you have problems now--caring for someone bedridden is no walk in the park with constant diapering and you will even have to manage their bowel movements..mom's bowels had to move every Tuesdays, Thursdays and Sundays--because if she did not go she would get IMPACTED on the 4th day. That means the stool is so hard it cannot pass, and requires emergency room visit. It is like a round hard ball stuck in there. It's a living nightmare.

If he has problems moving, then he will need CARDIAC REHAB, and adhere to a strict diet with no deviation. You just cannot eat whatever and lounge around all day with CHF, unless it is end-of-life care.

Let me emphasize he must try to maintain independence of movement. Walking is a gift. Trust me bedridden is pure horror..if a person can no longer walk they lose a lot including someone having to manage bowels, and being 100% dependent on care. People take going to the toilet on their own for granted.

Taking care of someone is no picnic and it is VERY SERIOUS. Bedridden means constant Hoyer lifts, diapering, bed baths, lactulose laxatives, enemas, and tons of diapers. TONS of it. Adult diapers are are NOT cheap--like a dollar a piece. I used about 5 to 6 diapers a day for mom, and tons of gloves and wipes. Those gloves are not cheap and neither are wipes. Go to the store and check out those prices. Then there are skin creams, ointments and if you do not turn and do skin care you will end up with bed sores which require AGGRESSIVE treatment. You must do STRICT ORAL CARE--the teeth must be brushed and kept clean because dirty teeth can cause PNEUMONIA. It's called aspiration pneumonia. Saliva with bacteria can get aspirated. Clean teeth are essential to prevent pneumonia. I kept my mom going to the dentist as long as I could, but I kept her mouth clean so she never had issues with dirty teeth, even with a feeding tube.

Mom died age 90 despite extremely advanced Alzheimer's and insulin-dependent diabetes, and I kept her blood glucose levels extremely well managed, and mom's skin was in perfect shape. But she was also 24/7 intensive care on my part.

When mom died it nearly destroyed me, because my life revolved around her 100%. Now do this for YEARS and YEARS and YEARS and see what it does to your mind. Every single moment of my life was about mom. I miss her very badly but her mind was totally gone, and survived on tube feedings, but she was very peaceful and died ironically of other natural causes not related to Alzheimer's. Her insulin-dependent diabetes also caused kidney disease.

However, I'm glad I took care of her and I learned to adapt to life without mom (no choice--people die). Mom's ordeal of living is over and she is in everlasting peace. The price of love is grief, and pain is only for the living.
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No way can you keep this schedule alone.
You need to hire sitters for ALL of them unless they can go to memory care. Hospice may be able to help with your husband depending on his health status.
I cared for my recently deceased dad, now my mom and a very elderly aunt. Mom and aunt are in their own homes but mom lives in a senior community. Both have dementia and mom has mobility issues. I order supplies, groceries and meds for them. Both have pill sorters that are put out weekly. Mom has a visiting geriatric physician that helps a lot. Ask their PCP's for a start.
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cetude Nov 2020
Hospice does not offer much help--just an aide comes in twice a week for about a half hour (and you have to wait all day sometimes), and they occasionally have volunteer sitters, but you are also letting a total stranger into your house. They generally have "respite care" but they may never recover from that. The only use I found with hospice was reordering her routine meds and free diapers/gloves and ointment supplies. I did all her mom's care 100% because I had to change mom about 5 times a day; sometimes even more, so a hospice aide was useless that I never used them.

Sitters do that--they just sit and they are about $20 an hour. Hands on care (CNA) is a lot more.
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I am so sorry that all these family members have chronic health issues that require A LOT of caregiving. You are right that you can not take care of all of them alone. You have a couple of choices - and you must make those choices soon - for their care and your continued health:

1 - Home help. Hire home health care aides for all of them and pay out of their assets. My MIL has dementia and has 2 caregivers round the clock since she chose to live out of state and BIL is handling her affairs. It is the least expensive option but not cheap.

2 - Placements. Your father may need to move to memory care since he creates problems for your husband and his care will only continue to get more and more difficult as the dementia progresses. Your MIL may need placement into assisted living if they will take her dog. You may need to hire somebody to care for the dog daily: walks and feeding. After placing these 2 family members, can you care for your husband's needs as well as building your home-based business. If not, decide with him if he needs placement into LTC and how to finance it.

Investigate resources: home health agencies, long term care facilities, assisted living/senior apartments in your area. You will get a better idea of which way to go after talking to these folks. Most of these resources have guides to list the types of care your family members require on a daily basis. After listing the care needed for each person, they can help guide you to which type of placement or care would best help you in your situation.
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Yes, I can relate to what you are experiencing with your loved ones. But let me say first that you must take care of you first or you will eventually have nothing left to give. I am taking care of my husband of 31 years full-time now. He has a heart condition and Type 2 diabetes which caused a septis infection in his left foot which got so infected that he had to have half of it removed. Now he has a prosthetic leg too. Now he too just wants to sit in his recyliner and his wheechair. These changes make our loved ones angry and sadly they take it out on us. You have to do what is best for you and your loved ones. If you need help to come in get it! I wish you luck and I hope this helped a little.
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Talk with your local Dept. of Aging which should be able to help you identify local resources. Talk with everyone's doctors to determine prognoses and needs for each. You might also talk with a lawyer who specializes in these kind of situations - as mentioned by another you probably should make sure that there are wills, POAs and Living wills for everyone. Determine what your financial resources are which will help when you start looking at options. It also sounds like you just need someone you can talk with - perhaps your minister or other religious contact. Any of the above people can probably help refer you to some type of counselor in your community - Check with your own Health insurance rep [if you have a plan] and/or your own doctor who can help point you in the right direction. It is most important that you take care of yourself before you care of anyone else. if you have children talk with them; also talk with family and even friends who might be able to help provide some assistance.

I also encourage you to start -at least with some of the suggested contacts as soon as possible.
I know this can be overwhelming and difficult to deal with, but taking that first step will make it easier to proceed. I would also suggest making a list of all the things you need to deal with -prioritize if you can, but at least make a start. It is only too easy for you to freeze up and then it becomes even more difficult to do anything,
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Wow, the LAST piece of advice I'd give you is to have all of these elders MOVE IN WITH YOU! Good grief. You're already feeling overwhelmed as it is!

You are not alone with these feelings, certainly not. Your mother in law can hire help to come into her home, that's a no brainer. Let her know that you have NO time to do more caregiving, so it's not an option. If she chooses not to move around, then the consequences of that decision will likely put her in a wheelchair at some point, and remove her power of decision as far as living at home alone goes.

If your father lives with you, it may be time to think about placing him in Assisted Living with a Memory Care annex for when the time comes. Let him know that if he does not move around on a schedule, the choice will be taken away from HIM as well, and he will require placement b/c you will be unable to handle an elder with dementia AND a wheelchair in your home. My mother also has 'selective hearing' and forces me to scream at her half the time, then gets her hackles up asking, 'why are you yelling at me?' all sweet an innocent like. Uh huh.

As far as your husband goes, lay down the law. Get him on a schedule of walking around the house every hour for 2 minutes. Set a timer; remind him to do it. CHF requires movement along with other behaviors if he'd like to live a longer life. If not, he can't choose to drag YOU down with him.........so shape up honey! My DH is home now for the past month after 2 very serious surgeries. He was sitting on the sofa all day feeling sorry for himself when I told him yesterday, GET UP, we're going to see my mother for a window visit at the ALF. Put on a coat and a mask so you don't have to breathe in cold air, and we're GOING. When we got home, he actually felt better. I told him he's lucky to be alive and to cut the crap! He's started walking the 2 minutes every hour like I suggested to you, and he even took the dog out this morning for the first time!!

Lay down the law to BOTH of them. Don't be a statistic. Caregivers often wind up dying BEFORE the elders they're caring for. Don't add your name to the list. Get out of the house daily, too......have your hair done, meet a friend for coffee, whatever. You are important too, not just these 3 elders!

GOOD LUCK!
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sounds like your plate is over flowing.  Is there anyone else that can help with your father? another sibling?  How old is the mother in law? is there someone else in her family that can help?  IF she would have to go into a NH, they won't take the dog so who would get the dog?  Does your father have the funds to have someone to come in daily to help him?  how about an Assisted living for him where he would be around other people but wouldn't be able to leave, etc?  It sounds like you need to call in resources for everyone other than your hubby.  Contact office of aging for information, You are NOT alone.......wishing you luck but get some help before YOU will need the help......then what will the others do??
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If your father has been diagnosed, you should be able to get him in assisted living or memory care. Get your power of attorney for him before he seriously declines, otherwise it will be guardianship. This will give you the ability to get him to a place that will be better able to take care of him. An elder care attorney can help you with that. The one I found will also help my brother get Medicare for assisted living and she already knows of a great place 😇 As far as your mom’s dog, you might be surprised. Some places allow a small pet. My sister-in-law delayed for years getting her aunt into assisted living because of her cat. It turns out she could have her cat there. Another writer had great suggestions for your husband with CHF. Having heart conditions can be depressing but it’s amazing what being outside can do. When I called the Alzheimer’s Association they emailed me a 90 page file with great information. One video I found was about communicating with someone with memory/dementia/Alzheimers. She said to not correct, argue, reason or test “do you remember...?” Chances are great that they’ll realize they should know how to respon but they can’t. Then they feel stupid and get angry. So far it’s working with my brother, who I suspect has early onset dementia. Waiting on Medicaid. Above don’t do all this yourself or feel bad because you can’t juggle all of this. No one can.
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Imho, your plate is overflowing. No one person is expected to perform miracles. Prayers sent.
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You don't handle it. Caregiving 24/7 for a single person is largely impossible for one caregive, much less 3.

Father to nursing home/AL

MiL, left to her own devices (didn't really say what her health is like, but not really your responsibility regardless).

Husband should be priority, but if he gets to the point where he needs 24/7 care, you will not be able to do that alone, so you'll either have to hire aids, or send him to a NH as well.
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